Patrick Aebischer

EPFL SV SV-DEC PH-SV
SV 3807 (Bâtiment SV)
Station 19
1015 Lausanne

Patrick Aebischer a achevé une formation en Médecine (1980) et en Neurosciences (1983) aux Universités de Genève et de Fribourg en Suisse. De 1984 à 1992, Patrick Aebischer a travaillé à Brown University (USA) au sein du Département des Neurosciences et au Département des Biomatériaux et des Organes Artificiels en tant que Professeur assistant, puis Professeur associé. En 1992, Patrick Aebischer a été nommé Professeur de la Division Autonome de Recherche Chirurgicale et du Centre de Thérapie Génique (DARC) au Centre Hospitalier Universitaire Vaudois (CHUV) à Lausanne. En 1999, Le Conseil Fédéral a nommé Patrick Aebischer en tant que Président de l'Ecole Polytechnique Fédérale de Lausanne (EPFL). Il a pris ses fonctions à la Présidence de l'EPFL en mars 2000, position qu'il a occupée jusqu'au 31 décembre 2016. Patrick Aebischer est membre de maintes sociétés professionnelles, tant en Europe qu'aux Etats-Unis. Patrick Aebischer a fondé trois start-up de biotechnologies. Il siège au conseil d'administration de Lonza, de Logitech et de Nestlé. Il préside également l'advisory board du Novartis Venture Fund. Patrick Aebischer est membre du conseil de fondation du Festival de Jazz de Montreux, du Festival de Verbier et de la Fondation Jacobs. Les recherches qu'il poursuit actuellement dans son laboratoire se concentrent sur le développement d'approches de thérapie cellulaire et de transfert génique pour le traitement des maladies neurodégénératives.

Urolithin A improves muscle strength, exercise performance, and biomarkers of mitochondrial health in a randomized trial in middle-aged adults

A. SinghD. D'AmicoP. A. AndreuxA. M. FouassierW. Blanco-Bose  et al.

Cell Reports Medicine. 2022. DOI : 10.1016/j.xcrm.2022.100633.

Effect of Urolithin A Supplementation on Muscle Endurance and Mitochondrial Health in Older Adults A Randomized Clinical Trial

S. LiuD. D'AmicoE. ShanklandS. BhayanaJ. M. Garcia  et al.

Jama Network Open. 2022. DOI : 10.1001/jamanetworkopen.2021.44279.

Astrocyte-targeting RNA interference against mutated superoxide dismutase 1 induces motoneuron plasticity and protects fast-fatigable motor units in a mouse model of amyotrophic lateral sclerosis

C. RochatN. Bernard-MarissalE. KaellstigS. PradervandF. E. Perrin  et al.

Glia. 2022. DOI : 10.1002/glia.24140.

Direct supplementation with Urolithin A overcomes limitations of dietary exposure and gut microbiome variability in healthy adults to achieve consistent levels across the population

A. SinghD. D'AmicoP. A. AndreuxG. DunngalvinT. Kern  et al.

European Journal Of Clinical Nutrition. 2021. DOI : 10.1038/s41430-021-00950-1.

Evolution of the neurochemical profiles in the G93A-SOD1 mouse model of amyotrophic lateral sclerosis

H. LeiE. A. DirrenC. Poitry-YamateB. SchneiderR. Gruetter  et al.

Journal of Cerebral Blood Flow & Metabolism. 2019. DOI : 10.1177/0271678X18756499.

The mitophagy activator urolithin A is safe and induces a molecular signature of improved mitochondrial and cellular health in humans

P. A. AndreuxW. Blanco-BoseD. RyuF. BurdetM. Ibberson  et al.

Nature Metabolism. 2019. DOI : 10.1038/s42255-019-0073-4.

A viral vector based in vivo model of tauopathy to explore therapeutic strategies against tau pathology

S. M. K. Nazeeruddin / B. SchneiderP. Aebischer (Dir.)

Lausanne, EPFL, 2019. DOI : 10.5075/epfl-thesis-9532.

Application of anti-amyloid beta immunization using encapsulated cell technology in mouse models of Alzheimer's disease

V. Laversenne / B. SchneiderP. Aebischer (Dir.)

Lausanne, EPFL, 2019. DOI : 10.5075/epfl-thesis-9751.

Cas9/gRNA selective targeting of the Beethoven tmc-1 mutant allele for treating progressive hearing loss by AAV-based delivery

P. SolanesY. AsaiB. PanC. A. Nist-LundP. Aebischer  et al.

2018. Conference on Changing the Face of Modern Medicine - Stem Cell and Gene Therapy, Lausanne, SWITZERLAND, Oct 16-19, 2018. p. A107 - A108.

Cas9/gRNAs Selective Targeting of the Beethoven Tmc-1 Mutant Allele for Treating Progressive Hearing Loss by AAV-Based Delivery

P. SolanesB. PanP. AebischerJ. R. HoltB. Schneider

2018. 21st Annual Meeting of the American-Society-of-Gene-and-Cell-Therapy (ASGCT), Chicago, IL, May 16-19, 2018. p. 138 - 139.

AAV based gene therapy for rare diseases : targeting astrocytes for functional recovery in Amyotrophic Lateral Sclerosis

C. C. Rochat / P. AebischerB. Schneider (Dir.)

Lausanne, EPFL, 2017. DOI : 10.5075/epfl-thesis-7888.

The effect of the functional interaction between PGC-1α and Parkin on mitochondrial quality control in Parkinson's disease

L. Zheng / P. AebischerB. Schneider (Dir.)

Lausanne, EPFL, 2016. DOI : 10.5075/epfl-thesis-6868.

Use of a Bicistronic Vector to Silence SOD1 in Motoneurons and Astrocytes for the Treatment of Familial Amyotrophic Lateral Sclerosis

J. Bobela-AebischerC. RochatN. Bernard-MarissalP. AebischerB. L. Schneider

2016. 19th Annual Meeting of the American-Society-of-Gene-and-Cell-Therapy (ASGCT), Washington, DC, MAY 04-07, 2016. p. S240 - S240.

Modulation of AMPK's activity via genetic tools and food-derived compounds as a novel approach to Parkinson's disease treatment

W. J. Bobela / P. AebischerB. Schneider (Dir.)

Lausanne, EPFL, 2016. DOI : 10.5075/epfl-thesis-6978.

In Vivo Evidence for a Lactate Gradient from Astrocytes to Neurons

P. MachlerM. T. WyssM. ElsayedJ. StobartR. Gutierrez  et al.

Cell Metabolism. 2016. DOI : 10.1016/j.cmet.2015.10.010.

Urolithin A induces mitophagy and prolongs lifespan in C. elegans and increases muscle function in rodents

D. RyuL. MouchiroudP. A. AndreuxE. KatsyubaN. Moullan  et al.

Nat Med. 2016. DOI : 10.1038/nm.4132.

A subcutaneous cellular implant for passive immunization against amyloid-beta reduces brain amyloid and tau pathologies

A. LathuiliereV. LaversenneA. AstolfoE. KopetzkiH. Jacobsen  et al.

Brain. 2016. DOI : 10.1093/brain/aww036.

Tmc gene therapy restores auditory function in deaf mice

C. AskewC. RochatB. PanY. AsaiH. Ahmed  et al.

Science Translational Medicine. 2015. DOI : 10.1126/scitranslmed.aab1996.

Alpha-Synuclein as a Mediator in the Interplay between Aging and Parkinson's Disease

W. BobelaP. AebischerB. L. Schneider

Biomolecules. 2015. DOI : 10.3390/biom5042675.

