Connexin 26 gene linked to a dominant deafness
Denoyelle, Françoise, Lina-Granade, Genevieve, Plauchu, Henri, Bruzzone, Roberto, Chaïb, Hassan, Lévi-Acobas, Fabienne, Weil, Dominique, Petit, Christine
Published in Nature (London) (28.05.1998)
Published in Nature (London) (28.05.1998)
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Journal Article
Interleukin 22 Is a Candidate Gene for Tmevp3, a Locus Controlling Theiler's Virus-Induced Neurological Diseases
Levillayer, F, Mas, M, Levi-Acobas, F, Brahic, M, Bureau, J. F
Published in Genetics (Austin) (01.07.2007)
Published in Genetics (Austin) (01.07.2007)
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Journal Article
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
Ayadi, Hammadi, Lévy, Gallia, Weil, Dominique, Levi-Acobas, Fabienne, Drira, Mohamed, Blanchard, Stéphane, Petit, Christine, Küssel, Polonca
Published in Nature genetics (01.06.1997)
Published in Nature genetics (01.06.1997)
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Journal Article
Adaptive evolution of interferon-γ in Glire lineage and evidence for a recent selective sweep in Mus. m. domesticus
Levi-Acobas, F, Mars, L T, Orth, A, Bureau, J-F, Bonhomme, F
Published in Genes and immunity (01.06.2009)
Published in Genes and immunity (01.06.2009)
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Journal Article
Human Myosin VIIA Responsible for the Usher 1B Syndrome: A Predicted Membrane-Associated Motor Protein Expressed in Developing Sensory Epithelia
Weil, Dominique, Lévy, Gallia, Sahly, Iman, Lévi-Acobas, Fabienne, Blanchard, Stéphane, El-Amraoui, Aziz, Crozet, Fabien, Philippe, Hervé, Abitbol, Marc, Petit, Christine
Published in Proceedings of the National Academy of Sciences - PNAS (16.04.1996)
Published in Proceedings of the National Academy of Sciences - PNAS (16.04.1996)
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Journal Article
Defective myosin VIIA gene responsible for Usher syndrome type 1B
WEIL, D, BLANCHARD, S, KELLEY, P. M, KIMBERLING, W. J, WAGENAAR, M, LEVI-ACOBAS, F, LARGET-PIET, D, MUNNICH, A, STEEL, K. P, BROWN, S. D. M, PETIT, C, KAPLAN, J, GUILFORD, P, GIBSON, F, WALSH, J, MBURU, P, VARELA, A, LEVILLIERS, J, WESTON, M. D
Published in Nature (London) (02.03.1995)
Published in Nature (London) (02.03.1995)
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Journal Article
Adaptive evolution of interferon-[gamma] in Glire lineage and evidence for a recent selective sweep in Mus. m. domesticus
Levi-acobas, F, Mars, L T, Orth, A, Bureau, J-f, Bonhomme, F
Published in Genes and immunity (01.06.2009)
Published in Genes and immunity (01.06.2009)
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Journal Article
Clustering of Mutations Responsible for Branchio-Oto-Renal (BOR) Syndrome in the Eyes Absent Homologous Region (eyaHR) of EYA1
Abdelhak, Sonia, Kalatzis, Vasiliki, Heilig, Roland, Compain, Sylvie, Samson, Delphine, Vincent, Christophe, Levi-Acobas, Fabienne, Cruaud, Corinne, Le Merrer, Martine, Mathieu, Michèle, König, Rainer, Vigneron, Jacqueline, Weissenbach, Jean, Petit, Christine, Weil, Dominique
Published in Human molecular genetics (01.12.1997)
Published in Human molecular genetics (01.12.1997)
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Journal Article
Cloning of the Genes Encoding Two Murine and Human Cochlear Unconventional Type I Myosins
Crozet, Fabien, Amraoui, Aziz El, Blanchard, Stéphane, Lenoir, Marc, Ripoll, Chantal, Vago, Philippe, Hamel, Christian, Fizames, Cécile, Levi-Acobas, Fabienne, Depétris, Danièle, Mattei, Marie-Genevı̀eve, Weil, Dominique, Pujol, Rémy, Petit, Christine
Published in Genomics (San Diego, Calif.) (01.03.1997)
Published in Genomics (San Diego, Calif.) (01.03.1997)
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Journal Article
Myosin VIIA Gene: Heterogeneity of the Mutations Responsible for Usher Syndrome Type IB
Lévy, Gallia, Levi-Acobas, Fabienne, Blanchard, Stéphane, Gerber, Sylvie, Larget-Piet, Dominique, Chenal, Viviane, Liu, Xue-Zhong, Newton, Valerie, Steel, Karen P., Brown, Steve D. M., Munnich, Arnold, Kaplan, Josseline, Petit, Christine, Weil, Dominique
Published in Human molecular genetics (01.01.1997)
Published in Human molecular genetics (01.01.1997)
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Journal Article
Sequence Characterization of a Newly Identified Human α-Tubulin Gene (TUBA2)
Dodé, Catherine, Weil, Dominique, Levilliers, Jacqueline, Crozet, Fabien, Chaı̈b, Hassan, Levi-Acobas, Fabienne, Guilford, Parry, Petit, Christine
Published in Genomics (San Diego, Calif.) (01.01.1998)
Published in Genomics (San Diego, Calif.) (01.01.1998)
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Journal Article
A YAC Contig and an EST Map in the Pericentromeric Region of Chromosome 13 Surrounding the Loci for Neurosensory Nonsyndromic Deafness (DFNB1 and DFNA3) and Limb-Girdle Muscular Dystrophy Type 2C (LGMD2C)
Guilford, Parry, Dodé, Catherine, Crozet, Fabien, Blanchard, Stéphane, Chaı̈b, Hassan, Levilliers, Jacqueline, Levi-Acobas, Fabienne, Weil, Dominique, Weissenbach, Jean, Cohen, Daniel, Le Paslier, Denis, Kaplan, Jean-Claude, Petit, Christine
Published in Genomics (San Diego, Calif.) (01.09.1995)
Published in Genomics (San Diego, Calif.) (01.09.1995)
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Journal Article
Syndrome de Usher de type IB : anomalie d'une myosine non conventionnelle: Les maladies génétiques sensorielles
WEIL, D, LEVY, G, BROWN, S, PETIT, C, SAHLY, I, LEVI-ACOBAS, F, BLANCHARD, S, CROZET, F, KAPLAN, J, MUNNICH, A, ABITBOL, M, STEEL, K
Published in Annales de l'Institut Pasteur. Actualités (1995)
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Published in Annales de l'Institut Pasteur. Actualités (1995)
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