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Augmented Indian hedgehog signaling in cranial neural crest cells leads to craniofacial abnormalities and dysplastic temporomandibular joint in mice
by
Song, Yingnan
, Gu, Shuping
, Chen, YiPing
, Ye, Wenduo
, Yang, Ling
in
alleles
/ Animals
/ Biomedical and Life Sciences
/ Biomedicine
/ Cellular biology
/ Craniofacial abnormalities
/ Craniofacial Abnormalities - embryology
/ Craniofacial Abnormalities - genetics
/ Craniofacial Abnormalities - pathology
/ Embryo, Mammalian - embryology
/ Embryo, Mammalian - pathology
/ gain-of-function mutation
/ gene overexpression
/ Genetic engineering
/ genetically modified organisms
/ Hedgehog Proteins - genetics
/ Hedgehog Proteins - metabolism
/ Human Genetics
/ Mice
/ Mice, Transgenic
/ Molecular Medicine
/ mutants
/ Mutation
/ neural crest
/ Neural Crest - metabolism
/ Neural Crest - pathology
/ palate
/ Proteomics
/ Regular Article
/ Rodents
/ Signal Transduction
/ skeleton
/ Studies
/ Temporomandibular Joint Disorders - embryology
/ Temporomandibular Joint Disorders - genetics
/ Temporomandibular Joint Disorders - pathology
2016
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Augmented Indian hedgehog signaling in cranial neural crest cells leads to craniofacial abnormalities and dysplastic temporomandibular joint in mice
by
Song, Yingnan
, Gu, Shuping
, Chen, YiPing
, Ye, Wenduo
, Yang, Ling
in
alleles
/ Animals
/ Biomedical and Life Sciences
/ Biomedicine
/ Cellular biology
/ Craniofacial abnormalities
/ Craniofacial Abnormalities - embryology
/ Craniofacial Abnormalities - genetics
/ Craniofacial Abnormalities - pathology
/ Embryo, Mammalian - embryology
/ Embryo, Mammalian - pathology
/ gain-of-function mutation
/ gene overexpression
/ Genetic engineering
/ genetically modified organisms
/ Hedgehog Proteins - genetics
/ Hedgehog Proteins - metabolism
/ Human Genetics
/ Mice
/ Mice, Transgenic
/ Molecular Medicine
/ mutants
/ Mutation
/ neural crest
/ Neural Crest - metabolism
/ Neural Crest - pathology
/ palate
/ Proteomics
/ Regular Article
/ Rodents
/ Signal Transduction
/ skeleton
/ Studies
/ Temporomandibular Joint Disorders - embryology
/ Temporomandibular Joint Disorders - genetics
/ Temporomandibular Joint Disorders - pathology
2016
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Augmented Indian hedgehog signaling in cranial neural crest cells leads to craniofacial abnormalities and dysplastic temporomandibular joint in mice
by
Song, Yingnan
, Gu, Shuping
, Chen, YiPing
, Ye, Wenduo
, Yang, Ling
in
alleles
/ Animals
/ Biomedical and Life Sciences
/ Biomedicine
/ Cellular biology
/ Craniofacial abnormalities
/ Craniofacial Abnormalities - embryology
/ Craniofacial Abnormalities - genetics
/ Craniofacial Abnormalities - pathology
/ Embryo, Mammalian - embryology
/ Embryo, Mammalian - pathology
/ gain-of-function mutation
/ gene overexpression
/ Genetic engineering
/ genetically modified organisms
/ Hedgehog Proteins - genetics
/ Hedgehog Proteins - metabolism
/ Human Genetics
/ Mice
/ Mice, Transgenic
/ Molecular Medicine
/ mutants
/ Mutation
/ neural crest
/ Neural Crest - metabolism
/ Neural Crest - pathology
/ palate
/ Proteomics
/ Regular Article
/ Rodents
/ Signal Transduction
/ skeleton
/ Studies
/ Temporomandibular Joint Disorders - embryology
/ Temporomandibular Joint Disorders - genetics
/ Temporomandibular Joint Disorders - pathology
2016
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Augmented Indian hedgehog signaling in cranial neural crest cells leads to craniofacial abnormalities and dysplastic temporomandibular joint in mice
Journal Article
Augmented Indian hedgehog signaling in cranial neural crest cells leads to craniofacial abnormalities and dysplastic temporomandibular joint in mice
2016
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Overview
Extensive studies have pinpointed the crucial role of Indian hedgehog (Ihh) signaling in the development of the appendicular skeleton and the essential function of Ihh in the formation of the temporomandibular joint (TMJ). In this study, we have investigated the effect of augmented Ihh signaling in TMJ development. We took a transgenic gain-of-function approach by overexpressing Ihh in the cranial neural crest (CNC) cells using a conditional Ihh transgenic allele and the Wnt1-Cre allele. We found that Wnt1-Cre-mediated tissue-specific overexpression of Ihh in the CNC lineage caused severe craniofacial abnormalities, including cleft lip/palate, encephalocele, anophthalmos, micrognathia, and defective TMJ development. In the mutant TMJ, the glenoid fossa was completely absent, whereas the condyle and the articular disc appeared relatively normal with slightly delayed chondrocyte differentiation. Our findings thus demonstrate that augmented Ihh signaling is detrimental to craniofacial development, and that finely tuned Ihh signaling is critical for TMJ formation. Our results also provide additional evidence that the development of the condyle and articular disc is independent of the glenoid fossa.
Publisher
Springer Berlin Heidelberg,Springer,Springer Nature B.V
Subject
/ Animals
/ Biomedical and Life Sciences
/ Craniofacial Abnormalities - embryology
/ Craniofacial Abnormalities - genetics
/ Craniofacial Abnormalities - pathology
/ Embryo, Mammalian - embryology
/ Embryo, Mammalian - pathology
/ genetically modified organisms
/ Hedgehog Proteins - genetics
/ Hedgehog Proteins - metabolism
/ Mice
/ mutants
/ Mutation
/ palate
/ Rodents
/ skeleton
/ Studies
/ Temporomandibular Joint Disorders - embryology
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