HuGE Literature Finder
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Records 1-5
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Genetic Analysis and Follow-Up of 25 Neonatal Diabetes Mellitus Patients in China.
Journal of diabetes research 2016 2016 6314368. Cao Bingyan, Gong Chunxiu, Wu Di, Lu Chaoxia, Liu Fang, Liu Xiaojing, Zhang Yingxian, Gu Yi, Qi Zhan, Li Xiaoqiao, Liu Min, Li Wenjing, Su Chang, Liang Xuejun, Feng M |
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Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.
European journal of endocrinology / European Federation of Endocrine Societies 2015 Jun 172 (6): 697-705. Demirbilek Huseyin, Arya Ved Bhushan, Ozbek Mehmet Nuri, Houghton Jayne A L, Baran Riza Taner, Akar Melek, Tekes Selahattin, Tuzun Heybet, Mackay Deborah J, Flanagan Sarah E, Hattersley Andrew T, Ellard Sian, Hussain Khal |
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Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach.
Molecular genetics and metabolism 2014 Dec 113 (4): 315-20. Alkorta-Aranburu G, Carmody D, Cheng Y W, Nelakuditi V, Ma L, Dickens Jazzmyne T, Das S, Greeley S A W, del Gaudio |
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Common variants in PERK, JNK, BIP and XBP1 genes are associated with the risk of prediabetes or diabetes-related phenotypes in a Chinese population.
Chinese medical journal 2014 127 (13): 2438-44. Feng Nan, Ma Xiaowei, Wei Xiaowei, Zhang Junqing, Dong Aimei, Jin Mengmeng, Zhang Hong, Guo Xiaoh |
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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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- Page last updated:Jul 11, 2019
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