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103. Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans

Author

Laissue, P, Lakhal, Besma, Vatin, M, Batista, Frank, Burgio, Gaetan, Mercier, Eric, Dos Santos, Esther, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, G, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A, Mehats, Celine, Fellous, Marc, Gris, Jean-Christophe, Cocquet, Julie, Vaiman, Daniel, Laissue, P, Lakhal, Besma, Vatin, M, Batista, Frank, Burgio, Gaetan, Mercier, Eric, Dos Santos, Esther, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, G, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A, Mehats, Celine, Fellous, Marc, Gris, Jean-Christophe, Cocquet, Julie, and Vaiman, Daniel

Abstract

Recurrent spontaneous abortion (RSA) is a common cause of infertility, but previous attempts at identifying RSA causative genes have been relatively unsuccessful. Such failure to describe RSA aetiological genes might be explained by the fact that reproductive phenotypes should be considered as quantitative traits resulting from the intricate interaction of numerous genetic, epigenetic and environmental factors. Here, we studied an interspecific recombinant congenic strain (IRCS) of Mus musculus from the C57BL6/J strain of mice harbouring an approximate 5 Mb DNA fragment from chromosome 13 from Mus spretus mice (66H-MMU13 strain), with a high rate of embryonic resorption (ER). Transcriptome analyses of endometrial and placental tissues from these mice showed a deregulation of many genes associated with the coagulation and inflammatory response pathways. Bioinformatics approaches led us to select Foxd1 as a candidate gene potentially related to ER and RSA. Sequencing analysis of Foxd1 in the 66H-MMU13 strain, and in 556 women affected by RSA and 271 controls revealed non-synonymous sequence variants. In vitro assays revealed that some led to perturbations in FOXD1 transactivation properties on promoters of genes having key roles during implantation/placentation, suggesting a role of this gene in mammalian implantation processes.

Published
2016

104. Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans

Author

Laissue, Paul, primary, Lakhal, Besma, additional, Vatin, Magalie, additional, Batista, Frank, additional, Burgio, Gaëtan, additional, Mercier, Eric, additional, Santos, Esther Dos, additional, Buffat, Christophe, additional, Sierra-Diaz, Diana Carolina, additional, Renault, Gilles, additional, Montagutelli, Xavier, additional, Salmon, Jane, additional, Monget, Philippe, additional, Veitia, Reiner A., additional, Méhats, Céline, additional, Fellous, Marc, additional, Gris, Jean-Christophe, additional, Cocquet, Julie, additional, and Vaiman, Daniel, additional

Published
2016
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105. Genome Editing and Dialogic Responsibility: “What's in a Name?”

Author

Blasimme, Alessandro, primary, Anegon, Ignacio, additional, Concordet, Jean-Paul, additional, De Vos, John, additional, Dubart-Kupperschmitt, Anne, additional, Fellous, Marc, additional, Fouchet, Pierre, additional, Frydman, Nelly, additional, Giovannangeli, Carine, additional, Jouannet, Pierre, additional, Serre, Jean-Loius, additional, Steffann, Julie, additional, Rial-Sebbag, Emmanuelle, additional, Thomsen, Mogens, additional, and Cambon-Thomsen, Anne, additional

Published
2015
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114. Prendre la mesure d’une culture ouverte et responsable

Author

Marris, Claire, Heams, Thomas, Kepes, Francois, Campos, Luis, Monsan, Pierre, Toussaint, Jean-François, Benoit-Browaeys, Dorothee, Haiech, Jacques, Alix, Jean-Pierre, Fellous, Marc, School of Social Science & Public Policy, Department of Social Science, Health & Medicine, Centre for Synthetic Biology and Innovation (CSynBI), King‘s College London, Génétique Animale et Biologie Intégrative (GABI), Institut National de la Recherche Agronomique (INRA)-AgroParisTech, Institut de biologie systémique et synthétique (ISSB), Université d'Évry-Val-d'Essonne (UEVE)-Génopole-Centre National de la Recherche Scientifique (CNRS), Department of History, Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA), Institut National des Sciences Appliquées - Toulouse (INSA Toulouse), Institut National des Sciences Appliquées (INSA), Independent, Faculté de Médecine, Laboratoire d'Innovation Thérapeutique, Université de Strasbourg (UNISTRA), AgroParisTech-Institut National de la Recherche Agronomique (INRA), Université d'Évry-Val-d'Essonne (UEVE)-Centre National de la Recherche Scientifique (CNRS), Laboratoire d'Innovation Thérapeutique (LIT), Université de Strasbourg (UNISTRA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), and Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)

