Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs

Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs

Item
http://www.wikidata.org/entity/Q24673860
Investigation of association between PFO complicated by cryptogenic stroke and a common variant of the cardiac transcription factor GATA4.The use of the twin model to investigate the genetics and epigenetics of skin diseases with genomic, transcriptomic and methylation data.Effects of disturbed flow on vascular endothelium: pathophysiological basis and clinical perspectivesForkhead box C2 promoter variant c.-512C>T is associated with increased susceptibility to chronic venous diseasesMatrix Metalloproteinases as Regulators of Vein Structure and Function: Implications in Chronic Venous Disease.Absence of venous valves in mice lacking Connexin37Matrix metalloproteinases as potential targets in the venous dilation associated with varicose veins.Segregated Foxc2, NFATc1 and Connexin expression at normal developing venous valves, and Connexin-specific differences in the valve phenotypes of Cx37, Cx43, and Cx47 knockout mice.A multicenter review of epidemiology and management of varicose veins for national guidance.Pathogenesis of varicose veins and implications for clinical management.What is the medical rationale for the treatment of varicose veins?Molecular Aspects of Wound Healing and the Rise of Venous Leg Ulceration: Omics Approaches to Enhance Knowledge and Aid Diagnostic Discovery.Biological findings from the PheWAS catalog: focus on connective tissue-related disorders (pelvic floor dysfunction, abdominal hernia, varicose veins and hemorrhoids).Association of polymorphisms near the FOXC2 gene with the risk of varicose veins in ethnic Russians.Matrix Metalloproteinases in Remodeling of Lower Extremity Veins and Chronic Venous Disease.Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
P2860

Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs

Item
http://www.wikidata.org/entity/Q24673860
description
2005 nî lūn-bûn
@nan
2005 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մարտին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@ast
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@en
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@nl
type
label
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@ast
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@en
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@nl
prefLabel
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@ast
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@en
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@nl
P1433
P1476
P2093
P2860
P304
P31
P3181
P356
P407
P433
P478
P50
P577
P5875
P698
P921
P932
P3181
P356
P1433
P1476
Linkage to the FOXC2 region of ...... lthy, unselected sibling pairs
@en
P2093
P2860
P304
P31
P3181
P356
P407
P433
P478
P50
P577
P5875
P698
P921
P932