Works matching IS 14345161 AND DT 2014 AND VI 59 AND IP 2

Results: 9

Common and rare single nucleotide polymorphisms in the LDLR gene are present in a black South African population and associate with low-density lipoprotein cholesterol levels.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 2, p. 88, doi. 10.1038/jhg.2013.123

By:

van Zyl, Tertia;
Jerling, Johann C;
Conradie, Karin R;
Feskens, Edith JM

Publication type:

Article

Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening.

Published in:: Journal of Human Genetics, 2014, v. 59, n. 2, p. 100, doi. 10.1038/jhg.2013.128
Publication type:: Article

Confounding by linkage disequilibrium.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 2, p. 110, doi. 10.1038/jhg.2013.130

By:

Aissani, Brahim

Publication type:

Article

Significant association between CYP3A5 polymorphism and blood concentration of tacrolimus in patients with connective tissue diseases.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 2, p. 107, doi. 10.1038/jhg.2013.129

By:

Tanaka, Kosuke;
Terao, Chikashi;
Ohmura, Koichiro;
Takahashi, Meiko;
Nakashima, Ran;
Imura, Yoshitaka;
Yoshifuji, Hajime;
Yukawa, Naoichiro;
Usui, Takashi;
Fujii, Takao;
Mimori, Tsuneyo;
Matsuda, Fumihiko

Publication type:

Article

The tumor-suppressive microRNA-143/145 cluster inhibits cell migration and invasion by targeting GOLM1 in prostate cancer.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 2, p. 78, doi. 10.1038/jhg.2013.121

By:

Kojima, Satoko;
Enokida, Hideki;
Yoshino, Hirofumi;
Itesako, Toshihiko;
Chiyomaru, Takeshi;
Kinoshita, Takashi;
Fuse, Miki;
Nishikawa, Rika;
Goto, Yusuke;
Naya, Yukio;
Nakagawa, Masayuki;
Seki, Naohiko

Publication type:

Article

Language isolates and their genetic identity: a commentary on mitochondrial DNA history of Sri Lankan ethnic people: their relations within the island and with the Indian subcontinental populations.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 2, p. 61, doi. 10.1038/jhg.2013.122

By:

Chaubey, Gyaneshwer

Publication type:

Article

The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 2, p. 66, doi. 10.1038/jhg.2013.120

By:

Bandelt, Hans-Jürgen;
Kloss-Brandstätter, Anita;
Richards, Martin B;
Yao, Yong-Gang;
Logan, Ian

Publication type:

Article

Molecular analysis of potassium ion channel genes in sudden death cases among patients administered psychotropic drug therapy: are polymorphisms in LQT genes a potential risk factor?

Published in:

Journal of Human Genetics, 2014, v. 59, n. 2, p. 95, doi. 10.1038/jhg.2013.125

By:

Kamei, Sayako;
Sato, Noriko;
Harayama, Yuta;
Nunotani, Miyako;
Takatsu, Kanae;
Shiozaki, Tetsuya;
Hayashi, Tokutaro;
Asamura, Hideki

Publication type:

Article

PLS3 expression and SMA phenotype: a commentary on correlation of PLS3 expression with disease severity in children with spinal muscular atrophy.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 2, p. 64, doi. 10.1038/jhg.2013.124

By:

Nishio, Hisahide

Publication type:

Article