UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Waardenburg syndrome type 2 with a de novo variant of the SOX10 gene: a case report

BMC medical genomics, 2024-04, Vol.17 (1), p.104-104, Article 104

2024

Volltextzugriff (PDF)

Polymorphism of tumor necrosis factor alpha (TNF-alpha) gene promoter, circulating TNF-alpha level, and cardiovascular risk factor for ischemic stroke

Journal of neuroinflammation, 2012-10, Vol.9 (1), p.235-235, Article 235

2012

Volltextzugriff (PDF)

A Functional Variant in APOA5/A4/C3/A1 Gene Cluster Contributes to Elevated Triglycerides and Severity of CAD by Interfering With MicroRNA 3201 Binding Efficiency

Journal of the American College of Cardiology, 2014-07, Vol.64 (3), p.267-277

2014

Volltextzugriff (PDF)

Aortic root aortopathy in bicuspid aortic valve associated with high genetic risk

BMC cardiovascular disorders, 2021-08, Vol.21 (1), p.413-413, Article 413

2021

Volltextzugriff (PDF)

Effects of Shuanghuanglian oral liquids on patients with COVID-19: a randomized, open-label, parallel-controlled, multicenter clinical trial

Frontiers of medicine, 2021-10, Vol.15 (5), p.704-717

2021

Volltextzugriff (PDF)

The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA

BMC medical genetics, 2019-05, Vol.20 (1), p.91-91, Article 91

2019

Volltextzugriff (PDF)

FBN1 Splice-Altering Mutations in Marfan Syndrome: A Case Report and Literature Review

Genes, 2022-10, Vol.13 (10), p.1842

2022

Volltextzugriff (PDF)

RBM20 Is a Candidate Gene for Hypertrophic Cardiomyopathy

Canadian journal of cardiology, 2021-11, Vol.37 (11), p.1751-1759

2021

Volltextzugriff (PDF)

MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway

Science China. Life sciences, 2020-09, Vol.63 (9), p.1347-1362

2020

Volltextzugriff (PDF)

FBN2 pathogenic variants in congenital contractural arachnodactyly with severe cardiovascular manifestations

Connective tissue research, 2024-05, Vol.65 (3), p.214-225

2024

Volltextzugriff (PDF)

Identification of COL3A1 variants associated with sporadic thoracic aortic dissection: a case--control study

Frontiers of medicine, 2021-06, Vol.15 (3), p.438-447

2021

Volltextzugriff (PDF)

Comparison of High-Resolution Melting Analysis, TaqMan Allelic Discrimination Assay, and Sanger Sequencing for Clopidogrel Efficacy Genotyping in Routine Molecular Diagnostics

The Journal of molecular diagnostics : JMD, 2013-09, Vol.15 (5), p.600-606

2013

Volltextzugriff (PDF)

Variants of genes encoding collagens and matrix metalloproteinase system increased the risk of aortic dissection

Science China. Life sciences, 2017, Vol.60 (1), p.57-65

2017

Volltextzugriff (PDF)

Association analysis of polymorphisms in ROCK2 with cardiovascular disease in a Chinese population

PloS one, 2013-01, Vol.8 (1), p.e53905-e53905

2013

Volltextzugriff (PDF)

Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism

Fertility and sterility, 2018-08, Vol.110 (3), p.486-495.e5

2018

Volltextzugriff (PDF)

A PLN nonsense variant causes severe dilated cardiomyopathy in a novel autosomal recessive inheritance mode

International journal of cardiology, 2019-03, Vol.279, p.122-125

2019

Volltextzugriff (PDF)

Association of TSR1 Variants and Spontaneous Coronary Artery Dissection

Journal of the American College of Cardiology, 2019-07, Vol.74 (2), p.167-176

2019

Volltextzugriff (PDF)

Genetic arrhythmias complicating patients with dilated cardiomyopathy

Heart rhythm, 2020-02, Vol.17 (2), p.305-312

2020

Volltextzugriff (PDF)

Novel URAT1 mutations caused acute renal failure after exercise in two Chinese families with renal hypouricemia

