Alexis Bemelmans, PhD
photo Alexis

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Last modification, january 14th, 2008
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Civil Status




39 years old, Married, 2 children, french citizenship
Address :  127 avenue Jean-Baptits Clément
F-92100 Boulogne-Billancourt
France
Phone: +33 (0)9 54 75 70 90
Skype : alexisbemelmans
E-mail







Education

1999 :

PhD in Molecular and Cellular Pharmacology, University Paris VI.
Obtained with the highest distinction.
Certificate (pdf file, 376 Ko)
Thesis dissertation (in french) (pdf file, 1.9 Mo)



1994 :

Postgraduate certificate in Molecular and Cellular Pharmacology (Diplôme d'Études Approfondies, University Paris VI, "good" distinction).



1992 :

Master's degree in Cellular Biology and Physiology (University Paris VI).



1991 :

Bachelor in Science's degree in  Cellular Biology and Physiology (University Paris VI, "good" distinction).



2000 :

Competence certificate for animal experimentation (University of Marseille).



2002 :

Supplementary competence certificate in animal surgery (University of Marseille).



2004 :

Swiss certificate for animal experimentation (CHUV, Lausanne).







Work
Experience

Since 2007:

Project Manager, Fovea Pharmaceuticals S.A., Paris, France.
www.fovea-pharma.com



2004-07:

Researcher in the Unit of Gene Therapy and Stem Cells Biology, Jules-Gonin Eye Hospital, Lausanne Switzerland. In charge of the gene therapy projects for Leber congenital amaurosis and ocular neovascularizations. Supervision of the work of 2 technicians and 1 PhD student.


(Detailled history, in french)

1999-2003:

Project leader "Business Development", for BioVectys SA, a biotech company dedicated to the treatment of neurological diseases by gene therapy.
* Writing up of the business plan and of grant applications (which were granted by ANVAR (French agency for research valorisation) in 2000, by French research ministry in 2000 and 2001, by Association Retina France in 2002 and 2003.
* Setting up of a network with academic partners for a project of gene therapy for retinal diseases.



1994-99:

PhD in a French academic lab, molecular genetic of neurotransmission (CNRS) headed by Dr J Mallet (la Pitié-Salpêtrière Hospital, Paris). Subject: neuroprotective gene transfer in in vitro and in vivo models of Huntington’s disease.







Linguistic
Skills




French : mother tongue. Very good writing (research project, activity report, etc..) as well as oral skills.
English: fluent. Good writing (scientific articles, patents, research project) and oral skills.







Technical
Skills



Molecular Biology (plasmid contruction, production of viral vector, quantitative pcr, etc...).
Cell Biology (cell line and primary culture of neural cells, flow cytometry).
In Vivo Experimentation (stereotaxic surgery, eye injections, behavioural tests, electroretinogram recordings, pupil light reflex recordings, functional testing of rodents models of neurological and retinal diseases.
Histology (cryostat and paraffin sectioning, immunostaining, in situ hybridization, morphometric analysis, confocal microscopy).
Computing (Windows and Mac OS, Microsoft Office, Adobe Photoshop, internet ressources for molecular biology, statistical analysis, etc...).







Publications
List

(PubMed)



  1. Bemelmans A.-P., Kostic C., Cachafeiro M., Crippa S.V., Wanner D., Tekaya M., Wenzel A., Arsenijevic Y. (2008) Lentiviral gene transfer-mediated cone vision restoration in RPE65 knockout mice. Advances in Experimental Medecine and Biology, 613:89-95

  2. Escartin C., Boyer F., Bemelmans A.-P., Hantraye P., Broullet E. (2007) IGF-1 exacerbates the neurotoxicity of the mitochondrial inhibitor 3NP in rats. Neuroscience Letters, 425:167-172

  3. Bemelmans A.-P., Kostic C., Hornfeld D., Jaquet M., Crippa S.V., Hauswirth W.W., Lem J., Wang Z., Schorderet D.E., Munier F.L., Wenzel A., Arsenijevic Y. (2006) Lentiviral vectors containing a retinal pigment epithelium specific promoter for leber congenital amaurosis gene therapy. Advances in Experimental Medicine and Biology, 572: 247-253

  4. Molles B.E., Maskos U., Pons S., Besson M., Guiard P., Guilloux J.-P., Evrad A., Cormier A., Mameli-Engvall M., Cloez-Tayarani I., Nakatani H., Dufour N., Bemelmans A.-P., Mallet J., Cazala P., Gardier A.-M., David V., Faure P., Granon S., Changeux J.-P. (2006) Targeted in vivo expression of nicotinic acetylcholine receptors in mouse brain using lentiviral expression vectors. Journal of molecular neuroscience , 30: 105-106. Editor site

