Works matching IS 09646906 AND DT 2021 AND VI 30 AND IP 21
Results: 12
Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1996, doi. 10.1093/hmg/ddab171
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- Article
Coordinated pyruvate kinase activity is crucial for metabolic adaptation and cell survival during mitochondrial dysfunction.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 2012, doi. 10.1093/hmg/ddab168
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- Article
Ten-eleven translocation 2 modulates allergic inflammation by 5-hydroxymethylcytosine remodeling of immunologic pathways.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1985, doi. 10.1093/hmg/ddab167
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- Article
Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormalities of the flagella.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1977, doi. 10.1093/hmg/ddab165
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- Article
Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1941, doi. 10.1093/hmg/ddab163
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- Article
Disulfide bond formation in microtubule-associated tau protein promotes tau accumulation and toxicity in vivo.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1955, doi. 10.1093/hmg/ddab162
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- Article
Genetic and in utero environmental contributions to DNA methylation variation in placenta.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1968, doi. 10.1093/hmg/ddab161
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- Article
Rheumatoid arthritis and osteoporosis: shared genetic effect, pleiotropy and causality.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1932, doi. 10.1093/hmg/ddab158
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- Article
Transcript isoforms of Reep6 have distinct functions in the retina.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1907, doi. 10.1093/hmg/ddab157
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- Article
Assessing the impact of alcohol consumption on the genetic contribution to mean corpuscular volume.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 2040, doi. 10.1093/hmg/ddab147
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- Article
novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1919, doi. 10.1093/hmg/ddab144
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- Article
Genome-wide association study of cardiac troponin I in the general population.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 2027, doi. 10.1093/hmg/ddab124
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- Article