Publications scientifiques
Les scientifiques de l'IGBMC publient régulièrement dans des revues dédiées à la recherche. Vous trouverez la liste de ces publications ci-dessous.
Publications
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2006
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The glutamate transporter EAAT5 works as a presynaptic receptor in mouse rod bipolar cells
- Eric Wersinger
- Yannick Schwab
- José-Alain Sahel
- Alvaro Rendon
- David Pow
- Serge Picaud
- Michel Roux
The Journal of Physiology ; Volume: 577 ; Page: 221-234
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CXorf6 is a causative gene for hypospadias
- Maki Fukami
- Yuka Wada
- Kanako Miyabayashi
- Ichizo Nishino
- Tomonobu Hasegawa
- Agneta Nordenskjöld
- Giovanna Camerino
- Christine Kretz
- Anna Buj-Bello
- Jocelyn Laporte
- Gen Yamada
- Ken-Ichirou Morohashi
- Tsutomu Ogata
Nature Genetics ; Volume: 38 ; Page: 1369-1371
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Biophysical characterization of an indolinone inhibitor in the ATP-binding site of DNA gyrase.
- Marko Oblak
- Simona Golic Grdadolnik
- Miha Kotnik
- Arnaud Poterszman
- Robert Andrew Atkinson
- Helene Nierengarten
- Dominique Desplancq
- Dino Moras
- Tom Solmajer
Biochemical and Biophysical Research Communications ; Volume: 349 ; Page: 1206-13
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Retinoic acid signalling is required for specification of pronephric cell fate.
- Jérôme Cartry
- Massimo Nichane
- Vanessa Ribes
- Alexandre Colas
- Jean-Francois Riou
- Tomas Pieler
- Pascal Dollé
- Eric J Bellefroid
- Muriel Umbhauer
Developmental Biology ; Volume: 299 ; Page: 35-51
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A novel PtdIns3P and PtdIns(3,5)P2 phosphatase with an inactivating variant in centronuclear myopathy.
- Valérie Tosch
- Holger M Rohde
- Hélène Tronchère
- Edmar Zanoteli
- Nancy Monroy
- Christine Kretz
- Nicolas Dondaine
- Bernard Payrastre
- Jean-Louis Mandel
- Jocelyn Laporte
Human Molecular Genetics ; Volume: 15 ; Page: 3098-106
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The columnar gene vnd is required for tritocerebral neuromere formation during embryonic brain development of Drosophila.
- Simon G Sprecher
- Rolf Urbach
- Gerhard M Technau
- Filippo M Rijli
- Heinrich Reichert
- Frank Hirth
Development (Cambridge, England) ; Volume: 133 ; Page: 4331-9
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PGC1alpha expression is controlled in skeletal muscles by PPARbeta, whose ablation results in fiber-type switching, obesity, and type 2 diabetes.
- Michael Schuler
- Faisal Ali
- Céline Chambon
- Delphine Duteil
- Jean-Marc Bornert
- Aubry Tardivel
- Béatrice Desvergne
- Walter Wahli
- Pierre Chambon
- Daniel Metzger
Cell Metabolism ; Volume: 4 ; Page: 407-14
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Pitfalls of homozygosity mapping: an extended consanguineous Bardet-Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism.
- Virginie Laurier
- Corinne Stoetzel
- Jean Muller
- Christelle Thibault
- Sandra Corbani
- Nadine Jalkh
- Nabiha Salem
- Eliane Chouery
- Olivier Poch
- Serge Licaire
- Jean-Marc Danse
- Patricia Amati-Bonneau
- Dominique Bonneau
- André Mégarbané
- Jean-Louis Mandel
- Hélène Dollfus
European Journal of Human Genetics ; Volume: 14 ; Page: 1195-203
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Bardet-Biedl syndrome: a unique family for a major gene (BBS10)
- Hélène Dollfus
- Jean Muller
- Corinne Stoetzel
- Virginie Laurier
- Dominique Bonneau
- André Mégarbané
- Olivier Poch
- Jean-Louis Mandel
Médecine/Sciences ; Volume: 22 ; Page: 901-4
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Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene.
- Céline Moutou
- Nadejda Machev
- Nathalie Gardes
- Stéphane Viville
Prenatal Diagnosis ; Volume: 26 ; Page: 1037-41
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