RERE deficiency contributes to the development of orofacial clefts in humans and mice.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 7, p. 595, doi. 10.1093/hmg/ddab084
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 2021 AND VI 30 AND IP 7
Results: 8
1
2
Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson–Forssman–Lehmann Syndrome.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 7, p. 575, doi. 10.1093/hmg/ddab081
- By:
- Publication type:
- Article
3
Humanization of a tandem repeat in IG-DMR causes stochastic restoration of paternal imprinting at mouse Dlk1-Dio3 domain.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 7, p. 564, doi. 10.1093/hmg/ddab071
- By:
- Publication type:
- Article
4
Nanopore direct RNA sequencing detects DUX4-activated repeats and isoforms in human muscle cells.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 7, p. 552, doi. 10.1093/hmg/ddab063
- By:
- Publication type:
- Article
5
Combinatorial glucose, nicotinic acid and N-acetylcysteine therapy has synergistic effect in preclinical C. elegans and zebrafish models of mitochondrial complex I disease.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 7, p. 536, doi. 10.1093/hmg/ddab059
- By:
- Publication type:
- Article
6
Single-cell RNA sequencing reveals species-specific time spans of cell cycle transitions in early oogenesis.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 7, p. 525, doi. 10.1093/hmg/ddab048
- By:
- Publication type:
- Article
7
Genome-wide identification of cis DNA methylation quantitative trait loci in three Southeast Asian Populations.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 7, p. 603, doi. 10.1093/hmg/ddab038
- By:
- Publication type:
- Article
8
Fate or coincidence: do COPD and major depression share genetic risk factors?
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 7, p. 619, doi. 10.1093/hmg/ddab068
- By:
- Publication type:
- Article