Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus-Reference-Cited by-同舟云学术

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Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus

Published:2014-04-01 Issue:16 Volume:23 Page:4302-4314
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Roberts N. A.,Woolf A. S.,Stuart H. M.,Thuret R.,McKenzie E. A.,Newman W. G.,Hilton E. N.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/23/16/4302/1744984/ddu147.pdf

Reference50 articles.

1. Genetic and diagnostic considerations in three families with abnormalities of facial expression and congenital urinary obstruction: “The Ochoa syndrome”

2. Can a congenital dysfunctional bladder be diagnosed from a smile? The Ochoa syndrome updated

3. Three new European cases of urofacial (Ochoa) syndrome

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Heparanase 2 regulates endothelial permeability and prevents from proteinuria via VEGFA and FGF signaling;2024-08-20

2. Urofacial (Ochoa) syndrome with a founder pathogenic variant in the HPSE2 gene: a case report and mutation origin;Journal of Applied Genetics;2024-08-16

3. Botulinum toxin to improve facial expression in a patient with Urofacial (Ochoa) Syndrome;American Journal of Medical Genetics Part A;2022-11-02

4. Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder;Frontiers in Genetics;2022-06-23

5. Urofacial (ochoa) syndrome: A literature review;Journal of Pediatric Urology;2021-04

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