Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: GFPT1[original query] |
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Molecular screening of the human glutamine-fructose-6-phosphate amidotransferase 1 (GFPT1) gene and association studies with diabetes and diabetic nephropathy. Molecular genetics and metabolism 2004 Aug 82 (4): 321-8. Elbein Steven C, Zheng Hailing, Jia Yiwen, Chu Winston, Cooper Judith J, Hale Terri, Zhang Zhengxi |
Common variants in glutamine:fructose-6-phosphate amidotransferase 2 (GFPT2) gene are associated with type 2 diabetes, diabetic nephropathy, and increased GFPT2 mRNA levels. The Journal of clinical endocrinology and metabolism 2004 Feb 89 (2): 748-55. Zhang Hailing, Jia Yiwen, Cooper Judith J, Hale Terri, Zhang Zhengxian, Elbein Steven |
Scrutiny of the glutamine-fructose-6-phosphate transaminase 1 (GFPT1) locus reveals conserved haplotype block structure not associated with diabetic nephropathy. Diabetes 2004 Mar 53 (3): 865-9. Ng Daniel P K, Walker William H, Chia Kee-Seng, Choo Serena, Warram James H, Krolewski Andrzej |
Effect of +36T>C in intron 1 on the glutamine: fructose-6-phosphate amidotransferase 1 gene and its contribution to type 2 diabetes in different populations. Journal of human genetics 2006 51 (12): 1100-9. Kunika Kiyoshi, Tanahashi Toshihito, Kudo Eiji, Mizusawa Noriko, Ichiishi Eiichiro, Nakamura Naoto, Yoshikawa Toshikazu, Yamaoka Takashi, Yasumo Hiroaki, Tsugawa Kazue, Moritani Maki, Inoue Hiroshi, Itakura Mits |
Glucose metabolism gene polymorphisms and clinical outcome in pancreatic cancer. Cancer 2011 Feb 117 (3): 480-91. Dong Xiaoqun, Tang Hongwei, Hess Kenneth R, Abbruzzese James L, Li Dongh |
Glucose metabolism gene variants modulate the risk of pancreatic cancer. Cancer prevention research (Philadelphia, Pa.) 2011 May 4 (5): 758-66. Dong Xiaoqun, Li Yanan, Chang Ping, Tang Hongwei, Hess Kenneth R, Abbruzzese James L, Li Dongh |
Congenital myasthenic syndrome in Israel: Genetic and clinical characterization. Neuromuscular disorders : NMD 2016 12 27 (2): 136-140. Aharoni Sharon, Sadeh Menachem, Shapira Yehuda, Edvardson Simon, Daana Muhannad, Dor-Wollman Talia, Mimouni-Bloch Aviva, Halevy Ayelet, Cohen Rony, Sagie Liora, Argov Zohar, Rabie Malcolm, Spiegel Ronen, Chervinsky Ilana, Orenstein Naama, Engel Andrew G, Nevo Yor |
Muscle magnetic resonance imaging in congenital myasthenic syndromes. Muscle & nerve 2016 Jan . Finlayson Sarah, Morrow Jasper M, Rodriguez Cruz Pedro M, Sinclair Christopher D J, Fischmann Arne, Thornton John S, Knight Steve, Norbury Ray, White Mel, Al-Hajjar Michal, Carboni Nicola, Jayawant Sandeep, Robb Stephanie A, Yousry Tarek A, Beeson David, Palace Jacqueli |
Genome-wide association study of subclinical interstitial lung disease in MESA.
Respiratory research 2017 May 18 (1): 97. Manichaikul Ani, Wang Xin-Qun, Sun Li, Dupuis Josée, Borczuk Alain C, Nguyen Jennifer N, Raghu Ganesh, Hoffman Eric A, Onengut-Gumuscu Suna, Farber Emily A, Kaufman Joel D, Rabinowitz Dan, Stukovsky Karen D Hinckley, Kawut Steven M, Hunninghake Gary M, Washko George R, O'Connor George T, Rich Stephen S, Barr R Graham, Lederer David |
Congenital Myasthenic Syndrome: Spectrum of Mutations in an Indian Cohort. Journal of clinical neuromuscular disease 2018 Sep 20 (1): 14-27. Selvam Pavalan, Arunachal Gautham, Danda Sumita, Chapla Aaron, Sivadasan Ajith, Alexander Mathew, Thomas Maya Mary, Thomas Nihal |
Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis. Pain 2021 Feb . Suri Pradeep, Stanaway Ian B, Zhang Yanfei, Freidin Maxim B, Tsepilov Yakov A, Carrell David S, Williams Frances M K, Aulchenko Yurii S, Hakonarson Hakon, Namjou Bahram, Crosslin David R, Jarvik Gail P, Lee Ming |
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- Page last updated:May 13, 2024
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