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Molecular and Cellular Biology
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May 5, 2010
Corepressor-directed preacetylation of histone H3 in promoter chromatin primes rapid transcriptional switching of cell-type-specific genes in yeast
Alec M Desimone, Jeffrey D Laney
Disease Models & Mechanisms
|
November 11, 2020
Cellular and animal models for facioscapulohumeral muscular dystrophy
Alec M DeSimone, Justin Cohen, Monkol Lek, et al.
Science Advances
|
December 18, 2019
Identification of the hyaluronic acid pathway as a therapeutic target for facioscapulohumeral muscular dystrophy
Alec M DeSimone, John Leszyk, Kathryn Wagner, et al.
Comprehensive Physiology
|
September 16, 2017
Facioscapulohumeral Muscular Dystrophy
Alec M DeSimone, Anna Pakula, Angela Lek, et al.
Trends in Genetics : TIG
|
July 31, 2022
Neuromuscular disorders: finding the missing genetic diagnoses
Katherine E Koczwara, Nicole J Lake, Alec M DeSimone, et al.
Nature Structural & Molecular Biology
|
June 19, 2012
Large-scale mapping of branchpoints in human pre-mRNA transcripts in vivo
Allison J Taggart, Alec M DeSimone, Janice S Shih, et al.
Genome Research
|
April 30, 2011
Combinatorial binding of transcription factors in the pluripotency control regions of the genome
Luciana Ferraris, Allan P Stewart, Jinsuk Kang, et al.
Cell Death & Disease
|
November 16, 2023
Flavones provide resistance to DUX4-induced toxicity via an mTor-independent mechanism
Justin Cohen, Shushu Huang, Katherine E Koczwara, et al.
Science Translational Medicine
|
March 28, 2020
Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy
Angela Lek, Yuanfan Zhang, Keryn G Woodman, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Molecular and Cellular Biology
|
May 5, 2010
Corepressor-directed preacetylation of histone H3 in promoter chromatin primes rapid transcriptional switching of cell-type-specific genes in yeast
Alec M Desimone, Jeffrey D Laney
Disease Models & Mechanisms
|
November 11, 2020
Cellular and animal models for facioscapulohumeral muscular dystrophy
Alec M DeSimone, Justin Cohen, Monkol Lek, et al.
Science Advances
|
December 18, 2019
Identification of the hyaluronic acid pathway as a therapeutic target for facioscapulohumeral muscular dystrophy
Alec M DeSimone, John Leszyk, Kathryn Wagner, et al.
Comprehensive Physiology
|
September 16, 2017
Facioscapulohumeral Muscular Dystrophy
Alec M DeSimone, Anna Pakula, Angela Lek, et al.
Trends in Genetics : TIG
|
July 31, 2022
Neuromuscular disorders: finding the missing genetic diagnoses
Katherine E Koczwara, Nicole J Lake, Alec M DeSimone, et al.
Nature Structural & Molecular Biology
|
June 19, 2012
Large-scale mapping of branchpoints in human pre-mRNA transcripts in vivo
Allison J Taggart, Alec M DeSimone, Janice S Shih, et al.
Genome Research
|
April 30, 2011
Combinatorial binding of transcription factors in the pluripotency control regions of the genome
Luciana Ferraris, Allan P Stewart, Jinsuk Kang, et al.
Cell Death & Disease
|
November 16, 2023
Flavones provide resistance to DUX4-induced toxicity via an mTor-independent mechanism
Justin Cohen, Shushu Huang, Katherine E Koczwara, et al.
Science Translational Medicine
|
March 28, 2020
Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy
Angela Lek, Yuanfan Zhang, Keryn G Woodman, et al.
Page
of 1