Found: 17
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Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy.
- Published in:
- Nature Genetics, 1999, v. 23, n. 2, p. 208, doi. 10.1038/13837
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- Publication type:
- Article
SIRT1 Polymorphisms Associate with Seasonal Weight Variation, Depressive Disorders, and Diastolic Blood Pressure in the General Population.
- Published in:
- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0141001
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- Publication type:
- Article
Genetic Loci Associated with Allergic Sensitization in Lithuanians.
- Published in:
- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0134188
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- Publication type:
- Article
<i>CRY2</i> Genetic Variants Associate with Dysthymia.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0071450
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- Publication type:
- Article
CRY1, CRY2 and PRKCDBP genetic variants in metabolic syndrome.
- Published in:
- Hypertension Research, 2015, v. 38, n. 3, p. 186, doi. 10.1038/hr.2014.157
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- Publication type:
- Article
STK39 variation predicts the ambulatory blood pressure response to losartan in hypertensive men.
- Published in:
- Hypertension Research, 2012, v. 35, n. 1, p. 107, doi. 10.1038/hr.2011.166
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- Publication type:
- Article
Genomics of asthma, allergy and chronic rhinosinusitis: novel concepts and relevance in airway mucosa.
- Published in:
- Clinical & Translational Allergy, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13601-020-00347-6
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- Publication type:
- Article
Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1055, doi. 10.1038/ejhg.2008.60
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- Publication type:
- Article
Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcripts.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 9, p. 744, doi. 10.1038/sj.ejhg.5201242
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- Publication type:
- Article
Generalized glucocorticoid resistance caused by a novel two nucleotide deletion in the hormone-binding domain of the glucocorticoid receptor gene NR3C1.
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- European Journal of Endocrinology, 2013, v. 167, n. 1, p. K9, doi. 10.1530/EJE-12-0532
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- Publication type:
- Article
Renin–Angiotensin System and α-Adducin Gene Polymorphisms and Their Relation to Responses to Antihypertensive Drugs: Results From the GENRES Study.
- Published in:
- American Journal of Hypertension, 2009, v. 22, n. 2, p. 169, doi. 10.1038/ajh.2008.343
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- Publication type:
- Article
Pharmacogenomics of hypertension: a genome‐wide, placebo‐controlled cross‐over study, using four classes of antihypertensive drugs.
- Published in:
- 2015
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- Publication type:
- journal article
Pharmacogenomics of Hypertension: A Genome-Wide, Placebo-Controlled Cross-Over Study, Using Four Classes of Antihypertensive Drugs.
- Published in:
- Journal of the American Heart Association, 2015, v. 4, n. 1, p. 1, doi. 10.1161/JAHA.114.001521
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- Publication type:
- Article
Characterisation of a LINE-1 Insertion in the RP1 Gene by Targeted Adaptive Nanopore Sequencing in a Family with Retinitis Pigmentosa.
- Published in:
- Human Mutation, 2024, v. 2024, p. 1, doi. 10.1155/2024/6580561
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- Publication type:
- Article
Mutation Update: The Spectra of Nebulin Variants and Associated Myopathies.
- Published in:
- Human Mutation, 2014, v. 35, n. 12, p. 1418, doi. 10.1002/humu.22693
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- Publication type:
- Article
Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy.
- Published in:
- Human Mutation, 2006, v. 27, n. 9, p. 946, doi. 10.1002/humu.20370
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- Publication type:
- Article
Heme oxygenase-1 repeat polymorphism in septic acute kidney injury.
- Published in:
- PLoS ONE, 2019, v. 14, n. 5, p. 1, doi. 10.1371/journal.pone.0217291
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- Publication type:
- Article