Perineuronal net digestion with chondroitinase restores memory in mice with tau pathology

S. YangM. CacquevelL. M. SaksidaT. J. BusseyB. L. Schneider  et al.

Experimental neurology. 2015. DOI : 10.1016/j.expneurol.2014.11.013.

Channel-Mediated Lactate Release by K+-Stimulated Astrocytes

T. Sotelo-HitschfeldM. I. NiemeyerP. MaechlerI. RuminotR. Lerchundi  et al.

The Journal of neuroscience. 2015. DOI : 10.1523/Jneurosci.5036-14.2015.

SOD1 silencing in motoneurons or glia rescues neuromuscular function in ALS mice

E. DirrenJ. AebischerC. RochatC. TowneB. L. Schneider  et al.

Annals Of Clinical And Translational Neurology. 2015. DOI : 10.1002/acn3.162.

Neuronal Matrix Metalloproteinase-9 Is a Determinant of Selective Neurodegeneration

A. KaplanK. J. SpillerC. TowneK. C. KanningG. T. Choe  et al.

Neuron. 2014. DOI : 10.1016/j.neuron.2013.12.009.

Genetic engineering of cell lines using lentiviral vectors to achieve antibody secretion following encapsulated implantation

A. LathuiliereB. BohrmannE. KopetzkiC. SchweitzerH. Jacobsen  et al.

Biomaterials. 2014. DOI : 10.1016/j.biomaterials.2013.10.026.

Intracerebroventricular Injection of Adeno-Associated Virus 6 and 9 Vectors for Cell Type-Specific Transgene Expression in the Spinal Cord

E. DirrenC. L. TowneV. SetolaD. E. J. RedmondB. L. Schneider  et al.

Human Gene Therapy. 2014. DOI : 10.1089/hum.2013.021.

A high-capacity cell macroencapsulation system supporting the long-term survival of genetically engineered allogeneic cells

A. LathuilièreS. CossonM. LütolfB. SchneiderP. Aebischer

Biomaterials. 2014. DOI : 10.1016/j.biomaterials.2013.09.071.

A Parkinson's disease gene regulatory network identifies the signaling protein RGS2 as a modulator of LRRK2 activity and neuronal toxicity

J. DusonchetH. LiM. GuillilyM. LiuK. Stafa  et al.

Human Molecular Genetics. 2014. DOI : 10.1093/hmg/ddu202.

AAV-mediated gene therapy against motoneuron diseases

E. A. Dirren / P. AebischerB. Schneider (Dir.)

Lausanne, EPFL, 2013. DOI : 10.5075/epfl-thesis-5821.

A novel encapsulation device for peripheral implantation of antibody-secreting cells : passive immunization against amyloid β

A. Lathuilière / P. AebischerB. Schneider (Dir.)

Lausanne, EPFL, 2013. DOI : 10.5075/epfl-thesis-5796.

Direct and Retrograde Transduction of Nigral Neurons with AAV6, 8, and 9 and Intraneuronal Persistence of Viral Particles

K. LoewP. AebischerB. L. Schneider

Human Gene Therapy. 2013. DOI : 10.1089/hum.2012.174.

Polo-like kinase 2 regulates selective autophagic α-synuclein clearance and suppresses its toxicity in vivo

A. OueslatiB. L. SchneiderP. AebischerH. A. Lashuel

Proceedings Of The National Academy Of Sciences Of The United States Of America (PNAS). 2013. DOI : 10.1073/pnas.1309991110.

Astrocyte–neuron co-culture on microchips based on the model of SOD mutation to mimic ALS

A. KunzeS. LengacherE. DirrenP. AebischerP. J. Magistretti  et al.

Integrative Biology. 2013. DOI : 10.1039/c3ib40022k.

Synergistic Effects of GDNF and VEGF on Lifespan and Disease Progression in a Familial ALS Rat Model

D. KrakoraP. MulcroneM. MeyerC. LewisK. Bernau  et al.

Molecular Therapy. 2013. DOI : 10.1038/mt.2013.108.

An in vivo ultrahigh field 14.1 T (1) H-MRS study on 6-OHDA and α-synuclein-based rat models of Parkinson's disease: GABA as an early disease marker

P. CouneM. CraveiroM. GauglerV. MlynárikB. Schneider  et al.

NMR in biomedicine. 2013. DOI : 10.1002/nbm.2817.

Focal expression of adeno-associated viral-mutant tau induces widespread impairment in an APP mouse model

E. DassieM. R. AndrewsJ.-C. BensadounM. CacquevelB. L. Schneider  et al.

Neurobiology Of Aging. 2013. DOI : 10.1016/j.neurobiolaging.2012.11.011.

Use of viral vectors to create animal models for Parkinson's disease

K. LoewP. Aebischer

Neurobiology Of Disease. 2012. DOI : 10.1016/j.nbd.2011.12.038.

Sustained expression of PGC-1α in the rat nigrostriatal system selectively impairs dopaminergic function

C. CironS. LengacherJ. DusonchetP. AebischerB. Schneider

Human Molecular Genetics. 2012. DOI : 10.1093/hmg/ddr618.

Proton and phosphorus magnetic resonance spectroscopy of a mouse model of Alzheimer's disease

V. MlynárikM. CacquevelL. Sun-ReimerS. JanssensC. Cudalbu  et al.

Journal of Alzheimer's disease : JAD. 2012. DOI : 10.3233/JAD-2012-112072.

Parkinson's Disease: Gene Therapies

P. G. CouneB. L. SchneiderP. Aebischer

Cold Spring Harbor Perspectives In Medicine. 2012. DOI : 10.1101/cshperspect.a009431.

α-Synuclein in central nervous system and from erythrocytes, mammalian cells, and Escherichia coli exists predominantly as disordered monomer

B. FauvetM. K. MbefoM.-B. FaresC. DesobryS. Michael  et al.

Journal of Biological Chemistry. 2012. DOI : 10.1074/jbc.M111.318949.

Imaging brain amyloid deposition using grating-based differential phase contrast tomography

B. R. PinzerM. CacquevelP. ModreggerS. A. McDonaldJ. C. Bensadoun  et al.

Neuroimage. 2012. DOI : 10.1016/j.neuroimage.2012.03.029.

Role of the FoxO3a Transcription Factor in alpha-synuclein Induced Neurodegeneration

E. Pino / P. AebischerB. Schneider (Dir.)

Lausanne, EPFL, 2012. DOI : 10.5075/epfl-thesis-5245.

Mimicking Phosphorylation at Serine 87 Inhibits the Aggregation of Human α-Synuclein and Protects against Its Toxicity in a Rat Model of Parkinson's Disease

A. OueslatiK. E. PaleologouB. L. SchneiderP. AebischerH. A. Lashuel

The Journal of neuroscience : the official journal of the Society for Neuroscience. 2012. DOI : 10.1523/JNEUROSCI.3784-11.2012.

How to build science capacity

B. FanaroffP. AebischerR. CamachoI. SerageldinN. Suetin  et al.

Nature. 2012. DOI : 10.1038/490331a.

Philanthropy: The price of charity

P. Aebischer

Nature. 2012. DOI : 10.1038/481260a.

