Lysine methyltransferase 2D regulates muscle fiber size and muscle cell differentiation-Reference-Cited by-同舟云学术

Lysine methyltransferase 2D regulates muscle fiber size and muscle cell differentiation

Published:2021-10-06 Issue:11 Volume:35 Page:
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Wright Alec¹,Hall Arielle¹,Daly Tara¹²,Fontelonga Tatiana¹,Potter Sarah³,Schafer Caitlin³,Lindsley Andrew³⁴,Hung Christina¹²,Bodamer Olaf¹²⁵,Gussoni Emanuela¹²⁶^ORCID

Affiliation:

1. Division of Genetics and Genomics Boston Children’s Hospital Boston Massachusetts USA

2. The Roya Kabuki Program Boston Children's Hospital Boston Massachusetts USA

3. Division of Allergy and Immunology Cincinnati Children’s Hospital Cincinnati Ohio USA

4. Amgen Thousand Oaks California USA

5. Division of Genetics and Genomics Broad Institute of MIT and Harvard University Cambridge Massachusetts USA

6. The Stem Cell Program Boston Children’s Hospital Boston Massachusetts USA

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.202100823R

Reference42 articles.

1. Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities

2. Mll3 and Mll4 Facilitate Enhancer RNA Synthesis and Transcription from Promoters Independently of H3K4 Monomethylation

3. Histone H3K4 monomethylation catalyzed by Trr and mammalian COMPASS-like proteins at enhancers is dispensable for development and viability

4. An essential role for UTX in resolution and activation of bivalent promoters

5. UTX-guided neural crest function underlies craniofacial features of Kabuki syndrome

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1. A non-invasive mouse model that recapitulates disuse-induced muscle atrophy in immobilized patients;Scientific Reports;2023-12-14

2. Lysine methylation signaling in skeletal muscle biology: from myogenesis to clinical insights;Biochemical Journal;2023-12-06

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4. Multidisciplinary clinical and translational approach for optimizing management for complex and rare conditions using Kabuki syndrome as example;Rare;2023

5. From Genotype to Phenotype—A Review of Kabuki Syndrome;Genes;2022-09-29