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...

Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery

Circulation (New York, N.Y.), 2019-01, Vol.139 (4), p.489-501

2019

Volltextzugriff (PDF)

Abstract 13546: Putative Titin Mutations Associated With Both Long QT Syndrome and Left Ventricular Noncompaction

Circulation (New York, N.Y.), 2021-11, Vol.144 (Suppl_1)

2021

Volltextzugriff (PDF)

Abstract 13147: Monitoring Central Arterial Pressure on the Chest Surface: Initial Results From Two Pilot Studies in Human Subjects

Circulation (New York, N.Y.), 2023-11, Vol.148 (Suppl_1)

2023

Volltextzugriff (PDF)

Abstract 16997: Reaffirmation of GPD1L-A280V as a Brugada Syndrome Disease-Causing Variant

Circulation (New York, N.Y.), 2020-11, Vol.142 (Suppl_3 Suppl 3), p.A16997-A16997

2020

Volltextzugriff (PDF)

Statins Decrease Oxidative Stress and ICD Therapies

Cardiology Research and Practice, 2010-01, Vol.2010 (2010), p.55-61

2010

Volltextzugriff (PDF)

Abstract 19030: High Mortality in Cardiomyopathy Patients Heterozygous for the CFTR ΔF508 Cystic Fibrosis Mutation

Circulation (New York, N.Y.), 2015-11, Vol.132 (Suppl_3 Suppl 3), p.A19030-A19030

2015

Volltextzugriff (PDF)

Abstract 17984: No Longer Silent: A Synonymous Coding SNP Modifying a Novel MicroRNA-24: SCN5A Interaction Associates With Non-Arrhythmic Death in Heart Failure

Circulation (New York, N.Y.), 2015-11, Vol.132 (Suppl_3 Suppl 3), p.A17984-A17984

2015

Volltextzugriff (PDF)

Array-Based Comparative Genomic Hybridization Identifies CDK4 and FOXM1 Alterations as Independent Predictors of Survival in Malignant Peripheral Nerve Sheath Tumor

Clinical cancer research, 2011-04, Vol.17 (7), p.1924-1934

2011

Volltextzugriff (PDF)

Tumor suppressor Tsc1 is a new Hsp90 co‐chaperone that facilitates folding of kinase and non‐kinase clients

The EMBO journal, 2017-12, Vol.36 (24), p.3650-3665

2017

Volltextzugriff (PDF)

Astrocyte-specific TSC1 conditional knockout mice exhibit abnormal neuronal organization and seizures

Annals of neurology, 2002-09, Vol.52 (3), p.285-296

2002

Volltextzugriff (PDF)

MicroRNA Profiling Reveals Marker of Motor Neuron Disease in ALS Models

The Journal of neuroscience, 2017-05, Vol.37 (22), p.5574-5586

2017

Volltextzugriff (PDF)

Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue Sarcomas

Cell, 2017-11, Vol.171 (4), p.950-965.e28

2017

Volltextzugriff (PDF)

Mutation in glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

Circulation (New York, N.Y.), 2007-11, Vol.116 (20), p.2260-2268

2007

Volltextzugriff (PDF)

The role of GPD1L, a sodium channel interacting gene, in the pathogenesis of Brugada Syndrome

Frontiers in medicine, 2024-06, Vol.10, p.1159586

2024

Volltextzugriff (PDF)

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Nature genetics, 2020-05, Vol.52 (5), p.473-481

2020

Volltextzugriff (PDF)

The High-resolution Intermediate Complexity Atmospheric Research (HICAR v1.1) model enables fast dynamic downscaling to the hectometer scale

Geoscientific Model Development, 2023-09, Vol.16 (17), p.5049-5068

2023

Volltextzugriff (PDF)

Immunohistochemical Analysis Supports a Role for INI1/SMARCB1 in Hereditary Forms of Schwannomas, but Not in Solitary, Sporadic Schwannomas

Brain pathology (Zurich, Switzerland), 2008-10, Vol.18 (4), p.517-519

2008

Volltextzugriff (PDF)

Effect of Angiotensin-Converting Enzyme Inhibitors and Receptor Blockers on Appropriate Implantable Cardiac Defibrillator Shock in Patients With Severe Systolic Heart Failure (from the GRADE Multicenter Study)

The American journal of cardiology, 2015-04, Vol.115 (7), p.924-931

2015

Volltextzugriff (PDF)

Oligodendrogliomas result from the expression of an activated mutant epidermal growth factor receptor in a RAS transgenic mouse astrocytoma model

Cancer research (Chicago, Ill.), 2003-03, Vol.63 (5), p.1106-1113

2003

Volltextzugriff (PDF)

