Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Syndrome and PTPN1[original query] |
---|
Protein tyrosine phosphatase-1B gene PTPN1: selection of tagging single nucleotide polymorphisms and association with body fat, insulin sensitivity, and the metabolic syndrome in a normal female population. Diabetes 2005 Nov 54 (11): 3296-304. Spencer-Jones Nicola J, Wang Xiaoling, Snieder Harold, Spector Tim D, Carter Nicholas D, O'Dell Sandra |
1484insG polymorphism of the PTPN1 gene is associated with insulin resistance in an Iranian population. Archives of medical research 2007 Jul 38 (5): 556-62. Meshkani Reza, Taghikhani Mohammad, Mosapour Abbas, Larijani Bagher, Khatami Shohreh, Khoshbin Ehteram, Ahmadvand Davood, Saeidi Parinaz, Maleki Ali, Yavari Kamal, Nasoohi Nikoo, Adeli Khosr |
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. European journal of endocrinology / European Federation of Endocrine Societies 2013 Sep 169 (3): 277-89. Clayton P, Chatelain P, Tatò L, Yoo H W, Ambler G R, Belgorosky A, Quinteiro S, Deal C, Stevens A, Raelson J, Croteau P, Destenaves B, Olivier |
The first PTPN1 1 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to previous studies. Turkish journal of medical sciences 2015 45 (2): 306-12. El Bouchikhi Ihssane, Samri Imane, Iraqui Houssaini Mohammed, Trhanint Saaid, Bouguenouch Laila, Sayel Hanane, Hida Moustapha, Atmani Samir, Ouldim Kar |
Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study. European journal of endocrinology 2016 Dec 175 (6): 633-643. Stevens Adam, Murray Philip, Wojcik Jerome, Raelson John, Koledova Ekaterina, Chatelain Pierre, Clayton Peter, |
Association of PTPN1 polymorphisms with breast cancer risk: A case-control study in Chinese females. Journal of cellular biochemistry 2019 Feb . Huang Shuya, Liu Liyuan, Xiang Yujuan, Wang Fei, Yu Lixiang, Zhou Fei, Cui Shude, Tian Fuguo, Fan Zhimin, Geng Cuizhi, Cao Xuchen, Yang Zhenlin, Wang Xiang, Liang Hong, Wang Shu, Jiang Hongchuan, Duan Xuening, Wang Haibo, Li Guolou, Wang Qitang, Zhang Jianguo, Jin Feng, Tang Jinhai, Li Liang, Zhu Shiguang, Zuo Wenshu, Ye Chunmiao, Zhou Wenzhong, Yin Gengshen, Ma Zhongbing, Yu Zhiga |
A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population. PLoS genetics 2020 Nov 16 (11): e1008802. Tcheandjieu Catherine, Aguirre Matthew, Gustafsson Stefan, Saha Priyanka, Potiny Praneetha, Haendel Melissa, Ingelsson Erik, Rivas Manuel A, Priest James |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: