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J Levilliers

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Cell|October 1, 1982
Undermethylation at the 5' end of the albumin gene is necessary but not sufficient for albumin production by rat hepatoma cells in cultureM O Ott, L Sperling, D Cassio, et al.
Human Molecular Genetics|December 1, 1994
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalH Chaïb, G Lina-Granade, P Guilford, et al.
Genomics|July 1, 1995
Prevalence and molecular analysis of two hot spots for ectopic recombination leading to XX malenessI Wang, D Weil, J Levilliers, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
The pseudoautosomal region of the human sex chromosomesF Rouyer, M C Simmler, G Vergnaud, et al.
Nature Genetics|January 1, 1994
A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13qP Guilford, S Ben Arab, S Blanchard, et al.
Journal of Cell Science|September 10, 1998
Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific mannerN Soussi-Yanicostas, C Faivre-Sarrailh, J P Hardelin, et al.
Human Genetics|February 1, 1992
Mutational analysis of SRY: nonsense and missense mutations in XY sex reversalJ R Hawkins, A Taylor, P Berta, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocationO Gabriel-Robez, Y Rumpler, C Ratomponirina, et al.
Genomics|January 1, 1993
Characterization and chromosomal assignment of a human cDNA encoding a protein related to the murine 102-kDa cadherin-associated protein (alpha-catenin)J M Claverie, J P Hardelin, R Legouis, et al.
Clinical Endocrinology|February 1, 1995
Hypogonadotrophic hypogonadism with hyposmia, X-linked ichthyosis, and renal malformation syndromeP Martul, J Pineda, J Levilliers, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Cell|October 1, 1982
Undermethylation at the 5' end of the albumin gene is necessary but not sufficient for albumin production by rat hepatoma cells in cultureM O Ott, L Sperling, D Cassio, et al.
Human Molecular Genetics|December 1, 1994
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalH Chaïb, G Lina-Granade, P Guilford, et al.
Genomics|July 1, 1995
Prevalence and molecular analysis of two hot spots for ectopic recombination leading to XX malenessI Wang, D Weil, J Levilliers, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
The pseudoautosomal region of the human sex chromosomesF Rouyer, M C Simmler, G Vergnaud, et al.
Nature Genetics|January 1, 1994
A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13qP Guilford, S Ben Arab, S Blanchard, et al.
Journal of Cell Science|September 10, 1998
Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific mannerN Soussi-Yanicostas, C Faivre-Sarrailh, J P Hardelin, et al.
Human Genetics|February 1, 1992
Mutational analysis of SRY: nonsense and missense mutations in XY sex reversalJ R Hawkins, A Taylor, P Berta, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocationO Gabriel-Robez, Y Rumpler, C Ratomponirina, et al.
Genomics|January 1, 1993
Characterization and chromosomal assignment of a human cDNA encoding a protein related to the murine 102-kDa cadherin-associated protein (alpha-catenin)J M Claverie, J P Hardelin, R Legouis, et al.
Clinical Endocrinology|February 1, 1995
Hypogonadotrophic hypogonadism with hyposmia, X-linked ichthyosis, and renal malformation syndromeP Martul, J Pineda, J Levilliers, et al.
Pageof 5