Scoping review of literature in urethral duplication

NIAID Data Ecosystem2026-03-13 收录

尿道重复

泌尿系统先天异常

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https://data.mendeley.com/datasets/8jy398xzhm 数据链接链接失效反馈

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资源简介：

This data is an excel spreadsheet of valuable information from publications in English language on urethral duplication from 2001 to 2021.

创建时间：

2022-02-24

Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies

基因调控

泌尿系统先天异常

Congenital anomalies of the kidney and urinary tract (CAKUT) are disorders resulting from defects in the development of the kidneys and their outflow tract. Copy number variations (CNVs) have been ide

DataCite Commons2023-07-05 更新190

Vesicoureteral Reflux and Other Urinary Tract Malformations in Mice Compound Heterozygous for Pax2 and Emx2

泌尿系统先天异常

发育遗传学

Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney disease in children. This disease group includes a spectrum of urinary tract defects including

NIAID Data Ecosystem80

Kids First: Genetics of kidney and urinary tract malformations. Kids First: Genetics of kidney and urinary tract malformations

儿科肾脏疾病遗传学

泌尿系统先天异常

Congenital defects of the kidney and urinary tract are a common cause of kidney failure in children and adults and elucidation of the genetics of these disorders will provide new opportunities for dia

NIAID Data Ecosystem40

of Transcriptome-wide based identification of miRs in congenital anomalies of the kidney and urinary tract (CAKUT) in children: the significant upregulation of tissue miR-144 expression

基因表达分析

泌尿系统先天异常

of Transcriptome-wide based identification of miRs in congenital anomalies of the kidney and urinary tract (CAKUT) in children: the significant upregulation of tissue miR-144 expression

DataCite Commons2020-08-26 更新80

Data_Sheet_9_SLC20A1 Is Involved in Urinary Tract and Urorectal Development.PDF

泌尿系统先天异常

基因功能研究

Previous studies in developing Xenopus and zebrafish reported that the phosphate transporter slc20a1a is expressed in pronephric kidneys. The recent identification of SLC20A1 as a monoallelic candidat

NIAID Data Ecosystem40

Scoping review of literature in urethral duplication

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