Global gene expression profiling in congenital diaphragmatic hernia (CDH) patients-Reference-Cited by-同舟云学术

Global gene expression profiling in congenital diaphragmatic hernia (CDH) patients

Published:2022-03-09 Issue:3 Volume:22 Page:359-369
ISSN:1438-793X
Container-title:Functional & Integrative Genomics
language:en
Short-container-title:Funct Integr Genomics

Author:

Gürünlüoğlu Kubilay^ORCID,Dündar Muhammed^ORCID,Unver Turgay^ORCID,Akpınar Necmettin^ORCID,Gokce Ismail Kürşad^ORCID,Gürünlüoğlu Semra^ORCID,Demircan Mehmet^ORCID,Koc Ahmet^ORCID

Funder

Inonu University

Publisher

Springer Science and Business Media LLC

Subject

Genetics,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s10142-022-00837-9.pdf

Reference43 articles.

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2. Amann R, Wyder S, Slavotinek AM, Trueb B (2014) The FgfrL1 receptor is required for development of slow muscle fibers. Dev Biol 394(2):228–241. https://doi.org/10.1016/j.ydbio.2014.08.016

3. Ameis D, Khoshgoo N, Keijzer R (2017) Abnormal lung development in congenital diaphragmatic hernia. Semin Pediatr Surg 26(3):123–128. https://doi.org/10.1053/j.sempedsurg.2017.04.011

4. Beck TF, Campeau PM, Jhangiani SN, Gambin T, Li AH, Abo-Zahrah R, Jordan VK, Hernandez-Garcia A, Wiszniewski WK, Muzny D, Gibbs RA, Boerwinkle E, Lupski JR, Lee B, Reardon W, Scott DA (2015) FBN1 contributing to familial congenital diaphragmatic hernia. Am J Med Genet A 167(4):831–836. https://doi.org/10.1002/ajmg.a.36960

5. Brady PD, Van Houdt J, Callewaert B, Deprest J, Devriendt K, Vermeesch JR (2014) Exome sequencing identifies ZFPM2 as a cause of familial isolated congenital diaphragmatic hernia and possibly cardiovascular malformations. Eur J Med Genet 57(6):247–252. https://doi.org/10.1016/j.ejmg.2014.04.006

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