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The Lancet. Diabetes & Endocrinology|April 16, 2014
Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysisKaixin Zhou, Louise Donnelly, Jian Yang, et al.
Plos One|December 14, 2011
The KCNJ11 E23K polymorphism and progression of glycaemia in Southern Chinese: a long-term prospective studyChloe Y Y Cheung, Annette W K Tso, Bernard M Y Cheung, et al.
BMC Medical Genomics|December 14, 2016
Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genesJohn K L Wong, Desmond Campbell, Ngoc Diem Ngo, et al.
Schizophrenia Bulletin|January 22, 2021
Neurological Soft Signs Are Associated With Altered Cerebellar-Cerebral Functional Connectivity in SchizophreniaXin-Lu Cai, Yong-Ming Wang, Yi Wang, et al.
European Journal of Endocrinology|April 25, 2014
Adiponectin gene variants and the risk of coronary heart disease: a 16-year longitudinal studyChloe Y Y Cheung, Elaine Y L Hui, Bernard M Y Cheung, et al.
Spine|December 24, 2005
The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degenerationJeffrey J T Jim, Noora Noponen-Hietala, Kenneth M C Cheung, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 16, 2009
Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese populationHon-Cheong So, Pui Y Fong, Ronald Y L Chen, et al.
Cell Reports|February 27, 2020
Directed Differentiation of Notochord-like and Nucleus Pulposus-like Cells Using Human Pluripotent Stem CellsYuelin Zhang, Zhao Zhang, Peikai Chen, et al.
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