Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: Albuminuria and ACR[original query] |
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RANTES promoter genotype is associated with diabetic nephropathy in type 2 diabetic subjects. Diabetes care 2003 Mar 26 (3): 892-8. Nakajima Kunihiro, Tanaka Yasushi, Nomiyama Takashi, Ogihara Takeshi, Ikeda Fuki, Kanno Rei, Iwashita Noseki, Sakai Ken, Watada Hirotaka, Onuma Tomio, Kawamori Ryu |
P-selectin gene haplotype associations with albuminuria in the Diabetes Heart Study. Kidney international 2005 Aug 68 (2): 741-6. Liu Yongmei, Burdon Kathryn P, Langefeld Carl D, Beck Stephanie R, Wagenknecht Lynne E, Rich Stephen S, Bowden Donald W, Freedman Barry |
Manganese superoxide dismutase gene polymorphism (V16A) is associated with stages of albuminuria in Korean type 2 diabetic patients. Metabolism: clinical and experimental 2006 Jan 55 (1): 1-7. Lee Seong Jin, Choi Moon Gi, Kim Dong-Sun, Kim Tae W |
Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes. American journal of kidney diseases : the official journal of the National Kidney Foundation 2008 Aug 52 (2): 242-50. Liu Yongmei, Freedman Barry I, Burdon Kathryn P, Langefeld Carl D, Howard Timothy, Herrington David, Goff David C, Bowden Donald W, Wagenknecht Lynne E, Hedrick Catherine C, Rich Stephen |
The association of podocin R229Q polymorphism with increased albuminuria or reduced estimated GFR in a large population-based sample of US adults. American journal of kidney diseases : the official journal of the National Kidney Foundation 2008 Nov 52 (5): 868-75. Köttgen Anna, Hsu Charles C, Coresh Josef, Shuldiner Alan R, Berthier-Schaad Yvette, Gambhir Tejal Rami, Smith Michael W, Boerwinkle Eric, Kao W H Lin |
Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study. American journal of nephrology 2009 29 (6): 626-32. Freedman Barry I, Kopp Jeffrey B, Winkler Cheryl A, Nelson George W, Rao D C, Eckfeldt John H, Leppert Mark F, Hicks Pamela J, Divers Jasmin, Langefeld Carl D, Hunt Steven |
The G protein ß3 subunit C825T polymorphism is associated with microalbuminuria in hypertensive women and cardiovascular disease in hypertensive men. American journal of hypertension 2010 Oct 23 (10): 1114-20. Romundstad Solfrid, Melien Oyvind, Holmen Joste |
Inflammation gene variants and susceptibility to albuminuria in the U.S. population: analysis in the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994. BMC medical genetics 2010 11 (1): 155. Ned Renée M, Yesupriya Ajay, Imperatore Giuseppina, Smelser Diane T, Moonesinghe Ramal, Chang Man-Huei, Dowling Nicole |
Chronic kidney disease and albuminuria in children with sickle cell disease. Clinical journal of the American Society of Nephrology : CJASN 2011 Nov 6 (11): 2628-33. McPherson Yee Marianne, Jabbar Shameem F, Osunkwo Ifeyinwa, Clement Lisa, Lane Peter A, Eckman James R, Guasch Anton |
Genetic variants in transient receptor potential cation channel, subfamily M 1 (TRPM1) and their risk of albuminuria-related traits in Mexican Americans. Clinica chimica acta; international journal of clinical chemistry 2011 Nov 412 (23-24): 2058-62. Thameem Farook, Puppala Sobha, Arar Nedal H, Blangero John, Duggirala Ravindranath, Abboud Hanna |
G501C polymorphism of the oxidized LDL receptor gene is associated with albuminuria in Chinese essential hypertension patients. Genetics and molecular research : GMR 2011 Oct 10 (4): 4. Hou X W, Yang R Q, Zhong Y G, Gao W, Sun S P, Wang N |
Genetic variation of glucose transporter-1 (GLUT1) and albuminuria in 10,278 European Americans and African Americans: a case-control study in the Atherosclerosis Risk in Communities (ARIC) study. BMC medical genetics 2011 12 (1): 16. Hsu Charles C, Kao Wenhong L, Steffes Michael W, Gambir Tejal, Brancati Frederick L, Heilig Charles W, Shuldiner Alan R, Boerwinkle Eric A, Coresh Jos |
Relationship between ADIPOQ gene, circulating high molecular weight adiponectin and albuminuria in individuals with normal kidney function: evidence from a family-based study. Diabetologia 2011 Apr 54 (4): 812-8. Menzaghi C, De Cosmo S, Copetti M, Salvemini L, De Bonis C, Mangiacotti D, Fini G, Pellegrini F, Trischitta |
Genetic variation in thrombin-activatable fibrinolysis inhibitor is associated with the risk of diabetic nephropathy. Journal of endocrinological investigation 2012 Jul 35 (7): 7. Xu CW, Wu XB, Ma XL, Wang YS, Zhang BC, Zhao JJ, Wang ZJ, Chen J |
KCNQ1 SNPS and susceptibility to diabetic nephropathy in East Asians with type 2 diabetes. Diabetologia 2012 Sep 55 (9): 2402-6. Lim X L, Nurbaya S, Salim A, Tai E S, Maeda S, Nakamura Y, Ng D P |
Glycated haemoglobin A1c is associated with low-grade albuminuria in Chinese adults. BMJ open 2015 5 (8): e007429. Huang Xiaolin, Zhou Yulin, Xu Baihui, Sun Wanwan, Lin Lin, Sun Jichao, Xu Min, Lu Jieli, Bi Yufang, Wang Weiqing, Xu Yu, Ning Gua |
