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Katherina Walz

Showing results (11-20 of 60) with videos related to

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American Journal of Medical Genetics. Part A|May 9, 2019
Arnold-Chiari type 1 malformation in Potocki-Lupski syndromeAlberto Varon, Zachary Whitt, Paige M Kalika, et al.
European Journal of Human Genetics : EJHG|August 11, 2011
Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenesBredford Kerr, Jessica Soto C, Mauricio Saez, et al.
Scientific Reports|June 22, 2026
Losartan shows limited benefit in preclinical models of Geleophysic dysplasiaAlejo A Morales, Vladimir Camarena, LéShon Peart, et al.
Biology|April 28, 2017
Rai1 Haploinsufficiency Is Associated with Social Abnormalities in MiceNalini R Rao, Clemer Abad, Irene C Perez, et al.
Journal of Molecular Medicine (Berlin, Germany)|October 4, 2018
Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientationOscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Human Molecular Genetics|October 2, 2004
Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndromeJiong Yan, Victoria W Keener, Weimin Bi, et al.
Human Molecular Genetics|November 13, 2013
Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memoryLei Cao, Jessica Molina, Clemer Abad, et al.
Human Molecular Genetics|April 1, 2021
Generation and characterization of a P2rx2 V60L mouse model for DFNA41Xiaoya Chen, Clemer Abad, Zheng-Yi Chen, et al.
Journal of Child Neurology|March 29, 2006
Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]Alica M Goldman, Lorraine Potocki, Katherina Walz, et al.
Human Genetics|November 27, 2004
Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndromeWeimin Bi, G Mustafa Saifi, Christine J Shaw, et al.
Pageof 6

Showing results (11-20 of 60) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|May 9, 2019
Arnold-Chiari type 1 malformation in Potocki-Lupski syndromeAlberto Varon, Zachary Whitt, Paige M Kalika, et al.
European Journal of Human Genetics : EJHG|August 11, 2011
Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenesBredford Kerr, Jessica Soto C, Mauricio Saez, et al.
Scientific Reports|June 22, 2026
Losartan shows limited benefit in preclinical models of Geleophysic dysplasiaAlejo A Morales, Vladimir Camarena, LéShon Peart, et al.
Biology|April 28, 2017
Rai1 Haploinsufficiency Is Associated with Social Abnormalities in MiceNalini R Rao, Clemer Abad, Irene C Perez, et al.
Journal of Molecular Medicine (Berlin, Germany)|October 4, 2018
Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientationOscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Human Molecular Genetics|October 2, 2004
Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndromeJiong Yan, Victoria W Keener, Weimin Bi, et al.
Human Molecular Genetics|November 13, 2013
Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memoryLei Cao, Jessica Molina, Clemer Abad, et al.
Human Molecular Genetics|April 1, 2021
Generation and characterization of a P2rx2 V60L mouse model for DFNA41Xiaoya Chen, Clemer Abad, Zheng-Yi Chen, et al.
Journal of Child Neurology|March 29, 2006
Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]Alica M Goldman, Lorraine Potocki, Katherina Walz, et al.
Human Genetics|November 27, 2004
Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndromeWeimin Bi, G Mustafa Saifi, Christine J Shaw, et al.
Pageof 6