Found: 8
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The RET51/FKBP52 complex and its involvement in Parkinson disease.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 14, p. 2804, doi. 10.1093/hmg/ddq181
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- Article
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients.
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- EMBO Molecular Medicine, 2014, v. 6, n. 12, p. 1639, doi. 10.15252/emmm.201404829
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- Article
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients.
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- EMBO Molecular Medicine, 2014, v. 6, n. 6, p. 795, doi. 10.1002/emmm.201303235
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- Article
Transcriptional regulation of TLX2 and impaired intestinal innervation: possible role of the PHOX2A and PHOX2B genes.
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- European Journal of Human Genetics, 2007, v. 15, n. 8, p. 848, doi. 10.1038/sj.ejhg.5201852
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- Article
The <i>KIT</i> Gene Is Associated with the <i>English Spotting</i> Coat Color Locus and Congenital Megacolon in Checkered Giant Rabbits (<i>Oryctolagus cuniculus</i>).
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0093750
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- Article
The Tyrosine Kinase Receptor RET Interacts in Vivo with Aryl Hydrocarbon Receptor-Interacting Protein to Alter Survivin Availability.
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- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 7, p. 2571, doi. 10.1210/jc.2008-1980
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- Article
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration.
- Published in:
- Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0164-1
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- Article
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma.
- Published in:
- International Journal of Cancer, 2014, v. 134, n. 9, p. 2098, doi. 10.1002/ijc.28543
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- Article