Gene, 2013-01, Vol.512 (1), p.97-101

2013

Volltextzugriff (PDF)

Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing

Journal of translational medicine, 2014-06, Vol.12 (1), p.173-173, Article 173

2014

Volltextzugriff (PDF)

A novel nonsense mutation in LMNA gene identified by Exome Sequencing in an atrial fibrillation family

European journal of medical genetics, 2016-08, Vol.59 (8), p.396-400

2016

Volltextzugriff (PDF)

Next-generation sequencing identifies novel mutations in the FBN1 gene for two Chinese families with Marfan syndrome

Molecular medicine reports, 2016-07, Vol.14 (1), p.151-158

2016

Volltextzugriff (PDF)

Stereoselective uptake and metabolism of prothioconazole caused oxidative stress in zebrafish (Danio rerio)

Journal of hazardous materials, 2020-09, Vol.396, p.122756, Article 122756

2020

Volltextzugriff (PDF)

Stereoselective endocrine-disrupting effects of the chiral triazole fungicide prothioconazole and its chiral metabolite

Environmental pollution (1987), 2019-08, Vol.251, p.30-36

2019

Volltextzugriff (PDF)

Maresin 1 Alleviates Diabetic Kidney Disease via LGR6-Mediated cAMP-SOD2-ROS Pathway

Oxidative medicine and cellular longevity, 2022, Vol.2022, p.7177889-15

2022

Volltextzugriff (PDF)

1 – 25 von 25

Suche als RSS-Feed

Aktive Filter

ThemaHumans

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(25)
Mit Volltextzugriff
(25)

Publikationsform

Artikel
(25)

Sprache

Englisch
(25)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Waardenburg syndrome type 2 with a de novo variant of the SOX10 gene: a case report

Polymorphism of tumor necrosis factor alpha (TNF-alpha) gene promoter, circulating TNF-alpha level, and cardiovascular risk factor for ischemic stroke

A Functional Variant in APOA5/A4/C3/A1 Gene Cluster Contributes to Elevated Triglycerides and Severity of CAD by Interfering With MicroRNA 3201 Binding Efficiency

Aortic root aortopathy in bicuspid aortic valve associated with high genetic risk

Effects of Shuanghuanglian oral liquids on patients with COVID-19: a randomized, open-label, parallel-controlled, multicenter clinical trial

The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA

FBN1 Splice-Altering Mutations in Marfan Syndrome: A Case Report and Literature Review

RBM20 Is a Candidate Gene for Hypertrophic Cardiomyopathy

MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway

FBN2 pathogenic variants in congenital contractural arachnodactyly with severe cardiovascular manifestations

Identification of COL3A1 variants associated with sporadic thoracic aortic dissection: a case--control study

Comparison of High-Resolution Melting Analysis, TaqMan Allelic Discrimination Assay, and Sanger Sequencing for Clopidogrel Efficacy Genotyping in Routine Molecular Diagnostics

Variants of genes encoding collagens and matrix metalloproteinase system increased the risk of aortic dissection

Association analysis of polymorphisms in ROCK2 with cardiovascular disease in a Chinese population

Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism

A PLN nonsense variant causes severe dilated cardiomyopathy in a novel autosomal recessive inheritance mode

Association of TSR1 Variants and Spontaneous Coronary Artery Dissection

Genetic arrhythmias complicating patients with dilated cardiomyopathy

Novel URAT1 mutations caused acute renal failure after exercise in two Chinese families with renal hypouricemia

Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing

A novel nonsense mutation in LMNA gene identified by Exome Sequencing in an atrial fibrillation family

Next-generation sequencing identifies novel mutations in the FBN1 gene for two Chinese families with Marfan syndrome

Stereoselective uptake and metabolism of prothioconazole caused oxidative stress in zebrafish (Danio rerio)

Stereoselective endocrine-disrupting effects of the chiral triazole fungicide prothioconazole and its chiral metabolite

Maresin 1 Alleviates Diabetic Kidney Disease via LGR6-Mediated cAMP-SOD2-ROS Pathway

Aktive Filter

Suchergebnisse filtern