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An A/C germline single-nucleotide polymorphism in the TNFAIP3 gene is associated with advanced disease stage and survival in only surgically treated esophageal cancer.
Published in:
Journal of Human Genetics, 2015, v. 60, n. 2, p. 107, doi. 10.1038/jhg.2014.106
By:
- Ghadban, Tarik;
- Schmidt-Yang, Magdalena;
- Uzunoglu, Faik G;
- Perez, Daniel R;
- Tsui, Tung Y;
- El Gammal, Alexander T;
- Erbes, Peter J;
- Zilbermints, Veacheslav;
- Wellner, Ulrich;
- Pantel, Klaus;
- Izbicki, Jakob R;
- Vashist, Yogesh K
Publication type:
Article
A powerful association test for qualitative traits incorporating imprinting effects using general pedigree data.
Published in:
Journal of Human Genetics, 2015, v. 60, n. 2, p. 77, doi. 10.1038/jhg.2014.109
By:
- Zhou, Ji-Yuan;
- He, Hai-Qiang;
- You, Xiao-Ping;
- Li, Shao-Zhan;
- Chen, Ping-Yan;
- Fung, Wing Kam
Publication type:
Article
Downregulation of the microRNA-1/133a cluster enhances cancer cell migration and invasion in lung-squamous cell carcinoma via regulation of Coronin1C.
Published in:
Journal of Human Genetics, 2015, v. 60, n. 2, p. 53, doi. 10.1038/jhg.2014.111
By:
- Mataki, Hiroko;
- Enokida, Hideki;
- Chiyomaru, Takeshi;
- Mizuno, Keiko;
- Matsushita, Ryosuke;
- Goto, Yusuke;
- Nishikawa, Rika;
- Higashimoto, Ikkou;
- Samukawa, Takuya;
- Nakagawa, Masayuki;
- Inoue, Hiromasa;
- Seki, Naohiko
Publication type:
Article
Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson's disease.
Published in:
Journal of Human Genetics, 2015, v. 60, n. 2, p. 85, doi. 10.1038/jhg.2014.110
By:
- Yu, Zhe;
- Wang, Ting;
- Xu, Jun;
- Wang, Wei;
- Wang, Guifang;
- Chen, Chao;
- Zheng, Lili;
- Pan, Li;
- Gong, Dianrong;
- Li, Xueli;
- Qu, Huaiqian;
- Li, Fang;
- Zhang, Bin;
- Le, Weidong;
- Han, Fabin
Publication type:
Article
Deep sequencing of RYR3 gene identifies rare and common variants associated with increased carotid intima-media thickness (cIMT) in HIV-infected individuals.
Published in:
Journal of Human Genetics, 2015, v. 60, n. 2, p. 63, doi. 10.1038/jhg.2014.104
By:
- Zhi, Degui;
- Shendre, Aditi;
- Scherzer, Rebecca;
- Irvin, Marguerite R;
- Perry, Rodney T;
- Levy, Shawn;
- Arnett, Donna K;
- Grunfeld, Carl;
- Shrestha, Sadeep
Publication type:
Article
Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy.
Published in:
Journal of Human Genetics, 2015, v. 60, n. 2, p. 97, doi. 10.1038/jhg.2014.103
By:
- Kodera, Hirofumi;
- Osaka, Hitoshi;
- Iai, Mizue;
- Aida, Noriko;
- Yamashita, Akio;
- Tsurusaki, Yoshinori;
- Nakashima, Mitsuko;
- Miyake, Noriko;
- Saitsu, Hirotomo;
- Matsumoto, Naomichi
Publication type:
Article
Silver-Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C.
Published in:
Journal of Human Genetics, 2015, v. 60, n. 2, p. 91, doi. 10.1038/jhg.2014.100
By:
- Nakashima, Shinichi;
- Kato, Fumiko;
- Kosho, Tomoki;
- Nagasaki, Keisuke;
- Kikuchi, Toru;
- Kagami, Masayo;
- Fukami, Maki;
- Ogata, Tsutomu
Publication type:
Article
Severe phenotypes in a Charcot-Marie-Tooth 1A patient with PMP22 triplication.
Published in:
Journal of Human Genetics, 2015, v. 60, n. 2, p. 103, doi. 10.1038/jhg.2014.102
By:
- Kim, Sung Min;
- Lee, Jinho;
- Yoon, Bo Ram;
- Kim, Ye Jin;
- Choi, Byung-Ok;
- Chung, Ki Wha
Publication type:
Article
Genetic structure among Fijian island populations.
Published in:
Journal of Human Genetics, 2015, v. 60, n. 2, p. 69, doi. 10.1038/jhg.2014.105
By:
- Shipley, Gerhard P;
- Taylor, Diana A;
- Tyagi, Anand;
- Tiwari, Geetanjali;
- Redd, Alan J
Publication type:
Article

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