Works matching IS 09646906 AND DT 2022 AND VI 31 AND IP 22
Results: 12
Embryo cryopreservation leads to sex-specific DNA methylation perturbations in both human and mouse placentas.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3855, doi. 10.1093/hmg/ddac138
- Publication type:
- Article
Protein misfolding and clearance in the pathogenesis of a new infantile onset ataxia caused by mutations in PRDX3.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3897, doi. 10.1093/hmg/ddac146
- Publication type:
- Article
Developmental genome-wide occupancy analysis of bZIP transcription factor NRL uncovers the role of c-Jun in early differentiation of rod photoreceptors in the mammalian retina.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3914, doi. 10.1093/hmg/ddac143
- Publication type:
- Article
Mutant VPS35-D620N induces motor dysfunction and impairs DAT-mediated dopamine recycling pathway.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3886, doi. 10.1093/hmg/ddac142
- Publication type:
- Article
De novo non-synonymous CTR9 variants are associated with motor delay and macrocephaly: human genetic and zebrafish experimental evidence.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3846, doi. 10.1093/hmg/ddac136
- Publication type:
- Article
Cerebellar contribution to threat probability in a SCA6 mouse model.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3807, doi. 10.1093/hmg/ddac135
- Publication type:
- Article
Novel genes and sex differences in COVID-19 severity.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3789, doi. 10.1093/hmg/ddac132
- Publication type:
- Article
critical role of the TB5 domain of fibrillin-1 in endochondral ossification.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3777, doi. 10.1093/hmg/ddac131
- Publication type:
- Article
Mesenchymal stem cell-derived extracellular vesicles alleviate cervical cancer by delivering microRNA-331-3p to reduce LIM zinc finger domain containing 2 methylation in tumor cells.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3829, doi. 10.1093/hmg/ddac130
- Publication type:
- Article
Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3769, doi. 10.1093/hmg/ddac129
- Publication type:
- Article
Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3873, doi. 10.1093/hmg/ddac117
- Publication type:
- Article
Identification of shared loci associated with both Crohn's disease and leprosy in East Asians.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 22, p. 3934, doi. 10.1093/hmg/ddac101
- Publication type:
- Article