Proton and phosphorus MRS of a 5xFAD mouse model of Alzheimer's disease

V. MlynarikL. Sun-ReimerS. JanssensM. CacquevelH. Lei  et al.

2011. ISMRM 19th Annual Meeting & Exhibition, Montreal, Canada, May 7-13, 2011.

Investigation of the role of PICALM on amyloid metabolism in a transgenic mouse model of Alzheimer’s disease

D. Rubi

2011

Early metabolic changes in the amyotrophic lateral sclerosis SOD1 mouse brain are revealed using 1H MRS rather than CASL and 18FDG PET

H. LeiE. DirrenC. Poitry-YamateB. SchneiderP. Aebischer  et al.

2011. 19th Scientific Meeting of the International Society for Magnetic Resonance in Medicine, 2011, Montréal, Québec, Canada.

A Rat Model of Progressive Nigral Neurodegeneration Induced by the Parkinson's Disease-Associated G2019S Mutation in LRRK2

J. DusonchetO. KochubeyK. StafaS. M. YoungR. Zufferey  et al.

Journal of Neuroscience. 2011. DOI : 10.1523/JNEUROSCI.5092-10.2011.

Chronic delivery of antibody fragments using immunoisolated cell implants as a passive vaccination tool

O. Marroquin BelaunzaranM. I. CorderoV. SetolaS. BianchiC. Galli  et al.

Plos One. 2011. DOI : 10.1371/journal.pone.0018268.

Alpha-Synuclein Effects at the ER-to-Golgi Level and Potential Biomarkers in Rat Models of the Early Phase of Parkinson's Disease

P. G. Coune / P. AebischerB. Schneider (Dir.)

Lausanne, EPFL, 2011. DOI : 10.5075/epfl-thesis-5176.

Rab1A Over-Expression Prevents Golgi Apparatus Fragmentation and Partially Corrects Motor Deficits in an Alpha-Synuclein Based Rat Model of Parkinson’s Disease

P. G. CouneJ.-C. BensadounP. AebischerB. Schneider

Journal of Parkinson's Disease. 2011. DOI : 10.3233/JPD-2011-11058.

Use of igf-1 and nt-3 in the treatment of x-linked adrenoleukodystrophy

R. MastroeniC. RaoulP. AebischerJ.-C. Bensadoun

WO2010089706 . 2010.

Efficient transduction of non-human primate motor neurons after intramuscular delivery of recombinant AAV serotype 6

C. TowneB. SchneiderD. KieranD. RedmondP. Aebischer

Gene Therapy. 2010. DOI : 10.1038/gt.2009.119.

Motor Deficits upon Alpha-Synuclein Expression in the Nigrostriatal System Are Due to a Loss of Dopaminergic Vesicles and Reduced Dopamine Release at an early Stage of Neurodegeneration

M. Gaugler / P. Aebischer (Dir.)

Lausanne, EPFL, 2010. DOI : 10.5075/epfl-thesis-4765.

Alpha-Synuclein Animal Models

M. GauglerP. G. CouneS. MohanaO. GencO. El-Agnaf  et al.

2010. 2nd World Parkinson Congress, Glasgow, UK, September 28 - October 1, 2010. p. S606 - S606.

Neuroprotection by Gene Therapy Targeting Mutant SOD1 in Individual Pools of Motor Neurons Does not Translate Into Therapeutic Benefit in fALS Mice

C. TowneV. SetolaB. L. SchneiderP. Aebischer

Molecular therapy : the journal of the American Society of Gene Therapy. 2010. DOI : 10.1038/mt.2010.260.

Neurodegenerative Disorders: Gene Therapy on Clinical Trial

P. Aebischer

Frontiers in Neuroscience. 2010.

Effective Delivery of the Neuroprotectant to the Brain

P. AebischerE. PinoM. CacquevelB. Schneider

2010. 2nd World Parkinson Congress, Glasgow, UK, September 28 - October 1, 2010. p. S602 - S602.

Phosphorylation at S87 is enhanced in synucleinopathies, inhibits alpha-synuclein oligomerization, and influences synuclein-membrane interactions

K. E. PaleologouA. OueslatiG. ShakkedC. C. RospigliosiH.-Y. Kim  et al.

The Journal of neuroscience : the official journal of the Society for Neuroscience. 2010. DOI : 10.1523/JNEUROSCI.5922-09.2010.

Adeno-Associated Virus-Mediated Gene Delivery for the Treatment of Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders

C. Towne / P. Aebischer (Dir.)

Lausanne, EPFL, 2010. DOI : 10.5075/epfl-thesis-4669.

Collapsin response médiator protein 4a(CRMP 4a) is upregulated in motoneurons of mutant SOD1 mice and can trigger motoneuron death

L. DuplanN. BernardW. CasseronK. DudleyE. Thouvenot  et al.

The Journal of neuroscience. 2010. DOI : 10.1523/JNEUROSCI.5411-09.2010.

AAV-mediated expression of wild-type and ALS-linked mutant VAPB selectively triggers death of motoneurons through a Ca2+-dependent ER-associated pathway

K. LangouA. MoumenC. PellegrinoJ. AebischerI. Medina  et al.

Journal of Neurochemistry (JNC). 2010. DOI : 10.1111/j.1471-4159.2010.06806.x.

Modeling Parkinson's Disease in Adult Rats Using Viral Vectors as Gene Delivery Tools

J. Dusonchet / P. Aebischer (Dir.)

Lausanne, EPFL, 2010. DOI : 10.5075/epfl-thesis-4758.

Grafts of Dopamine Neurons Can Send Neurites to the Striatum Under GDNF Inducement in a Nonhuman Primate

J. R. SladekJ. D. ElswonhR. H. RothC. LeranthT. J. Collier  et al.

2009. 16th Annual Meeting of the American-Society-for-Neural-Therapy-and-Repair, Clearwater Beach, FL, Apr 30-May 02, 2009. p. 234 - 235.

Dose optimization for long-term rAAV-mediated RNA interference in the nigrostriatal projection neurons

A. UlusoyG. ShainT. BjörklundP. AebischerD. Kirik

Molecular Therapy. 2009. DOI : 10.1038/mt.2009.142.

An in vivo culture system for human embryos using an encapsulation technology: a pilot study

C. BlockeelP. MockG. VerheyenN. BoucheP. Le Goff  et al.

Human Reproduction. 2009. DOI : 10.1093/humrep/dep005.

Targeted overexpression of the parkin substrate Pael-R in the nigrostriatal system of adult rats to model Parkinson's disease

J. DusonchetJ. BensadounB. SchneiderP. Aebischer

Neurobiology of disease. 2009. DOI : 10.1016/j.nbd.2009.03.013.

Implication of the JNK pathway in a rat model of Huntington's disease

V. PerrinN. DufourC. RaoulR. HassigE. Brouillet  et al.

Experimental Neurology. 2009. DOI : 10.1016/j.expneurol.2008.10.008.

Response of aged parkinsonian monkeys to in vivo gene transfer of GDNF

M. EmborgJ. MoiranoJ. RaschkeV. BondarenkoR. Zufferey  et al.

Neurobiology of Disease. 2009. DOI : 10.1016/j.nbd.2009.07.022.

Embryonic substantia nigra grafts in the mesencephalon send neurites to the host striatum in non-human primate after overexpression of GDNF

D. J. RedmondJ. ElsworthR. RothC. LeranthT. Collier  et al.

Journal of Comparative Neurology. 2009. DOI : 10.1002/cne.22028.

Alterations in lysosomal and proteasomal markers in Parkinson's disease: relationship to alpha-synuclein inclusions

Y. ChuH. DodiyaP. AebischerC. OlanowJ. Kordower

Neurobiology of Disease. 2009. DOI : 10.1016/j.nbd.2009.05.023.

