Analysis of PRICKLE 1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations-Reference-Cited by-同舟云学术

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Analysis of PRICKLE 1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations

Published:2013-12-17 Issue:2 Volume:2 Page:138-151
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Yang Tian¹,Jia Zhonglin²³⁴,Bryant‐Pike Whitney⁵,Chandrasekhar Anand⁵,Murray Jeffrey C.²,Fritzsch Bernd¹,Bassuk Alexander G.²

Affiliation:

1. Department of Biology University of Iowa Iowa City Iowa 52242

2. Department of Pediatrics University of Iowa Iowa City Iowa 52242

3. State Key Laboratory of Oral Diseases West China Hospital of Stomatology Sichuan University Chengdu China

4. Department of Cleft Lip and Palate Surgery West China Hospital of Stomatology Sichuan University Chengdu China

5. Division of Biological Sciences University of Missouri Columbia Missouri 65211

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.53

Reference64 articles.

1. Fine Tuning of Craniofacial Morphology by Distant-Acting Enhancers

2. Wnt/PCP signaling: A veritable polar star in establishing patterns of polarity in embryonic tissues

3. A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome

4. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

5. HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo

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1. Loss of PRICKLE1 leads to abnormal endometrial epithelial architecture, decreased embryo implantation, and reduced fertility in mice;2024-08-08

2. Prickle1‐driven basement membrane deposition of the iPSC‐derived embryoid bodies is separable from the establishment of apicobasal polarity;Cell Proliferation;2024-01-07

3. Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting;Genetics in Medicine;2023-10

4. The pathological and therapeutically role of mesenchymal stem cell (MSC)-derived exosome in degenerative diseases; Particular focus on LncRNA and microRNA;Pathology - Research and Practice;2023-10

5. Are palatal rugae reliable markers for 3D superimposition and forensic human identification after palatal expansion? A systematic review;Forensic Science International;2023-10

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