Works matching IS 09646906 AND DT 2018 AND VI 27 AND IP 10
Results: 14
Epigenome-wide association in adipose tissue from the METSIM cohort.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1830, doi. 10.1093/hmg/ddy093
- By:
- Publication type:
- Article
Leveraging lung tissue transcriptome to uncover candidate causal genes in COPD genetic associations.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1819, doi. 10.1093/hmg/ddy091
- By:
- Publication type:
- Article
A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relationship to chronic lymphocytic leukemia.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1809, doi. 10.1093/hmg/ddy094
- By:
- Publication type:
- Article
The TMEM127 human tumor suppressor is a component of the mTORC1 lysosomal nutrient-sensing complex.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1794, doi. 10.1093/hmg/ddy095
- By:
- Publication type:
- Article
Heteropolymerization of α-1-antitrypsin mutants in cell models mimicking heterozygosity.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1785, doi. 10.1093/hmg/ddy090
- By:
- Publication type:
- Article
Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1772, doi. 10.1093/hmg/ddy086
- By:
- Publication type:
- Article
Increased expression of microRNA-15a and microRNA-15b in skeletal muscle from adult offspring of women with diabetes in pregnancy.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1763, doi. 10.1093/hmg/ddy085
- By:
- Publication type:
- Article
Expression of C9orf72-related dipeptides impairs motor function in a vertebrate model.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1754, doi. 10.1093/hmg/ddy083
- By:
- Publication type:
- Article
Defective mitochondrial protease LonP1 can cause classical mitochondrial disease.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1743, doi. 10.1093/hmg/ddy080
- By:
- Publication type:
- Article
Secondary BH4 deficiency links protein homeostasis to regulation of phenylalanine metabolism.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1732, doi. 10.1093/hmg/ddy079
- By:
- Publication type:
- Article
Loss of CLN7 results in depletion of soluble lysosomal proteins and impaired mTOR reactivation.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1711, doi. 10.1093/hmg/ddy076
- By:
- Publication type:
- Article
Modulation of β-glucocerebrosidase increases α-synuclein secretion and exosome release in mouse models of Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1696, doi. 10.1093/hmg/ddy075
- By:
- Publication type:
- Article
PITX2 deficiency and associated human disease: insights from the zebrafish model.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1675, doi. 10.1093/hmg/ddy074
- By:
- Publication type:
- Article
A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1723, doi. 10.1093/hmg/ddy077
- By:
- Publication type:
- Article