Phenotypic and molecular description of an individual with a disruptive variant in the SULF2 gene-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Phenotypic and molecular description of an individual with a disruptive variant in the SULF2 gene

Published:2019-12-13 Issue:3 Volume:29 Page:144-147
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Kirola Laxmi,Edgar-Zarate Courtney L.,Rook Brita,Rowell Amy C.,Wood Tim,Uchimura Kenji,Schwartz Charles E.,Zarate Yuri A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health

Reference12 articles.

1. Substrate specificity and domain functions of extracellular heparan sulfate 6-O-endosulfatases, qsulf1 and qsulf2.;Ai;J Biol Chem,2006

2. SULF1 and SULF2 regulate heparan sulfate-mediated GDNF signaling for esophageal innervation.;Ai;Development,2007

3. Secreted sulfatases sulf1 and sulf2 have overlapping yet essential roles in mouse neonatal survival.;Holst;Plos One,2007

4. Mesomelia-synostoses syndrome results from deletion of SULF1 and SLCO5A1 genes at 8q13.;Isidor;Am J Hum Genet,2010

5. Sulf1 and sulf2 expression in the nervous system and its role in limiting neurite outgrowth in vitro.;Joy;Exp Neurol,2015

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP