Works matching IS 14345161 AND DT 2011 AND VI 56 AND IP 8
Results: 14
Association studies getting broader: A commentary on A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 550, doi. 10.1038/jhg.2011.70
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Association of interleukin-1β genetic polymorphisms with cognitive performance in elderly females without dementia.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 613, doi. 10.1038/jhg.2011.56
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Genetic features of ancient West Siberian people of the Middle Ages, revealed by mitochondrial DNA haplogroup analysis.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 602, doi. 10.1038/jhg.2011.68
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Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 589, doi. 10.1038/jhg.2011.65
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A eulogy to the late Professor Eiji Inouye.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 549, doi. 10.1038/jhg.2011.67
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Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 617, doi. 10.1038/jhg.2011.63
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A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 572, doi. 10.1038/jhg.2011.60
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- Article
Loss-of-function mutation of collybistin is responsible for X-linked mental retardation associated with epilepsy.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 561, doi. 10.1038/jhg.2011.58
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Autosomal dominant nocturnal frontal lobe epilepsy: a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 609, doi. 10.1038/jhg.2011.69
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Ancient links between Siberians and Native Americans revealed by subtyping the Y chromosome haplogroup Q1a.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 583, doi. 10.1038/jhg.2011.64
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Copy number polymorphisms in new HapMap III and Singapore populations.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 552, doi. 10.1038/jhg.2011.54
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Tumor suppressive microRNA-375 regulates oncogene AEG-1/MTDH in head and neck squamous cell carcinoma (HNSCC).
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 595, doi. 10.1038/jhg.2011.66
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Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 566, doi. 10.1038/jhg.2011.59
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Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 577, doi. 10.1038/jhg.2011.61
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- Article