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Author Details

Kuixing Zhang
2003
58
20
PMIDPaper TitleJournal TitlePublished Year
37161199Machine learning-based evaluation of application value of pulse wave parameter model in the diagnosis of hypertensive disorder in pregnancy.2023
36899567SAMS-Net: Fusion of attention mechanism and multi-scale features network for tumor infiltrating lymphocytes segmentation.2023
36680935Enhanced antibody-defucosylation capability of α-L-fucosidase by proximity-based protein fusion.2023
34331146Eosinophilic Gastritis/Gastroenteritis.Current Gastroenterology Reports2021
33682770Research on the classification of lymphoma pathological images based on deep residual neural network.Technology and Health Care2021
34254225SHA-MTL: soft and hard attention multi-task learning for automated breast cancer ultrasound image segmentation and classification.International journal of computer assisted radiology and surgery2021
31977863A multi-feature image retrieval scheme for pulmonary nodule diagnosis.Medicine (United States)2020
32060363Author Correction: A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function.Sci Rep2020
31405537Acute hepatitis and acute liver failure: Pathologic diagnosis and differential diagnosis.Seminars in Diagnostic Pathology2019
30601149Goblet Cell Carcinoid/Carcinoma: An Update.Advances in Anatomic Pathology2019
30342054Prolymphocytic transformation of lymphoplasmacytic lymphoma: an extremely unusual event.Human Pathology2019
30911067A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function.Sci Rep2019
28011710Identification of novel loci affecting circulating chromogranins and related peptides.Hum Mol Genet2017
28626544Atypical Hemolytic Uremic Syndrome: A Brief Review.Hematology Reports2017
26556564Analysis and validation of traits associated with a single nucleotide polymorphism Gly364Ser in catestatin using humanized chromogranin A mouse models.J Hypertens2016
26969407Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin system.BMC Med Genet2016
25392232Molecular Mechanism for Hypertensive Renal Disease: Differential Regulation of Chromogranin A Expression at 3'-Untranslated Region Polymorphism C+87T by MicroRNA-107.J Am Soc Nephrol2015
24509276Genetic implication of a novel thiamine transporter in human hypertension.J Am Coll Cardiol2014
24266713Chromogranin B: intra- and extra-cellular mechanisms to regulate catecholamine storage and release, in catecholaminergic cells and organisms.J Neurochem2014
24140660Human heart rate: heritability of resting and stress values in twin pairs, and influence of genetic variation in the adrenergic pathway at a microribonucleic acid (microrna) motif in the 3'-UTR of cytochrome b561 [corrected].J Am Coll Cardiol2014
24624250Large-cell neuroendocrine carcinoma (LCNEC) without pulmonary symptoms diagnosed in a cutaneous metastasis.American Journal of Case Reports2014
23674521MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension.Hum Mol Genet2013
23762491Zfp423 binds autoregulatory sites in p19 cell culture model.PLoS ONE2013
24391727Heritable influence of DBH on adrenergic and renal function: twin and disease studies.PLoS One2013
23786442Genetic variation at the delta-sarcoglycan (SGCD) locus elevates heritable sympathetic nerve activity in human twin pairs.J Neurochem2013
23149563Heredity and cardiometabolic risk: naturally occurring polymorphisms in the human neuropeptide Y(2) receptor promoter disrupt multiple transcriptional response motifs.J Hypertens2013
23021333Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses.J Am Coll Cardiol2012
22871890Genes and environment: novel, functional polymorphism in the human cathepsin L (CTSL1) promoter disrupts a xenobiotic response element (XRE) to alter transcription and blood pressure.J Hypertens2012
22676942Autonomic and hemodynamic origins of pre-hypertension: central role of heredity.J Am Coll Cardiol2012
22012986A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population.Circulation: Cardiovascular Genetics2011
21045684Contemporary approaches to genetic influences on hypertension.Curr Opin Nephrol Hypertens2011
21104344Catecholamine storage vesicles: role of core protein genetic polymorphisms in hypertension.Curr Hypertens Rep2011
20814407Human dopamine β-hydroxylase promoter variant alters transcription in chromaffin cells, enzyme secretion, and blood pressure.Am J Hypertens2011
21558123A common genetic variant in the 3'-UTR of vacuolar H+-ATPase ATP6V0A1 creates a micro-RNA motif to alter chromogranin A processing and hypertension risk.Circ Cardiovasc Genet2011
21551321Proteomic analysis yields an unexpected trans-acting point in control of the human sympathochromaffin phenotype.Circ Cardiovasc Genet2011
21597914Catecholamine biosynthesis and secretion: physiological and pharmacological effects of secretin.Cell Tissue Res2011
20359597Common functional genetic variants in catecholamine storage vesicle protein promoter motifs interact to trigger systemic hypertension.J Am Coll Cardiol2010
20888525Isoprostane, an "intermediate phenotype" for oxidative stress heritability, risk trait associations, and the influence of chromogranin B polymorphism.J Am Coll Cardiol2010
21079583Hypertension as a maladaptive "fight-or-flight" response?: confirmatory molecular genetic evidence from the human catecholamine biosynthetic pathway.Am J Hypertens2010
20729505Role of reactive oxygen species in hyperadrenergic hypertension: biochemical, physiological, and pharmacological evidence from targeted ablation of the chromogranin a (Chga) gene.Circ Cardiovasc Genet2010
21061160Naturally occurring genetic variants in human chromogranin A (CHGA) associated with hypertension as well as hypertensive renal disease.Cell Mol Neurobiol2010
20009769Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure.J Hypertens2010
20571875Human tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension.Cell Mol Neurobiol2010
20216088Genome-wide case/control studies in hypertension: only the 'tip of the iceberg'.J Hypertens2010
20124442Human tyrosine hydroxylase natural genetic variation: delineation of functional transcriptional control motifs disrupted in the proximal promoter.Circ Cardiovasc Genet2010
20204374Conserved regulatory motifs at phenylethanolamine N-methyltransferase (PNMT) are disrupted by common functional genetic variation: an integrated computational/experimental approach.Mamm Genome2010
20655339Human catestatin peptides differentially regulate infarct size in the ischemic-reperfused rat heart.Regul Pept2010
20668031Urocortin 2 lowers blood pressure and reduces plasma catecholamine levels in mice with hyperadrenergic activity.Endocrinology2010
20011129Autonomic function in hypertension; role of genetic variation at the catecholamine storage vesicle protein chromogranin B.Circ Cardiovasc Genet2009
19712806Neuropeptide Y(1) Receptor NPY1R discovery of naturally occurring human genetic variants governing gene expression in cella as well as pleiotropic effects on autonomic activity and blood pressure in vivo.J Am Coll Cardiol2009
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