Genetic modifiers of cardiovascular phenotype caused by elastin haploinsufficiency act by extrinsic noncomplementation.
about
Complex genetics and the etiology of human congenital heart disease.Validation of genetically matched wild-type strain and lysyl oxidase-like 1 knockout mouse model of pelvic organ prolapseNOX2 As a Target for Drug Development: Indications, Possible Complications, and Progress.Background differences in baseline and stimulated MMP levels influence abdominal aortic aneurysm susceptibility.Engineered zinc-finger proteins can compensate genetic haploinsufficiency by transcriptional activation of the wild-type allele: application to Willams-Beuren syndrome and supravalvular aortic stenosisModeling and rescue of the vascular phenotype of Williams-Beuren syndrome in patient induced pluripotent stem cells.Loss of Elastic Fiber Integrity Compromises Common Carotid Artery Function: Implications for Vascular Aging.Williams syndrome predisposes to vascular stiffness modified by antihypertensive use and copy number changes in NCF1Altered reactivity of resistance vasculature contributes to hypertension in elastin insufficiency.Molecular and phenotypic characterization of atypical Williams-Beuren syndrome.Minoxidil improves vascular compliance, restores cerebral blood flow and alters extracellular matrix gene expression in a model of chronic vascular stiffness.Elastin, arterial mechanics, and cardiovascular disease
P2860
Q33790650-12106B6A-6031-42F4-A082-91936F53CC04Q34139558-12B8C914-67B8-4336-BCFB-C7EC2B96721BQ35985407-17DC0A1E-9FC5-4AE3-900F-620D1B899D33Q36384137-4ECA3622-CD81-47E1-9D3E-4277E8970F08Q36401362-EB6A51E9-C786-4807-9B60-E5ACD024586FQ36861726-5165F9FC-F9E4-4EB8-B846-52F28EE1AD29Q37204699-DF7BC58B-6A9C-47C7-9B50-9FC912CEF064Q37598778-C71EA5EE-799E-4A3D-8AE7-4164F4F54A8CQ37629251-F9E9523F-CA06-45B4-9FC7-991D484EEBCBQ46221633-EF9964E9-7891-402C-9E60-72C6E5736208Q51766157-F798DD55-40A7-4274-A2FA-D68709BC602AQ57171390-5805AC8C-32B2-46AA-84CB-A3D02427BE60
P2860
Genetic modifiers of cardiovascular phenotype caused by elastin haploinsufficiency act by extrinsic noncomplementation.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Genetic modifiers of cardiovas ...... extrinsic noncomplementation.
@ast
Genetic modifiers of cardiovas ...... extrinsic noncomplementation.
@en
type
label
Genetic modifiers of cardiovas ...... extrinsic noncomplementation.
@ast
Genetic modifiers of cardiovas ...... extrinsic noncomplementation.
@en
prefLabel
Genetic modifiers of cardiovas ...... extrinsic noncomplementation.
@ast
Genetic modifiers of cardiovas ...... extrinsic noncomplementation.
@en
P2093
P2860
P356
P1476
Genetic modifiers of cardiovas ...... extrinsic noncomplementation.
@en
P2093
Beth A Kozel
Christopher H Ciliberto
Robert P Mecham
Russell H Knutsen
Thomas J Broekelmann
P2860
P304
44926-44936
P356
10.1074/JBC.M111.274779
P407
P577
2011-11-02T00:00:00Z