  5. Bemelmans A.-P., Kostic C., Crippa S.V., Hauswirth W.W., Lem J., Munier F.L., Seeliger M.W., Wenzel A., Arsenijevic Y. (2006) Lentiviral-mediated transfer of the RPE65 cDNA rescues both survival and function of cone photoreceptors in a mouse model of leber congenital amaurosis. PLoS Medicine, 3: 1892-1903. Editor site(open access)

  6. Bemelmans A.-P., Husson I., Mallet J., Kosofsky B.E. and Gressens P. (2006) Viral-mediated gene transfer of BDNF is neuroprotective in a mouse model of neonatal excitotoxic challenge. Journal of Neuroscience Research, 83: 50-60. Editor site

  7. Brizard M., Carcenac C., Bemelmans A.-P., Feuerstein C., Mallet J., Savasta M. (2006) Functional reinnervation from remaining DA terminals induced by GDNF lentivirus in a rat model of early Parkinson's disease. Neurobiology of Disease, 21: 90-101. Editor site

  8. Maskos U., Molles B.E., Pons S., Besson M., Guiard B.P., Guilloux J.P., Evrard A., Cazala P., Cormier A., Mameli-Engvall M., Dufour N., Cloez-Tayarani I., Bemelmans A.-P., Mallet J., Gardier A.M., David V., Faure P., Granon S., Changeux J.P. (2005) Nicotine reinforcement and cognition restored by targeted expression of nicotinic receptors. Nature, 436: 103-7. Editor site

  9. Bemelmans A.-P., Bonnel S., Houhou L., Dufour N., Nandrot E., Helmlinger D., Sarkis C., Abitbol M. and Mallet J. (2005) Retinal cell type expression specificity of HIV-1-derived gene transfer vectors upon subretinal injection in the adult rat: influence of pseudotyping and promoter. Journal of Gene Medicine, 7: 1367-1374. Editor site

  10. Girard C, Bemelmans A.-P., Dufour N, Mallet J, Bachelin C, Nait-Oumesmar B, Baron-Van Evercooren A, Lachapelle F. (2005) Grafts of brain-derived neurotrophic factor and neurotrophin 3-transduced primate Schwann cells lead to functional recovery of the demyelinated mouse spinal cord. Journal of Neuroscience, 25: 7924-33. Editor site (free of charge)

  11. Escartin C., Boyer F., Bemelmans A.-P., Hantraye P. and Brouillet E. (2004) Insulin Growth Factor-1 protects against excitotoxicity in the rat striatum, NeuroReport, 15: 2251-4

  12. Husson I., Rangon C.M., Lelièvre V., Bemelmans A.-P., Sachs P., Mallet J., Kosofsky B. E. and Gressens P. (2005) BDNF-induced white matter neuroprotection and stage-dependant neuronal survival following a neonatal excitotoxic challenge, Cerebral Cortex, 15: 250-61

  13. Bemelmans A.-P., Horellou P., Pradier L., Brunet I., Colin P., Mallet J. (1999) Brain-derived neurotrophic factor-mediated protection of striatal neurons in an excitotoxic rat model of Huntington's disease, as demonstrated by adenoviral gene transfer. Hum Gene Ther, 10: 2987-97

  14. Barkats M., Bemelmans A.-P., Geoffroy M.-C., Robert J.-J., Loquet I., Horellou P., Revah F., Mallet J. (1996) An adenovirus encoding CuZnSOD protects cultured striatal neurones against glutamate toxicity. Neuroreport, 7:497-501








Recent
Oral
Presentations



  1. Bemelmans A.-P., Kostic C., Hornfeld D., TekayaM., Crippa S.V., Hauswirth W.W., Lem J., Seeliger M., Wenzel A., Arsenijevic Y. Rescue of Cone Photoreceptors after Lentiviral Gene Transfer of Rpe65 cDNA in Knockout Mouse Models of Leber Congenital Amaurosis. 9th Annual Meeting of ASGT, Baltimore, Maryland. May 31th-June 4th, 2006.
  2. Bemelmans A.-P., Wenzel A., Afanasieva T., Kostic C., Jaquet M., Munier F.L., Arsenijevic Y. Neuroprotective properties of an Anti-VEGF single-chain antibody administered by gene transfer in the mouse retina. 13th Annual Congress of ESGT, Prague, Czech Republic. Oct 29th-Nov 1st, 2005.

  3. Bemelmans A.-P., Kostic C., Hornfeld D., Hauswirth W.W., Lem J., Schorderet D.F., Munier F.L., Seeliger M., Wenzel A., Arsenijevic Y. Transfert de gène par vecteur lentiviral de l'ADNc RPE65 dans deux lignées de souris knockout modélisant l'amaurose congénitale de Leber. 4ème congrès annuel de la société francophone de thérapie cellulaire et génique, Lyon, France. 28-29 juin 2005.

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