Effects of reduced connexin43 function on skull development in the Cx43I130T/+ mutant mouse that models oculodentodigital dysplasia-Reference-Cited by-同舟云学术

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Effects of reduced connexin43 function on skull development in the Cx43I130T/+ mutant mouse that models oculodentodigital dysplasia

Published:2020-07 Issue: Volume:136 Page:115365
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Jarvis Sommer E.,Lee Jae Eun,Jewlal Elizabeth,Barr Kevin,Kelly Gregory M.,Laird Dale W.,Willmore Katherine E.

Funder

Natural Sciences & Engineering Research Council

Canadian Institutes of Health Research

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference47 articles.

1. Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of Oculodentodigital dysplasia;Paznekas;Am. J. Hum. Genet.,2003

2. GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype;Paznekas;Hum. Mutat.,2009

3. Syndromic and non-syndromic disease-linked Cx43 mutations;Laird;FEBS Lett.,2014

4. A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia;Flenniken;Development,2005

5. The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans;Dobrowolski;Hum. Mol. Genet.,2007

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1. Discordant growth of nasal cartilage and bone contributes to phenotypic variability of the skull in a mouse model;Developmental Dynamics;2023-03-30

2. Human iPSC-Derived Astrocytes: A Powerful Tool to Study Primary Astrocyte Dysfunction in the Pathogenesis of Rare Leukodystrophies;International Journal of Molecular Sciences;2021-12-27

3. Connexin 43 contributes to phenotypic robustness of the mouse skull;Developmental Dynamics;2021-06-24

4. Effects of advanced maternal age and acute prenatal alcohol exposure on mouse offspring growth and craniofacial phenotype;Alcoholism: Clinical and Experimental Research;2021-06-04

5. Effects of Reduced Connexin43 Function on Mandibular Morphology and Osteogenesis in Mutant Mouse Models of Oculodentodigital Dysplasia;Calcified Tissue International;2020-09-09

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