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Judit Balog

Showing results (21-30 of 38) with videos related to

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Journal of Tissue Engineering|May 4, 2026
Fibro-adipogenic progenitors enhance functional and structural properties of human 3D tissue engineered skeletal musclesRoy Augustinus, Lotte A de Ridder, Dongxu Zheng, et al.
Skeletal Muscle|June 8, 2017
SMCHD1 regulates a limited set of gene clusters on autosomal chromosomesAmanda G Mason, Roderick C Slieker, Judit Balog, et al.
Epigenetics|April 9, 2016
Corrigendum. Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4Judit Balog, Peter E Thijssen, Sean Shadle, et al.
Epigenetics|November 18, 2015
Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4Judit Balog, Peter E Thijssen, Sean Shadle, et al.
Journal of Medical Genetics|January 13, 2021
Chromosome 10q-linked FSHD identifies <i>DUX4</i> as principal disease geneRichard J L F Lemmers, Patrick J van der Vliet, Ana Blatnik, et al.
The European Journal of Neuroscience|April 11, 2021
Hippocampal glucocorticoid target genes associated with enhancement of memory consolidationJacobus C Buurstede, Lisa T C M van Weert, Paola Colucci, et al.
Neurology|May 30, 2020
Homozygous nonsense variant in <i>LRIF1</i> associated with facioscapulohumeral muscular dystrophyKohei Hamanaka, Darina Šikrová, Satomi Mitsuhashi, et al.
European Journal of Human Genetics : EJHG|November 23, 2017
Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2Richard Jlf Lemmers, Patrick J van der Vliet, Judit Balog, et al.
Plos Genetics|April 18, 2013
Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHDYvonne D Krom, Peter E Thijssen, Janet M Young, et al.
American Journal of Human Genetics|October 1, 2013
The FSHD2 gene SMCHD1 is a modifier of disease severity in families affected by FSHD1Sabrina Sacconi, Richard J L F Lemmers, Judit Balog, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Journal of Tissue Engineering|May 4, 2026
Fibro-adipogenic progenitors enhance functional and structural properties of human 3D tissue engineered skeletal musclesRoy Augustinus, Lotte A de Ridder, Dongxu Zheng, et al.
Skeletal Muscle|June 8, 2017
SMCHD1 regulates a limited set of gene clusters on autosomal chromosomesAmanda G Mason, Roderick C Slieker, Judit Balog, et al.
Epigenetics|April 9, 2016
Corrigendum. Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4Judit Balog, Peter E Thijssen, Sean Shadle, et al.
Epigenetics|November 18, 2015
Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4Judit Balog, Peter E Thijssen, Sean Shadle, et al.
Journal of Medical Genetics|January 13, 2021
Chromosome 10q-linked FSHD identifies <i>DUX4</i> as principal disease geneRichard J L F Lemmers, Patrick J van der Vliet, Ana Blatnik, et al.
The European Journal of Neuroscience|April 11, 2021
Hippocampal glucocorticoid target genes associated with enhancement of memory consolidationJacobus C Buurstede, Lisa T C M van Weert, Paola Colucci, et al.
Neurology|May 30, 2020
Homozygous nonsense variant in <i>LRIF1</i> associated with facioscapulohumeral muscular dystrophyKohei Hamanaka, Darina Šikrová, Satomi Mitsuhashi, et al.
European Journal of Human Genetics : EJHG|November 23, 2017
Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2Richard Jlf Lemmers, Patrick J van der Vliet, Judit Balog, et al.
Plos Genetics|April 18, 2013
Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHDYvonne D Krom, Peter E Thijssen, Janet M Young, et al.
American Journal of Human Genetics|October 1, 2013
The FSHD2 gene SMCHD1 is a modifier of disease severity in families affected by FSHD1Sabrina Sacconi, Richard J L F Lemmers, Judit Balog, et al.
Pageof 4