HuGE Literature Finder
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Records 1-10
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Association of a disintegrin and metalloproteinase with a thrombospondin type 1 motif member 13 polymorphisms with severity of coronary stenosis in type 2 diabetes mellitus.
Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2018 23 59. Lasom Supakanya, Komanasin Nantarat, Settasatian Nongnuch, Settasatian Chatri, Kukongviriyapan Upa, Intharapetch Pongs |
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A novel Dock8 gene mutation confers diabetogenic susceptibility in the LEW.1AR1/Ztm-iddm rat, an animal model of human type 1 diabetes.
Diabetologia 2015 Sep . Arndt Tanja, Wedekind Dirk, Jörns Anne, Tsiavaliaris Georgios, Cuppen Edwin, Hedrich Hans-Jürgen, Lenzen Sigu |
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GTP cyclohydrolase I gene polymorphisms are associated with endothelial dysfunction and oxidative stress in patients with type 2 diabetes mellitus.
PloS one 2014 9 (11): e108587. Wolkow Pawel P, Kosiniak-Kamysz Wladyslaw, Osmenda Grzegorz, Wilk Grzegorz, Bujak-Gizycka Beata, Ignacak Adam, Kanitkar Mihir, Walus-Miarka Malgorzata, Harrison David G, Korbut Ryszard, Malecki Maciej T, Guzik Tomasz |
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ADAMTS13 predicts renal and cardiovascular events in type 2 diabetic patients and response to therapy.
Diabetes 2013 Oct 62 (10): 3599-609. Rurali Erica, Noris Marina, Chianca Antonietta, Donadelli Roberta, Banterla Federica, Galbusera Miriam, Gherardi Giulia, Gastoldi Sara, Parvanova Aneliya, Iliev Ilian, Bossi Antonio, Haefliger Carolina, Trevisan Roberto, Remuzzi Giuseppe, Ruggenenti Piero, |
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Association between variations in coagulation system genes and carotid plaque.
Journal of the neurological sciences 2012 Dec 323 (1-2): 93-8. Della-Morte David, Beecham Ashley, Dong Chuanhui, Wang Liyong, McClendon Mark S, Gardener Hannah, Blanton Susan H, Sacco Ralph L, Rundek Tatja |
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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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Accumulation of gene polymorphisms related to plaque disruption and thrombosis is associated with cerebral infarction in subjects with type 2 diabetes.
Diabetes care 2010 Feb 33 (2): 390-5. Katakami Naoto, Takahara Mitsuyoshi, Kaneto Hideaki, Shimizu Ikki, Ohno Keizo, Ishibashi Fukashi, Osonoi Takeshi, Kashiwagi Atsunori, Kawamori Ryuzo, Shimomura Iichiro, Matsuhisa Munehide, Yamasaki Yoshimit |
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Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.
Dementia and geriatric cognitive disorders 2009 27 (1): 59-68. Giedraitis Vilmantas, Kilander Lena, Degerman-Gunnarsson Malin, Sundelöf Johan, Axelsson Tomas, Syvänen Ann-Christine, Lannfelt Lars, Glaser An |
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Impact of the Thr789Ala variant of the von Willebrand factor levels, on ristocetin co-factor and collagen binding capacity and its association with coronary heart disease in patients with diabetes mellitus type 2.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2005 Dec 113 (10): 568-72. Klemm T, Mehnert A K, Siegemund A, Wiesner T D, Gelbrich G, Blüher M, Paschke |
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Polymorphisms in the von Willebrand factor gene are not associated with proliferative retinopathy in non-insulin-dependent diabetes mellitus.
Ophthalmic research 0 34 (5): 327-30. Beránek Michal, Kanková Katerina, Kolár Petr, Znojil Vladim |
- Page last reviewed:Jul 30, 2019
- Page last updated:Oct 31, 2019
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