Immunoisolated cell implants for intracerebral delivery of anti-Aß single chain Fv antibodies in the APP23 Alzheimer's mouse model

O. Marroquin Belaunzaran / P. Aebischer (Dir.)

Lausanne, EPFL, 2009. DOI : 10.5075/epfl-thesis-4464.

Regulation of Episomal Gene Expression by KRAB/KAP1-Mediated Histone Modifications

I. BardeE. LaurentiS. VerpA. C. GronerC. Towne  et al.

Journal of Virology. 2009. DOI : 10.1128/JVI.00001-09.

Lentiviral and Adeno-Associated Vector-Based Therapy for Motor Neuron Disease Through RNAi

C. TowneP. Aebischer

Therapeutic Applications of RNAi; 2009. p. 87 - 108.

Phosphorylation does not prompt, nor prevent, the formation of alpha-synuclein toxic species in a rat model of Parkinson's disease

S. Azeredo da SilveiraB. SchneiderC. Cifuentes-DiazD. SageT. Abbas-Terki  et al.

Human Molecular Genetics. 2009. DOI : 10.1093/hmg/ddn417.

Insulin-like growth factor-1 and neurotrophin-3 gene therapy prevents motor decline in an X-linked adrenoleukodystrophy mouse model

R. MastroeniJ.-C. BensadounD. CharvinP. AebischerA. Pujol  et al.

Annals of Neurology. 2009. DOI : 10.1002/ana.21677.

Recombinant adeno-associated virus serotype 6 (rAAV2/6)-mediated gene transfer to nociceptive neurons through different routes of delivery

C. TowneM. PertinA. BeggahP. AebischerI. Decosterd

Molecular Pain. 2009. DOI : 10.1186/1744-8069-5-52.

Hsp104 antagonizes alpha-synuclein aggregation and reduces dopaminergic degeneration in a rat model of Parkinson disease

C. Lo BiancoJ. ShorterE. RégulierH. LashuelT. Iwatsubo  et al.

The Journal of clinical investigation. 2008. DOI : 10.1172/JCI35781.

Systemic AAV6 delivery mediating RNA interference against SOD1: neuromuscular transduction does not alter disease progression in fALS mice

C. TowneC. RaoulB. L. SchneiderP. Aebischer

Molecular Therapy. 2008. DOI : 10.1038/mt.2008.73.

Delta-like 1 participates in the specification of ventral midbrain progenitor derived dopaminergic neurons

M. BauerJ. SzulcM. MeyerC. H. JensenT. A. Terki  et al.

Journal of Neurochemistry (JNC). 2008. DOI : 10.1111/j.1471-4159.2007.05037.x.

Feasibility of gene therapy for the treatment of neuropathic pain: downregulation of GTP cyclohydrolase 1 expression via RNA interference

S. JeanC. TowneP. AebischerI. Decosterd

2008. p. 3S - 3S.

Neuropathic pain: Gene therapy as a tool to transduce nociceptors

M. PertinC. TowneT. BertaA. BeggahP. Aebischer  et al.

2008. p. 12S - 12S.

Development Of A Cell Encapsulation Approach For Human Anti-Tumor Immunotherapy

F. SchwenterS. ZareiP. LuyP. MorelP. Aebischer  et al.

2008. XXXV Congress of the European Society for Artificial Organs: 'Towards Future Biomedical Technologies. p. 601 - 601.

Impact of phosphorylation of alpha-synuclein in Parkinson's disease

S. Azeredo da Silveira Lajaunias / P. Aebischer (Dir.)

Lausanne, EPFL, 2008. DOI : 10.5075/epfl-thesis-4069.

Intramuscular delivery of GDNF with human mesenchymal stem cells protects dying motor neurons and prolongs survival in a rat model of familial ALS

M. SuzukiJ. McHughC. TorkB. ShelleyA. Hayes  et al.

2008. 15th Annual Meeting of the American-Society-for-Neural-Therapy-and-Repair, Clearwater Beach, FL, May 01-03, 2008. p. 482 - 483.

Conditional gene expression and knockdown using lentivirus vectors encoding shRNA

J. SzulcP. Aebischer

Methods Mol Biol. 2008. DOI : 10.1007/978-1-60327-248-3_18.

Viral vectors: a potent approach to generate genetic models of Parkinson's disease

B. SchneiderM. GauglerP. Aebischer

Parkinson's disease: Molecular and therapeutics insights from model systems; New York: Academic Press, 2008. p. 269 - 284.

Viral vectors, animal models and new therapies for Parkinson's disease

B. SchneiderR. ZuffereyP. Aebischer

Parkinsonism Realted Disorders. 2008. DOI : 10.1016/j.parkreldis.2008.04.024.

GDNF-secreting human neural progenitor cells increase tyrosine hydroxylase and VMAT2 expression in MPTP-treated cynomolgus monkeys

M. E. EmborgA. D. EbertJ. MoiranoS. PengM. Suzuki  et al.

Cell Transplant. 2008. DOI : 10.3727/096368908784423300.

Direct Muscle Delivery of GDNF With Human Mesenchymal Stem Cells Improves Motor Neuron Survival and Function in a Rat Model of Familial ALS

M. SuzukiJ. McHughC. TorkB. ShelleyA. Hayes  et al.

Molecular Therapy. 2008. DOI : 10.1038/mt.2008.197.

Dysregulation of gene expression in primary neuron models of Huntington's disease shows that polyglutamine-related effects on the striatal transcriptome may not be dependent on brain circuitry

H. RunneE. RégulierA. KuhnD. ZalaO. Gokce  et al.

The Journal of neuroscience. 2008. DOI : 10.1523/JNEUROSCI.3044-08.2008.

Over-expression of alpha-synuclein in human neural progenitors leads to specific changes in fate and differentiation

B. L. SchneiderC. R. SeehusE. E. CapowskiP. AebischerS. C. Zhang  et al.

Human Molecular Genetics. 2007. DOI : 10.1093/hmg/ddm008.

From gene to gene therapy and pharmacotherapy, via transgenic animals

P. Aebischer

2007. 11th Congress of the European-Federation-of-Neurological-Societies, Brussels, BELGIUM, Aug 25-28, 2007. p. 2 - 2.

Expression of mutated huntingtin fragment in the putamen is sufficient to produce abnormal movement in non-human primates

S. PalfiE. BrouilletB. JarrayaJ. BlochC. Jan  et al.

Molecular Therapy. 2007. DOI : 10.1038/sj.mt.6300185.

Neuroprotection by Hsp104 and Hsp27 in lentiviral-based rat models of Huntington's disease

V. PerrinE. RégulierT. Abbas-TerkiR. HassigE. Brouillet  et al.

Molecular Therapy. 2007. DOI : 10.1038/mt.sj.6300141.

Lentiviral vector-mediated genetic modification of human neural progenitor cells for ex vivo gene therapy

E. E. CapowskiB. L. SchneiderA. D. EbertC. R. SeehusJ. Szulc  et al.

Journal of Neuroscience Methods. 2007. DOI : 10.1016/j.jneumeth.2007.02.022.

DJ-1 as a neuroprotective protein in models of Parkinson's disease

K. Piorkowska-Stanco / P. Aebischer (Dir.)

Lausanne, EPFL, 2007. DOI : 10.5075/epfl-thesis-3926.

