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Erratum: Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
- Published in:
- 2006
- By:
- Publication type:
- Correction Notice
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
- Published in:
- Nature Genetics, 2006, v. 38, n. 1, p. 93, doi. 10.1038/ng1683
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- Publication type:
- Article
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 120, doi. 10.1038/72769
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- Publication type:
- Article
Cdk1 phosphorylation of Esp1/Separase functions with PP2A and Slk19 to regulate pericentric Cohesin and anaphase onset.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 3, p. 1, doi. 10.1371/journal.pgen.1007029
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- Publication type:
- Article
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 1, p. 105, doi. 10.1038/sj.ejhg.5201920
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- Publication type:
- Article
Tissue‐Engineered Disease Modeling of Lymphangioleiomyomatosis Exposes a Therapeutic Vulnerability to HDAC Inhibition.
- Published in:
- Advanced Science, 2023, v. 10, n. 26, p. 1, doi. 10.1002/advs.202302611
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- Publication type:
- Article
5' flanking variants of resistin are associated with obesity.
- Published in:
- 2002
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- Publication type:
- journal article
Redundant Regulation of Cdk1 Tyrosine Dephosphorylation in Saccharomyces cerevisiae.
- Published in:
- Genetics, 2016, v. 202, n. 3, p. 903, doi. 10.1534/genetics.115.182469
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- Publication type:
- Article
Competition between Heterochromatic Loci Allows the Abundance of the Silencing Protein, Sir4, to Regulate de novo Assembly of Heterochromatin.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 11, p. 1, doi. 10.1371/journal.pgen.1005425
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- Publication type:
- Article
Mutations in the MMAA Gene in Patients With the cblA Disorder of Vitamin B<sub>12</sub> Metabolism.
- Published in:
- Human Mutation, 2005, v. 25, n. 3, p. 317, doi. 10.1002/humu.20149
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- Publication type:
- Article
Mutations in the MMAA gene in patients with the cblA disorder of vitamin B<sub>12</sub> metabolism.
- Published in:
- Human Mutation, 2004, v. 24, n. 6, p. 509, doi. 10.1002/humu.20104
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- Publication type:
- Article
Tah18 transfers electrons to Dre2 in cytosolic iron-sulfur protein biogenesis.
- Published in:
- Nature Chemical Biology, 2010, v. 6, n. 10, p. 758, doi. 10.1038/nchembio.432
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- Publication type:
- Article
Reprogramming progeria fibroblasts re-establishes a normal epigenetic landscape.
- Published in:
- Aging Cell, 2017, v. 16, n. 4, p. 870, doi. 10.1111/acel.12621
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- Publication type:
- Article