UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 87

Sortiert nach

When the Lyon(ized chromosome) roars: ongoing expression from an inactive X chromosome

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2017-11, Vol.372 (1733)

2017

Link zum Volltext

Verfügbarkeit prüfen

X-inactivation profile reveals extensive variability in X-linked gene expression in females

Nature, 2005-03, Vol.434 (7031), p.400-404

2005

Link zum Volltext

Verfügbarkeit prüfen

Escape from X chromosome inactivation is an intrinsic property of the Jarid1c locus

Proceedings of the National Academy of Sciences - PNAS, 2008-11, Vol.105 (44), p.17055-17060

2008

Link zum Volltext

Verfügbarkeit prüfen

Isolation of MECP2-nuLl Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation

Human molecular genetics, 2011-06, Vol.20 (11), p.2103-2115

2011

Link zum Volltext

Verfügbarkeit prüfen

Integrating 3D genomic and epigenomic data to enhance target gene discovery and drug repurposing in transcriptome-wide association studies

Nature communications, 2022-06, Vol.13 (1), p.3258-3258, Article 3258

2022

Link zum Volltext

Verfügbarkeit prüfen

Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus

Nature communications, 2023-02, Vol.14 (1), p.668-668, Article 668

2023

Link zum Volltext

Verfügbarkeit prüfen

Deletion of an X-inactivation boundary disrupts adjacent gene silencing

PLoS genetics, 2013-11, Vol.9 (11), p.e1003952-e1003952

2013

Link zum Volltext

Verfügbarkeit prüfen

Construction and Application of Polygenic Risk Scores in Autoimmune Diseases

Frontiers in immunology, 2022-06, Vol.13, p.889296-889296

2022

Link zum Volltext

Verfügbarkeit prüfen

Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family

EJHaem, 2021-08, Vol.2 (3), p.485-487

2021

Link zum Volltext

Verfügbarkeit prüfen

Molecular Evidence for a Relationship between LINE-1 Elements and X Chromosome Inactivation: The Lyon Repeat Hypothesis

Proceedings of the National Academy of Sciences - PNAS, 2000-06, Vol.97 (12), p.6634-6639

2000

Link zum Volltext

Verfügbarkeit prüfen

A First-Generation X-Inactivation Profile of the Human X Chromosome

Proceedings of the National Academy of Sciences - PNAS, 1999-12, Vol.96 (25), p.14440-14444

1999

Link zum Volltext

Verfügbarkeit prüfen

Genomic environment predicts expression patterns on the human inactive X chromosome

PLoS genetics, 2006-09, Vol.2 (9), p.e151-e151

2006

Link zum Volltext

Verfügbarkeit prüfen

A regulatory potential of the Xist gene promoter in vole M. rossiaemeridionalis

PloS one, 2012-05, Vol.7 (5), p.e33994-e33994

2012

Link zum Volltext

Verfügbarkeit prüfen

An Ectopic Human XIST Gene Can Induce Chromosome Inactivation in Postdifferentiation Human HT-1080 Cells

Proceedings of the National Academy of Sciences - PNAS, 2002-06, Vol.99 (13), p.8677-8682

2002

Link zum Volltext

Verfügbarkeit prüfen

X-chromosome inactivation in rett syndrome human induced pluripotent stem cells

Frontiers in psychiatry, 2012, Vol.3, p.24-24

2012

Link zum Volltext

Verfügbarkeit prüfen

Heterogeneous Gene Expression from the Inactive X Chromosome: An X-Linked Gene That Escapes X Inactivation in Some Human Cell Lines but Is Inactivated in Others

Proceedings of the National Academy of Sciences - PNAS, 1999-06, Vol.96 (13), p.7364-7369

1999

Link zum Volltext

Verfügbarkeit prüfen

Genes that escape from X inactivation

Human genetics, 2011-08, Vol.130 (2), p.237-245

2011

Link zum Volltext

Verfügbarkeit prüfen

Inferring genes that escape X-Chromosome inactivation reveals important contribution of variable escape genes to sex-biased diseases

Genome research, 2021-09, Vol.31 (9), p.1629

2021

Link zum Volltext

Verfügbarkeit prüfen

Elevated Von Willebrand Factor May Abrogate Bleeding Phenotype in a Male with a Non-Null F8 Mutation

Blood, 2018-11, Vol.132 (Supplement 1), p.3787-3787

2018

Link zum Volltext

Verfügbarkeit prüfen

Bleeding in Mild Hemophilia A Due to a Splice-Site F8 Mutation May be Fully Abrogated By Prothrombotic Gene Variants

