about
klf2a couples mechanotransduction and zebrafish valve morphogenesis through fibronectin synthesis.Dchs1-Fat4 regulation of polarized cell behaviours during skeletal morphogenesis.Genetics and Genomics of Congenital Heart Disease.Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse.Differential MicroRNA Expression Profile in Myxomatous Mitral Valve Prolapse and Fibroelastic Deficiency ValvesMatrix Metalloproteinase Polymorphisms in Patients with Floppy Mitral Valve/Mitral Valve Prolapse (FMV/MVP) and FMV/MVP Syndrome.A role for primary cilia in aortic valve development and disease.How to develop a clinic for sudden cardiac arrest survivors and families of non-survivors.The evolution of mitral valve prolapse: insights from the Framingham Heart Study.Analysis of Serum Metabolites to Diagnose Bicuspid Aortic ValveMitral Valve Prolapse: Multimodality Imaging and Genetic Insights.New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study.Hemodynamic Forces Sculpt Developing Heart Valves through a KLF2-WNT9B Paracrine Signaling Axis.Genetics of syndromic and non-syndromic mitral valve prolapse.Deleterious variants in DCHS1 are prevalent in sporadic cases of mitral valve prolapse.Heritability of Mitral Regurgitation: Observations From the Framingham Heart Study and Swedish Population.Atypical Cadherin Dachsous1b Interacts with Ttc28 and Aurora B to Control Microtubule Dynamics in Embryonic Cleavages.Mechanistic insights of the left ventricle structure and fibrosis in the arrhythmogenic mitral valve prolapse.
P2860
Q27316170-CD84385A-CA34-4AD3-9D06-ACE07A03B25FQ27318196-4E3D2E32-FE3D-43C7-9ED6-25685009A222Q30235241-B6C0639B-D327-4217-B651-FF56458B0092Q33718349-52780100-4271-4432-B187-E3B68D737AC1Q36939321-FD665AAE-523B-4B90-B170-99BAFBB885DAQ38657246-354F74C2-E855-4CB9-AABC-DB0E4A7454D6Q38757391-71403F71-A3CD-4899-ACD5-016C0F78FAC4Q39085578-89B3455E-A4FA-4437-B404-BEB31ABE82BCQ39399228-313D3739-70DA-4543-A2AC-3EF34437F229Q42368724-E98224F0-4D62-4C00-A7F0-011F3EC2B6E7Q46290208-B8315450-95EA-43D8-8280-A84205F53264Q46808997-26A70303-E674-4D91-9354-C8137F5BB1FDQ47619529-17FCF604-31B2-4E3A-9A0A-E0AD1AB9C8D9Q47722741-878A5292-7B31-4C43-9823-B903E9D2AA53Q47806929-E35520C1-67DA-42A6-8746-500881947EF6Q47832929-C74103BC-6222-48FC-B9E0-068985A826B6Q54979554-46B6B6E1-F834-467B-83E8-0EE4B849FEE7Q55333292-32C4CD4E-2A32-41DE-9326-23498B02C87F
P2860
description
2015 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Nature
@fr
artículu científicu espublizáu en 2015
@ast
scientific journal article
@en
vedecký článok (publikovaný 2015/09/03)
@sk
vědecký článek publikovaný v roce 2015
@cs
wetenschappelijk artikel (gepubliceerd op 2015/09/03)
@nl
наукова стаття, опублікована у вересні 2015
@uk
مقالة علمية (نشرت في 3-9-2015)
@ar
name
Mutations in DCHS1 cause mitral valve prolapse
@ast
Mutations in DCHS1 cause mitral valve prolapse
@en
Mutations in DCHS1 cause mitral valve prolapse
@nl
type
label
Mutations in DCHS1 cause mitral valve prolapse
@ast
Mutations in DCHS1 cause mitral valve prolapse
@en
Mutations in DCHS1 cause mitral valve prolapse
@nl
prefLabel
Mutations in DCHS1 cause mitral valve prolapse
@ast
Mutations in DCHS1 cause mitral valve prolapse
@en
Mutations in DCHS1 cause mitral valve prolapse
@nl
P2093
P2860
P50
P921
P3181
P356
P1433
P1476
Mutations in DCHS1 cause mitral valve prolapse
@en
P2093
Adrian Chester
Amanda Johnson
Andy Wessels
Annemarieke deVlaming
Charles Simpson
Christopher Jett
David J. Milan
David S. Peal
Donald R. Menick
Florie Charles
P2860
P2888
P304
P3181
P356
10.1038/NATURE14670
P407
P50
P577
2015-09-03T00:00:00Z
P5875
P6179
1053732697