Improvement of toughness and electrical properties of epoxy composites with carbon nanotubes prepared by industrially relevant processes

Nanotechnology, 2011-03, Vol.22 (12), p.125702-125702

2011

Volltextzugriff (PDF)

A new data effort to inform career choices in biomedicine

Science (American Association for the Advancement of Science), 2017-12, Vol.358 (6369), p.1388-1389

2017

Volltextzugriff (PDF)

COMPOUND SCN5A MUTATION AND FGF12 VARIATION CAUSE BRUGADA SYNDROME

Journal of the American College of Cardiology, 2017-03, Vol.69 (11), p.332-332

2017

Volltextzugriff (PDF)

MP88-13 TUMOR SUPPRESSOR TSC1 IS A NEW HSP90 COCHAPERONE THAT FACILITATES FOLDING OF KINASE AND NON-KINASE CLIENTS

The Journal of urology, 2018-04, Vol.199 (4), p.e1202-e1202

2018

Volltextzugriff (PDF)

Assessing non-Mendelian inheritance in inherited axonopathies

Genetics in medicine, 2020-12, Vol.22 (12), p.2114-2119

2020

Volltextzugriff (PDF)

1 – 25 von 54

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(49)

Publikationsform

Sprache

Englisch
(54)

Erscheinungsjahr

n.n

Thema

Science & Technology
(32)
Life Sciences & Biomedicine
(29)
Humans
(16)
Biological And Medical Sciences
(11)
Mutation
(11)
Animals
(10)
Female
(10)
Male
(9)
Aged
(7)
Cardiac & Cardiovascular Systems
(7)
Cardiovascular System & Cardiology
(7)
Medical Sciences
(7)
Mice
(7)
Middle Aged
(7)
Neurosciences & Neurology
(7)
Neurosciences
(6)
Risk Factors
(6)
Cardiovascular
(5)
Fundamental And Applied Biological Sciences. Psychology
(5)
Astrocytoma
(4)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery

Abstract 13546: Putative Titin Mutations Associated With Both Long QT Syndrome and Left Ventricular Noncompaction

Abstract 13147: Monitoring Central Arterial Pressure on the Chest Surface: Initial Results From Two Pilot Studies in Human Subjects

Abstract 16997: Reaffirmation of GPD1L-A280V as a Brugada Syndrome Disease-Causing Variant

Statins Decrease Oxidative Stress and ICD Therapies

Abstract 19030: High Mortality in Cardiomyopathy Patients Heterozygous for the CFTR ΔF508 Cystic Fibrosis Mutation

Abstract 17984: No Longer Silent: A Synonymous Coding SNP Modifying a Novel MicroRNA-24: SCN5A Interaction Associates With Non-Arrhythmic Death in Heart Failure

Array-Based Comparative Genomic Hybridization Identifies CDK4 and FOXM1 Alterations as Independent Predictors of Survival in Malignant Peripheral Nerve Sheath Tumor

Tumor suppressor Tsc1 is a new Hsp90 co‐chaperone that facilitates folding of kinase and non‐kinase clients

Astrocyte-specific TSC1 conditional knockout mice exhibit abnormal neuronal organization and seizures

MicroRNA Profiling Reveals Marker of Motor Neuron Disease in ALS Models

Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue Sarcomas

Mutation in glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

The role of GPD1L, a sodium channel interacting gene, in the pathogenesis of Brugada Syndrome

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

The High-resolution Intermediate Complexity Atmospheric Research (HICAR v1.1) model enables fast dynamic downscaling to the hectometer scale

Immunohistochemical Analysis Supports a Role for INI1/SMARCB1 in Hereditary Forms of Schwannomas, but Not in Solitary, Sporadic Schwannomas

Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy

Effect of Angiotensin-Converting Enzyme Inhibitors and Receptor Blockers on Appropriate Implantable Cardiac Defibrillator Shock in Patients With Severe Systolic Heart Failure (from the GRADE Multicenter Study)

Oligodendrogliomas result from the expression of an activated mutant epidermal growth factor receptor in a RAS transgenic mouse astrocytoma model

Improvement of toughness and electrical properties of epoxy composites with carbon nanotubes prepared by industrially relevant processes

A new data effort to inform career choices in biomedicine

COMPOUND SCN5A MUTATION AND FGF12 VARIATION CAUSE BRUGADA SYNDROME

MP88-13 TUMOR SUPPRESSOR TSC1 IS A NEW HSP90 COCHAPERONE THAT FACILITATES FOLDING OF KINASE AND NON-KINASE CLIENTS

Assessing non-Mendelian inheritance in inherited axonopathies

Suchergebnisse filtern