Subjects
[SDV]Life Sciences [q-bio]
Abstract

Discussion Session 2Discussion Session 2; Prendre la mesure d’une culture ouverte et responsable. 3. Colloque Sciences de la vie en société

Published
2012

116. Human genetic of premature ovarian failure: a mendelian and candidate genes approach

Author

Caburet, Sandrine, Batista, Frank, Laissue, Paul, Reiner, A. Veitia, Fellous, Marc, Bacq, Delphine, Heath, Simon, Lathrop, Mark, Mandon-Pepin, Béatrice, Christin-Maitre, Sophie, Bouchard, Philippe, Touraine, Philippe, Ben Neriah, Zivah, Shalev, Stavit, Coppelli, Silvia, Institut Cochin (IC UM3 (UMR 8104 / U1016)), Centre National de la Recherche Scientifique (CNRS)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre National de Génotypage (CNG), Biologie du développement et reproduction (BDR), Centre National de la Recherche Scientifique (CNRS)-École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Hôpital Hadassah, Partenaires INRAE, Medical Center, and Caece University

Subjects
PREMATURE OVARIAN FAILURE, [SDV]Life Sciences [q-bio], [INFO]Computer Science [cs], GENETIQUE, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2006

118. Molecular aspects of female and male gonodal development in mammals

Author

Pannetier, Maëlle, Mandon-Pepin, Béatrice, Copelli, S., Fellous, Marc, Biologie du développement et reproduction (BDR), and Centre National de la Recherche Scientifique (CNRS)-École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)

Subjects
[SDV]Life Sciences [q-bio], [INFO]Computer Science [cs], ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2004

119. Final analysis of European patients from the Global Investigation of Therapeutic Decisions in Hepatocellular Carcinoma and of its Treatment with Sorafenib (GIDEON) study: Baseline characteristics and staging systems.

Author

Daniele, Bruno, primary, Ratziu, Vlad, additional, Stal, Per I, additional, Serejo, Fatima, additional, Bodoky, Gyorgy, additional, Croitoru, Adina E, additional, Papandreou, Christos, additional, Turnes, Juan, additional, Fellous, Marc Mardoche, additional, Mathurin, Philippe, additional, and Bronowicki, Jean-Pierre, additional

Published
2014
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121. Molecular genetics of sex determination

Author

Cotinot, Corinne, Pailhoux, Eric, Jaubert, F., Fellous, Marc, Unité biologie du développement et biotechnologie, and École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)

Subjects
[SDV]Life Sciences [q-bio], REPRODUCTION SEXUEE
Abstract

68 ref.; International audience

Published
2002

122. Linkage and association of the glutamate receptor 6 gene with autism

Author

Jamain, Stéphane, Betancur, Catalina, Quach, Hélène, Philippe, Anne, Fellous, Marc, Giros, Bruno, Gillberg, Christopher, Leboyer, Marion, Bourgeron, Thomas, Génomique fonctionnelle et développement, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Neurobiologie et Psychiatrie, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Child and Adolescent Psychiatry, University of Gothenburg (GU), Département de Psychiatrie, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Albert Chenevier, This work was supported by the Délégation de la Recherche Clinique de l'Assistance Publique-Hôpitaux de Paris, the French Research Ministry (Actions Concertées Incitatives), France Télécom, and the Swedish Medical Research Council. C.B. was supported by a Cure Autism Now Foundation Award., Paris Autism Research International Sibpair (PARIS) Study, and Betancur, Catalina

Subjects
GluR6, MESH: Chromosomes, Human, Pair 6, MESH: Autistic Disorder, MESH: Amino Acid Sequence, [SDV.GEN] Life Sciences [q-bio]/Genetics, MESH: Genetic Markers, MESH: Genotype, MESH: Brain, single nucleotide polymorphism, MESH: Child, MESH: Family, TDT, GRIK2, [SDV.GEN]Life Sciences [q-bio]/Genetics, MESH: Humans, MESH: Molecular Sequence Data, affected sib-pair method, editing, MESH: Receptor, isoforms, mutation screening, MESH: Glutamic Acid, MESH: Open Reading Frames, MESH: Male, autistic disorder, MESH: Chromosome Mapping, MESH: Exons, MESH: Linkage (Genetics), MESH: Female, linkage disequilibrium
Abstract

