Craniofacial Diseases Caused by Defects in Intracellular Trafficking

dc.contributor.author Lu, Chung-Ling
dc.contributor.author Kim, Jinoh
dc.contributor.department Department of Biomedical Sciences
dc.date.accessioned 2023-04-26T20:56:31Z
dc.date.available 2023-04-26T20:56:31Z
dc.date.issued 2021-05-13
dc.description.abstract Cells use membrane-bound carriers to transport cargo molecules like membrane proteins and soluble proteins, to their destinations. Many signaling receptors and ligands are synthesized in the endoplasmic reticulum and are transported to their destinations through intracellular trafficking pathways. Some of the signaling molecules play a critical role in craniofacial morphogenesis. Not surprisingly, variants in the genes encoding intracellular trafficking machinery can cause craniofacial diseases. Despite the fundamental importance of the trafficking pathways in craniofacial morphogenesis, relatively less emphasis is placed on this topic, thus far. Here, we describe craniofacial diseases caused by lesions in the intracellular trafficking machinery and possible treatment strategies for such diseases.
dc.description.comments This article is published as Lu, Chung-Ling, and Jinoh Kim. "Craniofacial diseases caused by defects in intracellular trafficking." Genes 12, no. 5 (2021): 726. DOI: 10.3390/genes12050726. Copyright 2021 by the authors. Attribution 4.0 International (CC BY 4.0). Posted with permission.
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/3wxaeD0v
dc.language.iso en
dc.publisher MDPI
dc.source.uri https://doi.org/10.3390/genes12050726 *
dc.subject.disciplines DegreeDisciplines::Life Sciences::Genetics and Genomics::Genetics
dc.subject.disciplines DegreeDisciplines::Life Sciences::Physiology::Cellular and Molecular Physiology
dc.subject.keywords craniofacial diseases
dc.subject.keywords intracellular trafficking
dc.subject.keywords secretory pathway
dc.subject.keywords endosome/lysosome targeting
dc.subject.keywords endocytosis
dc.title Craniofacial Diseases Caused by Defects in Intracellular Trafficking
dc.type Article
dspace.entity.type Publication
relation.isAuthorOfPublication f91583bc-bf62-46a5-bcbc-549c8c6b588d
relation.isOrgUnitOfPublication 184db3f2-d93f-4571-8ad7-07c8a9e6a5c9
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