The association of ACE gene polymorphism with diabetic kidney disease and renoprotective efficacy of valsartan. Journal of the renin-angiotensin-aldosterone system : JRAAS 2016 Jul 17 (3): . Wang Yuying, Peng Wen, Zhang Xiaoxue, Qiao Huibo, Wang Li, Xu Zhigang, Wu Chengua |
KIDNEY DISEASE GENETICS AND THE IMPORTANCE OF DIVERSITY IN PRECISION MEDICINE. Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2016 21 285-96. Bailey Jessica N Cooke, Wilson Sarah, Brown-Gentry Kristin, Goodloe Robert, Crawford Dana |
Association of Angiotensin-Converting Enzyme Gene Polymorphisms and Nephropathy in Diabetic Patients at a Tertiary Care Centre in South India. Clinical medicine insights. Endocrinology and diabetes 2017 10 1179551417726779. Wyawahare Mukta, Neelamegam Revathy, Vilvanathan Saranya, Soundravally R, Das A K, Adithan |
Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon. British journal of haematology 2017 May . Geard Amy, Pule Gift D, Chetcha Chemegni Bernard, Ngo Bitoungui Valentina J, Kengne Andre P, Chimusa Emile R, Wonkam Ambroi |
Prognostic Value of Urinary Calprotectin, NGAL and KIM-1 in Chronic Kidney Disease. Kidney & blood pressure research 2018 8 43 (4): 1255-1262. Seibert Felix S, Sitz Maximilian, Passfall Jürgen, Haesner Martin, Laschinski Peter, Buhl Martin, Bauer Frederic, Babel Nina, Pagonas Nikolaos, Westhoff Timm |
L-FABP and IL-6 as markers of chronic kidney damage in children after hemolytic uremic syndrome. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2018 6 27 (7): 955-962. Lipiec Katarzyna, Adamczyk Piotr, ?wi?tochowska El?bieta, Ziora Katarzyna, Szczepa?ska Mar |
Endothelial nitric oxide synthase gene (T786C and G894T) polymorphisms in Egyptian patients with type 2 diabetes. Journal, genetic engineering & biotechnology 2017 Dec 15 (2): 431-436. Moguib Omneya, Raslan Hala M, Abdel Rasheed Inas, Effat Laila, Mohamed Nadia, El Serougy Safaa, Hussein Ghada, Tawfeek Salwa, AbdelRahman Amany H, Omar Khal |
Serum Carnosinase-1 and Albuminuria Rather than the CNDP1 Genotype Correlate with Urinary Carnosinase-1 in Diabetic and Nondiabetic Patients with Chronic Kidney Disease. Journal of diabetes research 2020 1 2019 6850628. Rodriguez-Niño Angelica, Hauske Sibylle J, Herold Anna, Qiu Jiedong, van den Born Jacob, Bakker Stephan J L, Krämer Bernhard K, Yard Benito |
The HSD17B13 rs72613567 variant is associated with lower levels of albuminuria in patients with biopsy-proven nonalcoholic fatty liver disease. Nutrition, metabolism, and cardiovascular diseases : NMCD 2021 Feb . Sun Dan-Qin, Wang Ting-Yao, Zheng Kenneth I, Zhang Hao-Yang, Wang Xiao-Dong, Targher Giovanni, Byrne Christopher D, Chen Yong-Ping, Yuan Wei-Jie, Jin Yan, Zheng Ming-H |
Prevalence of chronic kidney disease in Brazilians with arterial hypertension and/or diabetes mellitus. Journal of clinical hypertension (Greenwich, Conn.) 2021 1 22 (9): 1666-1673. Comini Luma de Oliveira, de Oliveira Laura Camargo, Borges Luiza Delazari, Dias Heloísa Helena, Batistelli Clara Regina Santos, Ferreira Emily de Souza, da Silva Luciana Saraiva, Moreira Tiago Ricardo, da Costa Glauce Dias, da Silva Rodrigo Gomes, Cotta Rosângela Minardi Mit |
Genetic Variants of APOL1 Are Major Determinants of Kidney Failure in People of African Ancestry With HIV. Kidney international reports 2022 Apr 7 (4): 786-796. Hung Rachel K Y, Binns-Roemer Elizabeth, Booth John W, Hilton Rachel, Harber Mark, Santana-Suarez Beatriz, Campbell Lucy, Fox Julie, Ustianowski Andrew, Cosgrove Catherine, Burns James E, Clarke Amanda, Price David A, Chadwick David, Onyango Denis, Hamzah Lisa, Bramham Kate, Sabin Caroline A, Winkler Cheryl A, Post Frank A, |
Kidney function, albuminuria, and their modification by genetic factors and risk of incident dementia in UK Biobank. Alzheimer's research & therapy 2023 8 15 (1): 138. Tian-Shin Yeh, Lei Clifton, Jennifer A Collister, Xiaonan Liu, David J Hunter, Thomas J Littlejoh |
Genetic variants of interferon-response factor 5 are associated with the incidence of chronic kidney disease: the D.E.S.I.R. study. Genes and immunity 2023 11 . Frédéric Fumeron, Gilberto Velho, Fawaz Alzaid, Ray El Boustany, Claire Vandiedonck, Amélie Bonnefond, Philippe Froguel, Louis Potier, Michel Marre, Beverley Balkau, Ronan Roussel, Nicolas Ventecl |
Effects of the ABCC8 R1420H loss-of-function variant on beta-cell function, diabetes incidence, and retinopathy. BMJ open diabetes research & care 2024 1 11 (6): . Elsa Vazquez Arreola, William C Knowler, Leslie J Baier, Robert L Hans |
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- Page last updated:Apr 16, 2024
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