Blood, 2019-11, Vol.134 (Supplement_1), p.1125-1125

2019

Link zum Volltext

Verfügbarkeit prüfen

Computational and Statistical Analyses of Insertional Polymorphic Endogenous Retroviruses in a Non-Model Organism

Computation, 2014, Vol.2 (4), p.221-245

2014

Link zum Volltext

Verfügbarkeit prüfen

Correlation of X Chromosome Inactivation Skewing and Bleeding Phenotype in Obligate Carriers of Hemophilia A

Blood, 2015-12, Vol.126 (23), p.2285-2285

2015

Link zum Volltext

Verfügbarkeit prüfen

Role of Von Willebrand Factor in Female Carriers from an Extended Family with Mild Hemophilia A

Blood, 2015-12, Vol.126 (23), p.3537-3537

2015

Link zum Volltext

Verfügbarkeit prüfen

Random X-Chromosome Inactivation in Hemophilia A Carriers Does Not Fully Attenuate Bleeding Risk

Blood, 2017-12, Vol.130, p.3676-3676

2017

Link zum Volltext

Verfügbarkeit prüfen

Deletion of an X-Inactivation Boundary Disrupts Adjacent Gene Silencing: e1003952

PLoS genetics, 2013-11, Vol.9 (11)

2013

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 87

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(82)
Mit Volltextzugriff
(80)

Publikationsform

Sprache

Englisch
(87)
Japanisch
(17)

Erscheinungsjahr

n.n

Thema

Science & Technology
(60)
Humans
(53)
Life Sciences & Biomedicine
(47)
Female
(31)
Animals
(29)
Genetics & Heredity
(27)
Biological And Medical Sciences
(23)
Male
(22)
Genes
(21)
Genetics
(20)
Fundamental And Applied Biological Sciences. Psychology
(19)
Mice
(18)
Cell Line
(17)
Gene Expression
(17)
X Chromosome
(16)
Biochemistry & Molecular Biology
(15)
Chromosomes
(15)
Dosage Compensation, Genetic
(15)
Molecular Sequence Data
(12)
Multidisciplinary Sciences
(12)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

When the Lyon(ized chromosome) roars: ongoing expression from an inactive X chromosome

X-inactivation profile reveals extensive variability in X-linked gene expression in females

Escape from X chromosome inactivation is an intrinsic property of the Jarid1c locus

Isolation of MECP2-nuLl Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation

Integrating 3D genomic and epigenomic data to enhance target gene discovery and drug repurposing in transcriptome-wide association studies

Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus

Deletion of an X-inactivation boundary disrupts adjacent gene silencing

Construction and Application of Polygenic Risk Scores in Autoimmune Diseases

Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family

Molecular Evidence for a Relationship between LINE-1 Elements and X Chromosome Inactivation: The Lyon Repeat Hypothesis

A First-Generation X-Inactivation Profile of the Human X Chromosome

Genomic environment predicts expression patterns on the human inactive X chromosome

A regulatory potential of the Xist gene promoter in vole M. rossiaemeridionalis

An Ectopic Human XIST Gene Can Induce Chromosome Inactivation in Postdifferentiation Human HT-1080 Cells

X-chromosome inactivation in rett syndrome human induced pluripotent stem cells

Heterogeneous Gene Expression from the Inactive X Chromosome: An X-Linked Gene That Escapes X Inactivation in Some Human Cell Lines but Is Inactivated in Others

Genes that escape from X inactivation

Inferring genes that escape X-Chromosome inactivation reveals important contribution of variable escape genes to sex-biased diseases

Elevated Von Willebrand Factor May Abrogate Bleeding Phenotype in a Male with a Non-Null F8 Mutation

Bleeding in Mild Hemophilia A Due to a Splice-Site F8 Mutation May be Fully Abrogated By Prothrombotic Gene Variants

Computational and Statistical Analyses of Insertional Polymorphic Endogenous Retroviruses in a Non-Model Organism

Correlation of X Chromosome Inactivation Skewing and Bleeding Phenotype in Obligate Carriers of Hemophilia A

Role of Von Willebrand Factor in Female Carriers from an Extended Family with Mild Hemophilia A

Random X-Chromosome Inactivation in Hemophilia A Carriers Does Not Fully Attenuate Bleeding Risk

Deletion of an X-Inactivation Boundary Disrupts Adjacent Gene Silencing: e1003952

Suchergebnisse filtern