International audience; A genome scan was previously performed and pointed to chromosome 6q21 as a candidate region for autism. This region contains the glutamate receptor 6 (GluR6 or GRIK2) gene, a functional candidate for the syndrome. Glutamate is the principal excitatory neurotransmitter in the brain and is directly involved in cognitive functions such as memory and learning. We used two different approaches, the affected sib-pair (ASP) method and the transmission disequilibrium test (TDT), to investigate the linkage and association between GluR6 and autism. The ASP method, conducted with additional markers on the 51 original families and in eight new sibling pairs, showed a significant excess of allele sharing, generating an elevated multipoint maximum LOD score (ASPEX MLS = 3.28). TDT analysis, performed in the ASP families and in an independent data set of 107 parent-offspring trios, indicated a significant maternal transmission disequilibrium (TDTall P = 0.0004). Furthermore, TDT analysis (with only one affected proband per family) showed significant association between GluR6 and autism (TDT association P = 0.008). In contrast to maternal transmission, paternal transmission of GluR6 alleles was as expected in the absence of linkage, suggesting a maternal effect such as imprinting. Mutation screening was performed in 33 affected individuals, revealing several nucleotide polymorphisms (SNPs), including one amino acid change (M867I) in a highly conserved domain of the intracytoplasmic C-terminal region of the protein. This change is found in 8% of the autistic subjects and in 4% of the control population and seems to be more maternally transmitted than expected to autistic males (P = 0.007). Taken together, these data suggest that GluR6 is in linkage disequilibrium with autism.

Published
2002

123. Génétique et infertilité humaine : 'une approche gènes candidats'

Author

Mandon-Pepin, Béatrice, Derbois, C., Matsuda, F., Cotinot, Corinne, Wolgemuth, D.J., Smith, K., McElreavey, K., Nicolas, A., Fellous, Marc, Unité biologie du développement et biotechnologie, and École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)

Subjects
[SDV]Life Sciences [q-bio], GENETIQUE, ComputingMilieux_MISCELLANEOUS
Abstract

National audience

Published
2002

124. Le déterminisme du sexe : son contrôle génetique

Author

Cotinot, Corinne, Pailhoux, Eric, Ottolenghi, C., Veitia, Reiner, Fellous, Marc, Unité biologie du développement et biotechnologie, École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA), C. Thibault (Editeur), and M.C. Levasseur (Editeur)

Subjects
INVERSION DU SEXE, [SDV]Life Sciences [q-bio]
Abstract

chap. 11; National audience

Published
2001

125. The Human Y Chromosome: The Biological Role of a 'Functional Wasteland'

Author

Quintana-Murci, Lluís and Fellous, Marc

Subjects
Article Subject
Abstract

“Functional wasteland,” “Nonrecombining desert” and “Gene-poor chromosome” are only some examples of the different definitions given to the Y chromosome in the last decade. In comparison to the other chromosomes, the Y is poor in genes, being more than 50% of its sequence composed of repeated elements. Moreover, the Y genes are in continuous decay probably due to the lack of recombination of this chromosome. But the human Y chromosome, at the same time, plays a central role in human biology. The presence or absence of this chromosome determines gonadal sex. Thus, mammalian embryos with a Y chromosome develop testes, while those without it develop ovaries (Polani [38]). What is responsible for the male phenotype is the testis-determining SRY gene (Sinclair [52]) which remains the most distinguishing characteristic of this chromosome. In addition to SRY, the presence of other genes with important functions has been reported, including a region associated to Turner estigmata, a gene related to the development of gonadoblastoma and, most important, genes related to germ cell development and maintenance and then, related with male fertility (Lahn and Page [31]). This paper reviews the structure and the biological functions of this peculiar chromosome.

