Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorder.
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Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosusMarfan's syndromeThe molecular genetics of Marfan syndrome and related disordersMatrix metalloproteinases and descending aortic aneurysms: parity, disparity, and switchLessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm.Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysmsA balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysmGenomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibshipsMYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin IIReport of the National Heart, Lung, and Blood Institute and National Marfan Foundation Working Group on research in Marfan syndrome and related disorders.Ascending thoracic aortic aneurysms protect against myocardial infarctionsRare copy number variants disrupt genes regulating vascular smooth muscle cell adhesion and contractility in sporadic thoracic aortic aneurysms and dissectionsCoronary arteriomegaly in a patient with Ehlers-Danlos syndrome and multiple aneurysms--a case report.Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD.Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve.Bicuspid aortic valve and thoracic aortic aneurysm: three patient populations, two disease phenotypes, and one shared genotype.Genetic basis of thoracic aortic aneurysms and aortic dissections.Pathobiology of idiopathic ascending aortic aneurysms.TGFβRIIb mutations trigger aortic aneurysm pathogenesis by altering transforming growth factor β2 signal transductionAortic disease in the young: genetic aneurysm syndromes, connective tissue disorders, and familial aortic aneurysms and dissectionsRecent progress in genetics of Marfan syndrome and Marfan-associated disorders.Surgery insight: the dilated ascending aorta--indications for surgical intervention.Etiology, pathogenesis and management of thoracic aortic aneurysm.Characterization of the inflammatory cells in ascending thoracic aortic aneurysms in patients with Marfan syndrome, familial thoracic aortic aneurysms, and sporadic aneurysms.A single nucleotide polymorphism in the matrix metalloproteinase 9 gene (-8202A/G) is associated with thoracic aortic aneurysms and thoracic aortic dissection.Familial thoracic aortic aneurysms and dissections: identification of a novel locus for stable aneurysms with a low risk for progression to aortic dissection.Acute aortic syndromes and thoracic aortic aneurysm.Molecular mechanisms of thoracic aortic dissection.Cellular and molecular mechanisms of thoracic aortic aneurysms.Epidemiology of thoracic aortic dissection.Review of molecular and mechanical interactions in the aortic valve and aorta: implications for the shared pathogenesis of aortic valve disease and aortopathy.The genetic architecture of non-syndromic thoracic aortic aneurysm.Aetiology and management of hereditary aortopathy.The genetics and genomics of thoracic aortic disease.Cardiovascular manifestations in men and women carrying a FBN1 mutation.TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies.Brain hemorrhages in Jacobsen syndrome: A retrospective review of six cases and clinical recommendations.Large deletions and uniparental disomy detected by SNP arrays in adults with thoracic aortic aneurysms and dissections.Familial thoracic aortic aneurysm/dissection with patent ductus arteriosus: genetic arguments for a particular pathophysiological entityFamilial thoracic aortic aneurysms and dissections: three families with early-onset ascending and descending aortic dissections in women
P2860
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P2860
Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorder.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Identification of a chromosome ...... ically heterogeneous disorder.
@en
type
label
Identification of a chromosome ...... ically heterogeneous disorder.
@en
prefLabel
Identification of a chromosome ...... ically heterogeneous disorder.
@en
P2093
P1433
P1476
Identification of a chromosome ...... ically heterogeneous disorder.
@en
P2093
Campagna R
Devereux RB
Henderson K
Milewicz DM
Vaughan CJ
P304
P356
10.1161/01.CIR.103.20.2469
P407
P577
2001-05-01T00:00:00Z