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J P Hardelin

Showing results (11-20 of 27) with videos related to

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Genomics|September 20, 1995
The human SOX11 gene: cloning, chromosomal assignment and tissue expressionP Jay, C Gozé, C Marsollier, 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.
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.
The Journal of Comparative Neurology|March 11, 1996
Migration of luteinizing hormone-releasing hormone (LHRH) neurons in early human embryosM Schwanzel-Fukuda, K L Crossin, D W Pfaff, et al.
Advances in Nephrology From the Necker Hospital|January 16, 1999
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndromeJ P Hardelin, N Soussi-Yanicostas, J Levilliers, et al.
The Journal of Biological Chemistry|July 13, 2000
Unconventional myosin VIIA is a novel A-kinase-anchoring proteinP Küssel-Andermann, A El-Amraoui, S Safieddine, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 13, 2000
KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathwayT Kharkovets, J P Hardelin, S Safieddine, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1993
Xp22.3 deletions in isolated familial Kallmann's syndromeJ P Hardelin, J Levilliers, J Young, et al.
Human Molecular Genetics|April 1, 1993
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndromeJ P Hardelin, J Levilliers, S Blanchard, et al.
American Journal of Medical Genetics|December 22, 1999
Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutationS Masmoudi, I Charfedine, M Hmani, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Genomics|September 20, 1995
The human SOX11 gene: cloning, chromosomal assignment and tissue expressionP Jay, C Gozé, C Marsollier, 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.
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.
The Journal of Comparative Neurology|March 11, 1996
Migration of luteinizing hormone-releasing hormone (LHRH) neurons in early human embryosM Schwanzel-Fukuda, K L Crossin, D W Pfaff, et al.
Advances in Nephrology From the Necker Hospital|January 16, 1999
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndromeJ P Hardelin, N Soussi-Yanicostas, J Levilliers, et al.
The Journal of Biological Chemistry|July 13, 2000
Unconventional myosin VIIA is a novel A-kinase-anchoring proteinP Küssel-Andermann, A El-Amraoui, S Safieddine, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 13, 2000
KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathwayT Kharkovets, J P Hardelin, S Safieddine, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1993
Xp22.3 deletions in isolated familial Kallmann's syndromeJ P Hardelin, J Levilliers, J Young, et al.
Human Molecular Genetics|April 1, 1993
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndromeJ P Hardelin, J Levilliers, S Blanchard, et al.
American Journal of Medical Genetics|December 22, 1999
Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutationS Masmoudi, I Charfedine, M Hmani, et al.
Pageof 3