UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 46

Sortiert nach

Expression of the familial cardiac valvular dystrophy gene, filamin‐A, during heart morphogenesis

Developmental dynamics, 2010-07, Vol.239 (7), p.2118-2127

2010

Link zum Volltext

Verfügbarkeit prüfen

Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram pattern

Heart rhythm, 2008-11, Vol.5 (11), p.1561-1564

2008

Link zum Volltext

Verfügbarkeit prüfen

Heritability of aortic valve stenosis and evidence of bicuspid enrichment in families with tricuspid aortic valve stenosis

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association meta-analysis in 652,134 participants identifies 9 novel susceptibility loci for aortic stenosis

European heart journal, 2020-11, Vol.41 (Supplement_2), p.1862

2020

Link zum Volltext

Verfügbarkeit prüfen

Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

Link zum Volltext

Verfügbarkeit prüfen

GENECHOC study: genetic markers of arrhythmic risk in heart failure

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

Link zum Volltext

Verfügbarkeit prüfen

Mutations in the gene encoding filamin a as a cause for familial cardiac valvular dystrophy

Circulation (New York, N.Y.), 2007-01, Vol.115 (1), p.40-49

2007

Link zum Volltext

Verfügbarkeit prüfen

Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation

Biochimica et biophysica acta, 2014-02, Vol.1843 (2), p.234-244

2014

Link zum Volltext

Verfügbarkeit prüfen

Myofibroblastic differentiation of rat valvular interstitial cells in culture

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.250-250

2020

Link zum Volltext

Verfügbarkeit prüfen

Variation In Lpa And Calcific Aortic Valve Stenosis In Patients Undergoing Cardiac Surgery And Familial Risk Of Aortic Valve Microcalcification

Atherosclerosis, 2019-08, Vol.287, p.e16-e17

2019

Link zum Volltext

Verfügbarkeit prüfen

Paradoxycal restricted motion in diastole is a frequent finding in mitral valve prolapse/dystrophy patients

Archives of Cardiovascular Diseases Supplements, 2019-06, Vol.11 (3), p.e315-e315

2019

Link zum Volltext

Verfügbarkeit prüfen

Relevance and diagnostic performance of genes involved in arrhythmogenic cardiomyopathy

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.261-261

2020

Link zum Volltext

Verfügbarkeit prüfen

Functional, structural and molecular characterization of a new mitral valve prolapse animal model: The FLNA-P637Q KI rat

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.251-252

2020

Link zum Volltext

Verfügbarkeit prüfen

Identification by Whole Genome Sequencing of a New Gene Causing Hereditary Sinus Node and Atrioventricular Conduction Dysfunction

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.263-263

2020

Link zum Volltext

Verfügbarkeit prüfen

Genechoc Study Genetic markers of arrhythmic risk in heart failure

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.264-264

2020

Link zum Volltext

Verfügbarkeit prüfen

Phenotypic and genotypic approach of a large family with early onset tricuspid aortic valve sclerosis-stenosis: A multimodality evaluation

Archives of Cardiovascular Diseases Supplements, 2019-01, Vol.11 (1), p.66-67

2019

Link zum Volltext

Verfügbarkeit prüfen

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome

Archives of Cardiovascular Diseases Supplements, 2018-04, Vol.10 (2), p.195-195

2018

Link zum Volltext

Verfügbarkeit prüfen

Familial Deafness, Congenital Heart Defects, and Posterior Embryotoxon Caused by Cysteine Substitution in the First Epidermal-Growth-Factor–Like Domain of Jagged 1

American journal of human genetics, 2002-07, Vol.71 (1), p.180-186

2002

Link zum Volltext

Verfügbarkeit prüfen

Methods for sampling and assessment in relation to the spatial pattern of phoma stem canker (Leptosphaeria maculans) in oilseed rape

