Common mechanisms in development and disease: BMP signaling in craniofacial development-Reference-Cited by-同舟云学术

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Common mechanisms in development and disease: BMP signaling in craniofacial development

Published:2016-02 Issue: Volume:27 Page:129-139
ISSN:1359-6101
Container-title:Cytokine & Growth Factor Reviews
language:en
Short-container-title:Cytokine & Growth Factor Reviews

Author:

Graf Daniel,Malik Zeba,Hayano Satoru,Mishina Yuji

Funder

School of Dentistry, University of Alberta

Swiss National Science Foundation

National Institutes of Health

Department of Defense

Japan Society for the Promotion of Science

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Endocrinology, Diabetes and Metabolism

Reference142 articles.

1. Signals from the brain induce variation in avian facial shape;Hu;Dev. Dyn.,2015

2. Noggin null allele mice exhibit a microform of holoprosencephaly;Lana-Elola;Hum. Mol. Genet.,2011

3. The mammalian twisted gastrulation gene functions in foregut and craniofacial development;Petryk;Dev. Biol.,2004

4. Holoprosencephaly: signaling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans;Petryk;Wiley Interdiscip. Rev. Dev. Biol.,2015

5. Signals and switches in Mammalian neural crest cell differentiation;Bhatt;Cold Spring Harb Perspect. Biol.,2013

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1. Craniofacial chondrogenesis in organoids from human stem cell-derived neural crest cells;iScience;2024-04

2. A BMP-controlled metabolic/epigenetic signaling cascade directs midfacial morphogenesis;Journal of Clinical Investigation;2024-03-11

3. Apoptotic Extracellular Vesicles Induced Endothelial Cell-Mediated Autologous Stem Cell Recruitment Dominates Allogeneic Stem Cell Therapeutic Mechanism for Bone Repair;ACS Nano;2024-03-11

4. Grainyhead-like 2 interacts with noggin to regulate tissue fusion in mouse;Development;2024-02-28

5. Genetic association and functional validation of ZFP36L2 in non-syndromic orofacial cleft subtypes;Journal of Human Genetics;2024-02-06

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