Scientific publications 2001

1. Achard, F., Vaysseix, G. and Barillot, E.: “XML, bioinformatics and data integration”. Bioinformatics 17 (2001) 115-125.

2. Aoki, M., Liu, J., Richard, I., Bashir, R., Britton, S., Keers, S.M., Oeltjen, J., Brown, H.E., Marchand, S., Bourg, N., Beley, C., McKenna-Yasek, D., Arahata, K., Bohlega, S., Cupler, E., Illa, I., Majneh, I., Barohn, R.J., Urtizberea, J.A., Fardeau, M., Amato, A., Angelini, C., Bushby, K., Beckmann, J.S. and Brown, R.H., Jr.: “Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy”. Neurology 57 (2001) 271-8.

3. Baghdiguian, S., Richard, I., Martin, M., Coopman, P., Beckmann, J.S., Mangeat, P. and Lefranc, G.: “Pathophysiology of limb girdle muscular dystrophy type 2A: hypothesis and new insights into the IkappaBalpha/NF-kappaB survival pathway in skeletal muscle”. J Mol Med 79 (2001) 254-61.

4. Balsa, A., Barrera, P., Westhovens, R., Alves, H., Maenaut, K., Pascual-Salcedo, D., Cornelis, F., Bardin, T., Riente, L., Radstake, T.R.D.J., De Almeida, G., Lepage, V., Stravopoulos, C., Spaepen, M., Lopes-Vaz, A., Charron, D., Martinez, M., Prud’homme, J.F., Migliorini, P. and Fritz, P.: “Clinical and immunogenetic characteristics of European multicase rheumatoid arthritis families”. Ann Rheum Dis 60 (2001) 573-576.

5. Barrera, P., Balsa, A., Alves, H., Westhovens, R., Maenaut, K., Cornelis, F., Fritz, P., Bardin, T., Ceu Maia, M., Lopes-Vaz, A., Pascual Salcedo, D., de la Concha, E., Radstake, T., van de Putte, L.B., Migliorini, P., Prud’homme, J.F., Charron, D., Spyropoulou, M., Mendes, A., Spaepen, M., Martinez, M. and Stavropoulos, C.: “Noninherited maternal antigens do not increase the susceptibility for familial rheumatoid arthritis. European Consortium on Rheumatoid Arthritis Families (ECRAF)”. J Rheumatol 28 (2001) 968-974.

6. Barrera, P., Faure, S., Prud’homme, J.F., Balsa, A., Migliorini, P., Chimenti, D., Radstake, T.R., van de Putte, L.B., Pascual-Salcedo, D., Westhovens, R., Maenaut, K., Alves, H., Lopes-Vaz, A., Stravopoulos, C., Spyropoulou, M., Fritz, P., Bardin, T., Charron, D., Lepage, V., Alibert, Martinez, M. and Cornelis, F.: “European genetic study on rheumatoid arthritis: is there a linkage of the interleukin-1 (IL-1), IL-10 or IL-4 genes to RA?”. Clin Exp Rheumatol 19 (2001) 709-714.

7. Baulac, S., Huberfeld, G., Gourfinkel-An, I., Mitropoulou, G., Beranger, A., Prud’homme, J.F., Baulac, M., Brice, A., Bruzzone, R. and LeGuern, E.: “First genetic evidence of GABAa receptor dysfunction in epilepsy: A mutation in the gamma2-subunit gene”. Nat Genet 28 (2001) 46-48.

8. Baulac, S., Picard, F., Herman, A., Feingold, J., Genin, E., Hirsch, E., Prud’homme, J.F., Baulac, M., Brice, A. and LeGuern, E.: “Evidence for a digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31”. Ann Neurol 49 (2001) 786-792.

9. Ben-Arieh, S.V., Zimerman, B., Smorodinsky, N.I., Yaacubovicz, M., Schechter, C., Bacik, I., Gibbs, J., Bennink, J.R., Yewdell, J.W., Coligan, J.E., Firat, H., Lemonnier, F. and Ehrlich, R.: “Human cytomegalovirus protein US2 interferes with the expression of human HFE, a nonclassical class I major histocompatibility complex molecule that regulates iron homeostasis”. J Virol 75 (2001) 10557-62.

