SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome.

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Cadherins function during the collective cell migration of Xenopus Cranial Neural Crest cells: revisiting the role of E-cadherin.CXCL12-CXCR4 signalling plays an essential role in proper patterning of aortic arch and pulmonary arteries.

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SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome.

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http://www.wikidata.org/entity/Q41901850

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

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2016年論文

@zh-tw

2016年论文

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2016年论文

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2016年论文

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name

SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome.

@en

type

Item

label

SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome.

@en

prefLabel

SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome.

@en

P1476

SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome

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Claire Fournier-Thibault

http://www.w3.org/2001/XMLSchema#string

Jean-Loup Duband

http://www.w3.org/2001/XMLSchema#string

Sophie Escot

http://www.w3.org/2001/XMLSchema#string

P2860

Impaired B-lymphopoiesis, myelopoiesis, and derailed cerebellar neuron migration in CXCR4- and SDF-1-deficient mice

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development

Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome

Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants

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scholarly article

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10.1080/21675511.2016.1195050

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Claire Fournier-Thibault

Jean-Loup Duband

Sophie Escot

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2016-06-01T00:00:00Z

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SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome.

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P2860

P2860

SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome.

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type

label

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932