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...

Towards Increasing the Clinical Relevance of In Silico Methods to Predict Pathogenic Missense Variants

PLoS computational biology, 2016-05, Vol.12 (5), p.e1004725

2016

Volltextzugriff (PDF)

Exome-Scale Discovery of Hotspot Mutation Regions in Human Cancer Using 3D Protein Structure

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (13), p.3719-3731

2016

Volltextzugriff (PDF)

Correlation of Somatic Mutation and Expression Identifies Genes Important in Human Glioblastoma Progression and Survival

Cancer research (Chicago, Ill.), 2011-07, Vol.71 (13), p.4550-4561

2011

Volltextzugriff (PDF)

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene

Nature genetics, 2013-10, Vol.45 (10), p.1160-1167

2013

Volltextzugriff (PDF)

CRAVAT 4: Cancer-Related Analysis of Variants Toolkit

Cancer research (Chicago, Ill.), 2017-11, Vol.77 (21), p.e35-e38

2017

Volltextzugriff (PDF)

Collections of Simultaneously Altered Genes as Biomarkers of Cancer Cell Drug Response

Cancer research (Chicago, Ill.), 2013-03, Vol.73 (6), p.1699-1708

2013

Volltextzugriff (PDF)

Phosphorylation‐dependent inhibition of mineralization by osteopontin ASARM peptides is regulated by PHEX cleavage

Journal of bone and mineral research, 2010-04, Vol.25 (4), p.695-705

2010

Volltextzugriff (PDF)

Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches

American journal of human genetics, 2018-02, Vol.102 (2), p.233-248

2018

Volltextzugriff (PDF)

Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel)

Human mutation, 2016-01, Vol.37 (1), p.28-35

2016

Volltextzugriff (PDF)

IPMNs with co-occurring invasive cancers: neighbours but not always relatives

Gut, 2018-09, Vol.67 (9), p.1652-1662

2018

Volltextzugriff (PDF)

Association of Baseline and Pharmacodynamic Biomarkers With Outcomes in Patients Treated With the PD-1 Inhibitor Budigalimab

Journal of immunotherapy (1997), 2022-04, Vol.45 (3), p.167-179

2022

Volltextzugriff (PDF)

Network Analysis of Protein Adaptation: Modeling the Functional Impact of Multiple Mutations

Molecular biology and evolution, 2018-06, Vol.35 (6), p.1507-1519

2018

Volltextzugriff (PDF)

Structure Prediction of Protein−Solid Surface Interactions Reveals a Molecular Recognition Motif of Statherin for Hydroxyapatite

Journal of the American Chemical Society, 2007-11, Vol.129 (44), p.13713-13722

2007

Volltextzugriff (PDF)

Partial High-Resolution Structure of Phosphorylated and Non-phosphorylated Leucine-Rich Amelogenin Protein Adsorbed to Hydroxyapatite

Journal of physical chemistry. C, 2011-07, Vol.115 (28), p.13775-13785

2011

Volltextzugriff (PDF)

Fast, accurate, and racially unbiased pan-cancer tumor-only variant calling with tabular machine learning

NPJ precision oncology, 2023-01, Vol.7 (1), p.4-4, Article 4

2023

Volltextzugriff (PDF)

A Combination of Molecular Markers and Clinical Features Improve the Classification of Pancreatic Cysts

Gastroenterology (New York, N.Y. 1943), 2015-11, Vol.149 (6), p.1501-1510

2015

Volltextzugriff (PDF)

Solution- and Adsorbed-State Structural Ensembles Predicted for the Statherin-Hydroxyapatite System

Biophysical journal, 2009-04, Vol.96 (8), p.3082-3091

2009

Volltextzugriff (PDF)

Predicting survival in head and neck squamous cell carcinoma from TP53 mutation

Human genetics, 2015-05, Vol.134 (5), p.497-507

2015

Volltextzugriff (PDF)

Modulation of Calcium Oxalate Dihydrate Growth by Selective Crystal-face Binding of Phosphorylated Osteopontin and Polyaspartate Peptide Showing Occlusion by Sectoral (Compositional) Zoning

