Rapid degradation of progressive ankylosis protein (ANKH) in craniometaphyseal dysplasia
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Title
Rapid degradation of progressive ankylosis protein (ANKH) in craniometaphyseal dysplasia
Authors
Keywords
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Journal
Scientific Reports
Volume 8, Issue 1, Pages -
Publisher
Springer Nature America, Inc
Online
2018-10-18
DOI
10.1038/s41598-018-34157-5
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Note: Only part of the references are listed.- Craniometaphyseal Dysplasia Mutations in ANKH Negatively Affect Human Induced Pluripotent Stem Cell Differentiation into Osteoclasts
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- A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD)
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- Evasion of Endoplasmic Reticulum Surveillance Makes Wsc1p an Obligate Substrate of Golgi Quality Control
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- Introduction of a Phe377del Mutation in ANK Creates a Mouse Model for Craniometaphyseal Dysplasia
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- Null mutations in human and mouse orthologs frequently result in different phenotypes
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