The etiology of cleft palate formation in BMP7-deficient mice. - Wikidata - wikimedia - TriplyDB

The etiology of cleft palate formation in BMP7-deficient mice.

The etiology of cleft palate formation in BMP7-deficient mice.

http://www.wikidata.org/entity/Q30456163

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Molecular basis of cleft palates in mice Divergent palate morphology in turtles and birds correlates with differences in proliferation and BMP2 expression during embryonic development BMPR1B mutation causes Pierre Robin sequence BMP7 Gene involved in nonsyndromic orofacial clefts in Western Han Chinese.Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.Common mechanisms in development and disease: BMP signaling in craniofacial development.Dislocated Tongue Muscle Attachment and Cleft Palate Formation.Bone morphogenetic protein type I receptor inhibition induces cleft palate associated with micrognathia and cleft lower lip in mice.

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P2860

The etiology of cleft palate formation in BMP7-deficient mice.

http://www.wikidata.org/entity/Q30456163

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2013 nî lūn-bûn

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2013 թուականի Մարտին հրատարակուած գիտական յօդուած

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2013 թվականի մարտին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

The etiology of cleft palate formation in BMP7-deficient mice.

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The etiology of cleft palate formation in BMP7-deficient mice.

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The etiology of cleft palate formation in BMP7-deficient mice.

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The etiology of cleft palate formation in BMP7-deficient mice.

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The etiology of cleft palate formation in BMP7-deficient mice.

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The etiology of cleft palate formation in BMP7-deficient mice.

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The etiology of cleft palate formation in BMP7-deficient mice.

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Anastasiia Kozlova

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Daniel Graf

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Maria Alexiou

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Susanne Blumer

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Thaleia Kouskoura

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Vasiliki Zouvelou

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P2860

Signal transduction of bone morphogenetic protein receptors

Regulation of BMP7 expression during kidney development

Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects

Clinical and Molecular genetics of Stickler syndrome

The genetic basis of craniofacial and dental abnormalities

Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction

Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest

Mandibular growth retardation as a cause of cleft palate in mice homozygous for the chondrodysplasia gene

Shox2-deficient mice exhibit a rare type of incomplete clefting of the secondary palate

Multiple functions of Snail family genes during palate development in mice

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