Zobrazeno 1 - 10
of 68
pro vyhledávání: '"N Chiannilkulchai"'
Autor:
Gerlinde Averous, Frédérique Penault-Llorca, Anne Floquet, Patricia Pautier, Catherine Genestie, S. Croce, As Bats, Eliane Mery, Isabelle Treilleux, N. Chiannilkulchai, G. Ferron, Isabelle Ray-Coquard, Christophe Pomel, Anne-Sophie Lemaire, Jean-Emmanuel Kurtz, Mc Vacher-Lavenu, C. Lefeuvre-Plesse, S. Henno, Eric Leblanc, Mojgan Devouassoux-Shisheboran
Publikováno v:
Annals of Oncology
Annals of Oncology, Elsevier, 2017, 28 (6), pp.1274-1279. ⟨10.1093/annonc/mdx099⟩
Annals of Oncology, 2017, 28 (6), pp.1274-1279. ⟨10.1093/annonc/mdx099⟩
Annals of Oncology, Elsevier, 2017, 28 (6), pp.1274-1279. ⟨10.1093/annonc/mdx099⟩
Annals of Oncology, 2017, 28 (6), pp.1274-1279. ⟨10.1093/annonc/mdx099⟩
Background Rare ovarian tumors represent >20% of all ovarian cancers. Given the rarity of these tumors, natural history, prognostic factors are not clearly identified. The extreme variability of patients (age, histological subtypes, stage) induces mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dd79aca666c45a930bdd3ebb46e09d0
https://hal.archives-ouvertes.fr/hal-01656484
https://hal.archives-ouvertes.fr/hal-01656484
Akademický článek
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Autor:
Orit Kollet, Helmut Holtmann, Victor Luria, Denis V. Rebrikov, Eugene Varfolomeev, Peter Lonai, Jacques S. Beckmann, Tama Sobe, David Wallach, Oliver Kemper, Igor Mett, Vadim M Brodianski, Karen B. Avraham, Dror Soffer, Tsvee Lapidot, Marcus Schuchmann, Tanya Goncharov, N. Chiannilkulchai
Publikováno v:
Scopus-Elsevier
Homozygous targeted disruption of the mouse Caspase 8 (Casp8) gene was found to be lethal in utero. The Caspase 8 null embryos exhibited impaired heart muscle development and congested accumulation of erythrocytes. Recovery of hematopoietic colony-fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c31e7fd2fdce1b239a8299814dfda7b
Autor:
Alain Bernot, Jean Weissenbach, Nizar Smaoui, Cécile Fizames, C. da Crola Silva, N. Chiannilkulchai, Roland Heilig, Catherine Devaud, Marc Delpech, Gabor Gyapay, Christophe Caloustian, Delphine Samson, Joëlle Petit, Christian Clepet, Corinne Cruaud
Publikováno v:
Genomics. 50:147-160
Familial Mediterranean fever (FMF) is a recessively inherited disorder characterized by attacks of fever and serositis, which affects primarily non-Ashkenazi Jews, Armenians, Turks, and Arabs. We present here a transcriptional map covering the FMF lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1190fe6aa62f4276d1f47d5b190b623c
https://doi.org/10.1006/geno.1998.5313
https://doi.org/10.1006/geno.1998.5313
Autor:
N. Chiannilkulchai, F. Quétier, Jacques S. Beckmann, V. Allamand, Haluk Topaloglu, O. Broux, Yoshihide Sunada, Fernando M.S. Tomé, Daniel Cohen, L. Brenguier, J. Meyer, Charles E. Jackson, Kevin P. Campbell, Gérard Lefranc, Françoise Fougerousse, Nathalie Bourg, Leland E. Lim, Carinne Roudaut, Michel Fardeau, Isabelle Richard, Pervin Dinçer, P. Pasturaud, Luciano Merlini, Franck Duclos
Publikováno v:
Neuromuscular Disorders. 6:455-462
The autosomal recessive forms of limb-girdle muscular dystrophies are encoded by at least five distinct genes. The work performed towards the identification of two of these is summarized in this report. This success illustrates the growing importance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2fc72d0c8bf4d70c9d1d502e9f9d9ba
https://doi.org/10.1016/s0960-8966(96)00386-0
https://doi.org/10.1016/s0960-8966(96)00386-0
Autor:
Christopher Mader, B. B. Birren, Jean Morissette, C. Sanders, K. Swanson, Xiao-Yu Wu, Thomas J. Hudson, Mark S. Boguski, A. Maratukulam, Midori A. Harris, L. Green, S. Hussain, C. East, Robert E. White, Andrew A. Hicks, K. R. Iorio, Andrew B. Castle, W.-L. Sun, Paul Harrison, Simone Duprat, Kate Rice, Eric S. Lander, X. She, Shanti M. Perkins, Ammon B. Peck, Mina Sandusky, John Quackenbush, L. Hui, David Bentley, K. B. McKusick, Anindya Dehejia, Gregory D. Schuler, Gabor Gyapay, T. Dibling, C M Clee, Amita Aggarwal, James R. Hudson, R. Torres, Eva Bajorek, Peter N. Goodfellow, Mark Piercy, Mark Raymond Adams, Jun Fan, Cheryl Phillips, Elizabeth A. Stewart, Nicole Y. Fang, N. Drouot, Ian Dunham, Donna K. Slonim, Mihael H. Polymeropoulos, N. Nomura, Andrew J. Mungall, K. Ishikawa, E. Holloway, J. Ma, P. J. R. Day, N. Seki, S. Bentolila, Jean Weissenbach, P. Rodriguez-Tomé, Adam Butler, Sid Cowles, Angela M. Chu, Karin Schmitt, R. Houlgatte, Panos Deloukas, Tim Reif, Michael R. James, C. Louis-Dit-Sully, S. Voyticky, P. Tabar, David R. Cox, A. MacGilvery, David C. Page, Carol Soderlund, C A Edwards, S A Ranby, Nicole A.R. Walter, Douglas Vollrath, T. E. Wilmer, Lincoln Stein, H. C. Nusbaum, Takahiro Nagase, Tara C. Matise, T. Thangarajah, Susan E. Ide, Fawn Qin, Richard M. Myers, Steve Rozen, Jacques S. Beckmann, Richard Berry, James M. Sikela, Charles Auffray, Shannon T. Brady, Cécile Fizames, Christine Garrett, David Hadley, Delphine Muselet, Nathalie Vega-Czarny, Rhonda Brandon, Wha‐Young Lee, N. Chiannilkulchai, J. C. Venter, James Silva
Publikováno v:
Science. 274:540-546
The human genome is thought to harbor 50,000 to 100,000 genes, of which about half have been sampled to date in the form of expressed sequence tags. An international consortium was organized to develop and map gene-based sequence tagged site markers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87abe38bd8f96de2a0d10feb38533d10
https://doi.org/10.1126/science.274.5287.540
https://doi.org/10.1126/science.274.5287.540
Autor:
Isabelle Richard, Jacques S. Beckmann, Charles Auffray, N. Chiannilkulchai, Patricia Pasturaud
Publikováno v:
Human Molecular Genetics. 4:717-725
Previous genetic and physical studies of LGMD2A, an autosomal recessive form of limb-girdle muscular dystrophy, have led to the establishment of a 10-12 Mb YAC contig encompassing the morbid locus. In order to progress toward the identification of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::080fee47761ec21d1d4f5c6eb421b238
https://doi.org/10.1093/hmg/4.4.717
https://doi.org/10.1093/hmg/4.4.717
Akademický článek
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Publikováno v:
Molecular and Cellular Biology. 12:4433-4440
RNA polymerase C (III) promotes the transcription of tRNA and 5S RNA genes. In Saccharomyces cerevisiae, the enzyme is composed of 15 subunits, ranging from 160 to about 10 kDa. Here we report the cloning of the gene encoding the 82-kDa subunit, RPC8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd520bdef54215665239bc21c0326a41
https://doi.org/10.1128/mcb.12.10.4433
https://doi.org/10.1128/mcb.12.10.4433
Publikováno v:
Cancer Chemotherapy and Pharmacology. 26:122-126
In our previous studies, doxorubicin-loaded polyisohexylcyanoacrylate nanoparticles have been proven to increase dramatically the antitumoral activity of the cytotoxic agent in metastasis-bearing mice. The experimental model consisted of metastases i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e97c3e9cf217bcac7ac5142cac3a0ade
https://doi.org/10.1007/bf02897257
https://doi.org/10.1007/bf02897257