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...

Control of telomere length in yeast by SUMOylated PCNA and the Elg1 PCNA unloader

eLife, 2023-08, Vol.12

2023

Volltextzugriff (PDF)

Early transmission of SARS-CoV-2 in South Africa: An epidemiological and phylogenetic report

International journal of infectious diseases, 2021-02, Vol.103, p.234-241

2021

Volltextzugriff (PDF)

A MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?

PLoS genetics, 2016-07, Vol.12 (7), p.e1006190-e1006190

2016

Volltextzugriff (PDF)

Rnr1, but not Rnr3, facilitates the sustained telomerase-dependent elongation of telomeres

PLoS genetics, 2017-10, Vol.13 (10), p.e1007082-e1007082

2017

Volltextzugriff (PDF)

The importance of being modified: PCNA modification and DNA damage response

Cell cycle (Georgetown, Tex.), 2012-07, Vol.11 (14), p.2620-2623

2012

Volltextzugriff (PDF)

Unsuppressed HIV infection impairs T cell responses to SARS-CoV-2 infection and abrogates T cell cross-recognition

eLife, 2022-07, Vol.11

2022

Volltextzugriff (PDF)

Image-Based Deep Learning Detection of High-Grade B-Cell Lymphomas Directly from Hematoxylin and Eosin Images

Cancers, 2023-10, Vol.15 (21), p.5205

2023

Volltextzugriff (PDF)

Genomic instability and repair mediated by common repeated sequences

Proceedings of the National Academy of Sciences - PNAS, 2013-12, Vol.110 (49), p.19664-19665

2013

Volltextzugriff (PDF)

Whole Genome Sequencing of SARS-CoV-2: Adapting Illumina Protocols for Quick and Accurate Outbreak Investigation during a Pandemic

Genes, 2020-08, Vol.11 (8), p.949

2020

Volltextzugriff (PDF)

Towards Mechanism-Based Treatments for Fragile X Syndrome

Brain sciences, 2019-08, Vol.9 (8), p.202

2019

Volltextzugriff (PDF)

TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair

PloS one, 2015-07, Vol.10 (7), p.e0134120-e0134120

2015

Volltextzugriff (PDF)

Pharmacological Reactivation of the Silenced FMR1 Gene as a Targeted Therapeutic Approach for Fragile X Syndrome

Brain sciences, 2019-02, Vol.9 (2), p.39

2019

Volltextzugriff (PDF)

CGG Repeat Expansion, and Elevated Fmr1 Transcription and Mitochondrial Copy Number in a New Fragile X PM Mouse Embryonic Stem Cell Model

Frontiers in cell and developmental biology, 2020-06, Vol.8, p.482-482

2020

Volltextzugriff (PDF)

Repeat Instability in the Fragile X-Related Disorders: Lessons from a Mouse Model

Brain sciences, 2019-03, Vol.9 (3), p.52

2019

Volltextzugriff (PDF)

Control of telomere length in yeast by SUMOylated PCNA and the Elg1 PCNA unloader

eLife, 2023-08, Vol.12

2023

Volltextzugriff (PDF)

Escape of SARS-CoV-2 501Y.V2 from neutralization by convalescent plasma

Nature (London), 2021-05, Vol.593 (7857), p.142-146

2021

Volltextzugriff (PDF)

Double-strand break repair plays a role in repeat instability in a fragile X mouse model

DNA repair, 2019-02, Vol.74, p.63-69

2019

Volltextzugriff (PDF)

Towards Mechanism-based Treatments for Fragile X Syndrome

2019

Volltextzugriff (PDF)

Image-based detection of FGFR3 -fusion in urothelial bladder cancer

Journal of clinical oncology, 2022-06, Vol.40 (16_suppl), p.3072-3072

2022

Volltextzugriff (PDF)

A year of genomic surveillance reveals how the SARS-CoV-2 pandemic unfolded in Africa

Science (American Association for the Advancement of Science), 2021-10, Vol.374 (6566), p.423-431

