Genome-wide analysis of renal gene expression during hyperoxaluria development

ChEBI2012-12-20 更新2026-07-21 收录

肝肾疾病分子机制

高草酸尿症基因表达

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Genome-wide analysis of renal gene expression during hyperoxaluria development

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2012-12-20

A single-nucleus RNA-sequencing pipeline to decipher the molecular anatomy and pathophysiology of human kidneys

肾脏单细胞转录组

肝肾疾病分子机制

Defining cellular and molecular identities within the kidney is necessary to understand its organization and function in health and disease. Here we demonstrate a reproducible method with minimal arti

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HMOX1 expression depending on the studied parameters.

肝肾疾病分子机制

丙型肝炎遗传学

ALT - alanine aminotransferase, genotypes of IL28B: CC and not CC (CT and TT). In liverbiopsy: G- grade of inflammation and necrosis, S-stage of fibrosis.*Genotype 1 versus 3 p = 0.0501, genotype 1 ve

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Protein Inhibitor of Activated STAT, PIASy Regulates α-Smooth Muscle Actin Expression by Interacting with E12 in Mesangial Cells

肝肾疾病分子机制

转录调控

Phenotypic transformation of mesangial cells (MCs) is implicated in the development of glomerular disease; however, the mechanisms underlying their altered genetic program is still unclear. α-smooth m

NIAID Data Ecosystem10

Mus musculus strain:C57BL6 Transcriptome or Gene expression. Mus musculus strain:C57BL6

肝肾疾病分子机制

突变体基因组学

Mis-sense mutations of Inverted Formin 2 (INF2) are among the most common causes of genetic FSGS with or without Charcot-Marie-Tooth (CMT) disease. Here, we extracted glomeruli from Heterozygous INF2

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Supplementary Material for: The Role of CXCL12 in Kidney Diseases: A Friend or Foe?

肝肾疾病分子机制

趋化因子CXCL12功能

Background: Chemokines are a family of proteins mainly mediating the homing and migration of various cells. The CXC chemokine CXCL12 is a member of low-weight-molecular chemokines. In the kidney, CXCL

Figshare2021-04-06 更新20

Genome-wide analysis of renal gene expression during hyperoxaluria development

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