Published
2001
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126. Contribution of domestic animals to the identification of new genes involved in sex determination

Author

Pailhoux, Eric, Vigier, Brigitte, Vaiman, Daniel, Schibler, Laurent, Vaiman, Anne, Cribiu, Edmond, Nezer, C., Georges, M., Sundström, J., Pelliniemi, L.J., Fellous, Marc, Cotinot, Corinne, Unité biologie du développement et biotechnologie, École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA), Unité de recherche Génétique Biochimique et Cytogénétique (LGBC), and Institut National de la Recherche Agronomique (INRA)

Subjects
[SDV]Life Sciences [q-bio], ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2001

127. A 11.7-kb delection triggers intersexuality and polledness in goats

Author

Pailhoux, Eric, Vigier, Brigitte, Chaffaux, Stéphane, Servel, N., Taourit, Sead, Furet, J.P., Fellous, Marc, Grosclaude, F., CRIBIU, E.P., Cotinot, Corinne, Vaiman, Daniel, Unité biologie du développement et biotechnologie, École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA), Unité de recherche Génétique Biochimique et Cytogénétique (LGBC), and Institut National de la Recherche Agronomique (INRA)

Subjects
[SDV]Life Sciences [q-bio], ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2001

128. sY116, a human Y-linked polymorphic STS

Author

Saifi, Mustafa G, Veitia, Reiner, El khil, Houssein Khodjet, Barbaux, Sandrine, Tilak, Preetha, Thomas, Manorama I, and Fellous, Marc

Subjects
Microbiology & Cell Biology
Abstract

During a study of deletions of Y-chromosomal DNA in infertile males, sY116, a Y-linked STS, showed different electrophoretic mobilities in three males, two infertile and one fertile. A study of this STS among 35 other normal males showed that this locus is polymorphic. sY116 has a polya-rich stretch whose instability appears to be the most likely cause of this polymorphism. The possible usefulness of sY116 polymorphism in the detection of subtle genome-wide instabilities in some types of cancer is discussed.

Published
2000

129. Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.

Author

Beysens, D., De Jaegere, Sarah, Amor, David, Bouchard, Ph., Christin-Maitre, Sophie, Fellous, Marc, Touraine, Philippe, Grix, Arthur W, Hennekam, R C, Meire, Françoise, Oyen, Nina, Wilson, Louise C, Barel, Dalit, Clayton-Smith, Jill, de Ravel, Thomy, Decock, Christian, Delbeke, Patricia, Ensenauer, Regina, Ebinger, Friedrich, Gillessen-Kaesbach, G., Hendriks, Yvonne, Kimonis, Virginia, Laframboise, Rachel, Laissue, Paul, Leppig, Kathleen, Leroy, Bart P, Miller, David T, Mowat, David, Neumann, Luitgard, Plompen, Arjan, Van Regemorter, Nicole, Wieczorek, Dagmar, Veitia, Reiner A, De Paepe, Anne, De Baere, Elfride, Beysens, D., De Jaegere, Sarah, Amor, David, Bouchard, Ph., Christin-Maitre, Sophie, Fellous, Marc, Touraine, Philippe, Grix, Arthur W, Hennekam, R C, Meire, Françoise, Oyen, Nina, Wilson, Louise C, Barel, Dalit, Clayton-Smith, Jill, de Ravel, Thomy, Decock, Christian, Delbeke, Patricia, Ensenauer, Regina, Ebinger, Friedrich, Gillessen-Kaesbach, G., Hendriks, Yvonne, Kimonis, Virginia, Laframboise, Rachel, Laissue, Paul, Leppig, Kathleen, Leroy, Bart P, Miller, David T, Mowat, David, Neumann, Luitgard, Plompen, Arjan, Van Regemorter, Nicole, Wieczorek, Dagmar, Veitia, Reiner A, De Paepe, Anne, and De Baere, Elfride

Abstract

Blepharophimosis syndrome (BPES) is caused by loss-of-function mutations in the single-exon forkhead transcription factor gene FOXL2 and by genomic rearrangements of the FOXL2 locus. Here, we focus on 92 new intragenic FOXL2 mutations, 34 of which are novel. Specifically, we found 10 nonsense mutations (11%), 13 missense mutations (14%), 40 deletions or insertions leading to a frameshift (43%), and 29 in-frame changes (32%), of which 28 (30%) lead to a polyalanine expansion. This study confirms the existence of two previously described mutational hotspots. Moreover, we gained novel insights in genotype-phenotype correlations, emphasizing the need to interpret genotype-phenotype correlations individually and always in the context of further clinical observations., Journal Article, Research Support, Non-U.S. Gov't, SCOPUS: ar.j, FLWIN, info:eu-repo/semantics/published

Published
2008

130. Sex reversal in man and domestic animal. Contribution to the understanding of mammalian sex differentiation

Author

Pailhoux, Eric, Vaiman, Daniel, Barbaux, S., Cribiu, Edmond, Cotinot, Corinne, Fellous, Marc, ProdInra, Migration, Unité de biologie cellulaire et moléculaire, Institut National de la Recherche Agronomique (INRA), and Unité de recherche Génétique Biochimique et Cytogénétique (LGBC)

