Genetics of hereditary large vessel diseases. - Wikidata - awgldk - TriplyDB

Genetics of hereditary large vessel diseases.

Genetics of hereditary large vessel diseases.

http://www.wikidata.org/entity/Q38601760

about

Molecular Regulation of Arterial Aneurysms: Role of Actin Dynamics and microRNAs in Vascular Smooth Muscle Left main coronary artery compression by a dilated main pulmonary artery and left coronary sinus of Valsalva aneurysm in a patient with heritable pulmonary arterial hypertension and FLNA mutation.Characterization of SMAD2 Activation in Human Thoracic Aortic Aneurysm.

P2860

Q41369096-D09AB63F-88F9-4F89-ADDD-E52E42F1C615 Q47975927-AB7173B0-F672-4DD9-BF46-4DCC26B5FDBE Q52313129-B26C5AB6-1C29-4D49-BA41-9C251E6DAADD

P2860

Genetics of hereditary large vessel diseases.

http://www.wikidata.org/entity/Q38601760

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Genetics of hereditary large vessel diseases.

@en

type

label

Genetics of hereditary large vessel diseases.

@en

prefLabel

Genetics of hereditary large vessel diseases.

@en

P1433

Q38601760-7153B039-05DC-41A0-92D3-1F797AD9E2BB

P1476

Q38601760-6D638F96-7944-4332-899E-11C4F1805B09

P2093

Q38601760-28A68C5A-B459-43F9-B1A8-BA109DA6E45C

Q38601760-EA93514A-6143-47EC-AC3A-2678CD345B0C

P2860

Q38601760-02038DA7-2CC8-4D72-B89D-66ED09AEEF29

Q38601760-07FDDCB8-EF4F-4FD9-B614-7958BAD6B7D5

Q38601760-0BDC94F2-A2EA-42F0-BCA4-FAE29F96E6E5

Q38601760-0CA25EF1-CD8F-4C86-B00C-56BE790373F2

Q38601760-15A5CC08-04A2-42BB-BAD2-FBD30ABE45E9

Q38601760-1E598880-115F-4597-B759-8991476B4AA4

Q38601760-21B2333C-01B9-41F3-96DB-51E69803CC43

Q38601760-27FBFB4C-16A5-4EF1-AA8F-90BFC52EC21A

Q38601760-2BFE21AA-7222-42A1-8ED4-6012854FB477

Q38601760-2FD691D5-51D2-45F3-B350-68C2F7209C94

P2888

Q38601760-1AB2F1A3-355B-4A25-BA5A-5A09E7A6FE09

P304

Q38601760-F0299E44-896D-42D8-B868-53B92A520403

P31

Q38601760-A3DA63DC-2BE6-4DD9-80F1-AC5980946BED

P356

Q38601760-CCF33F31-21A8-40ED-9276-192FCE40152B

P433

Q38601760-CDFCBE91-FEAE-4732-9667-105CB4819CED

P478

Q38601760-63AD93EF-6465-4046-9F5D-A6C2EEBED938

P577

Q38601760-F68E1B68-279C-4634-A2D4-7CD1B1DBF9ED

P698

Q38601760-9E772794-08A7-4893-BBD1-33CECA0B0039

P356

P1433

Journal of Human Genetics

P1476

Genetics of hereditary large vessel diseases.

@en

P2093

Hiroko Morisaki

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

Takayuki Morisaki

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

P2860

Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

Mutations in myosin light chain kinase cause familial aortic dissections

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome

Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease

Making sense of latent TGFbeta activation

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Aneurysm syndromes caused by mutations in the TGF-beta receptor

P2888

P304

21-26

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

P31

scholarly article

P356

10.1038/JHG.2015.119

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

P433

1

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

P478

61

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

P577

2015-10-08T00:00:00Z

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

P698

26446364

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