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M Fellous

Showing results (221-230 of 246) with videos related to

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Immunogenetics|January 1, 1996
The RAG cell line defines a new complementation group of MHC class II deficiencyA Lennon, C Ottone, A Peijnenburg, et al.
Journal of Medical Genetics|May 12, 2009
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2P Laissue, B Lakhal, B A Benayoun, et al.
Journal of Medical Genetics|December 10, 2002
Evolution and expression of FOXL2J Cocquet, E Pailhoux, F Jaubert, et al.
Genomics|April 15, 1997
Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility geneE Seboun, S Barbaux, T Bourgeron, et al.
Molecular Psychiatry|February 13, 2002
Y chromosome haplogroups in autistic subjectsS Jamain, H Quach, L Quintana-Murci, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 21, 2001
Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHC class II deficiencyA M Lennon-Duménil, M R Barbouche, J Vedrenne, et al.
Kidney International|May 3, 2000
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosisE Denamur, N Bocquet, V Baudouin, et al.
Genomics|February 26, 1999
High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS): the human homologue is contained in a human YAC from HSA3q23D Vaiman, L Schibler, A Oustry-Vaiman, et al.
Human Genetics|May 1, 1997
Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotypeR Veitia, A Ion, S Barbaux, et al.
The Journal of Experimental Zoology|December 19, 2001
Contribution of domestic animals to the identification of new genes involved in sex determinationE Pailhoux, B Vigier, D Vaiman, et al.
Pageof 25

Showing results (221-230 of 246) with videos related to

Sort By:
Pageof 25
Immunogenetics|January 1, 1996
The RAG cell line defines a new complementation group of MHC class II deficiencyA Lennon, C Ottone, A Peijnenburg, et al.
Journal of Medical Genetics|May 12, 2009
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2P Laissue, B Lakhal, B A Benayoun, et al.
Journal of Medical Genetics|December 10, 2002
Evolution and expression of FOXL2J Cocquet, E Pailhoux, F Jaubert, et al.
Genomics|April 15, 1997
Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility geneE Seboun, S Barbaux, T Bourgeron, et al.
Molecular Psychiatry|February 13, 2002
Y chromosome haplogroups in autistic subjectsS Jamain, H Quach, L Quintana-Murci, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 21, 2001
Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHC class II deficiencyA M Lennon-Duménil, M R Barbouche, J Vedrenne, et al.
Kidney International|May 3, 2000
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosisE Denamur, N Bocquet, V Baudouin, et al.
Genomics|February 26, 1999
High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS): the human homologue is contained in a human YAC from HSA3q23D Vaiman, L Schibler, A Oustry-Vaiman, et al.
Human Genetics|May 1, 1997
Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotypeR Veitia, A Ion, S Barbaux, et al.
The Journal of Experimental Zoology|December 19, 2001
Contribution of domestic animals to the identification of new genes involved in sex determinationE Pailhoux, B Vigier, D Vaiman, et al.
Pageof 25