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...

Mechanism of mismatch recognition revealed by human MutSβ bound to unpaired DNA loops

Nature structural & molecular biology, 2012-01, Vol.19 (1), p.72-78

2012

Volltextzugriff (PDF)

Exploiting the distinctive properties of the bacterial and human MutS homolog sliding clamps on mismatched DNA

The Journal of biological chemistry, 2022-11, Vol.298 (11), p.102505-102505, Article 102505

2022

Volltextzugriff (PDF)

Disease-associated repeat instability and mismatch repair

DNA repair, 2016-02, Vol.38, p.117-126

2016

Volltextzugriff (PDF)

Elevated MSH2 MSH3 expression interferes with DNA metabolism in vivo

Nucleic acids research, 2023-12, Vol.51 (22), p.12185-12206

2023

Volltextzugriff (PDF)

High-throughput sequencing and in-silico analysis confirm pathogenicity of novel MSH3 variants in African American colorectal cancer

Neoplasia (New York, N.Y.), 2024-03, Vol.49, p.100970, Article 100970

2024

Volltextzugriff (PDF)

Prerecognition Diffusion Mechanism of Human DNA Mismatch Repair Proteins along DNA: Msh2-Msh3 versus Msh2-Msh6

Biochemistry (Easton), 2020-12, Vol.59 (51), p.4822-4832

2020

Volltextzugriff (PDF)

Complex mutation profiles in mismatch repair and ribonucleotide reductase mutants reveal novel repair substrate specificity of MutS homolog (MSH) complexes

Genetics (Austin), 2022-07, Vol.221 (4)

2022

Volltextzugriff (PDF)

DNA Mismatch Repair Complex MutSβ Promotes GAA·TTC Repeat Expansion in Human Cells

The Journal of biological chemistry, 2012-08, Vol.287 (35), p.29958-29967

2012

Volltextzugriff (PDF)

Genomic Instability Promoted by Overexpression of Mismatch Repair Factors in Yeast: A Model for Understanding Cancer Progression

Genetics (Austin), 2018-06, Vol.209 (2), p.439-456

2018

Volltextzugriff (PDF)

MCM9 Is Required for Mammalian DNA Mismatch Repair

Molecular cell, 2015-09, Vol.59 (5), p.831-839

2015

Volltextzugriff (PDF)

Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer

Journal of clinical oncology, 2017-04, Vol.35 (10), p.1086-1095

2017

Volltextzugriff (PDF)

Dynamic human MutSα–MutLα complexes compact mismatched DNA

Proceedings of the National Academy of Sciences - PNAS, 2020-07, Vol.117 (28), p.16302-16312

2020

Volltextzugriff (PDF)

Suppression of long noncoding RNA NCK1‐AS1 increases chemosensitivity to cisplatin in cervical cancer

Journal of cellular physiology, 2019-04, Vol.234 (4), p.4302-4313

2019

Volltextzugriff (PDF)

Complex MSH2 and MSH6 mutations in hypermutated microsatellite unstable advanced prostate cancer

Nature communications, 2014-09, Vol.5 (1), p.4988-4988, Article 4988

2014

Volltextzugriff (PDF)

The Human DNA Mismatch Repair Protein MSH3 Contains Nuclear Localization and Export Signals That Enable Nuclear-Cytosolic Shuttling in Response to Inflammation

Molecular and cellular biology, 2020-06, Vol.40 (13)

2020

Volltextzugriff (PDF)

MutSβ Stimulates Holliday Junction Resolution by the SMX Complex

Cell reports (Cambridge), 2020-10, Vol.33 (3), p.108289-108289, Article 108289

2020

Volltextzugriff (PDF)

MutSβ and histone deacetylase complexes promote expansions of trinucleotide repeats in human cells

Nucleic acids research, 2012-11, Vol.40 (20), p.10324-10333

2012

Volltextzugriff (PDF)

MSH2 ATPase domain mutation affects CTGCAG repeat instability in transgenic mice

PLoS genetics, 2009-05, Vol.5 (5), p.e1000482

2009

Volltextzugriff (PDF)

MutSβ promotes trinucleotide repeat expansion by recruiting DNA polymerase β to nascent (CAG)n or (CTG)n hairpins for error-prone DNA synthesis

Cell research, 2016-07, Vol.26 (7), p.775-786

2016

Volltextzugriff (PDF)

