UB Paderborn / Katalog / Suche / in CDI

Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

PloS one, 2016-12, Vol.11 (12), p.e0167358

2016

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Functional and structural conservation of CBS domains from CLC chloride channels

The Journal of physiology, 2004-06, Vol.557 (2), p.363-378

2004

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Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology

PloS one, 2014-12, Vol.9 (12), p.e114894-e114894

2014

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Large Genomic Imbalances in Brugada Syndrome

PloS one, 2016-09, Vol.11 (9), p.e0163514-e0163514

2016

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Exploring early stages of the chemical unfolding of proteins at the proteome scale

PLoS computational biology, 2013-12, Vol.9 (12), p.e1003393-e1003393

2013

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Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP

PloS one, 2017-12, Vol.12 (12), p.e0189618-e0189618

2017

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consensus view of protein dynamics

Proceedings of the National Academy of Sciences - PNAS, 2007-01, Vol.104 (3), p.796-801

2007

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A Genetically Vulnerable Myocardium May Predispose to Myocarditis

Journal of the American College of Cardiology, 2015-12, Vol.66 (25), p.2913-2914

2015

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Approaching Elastic Network Models to Molecular Dynamics Flexibility

Journal of chemical theory and computation, 2010-09, Vol.6 (9), p.2910-2923

2010

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The catalytic site structural gate of adenosine deaminase allosterically modulates ligand binding to adenosine receptors

The FASEB journal, 2013-03, Vol.27 (3), p.1048-1061

2013

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The role of clinical, genetic and segregation evaluation in sudden infant death

Forensic science international, 2014-09, Vol.242, p.9-15

2014

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Allosteric regulation of PKCθ: Understanding multistep phosphorylation and priming by ligands in AGC kinases

Proteins, structure, function, and bioinformatics, 2012-01, Vol.80 (1), p.269-280

2012

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The Structure of Human 4F2hc Ectodomain Provides a Model for Homodimerization and Electrostatic Interaction with Plasma Membrane

The Journal of biological chemistry, 2007-10, Vol.282 (43), p.31444-31452

2007

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Essential Dynamics: A Tool for Efficient Trajectory Compression and Management

Journal of chemical theory and computation, 2006-03, Vol.2 (2), p.251-258

2006

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Characterization of Compensated Mutations in Terms of Structural and Physico-Chemical Properties

Journal of molecular biology, 2007-01, Vol.365 (1), p.249-256

2007

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Use of bioinformatics tools for the annotation of disease-associated mutations in animal models

Proteins, structure, function, and bioinformatics, 2005-12, Vol.61 (4), p.878-887

2005

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PMUT: a web-based tool for the annotation of pathological mutations on proteins

Bioinformatics, 2005-07, Vol.21 (14), p.3176-3178

2005

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A fast method for the determination of fractional contributions to solvation in proteins

Protein science, 2006-11, Vol.15 (11), p.2525-2533

2006

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Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties

Journal of molecular biology, 2002-01, Vol.315 (4), p.771-786

2002

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MoDEL (Molecular Dynamics Extended Library): A Database of Atomistic Molecular Dynamics Trajectories

Structure (London), 2010-11, Vol.18 (11), p.1399-1409

2010

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Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties 1 1Edited by J. Thornton

Journal of molecular biology, 2002-01, Vol.315 (4), p.771-786

2002

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Clinical impact of rare variants associated with inherited channelopathies: a 5-year update

Human genetics, 2022-10, Vol.141 (10), p.1579-1589

2022

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Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

Functional and structural conservation of CBS domains from CLC chloride channels

Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology

Large Genomic Imbalances in Brugada Syndrome

Ultra-deep pyrosequencing detects conserved genomic sites and quantifies linkage of drug-resistant amino acid changes in the hepatitis B virus genome

Exploring early stages of the chemical unfolding of proteins at the proteome scale

Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP

consensus view of protein dynamics

A Genetically Vulnerable Myocardium May Predispose to Myocarditis

Approaching Elastic Network Models to Molecular Dynamics Flexibility

The catalytic site structural gate of adenosine deaminase allosterically modulates ligand binding to adenosine receptors

The role of clinical, genetic and segregation evaluation in sudden infant death

Allosteric regulation of PKCθ: Understanding multistep phosphorylation and priming by ligands in AGC kinases

The Structure of Human 4F2hc Ectodomain Provides a Model for Homodimerization and Electrostatic Interaction with Plasma Membrane

Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

Essential Dynamics: A Tool for Efficient Trajectory Compression and Management

Characterization of Compensated Mutations in Terms of Structural and Physico-Chemical Properties

Use of bioinformatics tools for the annotation of disease-associated mutations in animal models

PMUT: a web-based tool for the annotation of pathological mutations on proteins

A fast method for the determination of fractional contributions to solvation in proteins

Blood Biomarkers for the Early Diagnosis of Stroke: The Stroke-Chip Study

Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties

MoDEL (Molecular Dynamics Extended Library): A Database of Atomistic Molecular Dynamics Trajectories

Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties 1 1Edited by J. Thornton

Clinical impact of rare variants associated with inherited channelopathies: a 5-year update

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