Metabolic correction in oligodendrocytes derived from metachromatic leukodystrophy mouse model by using encapsulated recombinant myoblasts

A. ConsiglioS. MartinoD. DolcettaG. CusellaM. Conese  et al.

J Neurol Sci. 2007. DOI : 10.1016/j.jns.2007.01.010.

The KRAB repressor domain can trigger de novo promoter methylation during mouse early embryogenesis

M. WiznerowiczJ. JakobssonJ. SzulcS. LiaoA. Quazzola  et al.

Journal of Biological Chemistry. 2007. DOI : 10.1074/jbc.M705898200.

Playing Defense Against Lou Gehrig's Disease

P. AebischerA. C. Kato

Scientific American. 2007. DOI : 10.1038/scientificamerican1107-86.

GDNF secreting human neural progenitor cells protect dying motor neurons, but not their projection to muscle, in a rat model of familial ALS

M. SuzukiJ. McHughC. TorkB. ShelleyS. M. Klein  et al.

PLoS ONE. 2007. DOI : 10.1371/journal.pone.0000689.

Inducing tolerance to a soluble foreign antigen by encapsulated cell transplants

W. E. Blanco-BoseB. L. SchneiderP. Aebischer

Molecular Therapy. 2006. DOI : 10.1016/j.ymthe.2005.08.010.

Human neural progenitors deliver glial cell line-derived neurotrophic factor to parkinsonian rodents and aged primates

S. BehrstockA. EbertJ. McHughS. VosbergJ. Moore  et al.

Gene Therapy. 2006. DOI : 10.1038/sj.gt.3302679.

A versatile tool for conditional gene expression and knockdown

J. SzulcM. WiznerowiczM.-O. SauvainD. TronoP. Aebischer

Nature Methods. 2006. DOI : 10.1038/nmeth846.

Transient striatal delivery of GDNF via encapsulated cells leads to sustained behavioral improvement in a bilateral model of Parkinson disease

A. SajadiJ. BensadounB. SchneiderC. Lo BiancoP. Aebischer

Neurobiol Dis. 2006. DOI : 10.1016/j.nbd.2005.10.006.

Chronic activation in presymptomatic amyotrophic lateral sclerosis (ALS) mice of a feedback loop involving Fas, Daxx, and FasL

C. RaoulE. BuhlerC. SadeghiA. JacquierP. Aebischer  et al.

Proceedings Of The National Academy Of Sciences Of The United States Of America (PNAS). 2006. DOI : 10.1073/pnas.0508774103.

Lentivirus-mediated expression of glutathione peroxidase: neuroprotection in murine models of Parkinson's disease

J. L. RidetJ. BensadounN. DeglonP. AebischerA. D. Zurn

Neurobiol Dis. 2006. DOI : 10.1016/j.nbd.2005.06.003.

The potential of gene therapy for motor neuron diseases

C. RaoulP. Aebischer

Amyotrophic Lateral Sclerosis; New York, NY: Taylor&Francis, 2006. p. 505 - 524.

Viral vectors as a tool to model and treat Parkinson's disease

J. BensadounP. Aebischer

Wien Klin Wochenschr. 2006. DOI : 10.1007/s00508-006-0736-5.

Inhibition of calcineurin by FK506 protects against polyglutamine-huntingtin toxicity through an increase of huntingtin phosphorylation at S421

R. PardoE. ColinE. RegulierP. AebischerN. Deglon  et al.

The Journal of neuroscience. 2006. DOI : 10.1523/JNEUROSCI.3706-05.2006.

Viral-based modelling and correction of neurodegenerative diseases by RNA interference

C. RaoulS. D. BarkerP. Aebischer

Gene therapy. 2006. DOI : 10.1038/sj.gt.3302690.

CA150 expression delays striatal cell death in overexpression and knock-in conditions for mutant huntingtin neurotoxicity

M. ArangoS. HolbertD. ZalaE. BrouilletJ. Pearson  et al.

The Journal of neuroscience. 2006. DOI : 10.1523/JNEUROSCI.5409-05.2006.

Progressive and selective striatal degeneration in primary neuronal cultures using lentiviral vector coding for a mutant huntingtin fragment

D. ZalaA. BenchouaE. BrouilletV. PerrinM. C. Gaillard  et al.

Neurobiol Dis. 2005. DOI : 10.1016/j.nbd.2005.05.017.

Transgenic SOD1 mice as a model for developing amyotrophic lateral sclerosis therapies

S. Guillot / P. Aebischer (Dir.)

Lausanne, EPFL, 2005. DOI : 10.5075/epfl-thesis-3331.

Use of lentiviral vectors for modelling and treating Parkinson's disease

C. Lo Bianco / P. Aebischer (Dir.)

Lausanne, EPFL, 2005. DOI : 10.5075/epfl-thesis-3167.

GDNF delivery using human neural progenitor cells in a rat model of ALS

S. M. KleinS. BehrstockJ. McHughK. HoffmannK. Wallace  et al.

Human Gene Therapy. 2005. DOI : 10.1089/hum.2005.16.509.

Akt is altered in an animal model of Huntington's disease and in patients

E. ColinE. RegulierV. PerrinA. DurrA. Brice  et al.

European Journal of Neuroscience. 2005. DOI : 10.1111/j.1460-9568.2005.03985.x.

Lentiviral-mediated silencing of SOD1 through RNA interference retards disease onset and progression in a mouse model of ALS

C. RaoulT. Abbas-TerkiJ. BensadounS. GuillotG. Haase  et al.

Nature Medicine. 2005. DOI : 10.1038/nm1207.

Increased fiber outgrowth from xeno-transplanted human embryonic dopaminergic neurons with co-implants of polymer-encapsulated genetically modified cells releasing glial cell line-derived neurotrophic factor

Y. H. AhnJ. BensadounP. AebischerA. D. ZurnA. Seiger  et al.

Brain Res Bull. 2005. DOI : 10.1016/j.brainresbull.2005.04.009.

Long-term glial cell line-derived neurotrophic factor overexpression in the intact nigrostriatal system in rats leads to a decrease of dopamine and increase of tetrahydrobiopterin production

A. SajadiM. BauerB. ThonyP. Aebischer

Journal of Neurochemistry (JNC). 2005. DOI : 10.1111/j.1471-4159.2005.03139.x.

Dopaminergic fiber protection and regeneration by Wlds protein and GDNF in rodent models of Parkinson disease

A. Etemad-Sajadi / P. Aebischer (Dir.)

Lausanne, EPFL, 2005. DOI : 10.5075/epfl-thesis-3265.

Huntington's disease modeling and treatment : from primary neuronal cultures to rodents

D. Zala / P. AebischerN. Déglon (Dir.)

Lausanne, EPFL, 2005. DOI : 10.5075/epfl-thesis-3137.

ALS, IGF-1 and gene therapy: 'it's never too late to mend'

C. RaoulP. Aebischer

Gene Therapy. 2004. DOI : 10.1038/sj.gt.3302204.

Local GDNF expression mediated by lentiviral vector protects facial nerve motoneurons but not spinal motoneurons in SOD1(G93A) transgenic mice

S. GuillotM. AzzouzN. DeglonA. ZurnP. Aebischer

Neurobiol Dis. 2004. DOI : 10.1016/j.nbd.2004.01.017.

Lentiviral nigral delivery of GDNF does not prevent neurodegeneration in a genetic rat model of Parkinson's disease

C. Lo BiancoN. DeglonW. PralongP. Aebischer

Neurobiol Dis. 2004. DOI : 10.1016/j.nbd.2004.06.008.

