徐

徐让 (Rang Xu)

Shanghai Jiao Tong University

H指数:15

被引数:807

个人简介

"学科代码：100202 性别：女学科名称：儿科学培养单位：附属新华医院三级学科导师类型：博士生导师专业领域名称：联系方式：专业领域代码：邮编：邮箱地址：rangxu@shsmu.edu.cn"

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Slo1 Deficient Myoblast Exosomes-Derived miR-222-3p Inhibits Osteogenic Differentiation via Targeting of STAT3

Slo1缺陷型成肌细胞外泌体来源的miR-222-3p通过靶向STAT3抑制成骨分化

JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE

IF9.1

2025-12-010

OAAI

Dlc1 deletion activates the canonical Wnt pathway at an early stage and affects subsequent cardiac differentiation in mouse embryonic stem cells

Dlc1基因的缺失在早期激活了经典Wnt通路，并影响小鼠胚胎干细胞随后的心脏分化。

Genes & Diseases

IF9.4

2025-09-090

OAAI

ccdc141 is required for left-right axis development by regulating cilia formation in the Kupffer's vesicle of zebrafish

JOURNAL OF GENETICS AND GENOMICS

IF7.1

2024-09-010

PRE

Variants in FOXC1 and FOXC2 identified in patients with conotruncal heart defects

在圆锥躯干心脏缺陷患者中鉴定出FOXC1和FOXC2的变异

GENOMICS

IF3

2024-05-010

OAAI

Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing

基于靶向测序的605例中国非综合征型心脏圆锥管缺损患儿致病变异分析

GENOMICS

IF3

2023-09-011

OAAI

LOF variants identifying candidate genes of laterality defects patients with congenital heart disease

PLOS GENETICS

IF3.7

2022-12-025

OAAI

De novo disruptive heterozygous MMP21 variants are potential predisposing genetic risk factors in Chinese Han heterotaxy children

HUMAN GENOMICS

IF4.3

2022-09-193

OAAI

Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation

圆锥躯干心脏缺陷患者中TBX1顺式调节元件的变异会损害GATA6-mediated的反式激活

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-07-3111

OAAI

SOX7 suppresses endothelial-to-mesenchymal transitions by enhancing VE-cadherin expression during outflow tract development

CLINICAL SCIENCE

IF7.7

2021-03-2610

Exome sequencing identifies a FHOD3 p.S527del mutation in a Chinese family with hypertrophic cardiomyopathy

JOURNAL OF GENE MEDICINE

IF2.2

2020-01-1410

PREAI

Tet inactivation disrupts YY1 binding and long-range chromatin interactions during embryonic heart development

Tet失活会破坏胚胎心脏发育过程中的YY1结合和长距离染色质相互作用

NATURE COMMUNICATIONS

IF15.7

2019-09-2050

OAAI

Smilagenin Protects Dopaminergic Neurons in Chronic MPTP/Probenecid-Lesioned Parkinson's Disease Models

FRONTIERS IN CELLULAR NEUROSCIENCE

IF4

2019-02-0521

OAAI

A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

JOURNAL OF TRANSLATIONAL MEDICINE

IF7.5

2018-09-213

OAAI

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity

SCIENTIFIC REPORTS

IF3.9

2017-03-082

OAAI

Identification of candidate genes for congenital heart defects on proximal chromosome 8p

SCIENTIFIC REPORTS

IF3.9

2016-11-038

OAAI

Using exome sequencing to identify the cause of myocardial hypertrophy in a Chinese family

MOLECULAR MEDICINE REPORTS

IF3.5

2015-05-221

OAAI

Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects

MOLECULAR MEDICINE REPORTS

IF3.5

2014-05-1628

OAAI

Coupling of 6-phosphogluconate dehydrogenase with NADPH oxidase in neutrophils: Nox2 activity regulation by NADPH availability

FASEB JOURNAL

IF4.2

2011-03-2816

PREAI

Involvement of miR-21 in resistance to daunorubicin by regulating PTEN expression in the leukaemia K562 cell line

FEBS LETTERS

IF3

2010-12-25103

PREAI

徐让 (Rang Xu)

个人简介

教育背景

工作经历

荣誉奖项

研究方向