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of 10
pro vyhledávání: '"Danlei Cai"'
Autor:
Ruijue Zhu, Mingming Zhu, Boye Wang, Enen Chen, Danlei Cai, Yinghong Yang, Yi Liang, Chuqi Su, Ding Wang, Xiaofang Sun, Linhuan Huang, Yingjun Xie
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-7 (2024)
Abstract Introduction Dent disease type I is a rare X-linked recessive renal tubular disease resulting from pathogenic variants in the CLCN5 gene. Due to the rarity of Dent disease type I and the diversity of its phenotypes, its clinical diagnosis is
Externí odkaz:
https://doaj.org/article/24b2b46efe41447c85ae44857f855aa3
Autor:
Shaobin Lin, Shanshan Shi, Linhuan Huang, Ting Lei, Danlei Cai, Wenlong Hu, Yi Zhou, Yanmin Luo
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-11 (2019)
Abstract Background This study aimed to estimate the associations of copy number variants (CNVs) with fetal kidney ultrasound anomalies. A total of 331 fetuses with kidney ultrasound anomalies who underwent prenatal chromosomal microarray analyses we
Externí odkaz:
https://doaj.org/article/3fe088c466ae4f3bb53a1ced864cdd38
Akademický článek
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Autor:
Linhuan, Huang, Danlei, Cai, Zhiming, He, Shu, Kong, Jiayi, Chen, Jiayi, Peng, Chuqi, Su, Yinghong, Yang, Ding, Wang, Yingjun, Xie, Yanmin, Luo
Publikováno v:
Journal of Maternal-Fetal & Neonatal Medicine; Dec2024, Vol. 37 Issue 1, p1-8, 8p
Publikováno v:
Applied Biochemistry and Biotechnology. 194:1340-1358
Ocimum tenuiflorum (KT) is a common ethnobotanical plant of Southeast Asia. The ethnic communities of these regions use the various parts of the plants, especially the leaves, for the treatment of various ailments like cold and flu, chronic infection
Publikováno v:
Doklady Biochemistry and Biophysics. 497:151-157
Acute kidney injury (AKI), one of the frequently diagnosed and serious sepsis induced complication has high morbidity and mortality. The present study investigated the effect of cynaropicrin on AKI induced pathological damage in rat model in vivo. Tr
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 59, Iss 1, Pp 123-126 (2020)
Objective: We present the prenatal diagnosis of a class II 1q21.1 microdeletion in monozygotic (MZ) twins with discordant phenotypes. Case report: A monochorionic diamniotic twin pair presented with discordant ultrasound anomalies; twin A had cardiov
Autor:
Linhuan Huang, Yi Zhou, Danlei Cai, Shanshan Shi, Shaobin Lin, Yanmin Luo, Wenlong Hu, Ting Lei
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-11 (2019)
Molecular Cytogenetics
Molecular Cytogenetics
Background This study aimed to estimate the associations of copy number variants (CNVs) with fetal kidney ultrasound anomalies. A total of 331 fetuses with kidney ultrasound anomalies who underwent prenatal chromosomal microarray analyses were enroll
Publikováno v:
Experimental and Therapeutic Medicine
The phenotypic variability associated with 22q11.2 deletion syndrome (22q11.2DS) is well known. In the present study, the cases of three unrelated adult patients with chromosome 22q11.2DS and nearly normal features are described, along with their rep
Publikováno v:
Experimental & Therapeutic Medicine; 2015, Vol. 9 Issue 3, p823-828, 6p