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Frank J Kaiser

Showing results (11-20 of 101) with videos related to

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Human Molecular Genetics|May 10, 2017
Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expressionRonja Hollstein, Benedikt Reiz, Lucas Kötter, et al.
Nucleic Acids Research|October 16, 2008
The Cohesin loading factor NIPBL recruits histone deacetylases to mediate local chromatin modificationsPhilipp Jahnke, Weizhen Xu, Manuela Wülling, et al.
Developmental Biology|April 25, 2009
Trps1, a regulator of chondrocyte proliferation and differentiation, interacts with the activator form of Gli3Manuela Wuelling, Frank J Kaiser, Laetitia A Buelens, et al.
American Journal of Medical Genetics. Part A|May 7, 2014
Exome sequencing identifies compound heterozygous mutations in C12orf57 in two siblings with severe intellectual disability, hypoplasia of the corpus callosum, chorioretinal coloboma, and intractable seizuresKonrad Platzer, Irina Hüning, Carolin Obieglo, et al.
Plos One|September 7, 2012
A novel MCPH1 isoform complements the defective chromosome condensation of human MCPH1-deficient cellsIoannis Gavvovidis, Isabell Rost, Marc Trimborn, et al.
Journal of Molecular Neuroscience : MN|March 17, 2017
In-depth Characterization of the Homodimerization Domain of the Transcription Factor THAP1 and Dystonia-Causing Mutations ThereinAlev Richter, Ronja Hollstein, Eva Hebert, et al.
Human Mutation|October 10, 2018
In vitro functional characterization of the novel DHH mutations p.(Asn337Lysfs*24) and p.(Glu212Lys) associated with gonadal dysgenesisAsma Tajouri, Maher Kharrat, Syrine Hizem, et al.
Human Molecular Genetics|May 23, 2003
Nuclear interaction of the dynein light chain LC8a with the TRPS1 transcription factor suppresses the transcriptional repression activity of TRPS1Frank J Kaiser, Kamiab Tavassoli, Gert-Jan Van den Bemd, et al.
Clinical Genetics|November 14, 2019
Chromatinopathies: A focus on Cornelia de Lange syndromeLaura Avagliano, Ilaria Parenti, Paolo Grazioli, et al.
JAMA Neurology|July 9, 2014
Woman with x-linked recessive dystonia-parkinsonism: clue to the epidemiology of parkinsonism in Filipino women?Aloysius Domingo, Lillian V Lee, Norbert Brüggemann, et al.
Pageof 11

Showing results (11-20 of 101) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|May 10, 2017
Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expressionRonja Hollstein, Benedikt Reiz, Lucas Kötter, et al.
Nucleic Acids Research|October 16, 2008
The Cohesin loading factor NIPBL recruits histone deacetylases to mediate local chromatin modificationsPhilipp Jahnke, Weizhen Xu, Manuela Wülling, et al.
Developmental Biology|April 25, 2009
Trps1, a regulator of chondrocyte proliferation and differentiation, interacts with the activator form of Gli3Manuela Wuelling, Frank J Kaiser, Laetitia A Buelens, et al.
American Journal of Medical Genetics. Part A|May 7, 2014
Exome sequencing identifies compound heterozygous mutations in C12orf57 in two siblings with severe intellectual disability, hypoplasia of the corpus callosum, chorioretinal coloboma, and intractable seizuresKonrad Platzer, Irina Hüning, Carolin Obieglo, et al.
Plos One|September 7, 2012
A novel MCPH1 isoform complements the defective chromosome condensation of human MCPH1-deficient cellsIoannis Gavvovidis, Isabell Rost, Marc Trimborn, et al.
Journal of Molecular Neuroscience : MN|March 17, 2017
In-depth Characterization of the Homodimerization Domain of the Transcription Factor THAP1 and Dystonia-Causing Mutations ThereinAlev Richter, Ronja Hollstein, Eva Hebert, et al.
Human Mutation|October 10, 2018
In vitro functional characterization of the novel DHH mutations p.(Asn337Lysfs*24) and p.(Glu212Lys) associated with gonadal dysgenesisAsma Tajouri, Maher Kharrat, Syrine Hizem, et al.
Human Molecular Genetics|May 23, 2003
Nuclear interaction of the dynein light chain LC8a with the TRPS1 transcription factor suppresses the transcriptional repression activity of TRPS1Frank J Kaiser, Kamiab Tavassoli, Gert-Jan Van den Bemd, et al.
Clinical Genetics|November 14, 2019
Chromatinopathies: A focus on Cornelia de Lange syndromeLaura Avagliano, Ilaria Parenti, Paolo Grazioli, et al.
JAMA Neurology|July 9, 2014
Woman with x-linked recessive dystonia-parkinsonism: clue to the epidemiology of parkinsonism in Filipino women?Aloysius Domingo, Lillian V Lee, Norbert Brüggemann, et al.
Pageof 11