Found: 7
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Association between missense variants of uncertain significance in the CHEK2 gene and hereditary breast cancer: a cosegregation and bioinformatics analysis.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2023.1274108
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- Publication type:
- Article
Targeted sequencing of selected functional genes in patients with wild-type transthyretin amyloidosis.
- Published in:
- BMC Research Notes, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13104-023-06491-z
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- Publication type:
- Article
Correction to: Study of Cellular Aging in a Cohort of Patients with Heart Failure.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Study of Cellular Aging in a Cohort of Patients with Heart Failure.
- Published in:
- High Blood Pressure & Cardiovascular Prevention, 2021, v. 28, n. 1, p. 49, doi. 10.1007/s40292-020-00421-x
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- Publication type:
- Article
Multiparametric analysis of anti-proliferative and apoptotic effects of gold nanoprisms on mouse and human primary and transformed cells, biodistribution and toxicity in vivo.
- Published in:
- Particle & Fibre Toxicology, 2017, v. 14, p. 1, doi. 10.1186/s12989-017-0222-4
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- Publication type:
- Article
Characterization of splice variants of the genes encoding human mitochondrial HMG-CoA lyase and HMG-CoA synthase, the main enzymes of the ketogenesis pathway.
- Published in:
- Molecular Biology Reports, 2012, v. 39, n. 4, p. 4777, doi. 10.1007/s11033-011-1270-8
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- Publication type:
- Article
Ten novel HMGCL mutations in 24 patients of different origin with 3-hydroxy-3-methyl-glutaric aciduria.
- Published in:
- Human Mutation, 2009, v. 30, n. 3, p. E520, doi. 10.1002/humu.20966
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- Publication type:
- Article