D
Delphine Samson
Researcher at Centre national de la recherche scientifique
Publications - 12
Citations - 7056
Delphine Samson is an academic researcher from Centre national de la recherche scientifique. The author has contributed to research in topics: Gene & Gene mapping. The author has an hindex of 12, co-authored 12 publications receiving 6856 citations.
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Journal ArticleDOI
A comprehensive genetic map of the human genome based on 5,264 microsatellites
Colette Dib,Sabine Fauré,Cécile Fizames,Delphine Samson,N. Drouot,Alain Vignal,P Millasseau,S Marc,Jamilé Hazan,Eric Seboun,Mark Lathrop,Gabor Gyapay,Jean Morissette,Jean Morissette,Jean Weissenbach +14 more
TL;DR: The last version of the Généthon human linkage map is reported, which consists of 5,264 short tandem repeat polymorphisms with a mean heterozygosity of 70%.
Journal ArticleDOI
A candidate gene for familial Mediterranean fever
Alain Bernot,Christian Clepet,Corinne Dasilva,Catherine Devaud,Jean-Louis Petit,Christophe Caloustian,Corinne Cruaud,Delphine Samson,Françoise Pulcini,Jean Weissenbach,Roland Heilig,Cécile Notanicola,Cécile Domingo,Michael Rozenbaum,Eldad Ben-Chetrit,Rezzan Topaloglu,Marie Dewalle,Christiane Dross,Philippe Hadjari,Madeleine Dupont,Jacques Demaille,Isabelle Touitou,Nizar Smaoui,Brigitte Nedelec,Jean-Philippe Mery,Habiba Chaabouni,Marc Delpech,Gilles Grateau +27 more
TL;DR: A minimal co-segregating region of 60 kb containing the FMF gene (MEFV) is defined and one of these transcripts encodes a new protein (marenostrin) related to the ret-finger protein and to butyrophilin.
Journal ArticleDOI
A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family
Sonia Abdelhak,Kalatzis,Roland Heilig,Sylvie Compain,Delphine Samson,Christophe Vincent,Dominique Weil,Corinne Cruaud,Iman Sahly,Michel Leibovici,Bitner-Glindzicz M,Francis M,Didier Lacombe,Jacqueline Vigneron,Charachon R,Boven K,Bedbeder P,Van Regemorter N,Jean Weissenbach,Christine Petit +19 more
TL;DR: The expression pattern of the murine EYA1 orthologue, Eya1, suggests a role in the development of all components of the inner ear, from the emergence of the otic placode, and in the developing kidney, the expression pattern is indicative of a role for Eya 1 in the metanephric cells surrounding the ‘just-divided’ ureteric branches.
Journal ArticleDOI
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
Jamilé Hazan,Nuria Fonknechten,Delphine Mavel,Caroline Paternotte,Delphine Samson,François Artiguenave,Claire-Sophie Davoine,Corinne Cruaud,Alexandra Durr,Patrick Wincker,Philippe Brottier,Laurence Cattolico,Valérie Barbe,Jean-Marc Burgunder,Jean-François Prud'homme,Alexis Brice,Bertrand Fontaine,Roland Heilig,Jean Weissenbach +18 more
TL;DR: The sequence homologies and putative subcellular localization of spastin suggest that this ATPase is involved in the assembly or function of nuclear protein complexes.
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Mechanisms of evolution in Rickettsia conorii and R. prowazekii.
Hiroyuki Ogata,Stéphane Audic,Patricia Renesto-Audiffren,Pierre-Edouard Fournier,Valérie Barbe,Delphine Samson,Véronique Roux,Pascale Cossart,Jean Weissenbach,Jean-Michel Claverie,Didier Raoult +10 more
TL;DR: The 1,268,755-nucleotide complete genome sequence of Rickettsia conorii is determined, containing 1374 open reading frames, and this genome exhibits 804 of the 834 genes of the previously determined R. prowazekii genome plus 552 supplementaryOpen reading frames and a 10-fold increase in the number of repetitive elements.