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Showing results (121-130 of 160) with videos related to

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Neurogastroenterology and Motility|May 12, 2020
Comparative expression profiling in the intestine of patients with Giardia-induced postinfectious functional gastrointestinal disordersCristina Martínez, Felix Lasitschka, Cornelia Thöni, et al.
Current Biology : CB|January 16, 1999
A selective difference between human Y-chromosomal DNA haplotypesM A Jobling, G A Williams, G A Schiebel, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
Genomics|March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)I Wang, B Franco, G B Ferrero, et al.
Human Molecular Genetics|April 6, 2000
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndromeM Clement-Jones, S Schiller, E Rao, et al.
Frontiers in Endocrinology|July 1, 2021
Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary GenesBirgit Weiss, Birgit Eberle, Ralph Roeth, et al.
Molecular Psychiatry|January 7, 2015
Identification and functional characterization of rare SHANK2 variants in schizophreniaS Peykov, S Berkel, M Schoen, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Y Chromosome Mapping 1997. Heidelberg, Germany, April 13-16, 1997P H Vogt, N Affara, P Davey, et al.
American Journal of Human Genetics|July 25, 2000
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationM Fukami, S Kirsch, S Schiller, et al.
The Journal of Biological Chemistry|May 18, 2004
The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytesAntonio Marchini, Tiina Marttila, Anja Winter, et al.
Pageof 16

Showing results (121-130 of 160) with videos related to

Sort By:
Pageof 16
Neurogastroenterology and Motility|May 12, 2020
Comparative expression profiling in the intestine of patients with Giardia-induced postinfectious functional gastrointestinal disordersCristina Martínez, Felix Lasitschka, Cornelia Thöni, et al.
Current Biology : CB|January 16, 1999
A selective difference between human Y-chromosomal DNA haplotypesM A Jobling, G A Williams, G A Schiebel, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
Genomics|March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)I Wang, B Franco, G B Ferrero, et al.
Human Molecular Genetics|April 6, 2000
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndromeM Clement-Jones, S Schiller, E Rao, et al.
Frontiers in Endocrinology|July 1, 2021
Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary GenesBirgit Weiss, Birgit Eberle, Ralph Roeth, et al.
Molecular Psychiatry|January 7, 2015
Identification and functional characterization of rare SHANK2 variants in schizophreniaS Peykov, S Berkel, M Schoen, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Y Chromosome Mapping 1997. Heidelberg, Germany, April 13-16, 1997P H Vogt, N Affara, P Davey, et al.
American Journal of Human Genetics|July 25, 2000
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationM Fukami, S Kirsch, S Schiller, et al.
The Journal of Biological Chemistry|May 18, 2004
The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytesAntonio Marchini, Tiina Marttila, Anja Winter, et al.
Pageof 16