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Kuixing Zhang

Showing results (41-50 of 60) with videos related to

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Journal of Neurochemistry|June 22, 2013
Genetic variation at the delta-sarcoglycan (SGCD) locus elevates heritable sympathetic nerve activity in human twin pairsC Makena Hightower, Kuixing Zhang, José P Miramontes-González, et al.
Journal of Hypertension|August 9, 2012
Genes and environment: novel, functional polymorphism in the human cathepsin L (CTSL1) promoter disrupts a xenobiotic response element (XRE) to alter transcription and blood pressureNzali Mbewe-Campbell, Zhiyun Wei, Kuixing Zhang, et al.
Diabetes, Obesity & Metabolism|October 10, 2006
Catecholamine storage vesicles and the metabolic syndrome: The role of the chromogranin A fragment pancreastatinKuixing Zhang, Fangwen Rao, Gen Wen, et al.
BMC Medical Genetics|March 13, 2016
Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin systemNilima Biswas, Adam X Maihofer, Saiful Anam Mir, et al.
Journal of Hypertension|December 17, 2009
Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressureYuqing Chen, Gen Wen, Fangwen Rao, et al.
Plos One|January 7, 2014
Heritable influence of DBH on adrenergic and renal function: twin and disease studiesDalal N Pasha, Jason T Davis, Fangwen Rao, et al.
Scientific Reports|March 27, 2019
A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine functionJose Pablo Miramontes-Gonzalez, C Makena Hightower, Kuixing Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2003
Divergence of the genes on human chromosome 21 between human and other hominoids and variation of substitution rates among transcription unitsJinxiu Shi, Huifeng Xi, Ying Wang, et al.
The Journal of Clinical Investigation|August 25, 2007
Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular riskLian Zhang, Fangwen Rao, Kuixing Zhang, et al.
Scientific Reports|February 16, 2020
Author Correction: A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine functionJose Pablo Miramontes-Gonzalez, C Makena Hightower, Kuixing Zhang, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Journal of Neurochemistry|June 22, 2013
Genetic variation at the delta-sarcoglycan (SGCD) locus elevates heritable sympathetic nerve activity in human twin pairsC Makena Hightower, Kuixing Zhang, José P Miramontes-González, et al.
Journal of Hypertension|August 9, 2012
Genes and environment: novel, functional polymorphism in the human cathepsin L (CTSL1) promoter disrupts a xenobiotic response element (XRE) to alter transcription and blood pressureNzali Mbewe-Campbell, Zhiyun Wei, Kuixing Zhang, et al.
Diabetes, Obesity & Metabolism|October 10, 2006
Catecholamine storage vesicles and the metabolic syndrome: The role of the chromogranin A fragment pancreastatinKuixing Zhang, Fangwen Rao, Gen Wen, et al.
BMC Medical Genetics|March 13, 2016
Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin systemNilima Biswas, Adam X Maihofer, Saiful Anam Mir, et al.
Journal of Hypertension|December 17, 2009
Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressureYuqing Chen, Gen Wen, Fangwen Rao, et al.
Plos One|January 7, 2014
Heritable influence of DBH on adrenergic and renal function: twin and disease studiesDalal N Pasha, Jason T Davis, Fangwen Rao, et al.
Scientific Reports|March 27, 2019
A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine functionJose Pablo Miramontes-Gonzalez, C Makena Hightower, Kuixing Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2003
Divergence of the genes on human chromosome 21 between human and other hominoids and variation of substitution rates among transcription unitsJinxiu Shi, Huifeng Xi, Ying Wang, et al.
The Journal of Clinical Investigation|August 25, 2007
Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular riskLian Zhang, Fangwen Rao, Kuixing Zhang, et al.
Scientific Reports|February 16, 2020
Author Correction: A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine functionJose Pablo Miramontes-Gonzalez, C Makena Hightower, Kuixing Zhang, et al.
Pageof 6