Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: NDN[original query] |
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Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation. International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 2001 Jun 25 (6): 767-9. Oeffner F, Korn T, Roth H, Ziegler A, Hinney A, Goldschmidt H, Siegfried W, Hebebrand J, Grzeschik K |
Genomic predictors of the maximal O2 uptake response to standardized exercise training programs. Journal of applied physiology (Bethesda, Md. : 1985) 2011 May 110 (5): 1160-70. Bouchard Claude, Sarzynski Mark A, Rice Treva K, Kraus William E, Church Timothy S, Sung Yun Ju, Rao D C, Rankinen Tuo |
Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites. Obesity (Silver Spring, Md.) 2011 Jun 19 (6): 1229-34. Chen Yuan, Liu Yong-Jun, Pei Yu-Fang, Yang Tie-Lin, Deng Fei-Yan, Liu Xiao-Gang, Li Ding-You, Deng Hong-W |
BsmI polymorphisms in vitamin D receptor gene are associated with diabetic nephropathy in type 2 diabetes in the Han Chinese population. Gene 2012 Mar 495 (2): 183-8. Zhang Hao, Wang Jianwen, Yi Bin, Zhao Yan, Liu Yan, Zhang Ke, Cai Xu, Sun Jian, Huang Lihua, Liao Q |
Vascular endothelial growth factor insertion/deletion gene polymorphism in West Indian patients of type 2 diabetes and diabetic nephropathy. Indian journal of biochemistry & biophysics 2015 Apr 52 (2): 209-12. Dabhi Brijesh, Mistry Kinnari N, Patel Hitesh, Lal Sanj |
Genetic Variation of MT-ND Genes in Frontotemporal Lobar Degeneration: Biochemical Phenotype-Genotype Correlation. Neuro-degenerative diseases 2015 15 (2): 70-80. Gaspar Rita, Santana Isabel, Mendes Cândida, Fernandes Ana Sofia, Duro Diana, Simões Marta, Luís Daniela, Santos Maria João, Grazina Manue |
Oxidative stress and its association with TNF-a-308 G/C and IL-1a-889 C/T gene polymorphisms in patients with diabetes and diabetic nephropathy. Gene 2015 May 562 (2): 197-202. Dabhi Brijesh, Mistry Kinnari |
Matrix Metalloproteinase-9 -1562C/T Gene Polymorphism Is Associated with Diabetic Nephropathy. BioMed research international 2016 2016 1627143. Feng Shufen, Ye Gang, Bai Shi, Wei Hongcheng, Liao Xueling, Li |
Association of Pentraxin 3 Gene Polymorphisms with Susceptibility to Diabetic Nephropathy. Medical science monitor : international medical journal of experimental and clinical research 2017 Jan 23 428-436. Zhu Hong, Yu Weihui, Xie Yuanyuan, Zhang Hailing, Bi Yan, Zhu Dalo |
Is prone sleeping dangerous for neonates? Polysomnographic characteristics and NDN gene analysis. Ci ji yi xue za zhi = Tzu-chi medical journal 0 31 (2): 113-117. Wong Shi-Bing, Zhao Lu-Lu, Chuang Shu-Hua, Tsai Wen-Hsin, Yu Chun-Hsien, Tsai Li-Pi |
Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome. The Journal of clinical endocrinology and metabolism 2020 6 105 (8): 2732-9. Meader Brooke N, Albano Alessandro, Sekizkardes Hilal, Delaney Ange |
Novel immune-related signature for risk stratification and prognosis in prostatic adenocarcinoma. Cancer science 2021 7 112 (10): 4365-4376. Zhao Hai-Bo, Zeng Yan-Ru, Han Zhao-Dong, Zhuo Yang-Jia, Liang Ying-Ke, Hon Chi Tin, Wan Song, Wu Shulin, Dahl Douglas, Zhong Wei-De, Wu Chin-L |
Genomic alterations caused by HPV integration in a cohort of Chinese endocervical adenocarcinomas. Cancer gene therapy 2021 1 28 (12): 1353-1364. Li Wenhui, Lei Wanjun, Chao Xiaopei, Song Xiaochen, Bi Yalan, Wu Huanwen, Wu Ming, Li L |
Genetic Modifiers of Age at Onset for Parkinson's Disease in Asians: A Genome-Wide Association Study.
Movement disorders : official journal of the Movement Disorder Society 2021 4 36 (9): 2077-2084. Li Chunyu, Ou Ruwei, Chen Yongping, Gu Xiaojing, Wei Qianqian, Cao Bei, Zhang Lingyu, Hou Yanbing, Liu Kuncheng, Chen Xueping, Song Wei, Zhao Bi, Wu Ying, Li Tao, Dong Xianjun, Shang Huifa |
Identification of potential crucial genes and therapeutic targets for epilepsy. European journal of medical research 2024 1 29 (1): 43. Shitao Wang, Zhenrong Xie, Tian Jun, Xuelu Ma, Mengen Zhang, Feng Rao, Hui Xu, Jinghong Lu, Xiangqian Ding, Zongyou |
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- Page last updated:Apr 22, 2024
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