UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 77

Sortiert nach

Genomic Tackling of Human Satellite DNA: Breaking Barriers through Time

International journal of molecular sciences, 2021-04, Vol.22 (9), p.4707

2021

Volltextzugriff (PDF)

Multiplexed pancreatic genome engineering and cancer induction by transfection-based CRISPR/Cas9 delivery in mice

Nature communications, 2016-02, Vol.7 (1), p.10770-13, Article 10770

2016

Volltextzugriff (PDF)

Human Satellite 1A analysis provides evidence of pericentromeric transcription

BMC biology, 2023-02, Vol.21 (1), p.28-28, Article 28

2023

Volltextzugriff (PDF)

Decoding the Role of Satellite DNA in Genome Architecture and Plasticity-An Evolutionary and Clinical Affair

Genes, 2020-01, Vol.11 (1), p.72

2020

Volltextzugriff (PDF)

Structural rearrangements generate cell-specific, gene-independent CRISPR-Cas9 loss of fitness effects

Genome Biology, 2019-02, Vol.20 (1), p.27-10, Article 27

2019

Volltextzugriff (PDF)

Answering the Cell Stress Call: Satellite Non-Coding Transcription as a Response Mechanism

Biomolecules (Basel, Switzerland), 2024-01, Vol.14 (1), p.124

2024

Volltextzugriff (PDF)

ALPK1 hotspot mutation as a driver of human spiradenoma and spiradenocarcinoma

Nature communications, 2019-05, Vol.10 (1), p.2213-2213, Article 2213

2019

Volltextzugriff (PDF)

Defining the sister rat mammary tumor cell lines HH-16 cl.2/1 and HH-16.cl.4 as an in vitro cell model for Erbb2

PloS one, 2012-01, Vol.7 (1), p.e29923

2012

Volltextzugriff (PDF)

Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome

Genome Biology, 2019-10, Vol.20 (1), p.207-207, Article 207

2019

Volltextzugriff (PDF)

Evolution of the rapidly mutating human salivary agglutinin gene (DMBT1) and population subsistence strategy

Proceedings of the National Academy of Sciences - PNAS, 2015-04, Vol.112 (16), p.5105-5110

2015

Volltextzugriff (PDF)

Structural variation of the malaria-associated human glycophorin A-B-E region

BMC genomics, 2020-06, Vol.21 (1), p.446-446, Article 446

2020

Volltextzugriff (PDF)

Quantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome association

PLoS genetics, 2014-11, Vol.10 (11), p.e1004798-e1004798

2014

Volltextzugriff (PDF)

Correction: Quantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome association

PLoS genetics, 2015-04, Vol.11 (4), p.e1005177-e1005177

2015

Volltextzugriff (PDF)

Genetic variation of glycophorins and infectious disease

Immunogenetics (New York), 2023-06, Vol.75 (3), p.201-206

2023

Volltextzugriff (PDF)

Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells

Nature (London), 2018-01, Vol.553 (7687), p.171-177

2018

Volltextzugriff (PDF)

Pericentromeric satellite RNAs as flexible protein partners in the regulation of nuclear structure

Wiley interdisciplinary reviews. RNA, 2024-07, Vol.15 (4), p.e1868

2024

Volltextzugriff (PDF)

Recurrent Rearrangements of Human Amylase Genes Create Multiple Independent CNV Series: HUMAN MUTATION

Human mutation, 2017-05, Vol.38 (5), p.532-539

2017

Volltextzugriff (PDF)

The Malaria-Protective Human Glycophorin Structural Variant DUP4 Shows Somatic Mosaicism and Association with Hemoglobin Levels

American journal of human genetics, 2018-11, Vol.103 (5), p.769-776

2018

Volltextzugriff (PDF)

A High-Resolution Comparative Chromosome Map of Cricetus cricetus and Peromyscus eremicus Reveals the Involvement of Constitutive Heterochromatin in Breakpoint Regions

Cytogenetic and genome research, 2015-01, Vol.145 (1), p.59-67

2015

Volltextzugriff (PDF)

Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome

Human molecular genetics, 2019-08, Vol.28 (16), p.2785-2798

2019

Volltextzugriff (PDF)

A new patient‐derived iPSC model for dystroglycanopathies validates a compound that increases glycosylation of α‐dystroglycan

EMBO reports, 2019-11, Vol.20 (11), p.e47967-n/a

2019

Volltextzugriff (PDF)

Recurrent Rearrangements of Human Amylase Genes Create Multiple Independent CNV Series

Human mutation, 2017-05, Vol.38 (5), p.532-539

2017

Volltextzugriff (PDF)

A novel satellite DNA sequence in the Peromyscus genome (PMSat): Evolution via copy number fluctuation

Molecular phylogenetics and evolution, 2015-11, Vol.92, p.193-203

2015

Volltextzugriff (PDF)

Copy number variation arising from gene conversion on the human Y chromosome

Human genetics, 2018, Vol.137 (1), p.73-83

2018

Volltextzugriff (PDF)

1 – 25 von 77

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(64)
Mit Volltextzugriff
(72)

Publikationsform

Artikel
(76)
Dissertationen
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Genomic Tackling of Human Satellite DNA: Breaking Barriers through Time

Multiplexed pancreatic genome engineering and cancer induction by transfection-based CRISPR/Cas9 delivery in mice

Human Satellite 1A analysis provides evidence of pericentromeric transcription

Decoding the Role of Satellite DNA in Genome Architecture and Plasticity-An Evolutionary and Clinical Affair

Structural rearrangements generate cell-specific, gene-independent CRISPR-Cas9 loss of fitness effects

Answering the Cell Stress Call: Satellite Non-Coding Transcription as a Response Mechanism

ALPK1 hotspot mutation as a driver of human spiradenoma and spiradenocarcinoma

Defining the sister rat mammary tumor cell lines HH-16 cl.2/1 and HH-16.cl.4 as an in vitro cell model for Erbb2

Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome

The pig X and Y Chromosomes: structure, sequence, and evolution

Evolution of the rapidly mutating human salivary agglutinin gene (DMBT1) and population subsistence strategy

Structural variation of the malaria-associated human glycophorin A-B-E region

Quantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome association

Correction: Quantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome association

Genetic variation of glycophorins and infectious disease

Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells

Pericentromeric satellite RNAs as flexible protein partners in the regulation of nuclear structure

Recurrent Rearrangements of Human Amylase Genes Create Multiple Independent CNV Series: HUMAN MUTATION

The Malaria-Protective Human Glycophorin Structural Variant DUP4 Shows Somatic Mosaicism and Association with Hemoglobin Levels

A High-Resolution Comparative Chromosome Map of Cricetus cricetus and Peromyscus eremicus Reveals the Involvement of Constitutive Heterochromatin in Breakpoint Regions

Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome

A new patient‐derived iPSC model for dystroglycanopathies validates a compound that increases glycosylation of α‐dystroglycan

Recurrent Rearrangements of Human Amylase Genes Create Multiple Independent CNV Series

A novel satellite DNA sequence in the Peromyscus genome (PMSat): Evolution via copy number fluctuation

Copy number variation arising from gene conversion on the human Y chromosome

Suchergebnisse filtern