Subjects
[SDV.SA]Life Sciences [q-bio]/Agricultural sciences, [SDV.SA] Life Sciences [q-bio]/Agricultural sciences
Abstract

3 tables 3 graph.; National audience

Published
1998

132. Genetic mapping of the polled/intersex locus (PIS) in goats

Author

CRIBIU, E.P., Vaiman, Daniel, Pailhoux, Eric, Chaffaux, Stéphane, Cotinot, Corinne, Elsen, Jean Michel, Manfredi, Eduardo, Oustry, Anne, Darré, Roland, Fellous, Marc, Grosclaude, F., ProdInra, Migration, Unité de recherche Génétique Biochimique et Cytogénétique (LGBC), Institut National de la Recherche Agronomique (INRA), Unité de biologie cellulaire et moléculaire, Station d'Amélioration Génétique des Animaux (SAGA), Cytogénétique des Populations Animales (CPA), Institut National de la Recherche Agronomique (INRA)-Ecole Nationale Vétérinaire de Toulouse (ENVT), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National Polytechnique (Toulouse) (Toulouse INP), and Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées

Subjects
[SDV] Life Sciences [q-bio], [SDV.GEN]Life Sciences [q-bio]/Genetics, [SDV]Life Sciences [q-bio], [SDV.GEN] Life Sciences [q-bio]/Genetics, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
1996

133. Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure

Author

Caburet, Sandrine, primary, Zavadakova, Petra, additional, Ben-Neriah, Ziva, additional, Bouhali, Kamal, additional, Dipietromaria, Aurélie, additional, Charon, Céline, additional, Besse, Céline, additional, Laissue, Paul, additional, Chalifa-Caspi, Vered, additional, Christin-Maitre, Sophie, additional, Vaiman, Daniel, additional, Levi, Giovanni, additional, Veitia, Reiner A., additional, and Fellous, Marc, additional

Published
2012
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134. Physiological and genetical study of polled/intersex goats. Genetic mapping of the chromosomal region involved

Author

CRIBIU, E.P., Vaiman, Daniel, Pailhoux, Eric, Chaffaux, Stéphane, Cotinot, Corinne, Elsen, Jean Michel, Manfredi, Eduardo, Fellous, Marc, Grosclaude, F., Unité de recherche Génétique Biochimique et Cytogénétique (LGBC), Institut National de la Recherche Agronomique (INRA), Unité de biologie cellulaire et moléculaire, Cytogénétique des Populations Animales (CPA), Institut National de la Recherche Agronomique (INRA)-Ecole Nationale Vétérinaire de Toulouse (ENVT), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées, Station d'Amélioration Génétique des Animaux (SAGA), and ProdInra, Migration

Subjects
[SDV] Life Sciences [q-bio], [SDV]Life Sciences [q-bio], ComputingMilieux_MISCELLANEOUS
Abstract

National audience

Published
1995

135. Distinct domains of the protein tyrosine kinase tyk2 required for binding of interferon-a/b and for signal transduction

Author

Velazquez, Laura, Mogensen, Knud Erik, Fellous, Marc, Uzé, Gilles, Pellegrini, Sandra, Expression des gènes du complexe majeur d'histocompatibilité, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), and Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)

Subjects
[SDV.MHEP.HEM]Life Sciences [q-bio]/Human health and pathology/Hematology, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
1995

136. Analyse moléculaire de chèvres 60, XX pseudohermaphrodite sans corne pour la présence de gènes SRY et ZFY

Author

Pailhoux, Eric, CRIBIU, E.P., Chaffaux, Stéphane, Darré, Roland, Fellous, Marc, Cotinot, Corinne, ProdInra, Migration, Unité de biologie cellulaire et moléculaire, Institut National de la Recherche Agronomique (INRA), Unité de recherche Génétique Biochimique et Cytogénétique (LGBC), Cytogénétique des Populations Animales (CPA), Institut National de la Recherche Agronomique (INRA)-Ecole Nationale Vétérinaire de Toulouse (ENVT), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National Polytechnique (Toulouse) (Toulouse INP), and Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées

Subjects
[SDV] Life Sciences [q-bio], [SDV]Life Sciences [q-bio], ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
1994