Lentiviral-mediated gene transfer to model triplet repeat disorders

E. RegulierD. ZalaP. AebischerN. Deglon

Methods Mol Biol. 2004. DOI : 10.1385/1-59259-804-8:199.

Neuroprotective gene therapy for Huntington's disease, using polymer-encapsulated cells engineered to secrete human ciliary neurotrophic factor: results of a phase I study

J. BlochA. C. Bachoud-LeviN. DeglonJ. P. LefaucheurL. Winkel  et al.

Human Gene Therapy. 2004. DOI : 10.1089/hum.2004.15.968.

Long-term lentiviral-mediated expression of ciliary neurotrophic factor in the striatum of Huntington's disease transgenic mice

D. ZalaJ. BensadounL. Pereira de AlmeidaB. R. LeavittC. A. Gutekunst  et al.

Exp Neurol. 2004. DOI : 10.1016/j.expneurol.2003.09.002.

Salivary glands and gene therapy: the mouth waters

R. ZuffereyP. Aebischer

Gene Therapy. 2004. DOI : 10.1038/sj.gt.3302321.

In vivo calcium deposition on polyvinyl alcohol matrix used in hollow fiber cell macroencapsulation devices

F. SchwenterN. BoucheW. F. PralongP. Aebischer

Biomaterials. 2004. DOI : 10.1016/j.biomaterials.2003.10.030.

Lentiviral vector delivery of parkin prevents dopaminergic degeneration in an alpha-synuclein rat model of Parkinson's disease

C. Lo BiancoB. L. SchneiderM. BauerA. SajadiA. Brice  et al.

Proceedings Of The National Academy Of Sciences Of The United States Of America (PNAS). 2004. DOI : 10.1073/pnas.0405313101.

Survival of encapsulated human primary fibroblasts and erythropoietin expression under xenogeneic conditions

F. SchwenterB. L. SchneiderW. F. PralongN. DeglonP. Aebischer

Human Gene Therapy. 2004. DOI : 10.1089/1043034041361172.

Wlds-mediated protection of dopaminergic fibers in an animal model of Parkinson disease

A. SajadiB. L. SchneiderP. Aebischer

Current Biology. 2004. DOI : 10.1016/S0960-9822(04)00050-8.

Encapsulated GDNF-producing C2C12 cells for Parkinson's disease: a pre-clinical study in chronic MPTP-treated baboons

H. KishimaT. PoyotJ. BlochJ. DauguetF. Conde  et al.

Neurobiol Dis. 2004. DOI : 10.1016/j.nbd.2004.03.012.

Cellular implants: pioneers in xenotransplantation?

B. L. SchneiderP. Aebischer

Xenotransplantation. 2003. DOI : 10.1034/j.1399-3089.2003.02086.x.

Enhancement of peripheral nerve regeneration by interactive biomaterials

E. G. Fine / P. Aebischer (Dir.)

Lausanne, EPFL, 2003. DOI : 10.5075/epfl-thesis-2423.

Early and reversible neuropathology induced by tetracycline-regulated lentiviral overexpression of mutant huntingtin in rat striatum

E. RegulierY. TrottierV. PerrinP. AebischerN. Deglon

Human Molecular Genetics. 2003. DOI : 10.1093/hmg/ddg305.

Cell therapy using encapsulated cells producing endostatin

R. BjerkvigT. A. ReadP. VajkoczyP. AebischerW. Pralong  et al.

Local Therapies for Glioma; New York, NY: Springer, 2003. p. 137 - 141.

Presence of Gal-alpha1,3Gal epitope on xenogeneic lines: implications for cellular gene therapy based on the encapsulation technology

N. DeglonV. AubertF. SpertiniL. WinkelP. Aebischer

Xenotransplantation. 2003. DOI : 10.1034/j.1399-3089.2003.00110.x.

Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retina

C. KosticF. ChiodiniP. SalmonM. WiznerowiczN. Deglon  et al.

Gene Therapy. 2003. DOI : 10.1038/sj.gt.3301948.

Optimization of human erythropoietin secretion from MLV-infected human primary fibroblasts used for encapsulated cell therapy

F. SchwenterN. DeglonP. Aebischer

J Gene Med. 2003. DOI : 10.1002/jgm.338.

Prevention of the initial host immuno-inflammatory response determines the long-term survival of encapsulated myoblasts genetically engineered for erythropoietin delivery

B. L. SchneiderF. SchwenterW. F. PralongP. Aebischer

Molecular Therapy. 2003. DOI : 10.1016/S1525-0016(03)00055-8.

Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors

J. BensadounL. Pereira de AlmeidaE. G. FineJ. L. TsengN. Deglon  et al.

J Control Release. 2003. DOI : 10.1016/S0168-3659(02)00353-X.

Lentiviral-mediated RNA interference

T. Abbas-TerkiW. Blanco-BoseN. DeglonW. PralongP. Aebischer

Human Gene Therapy. 2002. DOI : 10.1089/104303402320987888.

GDNF and NGF released by synthetic guidance channels support sciatic nerve regeneration across a long gap

E. G. FineI. DecosterdM. PapaloizosA. D. ZurnP. Aebischer

European Journal of Neuroscience. 2002. DOI : 10.1046/j.1460-9568.2002.01892.x.

Lentiviral-mediated delivery of mutant huntingtin in the striatum of rats induces a selective neuropathology modulated by polyglutamine repeat size, huntingtin expression levels, and protein length

L. P. de AlmeidaC. A. RossD. ZalaP. AebischerN. Deglon

The Journal of neuroscience. 2002. DOI : 10.1523/JNEUROSCI.22-09-03473.2002.

Allogeneic beta-islet cells correct diabetes and resist immune rejection

M. PericinA. AlthageS. FreigangH. HengartnerE. Rolland  et al.

Proceedings Of The National Academy Of Sciences Of The United States Of America (PNAS). 2002. DOI : 10.1073/pnas.122241299.

Long-term doxycycline-regulated secretion of erythropoietin by encapsulated myoblasts

B. SommerC. RinschE. PayenB. DalleB. Schneider  et al.

Molecular Therapy. 2002. DOI : 10.1006/mthe.2002.0646.

Encapsulation as a strategy for cell xenotransplantation

B. SchneiderP. Aebischer

Future strategies for tissue and organ replacement; London: Imperial College Press, 2002. p. 291 - 322.

Delivery of erythropoietin by encapsulated myoblasts in a genetic model of severe anemia

C. RinschP. DuprazB. L. SchneiderN. DeglonP. H. Maxwell  et al.

Kidney Int. 2002. DOI : 10.1111/j.1523-1755.2002.kid574.x.

Lentiviruses as vectors for CNS diseases

N. DeglonP. Aebischer

Current topics in microbiology and immunology. 2002. DOI : 10.1007/978-3-642-56114-6_10.

alpha -Synucleinopathy and selective dopaminergic neuron loss in a rat lentiviral-based model of Parkinson's disease

C. Lo BiancoJ. L. RidetB. L. SchneiderN. DeglonP. Aebischer

Proceedings Of The National Academy Of Sciences Of The United States Of America (PNAS). 2002. DOI : 10.1073/pnas.152339799.

Simultaneous GDNF and BDNF application leads to increased motoneuron survival and improved functional outcome in an experimental model for obstetric brachial plexus lesions

O. C. AszmannK. J. KorakN. KropfE. FineP. Aebischer  et al.

Plast Reconstr Surg. 2002. DOI : 10.1097/01.PRS.0000020990.82332.43.

