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A Rappold

Showing results (71-80 of 160) with videos related to

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Human Molecular Genetics|September 15, 1999
Transposition of SRY into the ancestral pseudoautosomal region creates a new pseudoautosomal boundary in a progenitor of simian primatesB Gläser, D Myrtek, Y Rumpler, et al.
Frontiers in Endocrinology|May 4, 2026
Linking shox/shox2 deficiency with fgfr3 gain-of-function and natriuretic peptidesSandra Hoffmann, Sabrina Diebold, Ralph Roeth, et al.
Journal of Medical Genetics|August 3, 2000
Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsyB C Gohlke, K Haug, M Fukami, et al.
Human Genetics|January 1, 1984
Sex chromosome positions in human interphase nuclei as studied by in situ hybridization with chromosome specific DNA probesG A Rappold, T Cremer, H D Hager, et al.
The Journal of Biological Chemistry|September 10, 2003
Transcriptional and translational regulation of the Leri-Weill and Turner syndrome homeobox gene SHOXRudiger J Blaschke, Christine Töpfer, Antonio Marchini, et al.
Frontiers in Molecular Neuroscience|October 16, 2018
Sex Hormones Regulate <i>SHANK</i> ExpressionSimone Berkel, Ahmed Eltokhi, Henning Fröhlich, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 19, 2013
Tbx4 interacts with the short stature homeobox gene Shox2 in limb developmentAnne Glaser, Ripla Arora, Sandra Hoffmann, et al.
Stem Cell Research|December 17, 2017
Murine transgenic embryonic stem cell lines for the investigation of sinoatrial node-related molecular pathwaysStefanie Schmitteckert, Anne Griesbeck, Simon Sumer, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2022
Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndromeJing Wang, Henning Fröhlich, Felipe Bodaleo Torres, et al.
American Journal of Medical Genetics|May 9, 2001
Cytogenetic and molecular characterization of two isodicentric Y chromosomesP Stankiewicz, Z Hélias-Rodzewicz, K Jakubów-Durska, et al.
Pageof 16

Showing results (71-80 of 160) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|September 15, 1999
Transposition of SRY into the ancestral pseudoautosomal region creates a new pseudoautosomal boundary in a progenitor of simian primatesB Gläser, D Myrtek, Y Rumpler, et al.
Frontiers in Endocrinology|May 4, 2026
Linking shox/shox2 deficiency with fgfr3 gain-of-function and natriuretic peptidesSandra Hoffmann, Sabrina Diebold, Ralph Roeth, et al.
Journal of Medical Genetics|August 3, 2000
Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsyB C Gohlke, K Haug, M Fukami, et al.
Human Genetics|January 1, 1984
Sex chromosome positions in human interphase nuclei as studied by in situ hybridization with chromosome specific DNA probesG A Rappold, T Cremer, H D Hager, et al.
The Journal of Biological Chemistry|September 10, 2003
Transcriptional and translational regulation of the Leri-Weill and Turner syndrome homeobox gene SHOXRudiger J Blaschke, Christine Töpfer, Antonio Marchini, et al.
Frontiers in Molecular Neuroscience|October 16, 2018
Sex Hormones Regulate <i>SHANK</i> ExpressionSimone Berkel, Ahmed Eltokhi, Henning Fröhlich, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 19, 2013
Tbx4 interacts with the short stature homeobox gene Shox2 in limb developmentAnne Glaser, Ripla Arora, Sandra Hoffmann, et al.
Stem Cell Research|December 17, 2017
Murine transgenic embryonic stem cell lines for the investigation of sinoatrial node-related molecular pathwaysStefanie Schmitteckert, Anne Griesbeck, Simon Sumer, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2022
Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndromeJing Wang, Henning Fröhlich, Felipe Bodaleo Torres, et al.
American Journal of Medical Genetics|May 9, 2001
Cytogenetic and molecular characterization of two isodicentric Y chromosomesP Stankiewicz, Z Hélias-Rodzewicz, K Jakubów-Durska, et al.
Pageof 16