European journal of plant pathology, 2004-02, Vol.110 (2), p.183-192

2004

Link zum Volltext

Verfügbarkeit prüfen

Magnetic resonance sounding (MRS) and resistivity characterisation of a mountain hard rock aquifer: the Ringelbach Catchment, Vosges Massif, France

Near surface geophysics (Online), 2005-11, Vol.3 (4), p.267-274

2005

Link zum Volltext

Verfügbarkeit prüfen

Apparent Polar Wander Path Smoothing with spherical splines

Physics of the earth and planetary interiors, 1994-08, Vol.85 (1), p.67-82

1994

Link zum Volltext

Verfügbarkeit prüfen

Paleomagnetism of Permo-Triassic red beds in the western Pyrenees: evidence for strong clockwise rotations of the Paleozoic units

Tectonophysics, 1988-12, Vol.156 (1), p.75-88

1988

Link zum Volltext

Verfügbarkeit prüfen

Paleomagnetism of the Lower Cretaceous redbeds from northern Spain: evidence for a multistage acquisition of magnetization

Tectonophysics, 1987-08, Vol.139 (3), p.239-253

1987

Link zum Volltext

Verfügbarkeit prüfen

Paleomagnetism of Permo-Triassic Redbeds from the Asturias and Cantabric Chain (northern Spain): evidence for strong lower Tertiary remagnetizations

Tectonophysics, 1987-09, Vol.140 (2), p.179-191

1987

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 46

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(40)
Mit Volltextzugriff
(43)

Publikationsform

Artikel
(45)
Bücher
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Expression of the familial cardiac valvular dystrophy gene, filamin‐A, during heart morphogenesis

Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram pattern

Heritability of aortic valve stenosis and evidence of bicuspid enrichment in families with tricuspid aortic valve stenosis

Genome-wide association meta-analysis in 652,134 participants identifies 9 novel susceptibility loci for aortic stenosis

Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25

GENECHOC study: genetic markers of arrhythmic risk in heart failure

Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome

Mutations in the gene encoding filamin a as a cause for familial cardiac valvular dystrophy

Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation

Myofibroblastic differentiation of rat valvular interstitial cells in culture

Variation In Lpa And Calcific Aortic Valve Stenosis In Patients Undergoing Cardiac Surgery And Familial Risk Of Aortic Valve Microcalcification

Paradoxycal restricted motion in diastole is a frequent finding in mitral valve prolapse/dystrophy patients

Relevance and diagnostic performance of genes involved in arrhythmogenic cardiomyopathy

Functional, structural and molecular characterization of a new mitral valve prolapse animal model: The FLNA-P637Q KI rat

Identification by Whole Genome Sequencing of a New Gene Causing Hereditary Sinus Node and Atrioventricular Conduction Dysfunction

Genechoc Study Genetic markers of arrhythmic risk in heart failure

Phenotypic and genotypic approach of a large family with early onset tricuspid aortic valve sclerosis-stenosis: A multimodality evaluation

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome

Familial Deafness, Congenital Heart Defects, and Posterior Embryotoxon Caused by Cysteine Substitution in the First Epidermal-Growth-Factor–Like Domain of Jagged 1

Methods for sampling and assessment in relation to the spatial pattern of phoma stem canker (Leptosphaeria maculans) in oilseed rape

Magnetic resonance sounding (MRS) and resistivity characterisation of a mountain hard rock aquifer: the Ringelbach Catchment, Vosges Massif, France

Apparent Polar Wander Path Smoothing with spherical splines

Paleomagnetism of Permo-Triassic red beds in the western Pyrenees: evidence for strong clockwise rotations of the Paleozoic units

Paleomagnetism of the Lower Cretaceous redbeds from northern Spain: evidence for a multistage acquisition of magnetization

Paleomagnetism of Permo-Triassic Redbeds from the Asturias and Cantabric Chain (northern Spain): evidence for strong lower Tertiary remagnetizations

Suchergebnisse filtern