10. Brockington, M., Yuva, Y., Prandini, P., Brown, S.C., Torelli, S., Benson, M.A., Herrmann, R., L.V., A., Bashir, R., Burgunder, J.M., Fallet, S., Romero, N., Fardeau, M., Straub, V., Storey, G., Pollitt, C., Richard, I., Sewry, C.A., Bushby, K., Voit, T., Blake, D.J. and Muntoni, F.:“Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C”. Hum Mol Genet 10 (2001) 2851-2859.

11. Chillon, M. and Kremer, E.J.: “Trafficking and propagation of canine adenovirus vectors lacking a known integrin-interacting motif”. Hum Gene Ther 12 (2001) 1815-1823.

12. Chillon, M. and Kremer, E.J.: “Trafficking and propagation of canine adenovirus vectors lacking a known integrin-interacting motif”. Human Gene Therapy 12 (2001) 1815-1823.

13. Coutelle, C., Themis, M., Schneider, H., Kieserud, T., Cook, T., Douar, A.M., Hanson, M., Pavirani, A. and Rodeck, C.: “Fetal somatic gene therapy – A preventive approach to the treatment of genetic disease”. In: Holzgreve, W. and Lessl, M. (Eds.), Stem cells from cord blood, in utero stem cell development, and transplantation-inclusive gene therapy. Springer-Verlag, Berlin, 2001, pp. 99-114.

14. Douar, A.M. and Danos, O.: “Transfert de gène au moyen de vecteurs adéno-associés”. In: Cohen-Haguenauer, O. (Ed.), Thérapie Génique. Editions Tec & Doc/Editions Médicales Internationales, Paris, 2001, pp. 145-154.

15. Douar, A.M., Poulard, K., Stockholm, D. and Danos, O.: “Intracellular trafficking of adeno-associated virus vectors: Routing to the late endosomal compartment and proteasome degradation”. J Virol 75 (2001) 1824-1833.

16. Drittanti, L., Jenny, C., Poulard, K., Samba, A., Manceau, P., Soria, N., Vincent, N., Danos, O. and Vega, M.: “Optimised helper virus-free production of high-quality adeno-associated virus vectors”. J Gene Med 3 (2001) 59-71.

17. Duyckaerts, C., Joly, B., Sazdovitch, V., Hauw, J.J. and Di Donato, J.H.: “Associations of patients and tissue banks”. Bull Acad Natl Med 185 (2001) 857-866.

18. Firat, H., Favier, R., Adam, M., Leverger, G., Landman-Parker, J., Cayre, Y. and Douay, L.: “Determination of myeloid antigen expression on childhood acute lymphoblastic leukaemia cells: discrepancies using different monoclonal antibody clones”. Leuk Lymphoma 42 (2001) 675-682.

19. Firat, H., Tourdot, S., Ureta-Vidal, A., Scardino, A., Suhrbier, A., Buseyne, F., Riviere, Y., Danos, O., Michel, M.L., Kosmatopoulos, K. and Lemonnier, F.A.: “Design of a polyepitope construct for the induction of HLA-A0201-restricted HIV 1-specific CTL responses using HLA-A*0201 transgenic, H-2 class I KO mice”. Eur J Immunol 31 (2001) 3064-3074.

20. Fischer, J., Bouadjar, B., Heilig, R., Huber, M., Lefevre, C., Jobard, F., Macari, F., Bakija-Konsuo, A., Ait-Belkacem, F., Weissenbach, J., Lathrop, M., Hohl, D. and Prud’homme, J.F.: “Mutations in the gene encoding SLURP-1 in Mal de Meleda”. Hum Mol Genet 10 (2001) 875-880.