The Journal of biological chemistry, 2009-08, Vol.284 (35), p.23491-23501

2009

Volltextzugriff (PDF)

Missense variants in CFTR nucleotide-binding domains predict quantitative phenotypes associated with cystic fibrosis disease severity

Human molecular genetics, 2015-04, Vol.24 (7), p.1908-1917

2015

Volltextzugriff (PDF)

Neutron Reflectometry Studies of the Adsorbed Structure of the Amelogenin, LRAP

The journal of physical chemistry. B, 2013-03, Vol.117 (11), p.3098-3109

2013

Volltextzugriff (PDF)

Toward a Structure Determination Method for Biomineral-Associated Protein Using Combined Solid- State NMR and Computational Structure Prediction

Structure (London), 2010-12, Vol.18 (12), p.1678-1687

2010

Volltextzugriff (PDF)

Caspase-1 from Human Myeloid-Derived Suppressor Cells Can Promote T Cell-Independent Tumor Proliferation

Cancer immunology research, 2018-05, Vol.6 (5), p.566-577

2018

Volltextzugriff (PDF)

De Novo Design of Peptide−Calcite Biomineralization Systems

Journal of the American Chemical Society, 2010-09, Vol.132 (35), p.12252-12262

2010

Volltextzugriff (PDF)

Phenotype-optimized sequence ensembles substantially improve prediction of disease-causing mutation in cystic fibrosis

Human mutation, 2012-08, Vol.33 (8), p.1267-1274

2012

Volltextzugriff (PDF)

1 – 25 von 66

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(60)
Mit Volltextzugriff
(53)

Publikationsform

Sprache

Englisch
(66)
Japanisch
(16)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Towards Increasing the Clinical Relevance of In Silico Methods to Predict Pathogenic Missense Variants

Exome-Scale Discovery of Hotspot Mutation Regions in Human Cancer Using 3D Protein Structure

Correlation of Somatic Mutation and Expression Identifies Genes Important in Human Glioblastoma Progression and Survival

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene

CRAVAT 4: Cancer-Related Analysis of Variants Toolkit

Collections of Simultaneously Altered Genes as Biomarkers of Cancer Cell Drug Response

Phosphorylation‐dependent inhibition of mineralization by osteopontin ASARM peptides is regulated by PHEX cleavage

Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches

Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel)

IPMNs with co-occurring invasive cancers: neighbours but not always relatives

Association of Baseline and Pharmacodynamic Biomarkers With Outcomes in Patients Treated With the PD-1 Inhibitor Budigalimab

Network Analysis of Protein Adaptation: Modeling the Functional Impact of Multiple Mutations

Structure Prediction of Protein−Solid Surface Interactions Reveals a Molecular Recognition Motif of Statherin for Hydroxyapatite

Partial High-Resolution Structure of Phosphorylated and Non-phosphorylated Leucine-Rich Amelogenin Protein Adsorbed to Hydroxyapatite

Fast, accurate, and racially unbiased pan-cancer tumor-only variant calling with tabular machine learning

A Combination of Molecular Markers and Clinical Features Improve the Classification of Pancreatic Cysts

Solution- and Adsorbed-State Structural Ensembles Predicted for the Statherin-Hydroxyapatite System

Predicting survival in head and neck squamous cell carcinoma from TP53 mutation

Modulation of Calcium Oxalate Dihydrate Growth by Selective Crystal-face Binding of Phosphorylated Osteopontin and Polyaspartate Peptide Showing Occlusion by Sectoral (Compositional) Zoning

Missense variants in CFTR nucleotide-binding domains predict quantitative phenotypes associated with cystic fibrosis disease severity

Neutron Reflectometry Studies of the Adsorbed Structure of the Amelogenin, LRAP

Toward a Structure Determination Method for Biomineral-Associated Protein Using Combined Solid- State NMR and Computational Structure Prediction

Caspase-1 from Human Myeloid-Derived Suppressor Cells Can Promote T Cell-Independent Tumor Proliferation

De Novo Design of Peptide−Calcite Biomineralization Systems

Phenotype-optimized sequence ensembles substantially improve prediction of disease-causing mutation in cystic fibrosis

Suchergebnisse filtern