Zobrazeno 1 - 10 of 24 pro vyhledávání: '"Jiazhen Chang"'
1
Akademický článek
Hypoxia reduces mouse urine output via HIF1α–mediated up–regulation of renal AQP1
Autor: Rongfang Qiao, Xiaohui Cui, Yitong Hu, Haoqing Wei, Hu Xu, Cong Zhang, Chunxiu Du, Jiazhen Chang, Yaqing Li, Wenhua Ming, Yinghui Qi, Youfei Guan, Xiaoyan Zhang
Publikováno v: Kidney Diseases, Pp 1-26 (2024)
Introduction: Patients with acute mountain sickness (AMS) due to hypoxia at high altitudes often exhibit abnormal water metabolism. Hypoxia-inducible factors (HIFs) are major regulators of adaptive responses to hypoxia. As transcription factors, HIFs
Externí odkaz: https://doaj.org/article/b332f9f6733943caac920c8cab7854bd
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2
Akademický článek
Gene Analysis of Four Families with Severe Peripartum Cardiomyopathy Reveals Known Gene Mutations and Supports the Recent Call for Screening
Autor: Mengmeng Li, Kaili Yin, Liang Chen, Jiazhen Chang, Na Hao
Publikováno v: Reviews in Cardiovascular Medicine, Vol 25, Iss 11, p 399 (2024)
Background: Peripartum cardiomyopathy (PPCM) is a rare disease that causes maternal morbidity and mortality worldwide. However, the etiology of PPCM is still unclear, and the rate of recovery varies between patients. Understanding the genetic factors
Externí odkaz: https://doaj.org/article/4ba124043ebb4e09a158910436ac2422
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3
Akademický článek
Detection of Mosaic Absence of Heterozygosity (AOH) Using Low-Pass Whole Genome Sequencing in Prenatal Diagnosis: A Preliminary Report
Autor: Yan Lü, Yulin Jiang, Xiya Zhou, Na Hao, Chenlu Xu, Ruidong Guo, Jiazhen Chang, Mengmeng Li, Hanzhe Zhang, Jing Zhou, Wei (Victor) Zhang, Qingwei Qi
Publikováno v: Diagnostics, Vol 13, Iss 18, p 2895 (2023)
Objective: Mosaicism is a common biological phenomenon in organisms and has been reported in many types of chromosome abnormalities, including the absence of heterozygosity (AOH). Due to the detection limitations of the sequencing approach, mosaic AO
Externí odkaz: https://doaj.org/article/d54c3eeabd874354bfafb9c0417408fa
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4
Akademický článek
Evaluation and Analysis of Absence of Homozygosity (AOH) Using Chromosome Analysis by Medium Coverage Whole Genome Sequencing (CMA-seq) in Prenatal Diagnosis
Autor: Yan Lü, Yulin Jiang, Xiya Zhou, Na Hao, Guizhen Lü, Xiangxue Guo, Ruidong Guo, Wenjie Liu, Chenlu Xu, Jiazhen Chang, Mengmeng Li, Hanzhe Zhang, Jing Zhou, Wei (Victor) Zhang, Qingwei Qi
Publikováno v: Diagnostics, Vol 13, Iss 3, p 560 (2023)
Objective: Absence of homozygosity (AOH) is a genetic characteristic known to cause human diseases mainly through autosomal recessive or imprinting mechanisms. The importance and necessity of accurate AOH detection has become more clinically signific
Externí odkaz: https://doaj.org/article/91e683b5e4e54e4aa40718e40177b55f
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5
Akademický článek
Automatic Measurement of Inclination Angle of Utility Poles Using 2D Image and 3D Point Cloud
Autor: Lei Chen, Jiazhen Chang, Jinli Xu, Zuowei Yang
Publikováno v: Applied Sciences, Vol 13, Iss 3, p 1688 (2023)
The utility pole inclination angle is an important parameter for determining pole health conditions. Without depth information, the angle cannot be estimated from a 2D image, and without large labeled reference pole data, it is time consuming to loca
Externí odkaz: https://doaj.org/article/8fa1c3bf374a4786998d7828f7c77738
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6
Akademický článek
Expression and localization of HSD17B13 along mouse urinary tract.
Autor: Haibo Zhang, Jiazhen Chang, Zhihong Dai, Qiuming Wang, Rongfang Qiao, Yingzhi Huang, Beibei Ma, Jiuchao Jiang, Chunhua Zhu, Wen Su, Xiaoyan Zhang, Youfei Guan
Publikováno v: American Journal of Physiology: Renal Physiology; Jul2024, Vol. 327 Issue 1, pF146-F157, 12p
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9
Factors associated with test failure in pregnant women undergoing cell-free DNA-based testing for fetal trisomy
Autor: Xiya Zhou, Jiazhen Chang, Yulin Jiang, Juntao Liu, Na Hao, Qingwei Qi
Publikováno v: Journal of medical screening. 28(4)
Objective To investigate the factors associated with cell-free DNA test failure, and the optimal subsequent management of these pregnancies. Methods This was a retrospective study of 27,363 singleton pregnancies undergoing cell-free DNA testing. Wome
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::894a03b90c316697ba8f0bb5ef307ba8
https://pubmed.ncbi.nlm.nih.gov/33884933
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10
Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes
Autor: Juntao Liu, Hua Meng, Yulin Jiang, Jiazhen Chang, Chunli Wang, Qingwei Qi, Junjie Bai, Jiangshan Guo, Mengsu Xiao, Na Hao, Mingming Wang, Xiya Zhou, Victor Wei Zhang, Zhonghui Xu, Yunshu Ouyang
Publikováno v: Genes
Volume 11
Issue 12
Genes, Vol 11, Iss 1397, p 1397 (2020)
The routine assessment to determine the genetic etiology for fetal ultrasound anomalies follows a sequential approach, which usually takes about 6&ndash
8 weeks turnaround time (TAT). We evaluated the clinical utility of simultaneous detection o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15925d9d7be8afa4588c5b69d14232d3
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