MSH2 Loss in Primary Prostate Cancer

Clinical cancer research, 2017-11, Vol.23 (22), p.6863-6874

2017

Volltextzugriff (PDF)

MSH2 Gene Point Mutations Are Not Antifungal Resistance Markers in Candida glabrata

Antimicrobial agents and chemotherapy, 2019-01, Vol.63 (1)

2019

Volltextzugriff (PDF)

Expansion and improvement of ChinaMu by MuT‐seq and chromosome‐level assembly of the Mu‐starter genome

Journal of integrative plant biology, 2024-04, Vol.66 (4), p.645-659

2024

Volltextzugriff (PDF)

Ultrasensitive and Quantitative DNA Methylation Detection Method Based on the MutS Protein

Analytical chemistry (Washington), 2023-12, Vol.95 (51), p.18828-18835

2023

Volltextzugriff (PDF)

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome

JAMA : the journal of the American Medical Association, 2011-06, Vol.305 (22), p.2304

2011

Volltextzugriff (PDF)

Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood

Clinical cancer research, 2017-06, Vol.23 (11), p.e32-e37

2017

Volltextzugriff (PDF)

1 – 25 von 3.008

Suche als RSS-Feed

Aktive Filter

ThemaHumans

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.723)
Mit Volltextzugriff
(2.483)

Publikationsform

Sprache

12 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(2.566)
Life Sciences & Biomedicine
(2.466)
Female
(1.544)
Mutl Protein Homolog 1
(1.340)
Male
(1.294)
Middle Aged
(1.237)
Muts Homolog 2 Protein - Genetics
(1.200)
Adult
(1.039)
Colorectal Neoplasms, Hereditary Nonpolyposis - Genetics
(1.017)
Oncology
(1.015)
Muts Homolog 2 Protein
(989)
Mutation
(927)
Aged
(911)
Biological And Medical Sciences
(904)
Dna-Binding Proteins - Genetics
(865)
Tumors
(864)
Medical Sciences
(806)
Adaptor Proteins, Signal Transducing
(752)
Proto-Oncogene Proteins - Genetics
(711)

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mechanism of mismatch recognition revealed by human MutSβ bound to unpaired DNA loops

Exploiting the distinctive properties of the bacterial and human MutS homolog sliding clamps on mismatched DNA

Disease-associated repeat instability and mismatch repair

Elevated MSH2 MSH3 expression interferes with DNA metabolism in vivo

High-throughput sequencing and in-silico analysis confirm pathogenicity of novel MSH3 variants in African American colorectal cancer

Prerecognition Diffusion Mechanism of Human DNA Mismatch Repair Proteins along DNA: Msh2-Msh3 versus Msh2-Msh6

Complex mutation profiles in mismatch repair and ribonucleotide reductase mutants reveal novel repair substrate specificity of MutS homolog (MSH) complexes

DNA Mismatch Repair Complex MutSβ Promotes GAA·TTC Repeat Expansion in Human Cells

Genomic Instability Promoted by Overexpression of Mismatch Repair Factors in Yeast: A Model for Understanding Cancer Progression

MCM9 Is Required for Mammalian DNA Mismatch Repair

Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer

Dynamic human MutSα–MutLα complexes compact mismatched DNA

Suppression of long noncoding RNA NCK1‐AS1 increases chemosensitivity to cisplatin in cervical cancer

Complex MSH2 and MSH6 mutations in hypermutated microsatellite unstable advanced prostate cancer

The Human DNA Mismatch Repair Protein MSH3 Contains Nuclear Localization and Export Signals That Enable Nuclear-Cytosolic Shuttling in Response to Inflammation

MutSβ Stimulates Holliday Junction Resolution by the SMX Complex

MutSβ and histone deacetylase complexes promote expansions of trinucleotide repeats in human cells

MSH2 ATPase domain mutation affects CTGCAG repeat instability in transgenic mice

MutSβ promotes trinucleotide repeat expansion by recruiting DNA polymerase β to nascent (CAG)n or (CTG)n hairpins for error-prone DNA synthesis

MSH2 Loss in Primary Prostate Cancer

MSH2 Gene Point Mutations Are Not Antifungal Resistance Markers in Candida glabrata

Expansion and improvement of ChinaMu by MuT‐seq and chromosome‐level assembly of the Mu‐starter genome

Ultrasensitive and Quantitative DNA Methylation Detection Method Based on the MutS Protein

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome

Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood

Aktive Filter

Suchergebnisse filtern