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Gerd Scherer

Showing results (11-20 of 44) with videos related to

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Human Genetics|April 5, 2005
A homozygous nonsense mutation in SOX9 in the dominant disorder campomelic dysplasia: a case of mitotic gene conversionRamona Pop, Michael V Zaragoza, Mara Gaudette, et al.
Reproductive Biology and Endocrinology : RB&E|December 25, 2010
Profiling spermatogenic failure in adult testes bearing Sox9-deficient Sertoli cells identifies genes involved in feminization, inflammation and stressAurélie Lardenois, Frédéric Chalmel, Francisco Barrionuevo, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 1, 2017
Four Novel NR5A1 Mutations in 46,XY Gonadal Dysgenesis Patients Including Frameshift Mutations with Altered Subcellular SF-1 LocalizationJan Rehkämper, Ann-Christin Tewes, Judit Horvath, et al.
Human Molecular Genetics|June 5, 2003
Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasiaElisabeth Sock, Roberta A Pagon, Kathelijn Keymolen, et al.
Genesis (New York, N.Y. : 2000)|January 13, 2005
Normal lung development and function after Sox9 inactivation in the respiratory epitheliumAnne-Karina T Perl, Ralf Kist, Zhengyuan Shan, et al.
Prenatal Diagnosis|March 3, 2009
Diagnosis of true hermaphroditism in a fetus with acampomelic campomelic dysplasiaMélanie Beaulieu Bergeron, Emmanuelle Lemyre, Françoise Rypens, et al.
Molecules (Basel, Switzerland)|July 24, 2021
Double Proton Tautomerism via Intra- or Intermolecular Pathways? The Case of Tetramethyl Reductic Acid Studied by Dynamic NMR: Hydrogen Bond Association, Solvent and Kinetic H/D Isotope EffectsHans-Heinrich Limbach, Simone Baumgärtner, Roland Franke, et al.
Molecular Genetics and Metabolism|October 6, 2012
Tyrosinemia Type III detected via neonatal screening: management and outcomeEvelyne Heylen, Gerd Scherer, Marie-Françoise Vincent, et al.
The International Journal of Developmental Biology|April 17, 2008
Loss of Sox9 function results in defective chondrocyte differentiation of mouse embryonic stem cells in vitroGunnar Hargus, Ralf Kist, Jan Kramer, et al.
Indian Journal of Pediatrics|April 9, 2013
Acampomelic form of campomelic dysplasia with SOX9 missense mutationHariharan Gopakumar, Andrea Superti-Furga, Sheila Unger, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Human Genetics|April 5, 2005
A homozygous nonsense mutation in SOX9 in the dominant disorder campomelic dysplasia: a case of mitotic gene conversionRamona Pop, Michael V Zaragoza, Mara Gaudette, et al.
Reproductive Biology and Endocrinology : RB&E|December 25, 2010
Profiling spermatogenic failure in adult testes bearing Sox9-deficient Sertoli cells identifies genes involved in feminization, inflammation and stressAurélie Lardenois, Frédéric Chalmel, Francisco Barrionuevo, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 1, 2017
Four Novel NR5A1 Mutations in 46,XY Gonadal Dysgenesis Patients Including Frameshift Mutations with Altered Subcellular SF-1 LocalizationJan Rehkämper, Ann-Christin Tewes, Judit Horvath, et al.
Human Molecular Genetics|June 5, 2003
Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasiaElisabeth Sock, Roberta A Pagon, Kathelijn Keymolen, et al.
Genesis (New York, N.Y. : 2000)|January 13, 2005
Normal lung development and function after Sox9 inactivation in the respiratory epitheliumAnne-Karina T Perl, Ralf Kist, Zhengyuan Shan, et al.
Prenatal Diagnosis|March 3, 2009
Diagnosis of true hermaphroditism in a fetus with acampomelic campomelic dysplasiaMélanie Beaulieu Bergeron, Emmanuelle Lemyre, Françoise Rypens, et al.
Molecules (Basel, Switzerland)|July 24, 2021
Double Proton Tautomerism via Intra- or Intermolecular Pathways? The Case of Tetramethyl Reductic Acid Studied by Dynamic NMR: Hydrogen Bond Association, Solvent and Kinetic H/D Isotope EffectsHans-Heinrich Limbach, Simone Baumgärtner, Roland Franke, et al.
Molecular Genetics and Metabolism|October 6, 2012
Tyrosinemia Type III detected via neonatal screening: management and outcomeEvelyne Heylen, Gerd Scherer, Marie-Françoise Vincent, et al.
The International Journal of Developmental Biology|April 17, 2008
Loss of Sox9 function results in defective chondrocyte differentiation of mouse embryonic stem cells in vitroGunnar Hargus, Ralf Kist, Jan Kramer, et al.
Indian Journal of Pediatrics|April 9, 2013
Acampomelic form of campomelic dysplasia with SOX9 missense mutationHariharan Gopakumar, Andrea Superti-Furga, Sheila Unger, et al.
Pageof 5