Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and HK1[original query] |
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Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.
PLoS genetics 2008 Dec 4 (12): e1000312. Paré Guillaume, Chasman Daniel I, Parker Alexander N, Nathan David M, Miletich Joseph P, Zee Robert Y, Ridker Paul |
| mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas. Yonsei medical journal 2018 Aug 59 (6): 746-753. Suh Sunghwan, Kim Yun Hak, Goh Tae Sik, Jeong Dae Cheon, Lee Chi Seung, Jang Jeon Yeob, Cha Wonjae, Han Myoung Eun, Kim Seong Jang, Kim In Joo, Pak Kyoungju |
| Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep. PLoS genetics 2019 Apr 15 (4): e1007739. Cade Brian E, Chen Han, Stilp Adrienne M, Louie Tin, Ancoli-Israel Sonia, Arens Raanan, Barfield Richard, Below Jennifer E, Cai Jianwen, Conomos Matthew P, Evans Daniel S, Frazier-Wood Alexis C, Gharib Sina A, Gleason Kevin J, Gottlieb Daniel J, Hillman David R, Johnson W Craig, Lederer David J, Lee Jiwon, Loredo Jose S, Mei Hao, Mukherjee Sutapa, Patel Sanjay R, Post Wendy S, Purcell Shaun M, Ramos Alberto R, Reid Kathryn J, Rice Ken, Shah Neomi A, Sofer Tamar, Taylor Kent D, Thornton Timothy A, Wang Heming, Yaffe Kristine, Zee Phyllis C, Hanis Craig L, Palmer Lyle J, Rotter Jerome I, Stone Katie L, Tranah Gregory J, Wilson James G, Sunyaev Shamil R, Laurie Cathy C, Zhu Xiaofeng, Saxena Richa, Lin Xihong, Redline Sus |
| An EGLN1 mutation may regulate hypoxic response in cyanotic congenital heart disease through the PHD2/HIF-1A pathway. Genes & diseases 2019 3 6 (1): 35-42. Zhou Yuanlin, Ouyang Na, Liu Lingjuan, Tian Jie, Huang Xupei, Lu Tiew |
| Characterization of glycolysis-related gene expression in malignant melanoma. Pathology, research and practice 2019 12 216 (1): 152752. Koch Andreas, Ebert Eva Vanessa, Seitz Tatjana, Dietrich Peter, Berneburg Mark, Bosserhoff Anja, Hellerbrand Cla |
| Condemned or Not to Die? Gene Polymorphisms Associated With Cell Death in Pemphigus Foliaceus. Frontiers in immunology 2019 10 2416. Bumiller-Bini Valéria, Cipolla Gabriel Adelman, Spadoni Mariana Basso, Augusto Danillo Gardenal, Petzl-Erler Maria Luiza, Beltrame Marcia Holsbach, Boldt Angelica Beate Wint |
| Novel homozygous mutations in Pakistani families with Charcot-Marie-Tooth disease. BMC medical genomics 2021 7 14 (1): 174. Kanwal Sumaira, Choi Yu JIn, Lim Si On, Choi Hee Ji, Park Jin Hee, Nuzhat Rana, Khan Aneela, Perveen Shazia, Choi Byung-Ok, Chung Ki W |
| Multiple-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
The Journal of clinical investigation 2021 May . Page Grier P, Kanias Tamir, Guo Yuelong J, Lanteri Marion C, Zhang Xu, Mast Alan E, Cable Ritchard G, Spencer Bryan R, Kiss Joseph E, Fang Fang, Endres-Dighe Stacy M, Brambilla Donald, Nouraie Mehdi, Gordeuk Victor R, Kleinman Steve, Busch Michael P, Gladwin Mark T, |
| Latent trait modeling of tau neuropathology in progressive supranuclear palsy.
Acta neuropathologica 2021 2 141 (5): 667-680. Kouri Naomi, Murray Melissa E, Reddy Joseph S, Serie Daniel J, Soto-Beasley Alexandra, Allen Mariet, Carrasquillo Minerva M, Wang Xue, Castanedes Monica Casey, Baker Matthew C, Rademakers Rosa, Uitti Ryan J, Graff-Radford Neill R, Wszolek Zbigniew K, Schellenberg Gerard D, Crook Julia E, Ertekin-Taner Nilüfer, Ross Owen A, Dickson Dennis |
| Variants influencing age at diagnosis of HNF1A-MODY. Molecular medicine (Cambridge, Mass.) 2022 9 28 (1): 113. Ludwig-S?omczy?ska Agnieszka H, Seweryn Micha? T, Radkowski Piotr, Kapusta Przemys?aw, Machlowska Julita, Pruhova Stepanka, Gasperikova Daniela, Bellanne-Chantelot Christine, Hattersley Andrew, Kandasamy Balamurugan, Letourneau-Freiberg Lisa, Philipson Louis, Doria Alessandro, Wo?kow Pawe? P, Ma?ecki Maciej T, Klupa Toma |
| Driving with retinitis pigmentosa. Ophthalmic genetics 2023 4 1-9. Heath Jeffery Rachael C, Lo Johnny, Thompson Jennifer A, Lamey Tina M, McLaren Terri L, DeRoach John N, Kabilio Miguel S, Chen Fred |
| Clinical and genetic characteristics of congenital hyperinsulinism in Norway: A nationwide cohort study. The Journal of clinical endocrinology and metabolism 2024 7 . Christoffer Drabløs Velde, Janne Molnes, Siren Berland, Pål Rasmus Njølstad, Anders Molv |
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