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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Ronja Hollstein
American Journal of Medical Genetics. Part A
|
April 4, 2017
Molecular analysis of a novel intragenic deletion in GPC3 in three cousins with Simpson-Golabi-Behmel syndrome
Julia Schmidt, Ronja Hollstein, Frank J Kaiser, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Ronja Hollstein, Nina Ishorst, Annette Lischka, et al.
Cerebellum (London, England)
|
March 3, 2018
A Novel Frameshift CACNA1A Mutation Causing Episodic Ataxia Type 2
Alexander Balck, Sinem Tunc, Johanna Schmitz, et al.
Human Molecular Genetics
|
May 10, 2017
Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expression
Ronja Hollstein, Benedikt Reiz, Lucas Kötter, 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 Therein
Alev Richter, Ronja Hollstein, Eva Hebert, et al.
Scientific Reports
|
February 3, 2022
Allele-specific transcription factor binding in a cellular model of orofacial clefting
Katharina L M Ruff, Ronja Hollstein, Julia Fazaal, et al.
Scientific Reports
|
October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formation
Enrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
Biochimica Et Biophysica Acta
|
August 5, 2014
THAP1, the gene mutated in DYT6 dystonia, autoregulates its own expression
Alev Erogullari, Ronja Hollstein, Philip Seibler, et al.
European Journal of Medical Genetics
|
February 4, 2014
A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression
Katrin Bürk, Frank J Kaiser, Stephanie Tennstedt, et al.
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Search research articles
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Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Ronja Hollstein
American Journal of Medical Genetics. Part A
|
April 4, 2017
Molecular analysis of a novel intragenic deletion in GPC3 in three cousins with Simpson-Golabi-Behmel syndrome
Julia Schmidt, Ronja Hollstein, Frank J Kaiser, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Ronja Hollstein, Nina Ishorst, Annette Lischka, et al.
Cerebellum (London, England)
|
March 3, 2018
A Novel Frameshift CACNA1A Mutation Causing Episodic Ataxia Type 2
Alexander Balck, Sinem Tunc, Johanna Schmitz, et al.
Human Molecular Genetics
|
May 10, 2017
Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expression
Ronja Hollstein, Benedikt Reiz, Lucas Kötter, 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 Therein
Alev Richter, Ronja Hollstein, Eva Hebert, et al.
Scientific Reports
|
February 3, 2022
Allele-specific transcription factor binding in a cellular model of orofacial clefting
Katharina L M Ruff, Ronja Hollstein, Julia Fazaal, et al.
Scientific Reports
|
October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formation
Enrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
Biochimica Et Biophysica Acta
|
August 5, 2014
THAP1, the gene mutated in DYT6 dystonia, autoregulates its own expression
Alev Erogullari, Ronja Hollstein, Philip Seibler, et al.
European Journal of Medical Genetics
|
February 4, 2014
A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression
Katrin Bürk, Frank J Kaiser, Stephanie Tennstedt, et al.
Page
of 2