Expression analysis of Runx3 and other Runx family members during Xenopus development - Wikidata - wikimedia - TriplyDB

Expression analysis of Runx3 and other Runx family members during Xenopus development

Expression analysis of Runx3 and other Runx family members during Xenopus development

http://www.wikidata.org/entity/Q33957215

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A new mechanistic scenario for the origin and evolution of vertebrate cartilage Six1 is a key regulator of the developmental and evolutionary architecture of sensory neurons in craniates Characterization of the Runx gene family in a jawless vertebrate, the Japanese lamprey (Lethenteron japonicum).Xaml1/Runx1 is required for the specification of Rohon-Beard sensory neurons in Xenopus.Expression of periostin during Xenopus laevis embryogenesis.prdm1a Regulates sox10 and islet1 in the development of neural crest and Rohon-Beard sensory neurons.Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning.EBF factors drive expression of multiple classes of target genes governing neuronal development Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos.

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P2860

Expression analysis of Runx3 and other Runx family members during Xenopus development

http://www.wikidata.org/entity/Q33957215

description

2010 nî lūn-bûn

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2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Expression analysis of Runx3 and other Runx family members during Xenopus development

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Expression analysis of Runx3 and other Runx family members during Xenopus development

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type

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Expression analysis of Runx3 and other Runx family members during Xenopus development

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Expression analysis of Runx3 and other Runx family members during Xenopus development

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prefLabel

Expression analysis of Runx3 and other Runx family members during Xenopus development

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Expression analysis of Runx3 and other Runx family members during Xenopus development

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J.GEP.2010.04.004

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Gene Expression Patterns

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Expression analysis of Runx3 and other Runx family members during Xenopus development

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Byung-Yong Park

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Jean-Pierre Saint-Jeannet

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P2860

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

AML1, AML2, and AML3, the human members of the runt domain gene-family: cDNA structure, expression, and chromosomal localization

Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pter

Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

The RUNX genes: gain or loss of function in cancer

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

Causal relationship between the loss of RUNX3 expression and gastric cancer

Runx3 controls the axonal projection of proprioceptive dorsal root ganglion neurons

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