Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

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Corrigendum: Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

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Q53097211-E9122A68-48D3-4674-9319-5151286D42B8

P921

Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

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http://www.wikidata.org/entity/Q50441391

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

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Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

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Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

@en

Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

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Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

@en

Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

@nl

P1476

Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

@en

P2093

Daisuke Kurokawa

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

Hidehito Inagaki

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

Hiroki Kurahashi

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

Ichiro Morioka

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

Kandai Nozu

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

Kazumoto Iijima

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

Keiji Yamana

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

Mariko Taniguchi-Ikeda

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

Miwako Nagasaka

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

Risa Harada

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P2507

Corrigendum: Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

P2860

Regulation of Notch1 and Dll4 by vascular endothelial growth factor in arterial endothelial cells: implications for modulating arteriogenesis and angiogenesis

Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies

Structural Analysis Uncovers Lipid-Binding Properties of Notch Ligands

Notch ligand delta-like1: X-ray crystal structure and binding affinity

Recessive mutations in DOCK6, encoding the guanidine nucleotide exchange factor DOCK6, lead to abnormal actin cytoskeleton organization and Adams-Oliver syndrome

Mutations in NOTCH1 cause Adams-Oliver syndrome

Adams-Oliver syndrome revisited

Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies

Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome

RBPJ mutations identified in two families affected by Adams-Oliver syndrome

P2888

jhg.2017.48

P304

851-855

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

P31

scholarly article

P356

10.1038/JHG.2017.48

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

P433

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

P478

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

P577

2017-04-27T00:00:00Z

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P698

28446798

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Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

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P921

P921

Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.

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P1433

P1476

P2093

P2507

P2860

P2888

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2507

P2860

P2888

P304

P31

P356

P433

P478

P577

P698