21. Fougerousse, F., Edom-Vovard, F., Merkulova, T., Ott, M.O., Durand, M., Butler-Browne, G. and Keller, A.: “The muscle-specific enolase is an early marker of human myogenesis”. J Muscle Res Cell Motil 22 (2001) 535-544.

22. Gücüyener, K., Özgül, K., Paternotte, C., Erdem, H., Prud’homme, J.F., Özgüc, M. and Topaloglu, H.: “Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families”. Neuropediatrics 32 (2001) 142-146.

23. Haravuori, H., Vihola, A., Straub, V., Auranen, M., Richard, I., Marchand, S., Voit, T., Labeit, S., Somer, H., Peltonen, L., Beckmann, J.S. and Udd, B.: “Secondary calpain 3 deficiency in 2q-linked muscular dystrophy: Titin is the candidate gene”. Neurology 56 (2001) 869-877.

24. Jooss, K., Gjata, B., Danos, O., Von Boehmer, H. and Sarukhan, A.: “Regulatory function of in vivo anergized CD4+ T cells”. Proc Natl Acad Sci USA 98 (2001) 8738-8743.

25. Kichler, A., Leborgne, C., Coeytaux, E. and Danos, O.: “Polyethylenimine-mediated gene delivery: a mechanistic study”. J Gene Med 3 (2001) 135-144.

26. Lefèvre, C., Blanchet-Bardon, C., Jobard, F., Bouadjar, B., Stalder, J.F., Cure, S., Hoffmann, A., Prud’homme, J.F. and Fischer, J.: “Novel point mutations, deletions, and polymorphisms in the cathepsin C gene in nine families from Europe and North Africa with Papillon-Lefèvre syndrome”. J Invest Dermatol 117 (2001) 1657-1661.

27. Lefèvre, C., Jobard, F., Caux, F., Bouadjar, B., Karaduman, A., Heilig, R., Lakhdar, H., Wollenberg, A., Verret, J.L., Weissenbach, J., Özgüc, M., Lathrop, M., Prud’homme, J.F. and Fischer, J.: “Mutations in CGI-58, the gene encoding a new protein of the esterase/Lipase/Thioesterase subfamily, in Chanarin-Dorfman syndrome”. Am J Hum Genet 69 (2001) 1002-1012.

28. Martinez-Arca, S., Coco, S., Mainguy, G., Schenk, U., Alberts, P., Bouille, P., Mezzina, M., Prochiantz, A., Matteoli, M., Louvard, D. and Galli, T.: “A common exocytotic mechanism mediates axonal and dendritic outgrowth”. J Neurosci 21 (2001) 3830-3838.

29. Merten, O.-W., Cruz, P.E., Rochette, C., Geny-Fiamma, C., Bouquet, C., Gonçalves, D., Danos, O. and Carrondo, M.J.T.: “Comparison of different bioreactor systems for the production of high titer retroviral vectors”. Biotechnol Prog 17 (2001) 326-335.

30. Merten, O.-W., Landric, L. and Danos, O.: “Influence of the metabolic state of packaging cells on retroviral vector production”. In: Merten, O.W., Mattanovich, D., Lang, C., Larsson, G., Neubauer, P., Porro, D., Postma, P., Teixeira de Mattos, J. and Cole, J.A. (Eds.), Recombinant protein production with prokaryotic and eukaryotic cells: a comparative view on host physiology. Kluwer Academic Press, Dordrecht, 2001, pp. 301-316.

31. Mologni, L., Salmikangas, P., Fougerousse, F., Beckmann, J.S. and Carpén, O.: “Developmental expression of myotilin, a gene mutated in limb-girdle muscular distrophy type 1A”. Mech Dev 103 (2001) 121-125.

32. Moore, T., Hecquet, S., McLellann, A., Ville, D., Grid, D., Picard, F., Moulard, B., Asherson, P., Makoff, A.J., McCormick, D., Nashef, L., Froguel, P., Arzimanoglou, A., LeGuern, E. and Bailleul, B.: “Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME”. Epilepsy Res 46 (2001) 157-167.