Dose-dependent neuroprotective effect of ciliary neurotrophic factor delivered via tetracycline-regulated lentiviral vectors in the quinolinic acid rat model of Huntington's disease

E. RegulierL. Pereira de AlmeidaB. SommerP. AebischerN. Deglon

Human Gene Therapy. 2002. DOI : 10.1089/10430340260355383.

Neurospheres modified to produce glial cell line-derived neurotrophic factor increase the survival of transplanted dopamine neurons

T. OstenfeldY. T. TaiP. MartinN. DeglonP. Aebischer  et al.

Journal of Neuroscience Res. 2002. DOI : 10.1002/jnr.10396.

Glial cell line-derived neurotrophic factor released by synthetic guidance channels promotes facial nerve regeneration in the rat

F. M. BarrasP. PascheN. BoucheP. AebischerA. D. Zurn

Journal of Neuroscience Res. 2002. DOI : 10.1002/jnr.10434.

Seizure suppression by adenosine-releasing cells is independent of seizure frequency

D. BoisonA. HuberV. PadrunN. DeglonP. Aebischer  et al.

Epilepsia. 2002. DOI : 10.1046/j.1528-1157.2002.33001.x.

Lentivirally delivered glial cell line-derived neurotrophic factor increases the number of striatal dopaminergic neurons in primate models of nigrostriatal degeneration

S. PalfiL. LeventhalY. ChuS. Y. MaM. Emborg  et al.

The Journal of neuroscience. 2002. DOI : 10.1523/JNEUROSCI.22-12-04942.2002.

Isolation of multipotent neural precursors residing in the cortex of the adult human brain

Y. ArsenijevicJ. G. VillemureJ. F. BrunetJ. J. BlochN. Deglon  et al.

Exp Neurol. 2001. DOI : 10.1006/exnr.2001.7691.

Inducing host acceptance to encapsulated xenogeneic myoblasts

C. RinschG. PedutoB. L. SchneiderP. Aebischer

Transplantation. 2001. DOI : 10.1097/00007890-200102150-00002.

Grafts of adenosine-releasing cells suppress seizures in kindling epilepsy

A. HuberV. PadrunN. DeglonP. AebischerH. Mohler  et al.

Proceedings Of The National Academy Of Sciences Of The United States Of America (PNAS). 2001. DOI : 10.1073/pnas.131102898.

A self-immunomodulating myoblast cell line for erythropoietin delivery

B. L. SchneiderG. PedutoP. Aebischer

Gene Therapy. 2001. DOI : 10.1038/sj.gt.3301356.

Neuroprotective effect of a CNTF-expressing lentiviral vector in the quinolinic acid rat model of Huntington's disease

L. P. de AlmeidaD. ZalaP. AebischerN. Deglon

Neurobiol Dis. 2001. DOI : 10.1006/nbdi.2001.0388.

Insulin-like growth factor-I is necessary for neural stem cell proliferation and demonstrates distinct actions of epidermal growth factor and fibroblast growth factor-2

Y. ArsenijevicS. WeissB. SchneiderP. Aebischer

The Journal of neuroscience. 2001. DOI : 10.1523/JNEUROSCI.21-18-07194.2001.

Neuroprotective effect of interleukin-6 and IL6/IL6R chimera in the quinolinic acid rat model of Huntington's syndrome

J. BensadounL. P. de AlmeidaM. DreanoP. AebischerN. Deglon

European Journal of Neuroscience. 2001. DOI : 10.1046/j.0953-816x.2001.01802.x.

Encapsulated cell implants as a novel treatment for Parkinson’s disease

J. TsengP. Aebischer

Parkinson's disease: Methods and Protocols; Totowa, NJ: Humana Press, 2001. p. 279 - 288.

Nerve growth factor- and neurotrophin-3-releasing guidance channels promote regeneration of the transected rat dorsal root

J. BlochE. G. FineN. BoucheA. D. ZurnP. Aebischer

Exp Neurol. 2001. DOI : 10.1006/exnr.2001.7778.

Delivery of FGF-2 but not VEGF by encapsulated genetically engineered myoblasts improves survival and vascularization in a model of acute skin flap ischemia

C. RinschP. QuinodozB. PittetN. AlizadehD. Baetens  et al.

Gene Therapy. 2001. DOI : 10.1038/sj.gt.3301436.

Viral vector-mediated gene therapy for Parkinson's disease

M. EmborgN. DeglonL. LeventhalP. AebischerJ. Kordower

Clin Neurosci Res. 2001. DOI : 10.1016/S1566-2772(01)00027-5.

Sustained delivery of GDNF: towards a treatment for Parkinson's disease

A. D. ZurnH. R. WidmerP. Aebischer

Brain Res Brain Res Rev. 2001. DOI : 10.1016/S0165-0173(01)00098-4.

Recombinant proteins for neurodegenerative diseases: the delivery issue

P. AebischerJ. Ridet

Trends in Neurosciences. 2001. DOI : 10.1016/S0166-2236(00)01899-3.

Restoration of cognitive and motor functions by ciliary neurotrophic factor in a primate model of Huntington's disease

V. MittouxJ. M. JosephF. CondeS. PalfiC. Dautry  et al.

Human Gene Therapy. 2000. DOI : 10.1089/10430340050015220.

Self-inactivating lentiviral vectors with enhanced transgene expression as potential gene transfer system in Parkinson's disease

N. DéglonJ. L. TsengJ. BensadounA. D. ZurnY. Arsenijevic  et al.

Human Gene Therapy. 2000. DOI : 10.1089/10430340050016256.

Lentiviral vectors as a gene delivery system in the mouse midbrain: cellular and behavioral improvements in a 6-OHDA model of Parkinson's disease using GDNF

J. BensadounN. DeglonJ. L. TsengJ. L. RidetA. D. Zurn  et al.

Exp Neurol. 2000. DOI : 10.1006/exnr.2000.7409.

Encapsulated neural transplants

J. L. TsengP. Aebischer

Progress in Brain Research. 2000. DOI : 10.1016/S0079-6123(00)27010-6.

Complete and long-term rescue of lesioned adult motoneurons by lentiviral-mediated expression of glial cell line-derived neurotrophic factor in the facial nucleus

A. F. HottingerM. AzzouzN. DeglonP. AebischerA. D. Zurn

The Journal of neuroscience. 2000. DOI : 10.1523/JNEUROSCI.20-15-05587.2000.

Efficient gene transfer and expression of biologically active glial cell line-derived neurotrophic factor in rat motoneurons transduced wit lentiviral vectors

C. CisterniC. E. HendersonP. AebischerB. PettmannN. Deglon

Journal of Neurochemistry (JNC). 2000. DOI : 10.1046/j.1471-4159.2000.0741820.x.

Increased motoneuron survival and improved neuromuscular function in transgenic ALS mice after intraspinal injection of an adeno-associated virus encoding Bcl-2

M. AzzouzA. HottingerJ. C. PaternaA. D. ZurnP. Aebischer  et al.

Human Molecular Genetics. 2000. DOI : 10.1093/hmg/9.5.803.

Neuroprotective gene therapy for Huntington's disease using a polymer encapsulated BHK cell line engineered to secrete human CNTF

A. C. Bachoud-LeviN. DeglonJ. P. NguyenJ. BlochC. Bourdet  et al.

Human Gene Therapy. 2000. DOI : 10.1089/10430340050111377.

Long-term host unresponsiveness to encapsulated xenogeneic myoblasts after transient immunosuppression

G. PedutoC. RinschB. L. SchneiderE. RollandP. Aebischer

Transplantation. 2000.

