Found: 15
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Generation of mesothelial progenitor‐like cells from mouse‐induced pluripotent stem cells.
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- FEBS Letters, 2019, v. 593, n. 4, p. 386, doi. 10.1002/1873-3468.13325
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- Article
LPCAT3/LPLAT12 deficiency in the liver ameliorates acetaminophen‐induced acute liver injury.
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- FASEB Journal, 2024, v. 38, n. 1, p. 1, doi. 10.1096/fj.202301744R
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- Article
Role of HCN4 channel in preventing ventricular arrhythmia.
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- Journal of Human Genetics, 2009, v. 54, n. 2, p. 115, doi. 10.1038/jhg.2008.16
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- Article
Cardiac Complications Caused by Respiratory Syncytial Virus Infection: Questionnaire Survey and a Literature Review.
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- Global Pediatric Health, 2021, p. 1, doi. 10.1177/2333794X211044114
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- Article
Cell-based therapy for preventing postoperative adhesion and promoting regeneration after hepatectomy.
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- Journal of Hepato -- Biliary -- Pancreatic Sciences, 2015, v. 22, n. 7, p. 524, doi. 10.1002/jhbp.247
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- Article
A structural constraint for functional interaction between N-terminal and C-terminal domains in simian immunodeficiency virus capsid proteins.
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- Retrovirology, 2010, v. 7, p. 90, doi. 10.1186/1742-4690-7-90
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- Article
Pediatric hypertrophic cardiomyopathy caused by a novel TNNI3 variant.
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- Human Genome Variation, 2024, v. 11, n. 1, p. 1, doi. 10.1038/s41439-024-00272-1
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- Article
Pathogenic variant of RBM20 in a multiplex family with hypertrophic cardiomyopathy.
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- Human Genome Variation, 2022, v. 9, n. 1, p. 1, doi. 10.1038/s41439-022-00183-z
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- Article
A Case of Primary Ciliary Dyskinesia Caused by a Mutation in OFD1, Which Was Diagnosed Owing to Clostridium difficile Infection.
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- Pediatric Reports, 2021, v. 13, n. 2, p. 241, doi. 10.3390/pediatric13020033
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- Article
Case report: Rare heterozygous variant in the NR5A1 gene causing 46,XY complete gonadal dysgenesis with a non-communicating rudimentary uterus.
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- Frontiers in Medicine, 2024, p. 1, doi. 10.3389/fmed.2024.1441990
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- Article
Lipidomic Analyses Reveal Specific Alterations of Phosphatidylcholine in Dystrophic Mdx Muscle.
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- Frontiers in Physiology, 2022, v. 12, p. 1, doi. 10.3389/fphys.2021.698166
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- Article
Late-onset Hailey-Hailey disease with a novel frame-shift variant in the ATP2C1 gene.
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- Journal of Cutaneous Immunology & Allergy, 2024, p. 1, doi. 10.3389/jcia.2024.13246
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- Article
Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy.
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- Cardiovascular Research, 2009, v. 83, n. 1, p. 80, doi. 10.1093/cvr/cvp119
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- Article
Clock mechanisms for seasonal adaptation: Morning and evening oscillators in the suprachiasmatic nucleus.
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- Sleep & Biological Rhythms, 2008, v. 6, n. 2, p. 84, doi. 10.1111/j.1479-8425.2008.00347.x
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- Article
Truncated KCNQ1 mutant, A178fs/105, forms hetero-multimer channel with wild-type causing a dominant-negative suppression due to trafficking defect
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- FEBS Letters, 2004, v. 574, n. 1-3, p. 145, doi. 10.1016/j.febslet.2004.08.018
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- Article