33. Nabbout, R.: “A risk-benefit assessment of treatments for infantile spasms”. Drug Saf 24 (2001) 813-828.

34. Pizzato, M., Merten, O.-W., Blair, E.D. and Takeuchi, Y.: “Development of a suspension packaging cell line for production of high titre, serum-resistant murine leukemia virus vectors”. Gene Ther 8 (2001) 737-745.

35. Richard, I. and Beckmann, J.S.: “Molecular diagnosis of calpainopathies: methods used for detection of mutations in the CAPN3 gene implicated in limb-girdle muscular dystrophy type 2A”. In: Anderson, L.V.B. and Bushby, K.M.D. (Eds.), Muscular dystrophy: Methods and protocols. Humana Press, Totowa, USA, 2001, pp. 273-288.

36. Samakoglu, S., Fattori, E., Lamartina, S., Toniatti, C., Stockholm, D., Heard, J.M. and Bohl, D.: “BetaMinor-globin messenger RNA accumulation in reticulocytes governs improved erythropoiesis in beta-thalassemic mice after erythropoietin complementary DNA electrotransfer in muscles”. Blood 97 (2001) 2213-2220.

37. Sarukhan, A., Camugli, S., Gjata, B., Von Boehmer, H., Danos, O. and Jooss, K.: “Successful interference with cellular immune responses to immunogenic proteins encoded by recombinant viral vectors”. J Virol 75 (2001) 269-277.

38. Sarukhan, A., Soudais, C., Danos, O. and Jooss, K.: “Factors influencing cross-presentation of non-self antigens expressed from recombinant adeno-associated virus vectors”. J Gene Med 3 (2001) 260-270.

39. Scardino, A., Alves, P., Gross, D.A., Tourdot, S., Graff-Dubois, S., Angevin, E., Firat, H., Chouaib, S., Lemonnier, F., Nadler, L.M., Cardoso, A.A. and Kosmatopoulos, K.: “Identification of HER-2/neu immunogenic epitopes presented by renal cell carcinoma and other human epithelial tumors”. Eur J Immunol 31 (2001) 3261-3270.

40. Soudais, C., Boutin, S. and Kremer, E.J.: “Characterization of cis-acting sequences involved in canine adenovirus packaging”. Mol Ther 3 (2001) 631-640.

41. Soudais, C., Laplace-Builhe, C., Kissa, K. and Kremer, E.J.: “Preferential transduction of neurons by canine adenovirus vectors and their efficient retrograde transport in vivo”. FASEB J 15 (2001) 2283-2285.

42. Spirito, F., Meneguzzi, G., Danos, O. and Mezzina, M.: “Cutaneous gene transfer and therapy: the present and the future”. J Gene Med 3 (2001) 21-31.

43. Sylvius, N., Tesson, F., Gayet, C., Charron, P., Benaiche, A., Mangin, L., Peuchmaurd, M., Duboscq-Bidot, L., Feingold, J., Beckmann, J.S., Bouchier, C. and Komajda, M.: “A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q14”. American Journal Of Human Genetics 68 (2001) 241-246.

44. Talim, B., Ognibene, A., Mattioli, E., Richard, I., Anderson, L.V. and Merlini, L.: “Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A”. Neurology 56 (2001) 692-3.

45. Tiger, C.F., Fougerousse, F., Grundstrom, G., Velling, T. and Gullberg, D.: “Alpha11beta1 integrin is a receptor for interstitial collagens involved in cell migration and collagen reorganization on mesenchymal nonmuscle cells”. Dev Biol 237 (2001) 116-129.

46. Tores, F. and Barillot, E.: “The art of pedigree drawing: algorithmic aspects”. Bioinformatics 17 (2001) 174-179.

47. Stockholm D, Herasse M, Marchand S, Praud C, Roudaut C, Richard I, Sebille A, Beckmann JS., “Calpain 3 mRNA expression in mice after denervation and during muscle regeneration” , Am J Physiol Cell Physiol. 2001.