Arginylation-dependent neural crest cell migration is essential for mouse development

10.1371/journal.pgen.1000878

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Main Authors:	Kurosaka S., Leu N.A., Zhang F., Bunte R., Saha S., Wang J., Guo C., He W., Kashina A.
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	2019
Subjects:	arginyltransferase cre recombinase Wnt1 protein aminoacyltransferase arginine Wnt1 protein, mouse animal cell animal experiment animal model animal tissue arginylation article behavior disorder brain development breathing disorder cell cycle regulation cell migration cell motility cell motion chemical modification controlled study embryo gene deletion growth retardation in situ hybridization knockout mouse lethality morphogenesis mouse neural crest cell nonhuman palate disease pathogenesis pharynx disease promoter region protein protein interaction signal transduction skull defect animal biological model bone cell adhesion cell culture coculture congenital malformation craniofacial malformation enzymology gene inactivation growth, development and aging mesoderm metabolism mouse mutant neural crest newborn palate pathology survival Mus Aminoacyltransferases Animals Animals, Newborn Arginine Bone and Bones Cell Adhesion Cell Movement Cells, Cultured Coculture Techniques Craniofacial Abnormalities Gene Knockout Techniques Growth and Development Mesoderm Mice Mice, Knockout Models, Biological Neural Crest Palate Survival Analysis Wnt1 Protein
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/161666
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1616662023-11-01T07:29:23Z Arginylation-dependent neural crest cell migration is essential for mouse development Kurosaka S. Leu N.A. Zhang F. Bunte R. Saha S. Wang J. Guo C. He W. Kashina A. DUKE-NUS MEDICAL SCHOOL arginyltransferase cre recombinase Wnt1 protein aminoacyltransferase arginine arginyltransferase Wnt1 protein Wnt1 protein, mouse animal cell animal experiment animal model animal tissue arginylation article behavior disorder brain development breathing disorder cell cycle regulation cell migration cell motility cell motion chemical modification controlled study embryo gene deletion growth retardation in situ hybridization knockout mouse lethality morphogenesis mouse neural crest cell nonhuman palate disease pathogenesis pharynx disease promoter region protein protein interaction signal transduction skull defect animal biological model bone cell adhesion cell culture cell motion coculture congenital malformation craniofacial malformation enzymology gene inactivation growth, development and aging mesoderm metabolism mouse mutant neural crest newborn palate pathology survival Mus Aminoacyltransferases Animals Animals, Newborn Arginine Bone and Bones Cell Adhesion Cell Movement Cells, Cultured Coculture Techniques Craniofacial Abnormalities Gene Knockout Techniques Growth and Development Mesoderm Mice Mice, Knockout Models, Biological Neural Crest Palate Survival Analysis Wnt1 Protein 10.1371/journal.pgen.1000878 PLoS Genetics 6 3 e1000878 2019-11-06T09:34:15Z 2019-11-06T09:34:15Z 2010 Article Kurosaka S., Leu N.A., Zhang F., Bunte R., Saha S., Wang J., Guo C., He W., Kashina A. (2010). Arginylation-dependent neural crest cell migration is essential for mouse development. PLoS Genetics 6 (3) : e1000878. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1000878 15537390 https://scholarbank.nus.edu.sg/handle/10635/161666 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20191101
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	arginyltransferase cre recombinase Wnt1 protein aminoacyltransferase arginine arginyltransferase Wnt1 protein Wnt1 protein, mouse animal cell animal experiment animal model animal tissue arginylation article behavior disorder brain development breathing disorder cell cycle regulation cell migration cell motility cell motion chemical modification controlled study embryo gene deletion growth retardation in situ hybridization knockout mouse lethality morphogenesis mouse neural crest cell nonhuman palate disease pathogenesis pharynx disease promoter region protein protein interaction signal transduction skull defect animal biological model bone cell adhesion cell culture cell motion coculture congenital malformation craniofacial malformation enzymology gene inactivation growth, development and aging mesoderm metabolism mouse mutant neural crest newborn palate pathology survival Mus Aminoacyltransferases Animals Animals, Newborn Arginine Bone and Bones Cell Adhesion Cell Movement Cells, Cultured Coculture Techniques Craniofacial Abnormalities Gene Knockout Techniques Growth and Development Mesoderm Mice Mice, Knockout Models, Biological Neural Crest Palate Survival Analysis Wnt1 Protein
spellingShingle	arginyltransferase cre recombinase Wnt1 protein aminoacyltransferase arginine arginyltransferase Wnt1 protein Wnt1 protein, mouse animal cell animal experiment animal model animal tissue arginylation article behavior disorder brain development breathing disorder cell cycle regulation cell migration cell motility cell motion chemical modification controlled study embryo gene deletion growth retardation in situ hybridization knockout mouse lethality morphogenesis mouse neural crest cell nonhuman palate disease pathogenesis pharynx disease promoter region protein protein interaction signal transduction skull defect animal biological model bone cell adhesion cell culture cell motion coculture congenital malformation craniofacial malformation enzymology gene inactivation growth, development and aging mesoderm metabolism mouse mutant neural crest newborn palate pathology survival Mus Aminoacyltransferases Animals Animals, Newborn Arginine Bone and Bones Cell Adhesion Cell Movement Cells, Cultured Coculture Techniques Craniofacial Abnormalities Gene Knockout Techniques Growth and Development Mesoderm Mice Mice, Knockout Models, Biological Neural Crest Palate Survival Analysis Wnt1 Protein Kurosaka S. Leu N.A. Zhang F. Bunte R. Saha S. Wang J. Guo C. He W. Kashina A. Arginylation-dependent neural crest cell migration is essential for mouse development
description	10.1371/journal.pgen.1000878
author2	DUKE-NUS MEDICAL SCHOOL
author_facet	DUKE-NUS MEDICAL SCHOOL Kurosaka S. Leu N.A. Zhang F. Bunte R. Saha S. Wang J. Guo C. He W. Kashina A.
format	Article
author	Kurosaka S. Leu N.A. Zhang F. Bunte R. Saha S. Wang J. Guo C. He W. Kashina A.
author_sort	Kurosaka S.
title	Arginylation-dependent neural crest cell migration is essential for mouse development
title_short	Arginylation-dependent neural crest cell migration is essential for mouse development
title_full	Arginylation-dependent neural crest cell migration is essential for mouse development
title_fullStr	Arginylation-dependent neural crest cell migration is essential for mouse development
title_full_unstemmed	Arginylation-dependent neural crest cell migration is essential for mouse development
title_sort	arginylation-dependent neural crest cell migration is essential for mouse development
publishDate	2019
url	https://scholarbank.nus.edu.sg/handle/10635/161666
_version_	1781791816477048832

Arginylation-dependent neural crest cell migration is essential for mouse development

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