Gene transfer techniques for the delivery of GDNF in Parkinson's disease

J. L. RidetN. DeglonP. Aebischer

Novartis Foundation symposium. 2000.

Enzymatic incorporation of bioactive peptides into fibrin matrices enhances neurite extension

J. C. SchenseJ. BlochP. AebischerJ. A. Hubbell

Nature biotechnology. 2000. DOI : 10.1038/74473.

Evaluation of an intrathecal immune response in amyotrophic lateral sclerosis patients implanted with encapsulated genetically engineered xenogeneic cells

A. D. ZurnH. HenryM. SchluepV. AubertL. Winkel  et al.

Cell Transplant. 2000. DOI : 10.1177/096368970000900404.

Neurodegeneration prevented by lentiviral vector delivery of GDNF in primate models of Parkinson's disease

J. H. KordowerM. E. EmborgJ. BlochS. Y. MaY. Chu  et al.

Science. 2000. DOI : 10.1126/science.290.5492.767.

Treatment of diseases of the central nervous system using encapsulated cells

A. F. HottingerP. Aebischer

Advances and Technical Standards in Neurosurgery; 1999. p. 3 - 20.

Highlights of the cell transplantation meeting at Montreux, March 1999

C. RinschB. L. SchneiderP. Aebischer

Cell Transplant. 1999. DOI : 10.1177/096368979900800601.

Sniff nasal pressure: a sensitive respiratory test to assess progression of amyotrophic lateral sclerosis

J. W. FittingR. PaillexL. HirtP. AebischerM. Schluep

Annals of Neurology. 1999. DOI : 10.1002/1531-8249(199912)46:6<887::AID-ANA11>3.0.CO;2-L.

A surface engineering approach towards the development of cell-based biochip sensors

S. Makohliso / P. Aebischer (Dir.)

Lausanne, EPFL, 1998. DOI : 10.5075/epfl-thesis-1848.

Continuous delivery of human and mouse erythropoietin in mice by genetically engineered polymer encapsulated myoblasts

E. RegulierB. L. SchneiderN. DeglonY. BeuzardP. Aebischer

Gene Therapy. 1998. DOI : 10.1038/sj.gt.3300687.

Attenuation of 6-OHDA-induced neurotoxicity in glutathione peroxidase transgenic mice

J. BensadounO. MirochnitchenkoM. InouyeP. AebischerA. D. Zurn

European Journal of Neuroscience. 1998. DOI : 10.1046/j.1460-9568.1998.00345.x.

Neurturin protects dopaminergic neurons following medial forebrain bundle axotomy

J. L. TsengS. L. BruhnA. D. ZurnP. Aebischer

Neuroreport. 1998. DOI : 10.1097/00001756-199806010-00027.

Three-dimensional extracellular matrix engineering in the nervous system

M. BorkenhagenJ. F. ClemenceH. SigristP. Aebischer

J Biomed Mater Res. 1998. DOI : 10.1002/(SICI)1097-4636(19980603)40:3<392::AID-JBM8>3.0.CO;2-C.

Application of Teflon-AF thin films for bio-patterning of neural cell adhesion

S. A. MakohlisoL. GiovangrandiD. LeonardH. J. MathieuM. Ilegems  et al.

Biosens Bioelectron. 1998. DOI : 10.1016/S0956-5663(98)00036-0.

A gene therapy approach for the treatment of amyotrophic lateral sclerosis and Parkinson's disease

A. D. ZurnJ. L. TsengN. DeglonJ. M. JosephP. Aebischer

Advances in Pharmacology. 1998. DOI : 10.1016/S1054-3589(08)60899-6.

Intrathecal implants of bovine chromaffin cells alleviate mechanical allodynia in a rat model of neuropathic pain

I. DecosterdE. BuchserN. GilliardJ. SaydoffA. D. Zurn  et al.

Pain. 1998. DOI : 10.1016/S0304-3959(98)00044-X.

In vivo performance of a new biodegradable polyester urethane system used as a nerve guidance channel

M. BorkenhagenR. C. StollP. NeuenschwanderU. W. SuterP. Aebischer

Biomaterials. 1998. DOI : 10.1016/S0142-9612(98)00122-7.

A gene therapy approach to regulated delivery of erythropoietin as a function of oxygen tension

C. RinschE. RegulierN. DeglonB. DalleY. Beuzard  et al.

Human Gene Therapy. 1997. DOI : 10.1089/hum.1997.8.16-1881.

Tissue engineering approaches for peripheral nerve regeneration

M. Borkenhagen / P. Aebischer (Dir.)

Lausanne, EPFL, 1997. DOI : 10.5075/epfl-thesis-1688.

The copper chelator d-penicillamine delays onset of disease and extends survival in a transgenic mouse model of familial amyotrophic lateral sclerosis

A. F. HottingerE. G. FineM. E. GurneyA. D. ZurnP. Aebischer

European Journal of Neuroscience. 1997. DOI : 10.1111/j.1460-9568.1997.tb01511.x.

GDNF reduces drug-induced rotational behavior after medial forebrain bundle transection by a mechanism not involving striatal dopamine

J. L. TsengE. E. BaetgeA. D. ZurnP. Aebischer

The Journal of neuroscience. 1997. DOI : 10.1523/JNEUROSCI.17-01-00325.1997.

Neuronal GDNF expression in the adult rat nervous system identified by in situ hybridization

N. A. PochonA. MenoudJ. L. TsengA. D. ZurnP. Aebischer

European Journal of Neuroscience. 1997. DOI : 10.1111/j.1460-9568.1997.tb01623.x.

Treatment of Parkinson's disease. Symptomatic cell therapies: cells as biological minipumps

A. D. ZurnJ. TsengP. Aebischer

European Neurology. 1996.

Gene therapy for amyotrophic lateral sclerosis (ALS) using a polymer encapsulated xenogenic cell line engineered to secrete hCNTF

P. AebischerN. A. PochonB. HeydN. DeglonJ. M. Joseph  et al.

Human Gene Therapy. 1996. DOI : 10.1089/hum.1996.7.7-851.

Immunoisolated xenogenic chromaffin cell therapy for chronic pain. Initial clinical experience

E. BuchserM. GoddardB. HeydJ. M. JosephJ. Favre  et al.

Anesthesiology. 1996. DOI : 10.1097/00000542-199611000-00007.

Combined effects of GDNF, BDNF, and CNTF on motoneuron differentiation in vitro

A. D. ZurnL. WinkelA. MenoudK. DjabaliP. Aebischer

Journal of Neuroscience Res. 1996. DOI : 10.1002/(SICI)1097-4547(19960415)44:2<133::AID-JNR5>3.0.CO;2-E.

Central nervous system delivery of recombinant ciliary neurotrophic factor by polymer encapsulated differentiated C2C12 myoblasts

N. DeglonB. HeydS. A. TanJ. M. JosephA. D. Zurn  et al.

Human Gene Therapy. 1996. DOI : 10.1089/hum.1996.7.17-2135.

The problems of delivering neuroactive molecules to the CNS

S. A. TanP. Aebischer

Ciba Found Symp. 1996. DOI : 10.1002/9780470514863.ch14.

Intrathecal delivery of CNTF using encapsulated genetically modified xenogeneic cells in amyotrophic lateral sclerosis patients

P. AebischerM. SchluepN. DeglonJ. M. JosephL. Hirt  et al.

Nature Medicine. 1996. DOI : 10.1038/nm0696-696.

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