137. Genetic male infertility and mutation of CATSPER ion channels

Author

Hildebrand, Michael S, primary, Avenarius, Matthew R, additional, Fellous, Marc, additional, Zhang, Yuzhou, additional, Meyer, Nicole C, additional, Auer, Jana, additional, Serres, Catherine, additional, Kahrizi, Kimia, additional, Najmabadi, Hossein, additional, Beckmann, Jacques S, additional, and Smith, Richard J H, additional

Published
2010
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138. Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)

Author

Benayoun, Bérénice A., primary, Caburet, Sandrine, additional, Dipietromaria, Aurélie, additional, Georges, Adrien, additional, D'Haene, Barbara, additional, Pandaranayaka, P. J. Eswari, additional, L'Hôte, David, additional, Todeschini, Anne-Laure, additional, Krishnaswamy, Sankaran, additional, Fellous, Marc, additional, De Baere, Elfride, additional, and Veitia, Reiner A., additional

Published
2010
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140. Sex determination : genetic control

Author

Cotinot, Corinne, Mc Elreavey, K., Fellous, Marc, ProdInra, Migration, C. Thibault (Editeur), M.C. Levasseur (Editeur), R.H.F. Hunter (Editeur), Unité de biologie cellulaire et moléculaire, and Institut National de la Recherche Agronomique (INRA)

Subjects
[SDV] Life Sciences [q-bio], [SDV]Life Sciences [q-bio]
Abstract

chap. 12; International audience

Published
1993

142. Identification of Quantitative Trait Loci responsible for embryonic lethality in mice assessed by ultrasonography

Author

Laissue, Paul, primary, Burgio, Gaetan, additional, l'Hote, David, additional, Renault, Gilles, additional, Marchiol-Fournigault, Carmen, additional, Fradelizi, Didier, additional, Fellous, Marc, additional, Serres, Catherine, additional, Montagutelli, Xavier, additional, Monget, Philippe, additional, and Vaiman, Daniel, additional

Published
2009
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144. Identification of 34 novel and 56 knownFOXL2mutations in patients with blepharophimosis syndrome

Author

Beysen, Diane, primary, De Jaegere, Sarah, additional, Amor, David, additional, Bouchard, Philippe, additional, Christin-Maitre, Sophie, additional, Fellous, Marc, additional, Touraine, Philippe, additional, Grix, Arthur W., additional, Hennekam, Raoul, additional, Meire, Françoise, additional, Oyen, Nina, additional, Wilson, Louise C., additional, Barel, Dalit, additional, Clayton-Smith, Jill, additional, de Ravel, Thomy, additional, Decock, Christian, additional, Delbeke, Patricia, additional, Ensenauer, Regina, additional, Ebinger, Friedrich, additional, Gillessen-Kaesbach, Gabriele, additional, Hendriks, Yvonne, additional, Kimonis, Virginia, additional, Laframboise, Rachel, additional, Laissue, Paul, additional, Leppig, Kathleen, additional, Leroy, Bart P., additional, Miller, David T., additional, Mowat, David, additional, Neumann, Luitgard, additional, Plomp, Astrid, additional, Van Regemorter, Nicole, additional, Wieczorek, Dagmar, additional, Veitia, Reiner A., additional, De Paepe, Anne, additional, and De Baere, Elfride, additional

Published
2008
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147. La determination du sexe dans l'espece humaine

Author

Richaud, F., McElreavey, K., Vilain, E., Abbas, N., Cotinot, Corinne, Boucekkine, C., Fellous, Marc, Unité de biologie cellulaire et moléculaire, and Institut National de la Recherche Agronomique (INRA)

Subjects
[SDV]Life Sciences [q-bio], ComputingMilieux_MISCELLANEOUS
Abstract

National audience

Published
1992

150. Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure

Author

Laissue, Paul, primary, Christin-Maitre, Sophie, additional, Touraine, Philippe, additional, Kuttenn, Frederique, additional, Ritvos, Olli, additional, Aittomaki, Kristiina, additional, Bourcigaux, Nathalie, additional, Jacquesson, Laetitia, additional, Bouchard, Philippe, additional, Frydman, Rene, additional, Dewailly, Didier, additional, Reyss, Anne-Céline, additional, Jeffery, Luke, additional, Bachelot, Anne, additional, Massin, Nathalie, additional, Fellous, Marc, additional, and Veitia, Reiner A, additional

Published
2006
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