Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and PCSK2[original query] |
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| Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population. Molecular genetics and metabolism 0 92 (1-2): 145-50. Leak Tennille S, Keene Keith L, Langefeld Carl D, Gallagher Carla J, Mychaleckyj Josyf C, Freedman Barry I, Bowden Donald W, Rich Stephen S, Sale Michèle |
Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.
BMC medical genetics 2007 8 Suppl 1 S4. O'Donnell Christopher J, Cupples L Adrienne, D'Agostino Ralph B, Fox Caroline S, Hoffmann Udo, Hwang Shih-Jen, Ingellson Erik, Liu Chunyu, Murabito Joanne M, Polak Joseph F, Wolf Philip A, Demissie Serkal |
| Association of gene polymorphisms with chronic kidney disease in Japanese individuals. International journal of molecular medicine 2009 Oct 24 (4): 539-47. Yoshida Tetsuro, Kato Kimihiko, Yokoi Kiyoshi, Oguri Mitsutoshi, Watanabe Sachiro, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Aoyagi Yukitoshi, Nozawa Yoshinori, Yamada Yoshi |
| Association of common variants of TCF7L2 and PCSK2 with gestational diabetes mellitus in West Bengal, India. Nucleosides, nucleotides & nucleic acids 2023 8 1-18. Jayita Basu, Ruchira Mukherjee, Pooja Sahu, Chhanda Datta, Subhankar Chowdhury, Debasmita Mandal, Amlan Gho |
| Susceptibility of PCSK2 Polymorphism to Hirschsprung Disease in Southern Chinese Children. Clinical and experimental gastroenterology 2023 5 16 59-64. Bingtong Wang, Wenlin Fang, Dingjiang Qin, Qiuming He, Chaoting L |
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