2021

Volltextzugriff (PDF)

Direct identification of ALK and ROS1 fusions in non-small cell lung cancer from hematoxylin and eosin-stained slides using deep learning algorithms

Modern pathology, 2022-12, Vol.35 (12), p.1882-1887

2022

Volltextzugriff (PDF)

High-confidence AI-based biomarker profiling for H&E slides to optimize pathology workflow in lung cancer

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.e21207-e21207

2023

Volltextzugriff (PDF)

Elg1, a central player in genome stability

Mutation research. Reviews in mutation research, 2015-01, Vol.763, p.267-279

2015

Volltextzugriff (PDF)

1 – 25 von 31

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(29)
Mit Volltextzugriff
(28)

Publikationsform

Sprache

Englisch
(31)
Japanisch
(3)

Erscheinungsjahr

n.n

Thema

Science & Technology
(22)
Life Sciences & Biomedicine
(19)
Humans
(13)
Genomes
(9)
Coronaviruses
(7)
Fragile X Syndrome
(7)
Mutation
(7)
Sars-Cov-2
(7)
Covid-19
(6)
Deoxyribonucleic Acid
(6)
Disease Transmission
(6)
Dna
(6)
Dna Repair
(6)
Genetics & Heredity
(6)
Severe Acute Respiratory Syndrome Coronavirus 2
(6)
Proteins
(5)
South Africa
(5)
Animals
(4)
Biology
(4)
Dna Sequencing
(4)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Elife
(5)
Brain Sciences
(3)
Plos Genetics
(3)
Journal Of Clinical Oncology
(2)
Plos One
(2)
Cancers
(1)
Cell Cycle
(1)
Cell Cycle/cell Cycle
(1)
Dna Repair
(1)
Frontiers In Cell And Developmental Biology
(1)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Control of telomere length in yeast by SUMOylated PCNA and the Elg1 PCNA unloader

Sixteen novel lineages of SARS-CoV-2 in South Africa

Early transmission of SARS-CoV-2 in South Africa: An epidemiological and phylogenetic report

HIV skews the SARS-CoV-2 B cell response towards an extrafollicular maturation pathway

A MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?

Rnr1, but not Rnr3, facilitates the sustained telomerase-dependent elongation of telomeres

The importance of being modified: PCNA modification and DNA damage response

Unsuppressed HIV infection impairs T cell responses to SARS-CoV-2 infection and abrogates T cell cross-recognition

Image-Based Deep Learning Detection of High-Grade B-Cell Lymphomas Directly from Hematoxylin and Eosin Images

Genomic instability and repair mediated by common repeated sequences

Whole Genome Sequencing of SARS-CoV-2: Adapting Illumina Protocols for Quick and Accurate Outbreak Investigation during a Pandemic

Towards Mechanism-Based Treatments for Fragile X Syndrome

TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair

Pharmacological Reactivation of the Silenced FMR1 Gene as a Targeted Therapeutic Approach for Fragile X Syndrome

CGG Repeat Expansion, and Elevated Fmr1 Transcription and Mitochondrial Copy Number in a New Fragile X PM Mouse Embryonic Stem Cell Model

Repeat Instability in the Fragile X-Related Disorders: Lessons from a Mouse Model

Control of telomere length in yeast by SUMOylated PCNA and the Elg1 PCNA unloader

Escape of SARS-CoV-2 501Y.V2 from neutralization by convalescent plasma

Double-strand break repair plays a role in repeat instability in a fragile X mouse model

Towards Mechanism-based Treatments for Fragile X Syndrome

Image-based detection of FGFR3 -fusion in urothelial bladder cancer

A year of genomic surveillance reveals how the SARS-CoV-2 pandemic unfolded in Africa

Direct identification of ALK and ROS1 fusions in non-small cell lung cancer from hematoxylin and eosin-stained slides using deep learning algorithms

High-confidence AI-based biomarker profiling for H&E slides to optimize pathology workflow in lung cancer

Elg1, a central player in genome stability

Suchergebnisse filtern