Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans-Reference-Cited by-同舟云学术

Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans

Published:2021-01-14 Issue:3 Volume:185 Page:836-840
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Gofin Yoel¹²^ORCID,Mackay Laura Palmer¹²,Machol Keren¹²^ORCID,Keswani Sundeep²³,Potocki Lorraine¹²,Di Gregorio Eleonora⁴,Naretto Valeria Giorgia⁴,Brusco Alfredo⁴⁵^ORCID,Hernandez‐Garcia Andres¹,Scott Daryl A.¹²⁶^ORCID

Affiliation:

1. Department of Molecular and Human Genetics Baylor College of Medicine Houston Texas USA

2. Texas Children's Hospital Houston Texas USA

3. Department of Surgery Baylor College of Medicine Houston Texas USA

4. Medical Genetics Unit Città della Salute e della Scienza University Hospital Torino Italy

5. Department of Medical Sciences University of Turin Torino Italy

6. Department of Molecular Physiology and Biophysics Baylor College of Medicine Houston Texas USA

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62066

Reference19 articles.

1. Mice with a targeted disruption of the Fgfrl1 gene die at birth due to alterations in the diaphragm

2. Molecular Mechanisms of Fibroblast Growth Factor Signaling in Physiology and Pathology

3. Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning Algorithm

4. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia

5. Downregulation of FGFRL1 Contributes to the Development of the Diaphragmatic Defect in the Nitrofen Model of Congenital Diaphragmatic Hernia

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