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...

Transposon Reactivation in the Germline May Be Useful for Both Transposons and Their Host Genomes

Cells (Basel, Switzerland), 2020-05, Vol.9 (5), p.1172

2020

Volltextzugriff (PDF)

Deep sequencing and de novo assembly of the mouse oocyte transcriptome define the contribution of transcription to the DNA methylation landscape

Genome Biology, 2015-09, Vol.16 (1), p.209-209, Article 209

2015

Volltextzugriff (PDF)

Reactivation of a somatic errantivirus and germline invasion in Drosophila ovaries

Nature communications, 2023-09, Vol.14 (1), p.6096-6096, Article 6096

2023

Volltextzugriff (PDF)

Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type Ib

Journal of medical genetics, 2011-01, Vol.48 (1), p.55-63

2011

Volltextzugriff (PDF)

The interplay between the Argonaute proteins Piwi and Aub within Drosophila germarium is critical for oogenesis, piRNA biogenesis and TE silencing

Nucleic acids research, 2018-11, Vol.46 (19), p.10052-10065

2018

Volltextzugriff (PDF)

A Maternal Epimutation of GNAS Leads to Albright Osteodystrophy and Parathyroid Hormone Resistance

The journal of clinical endocrinology and metabolism, 2008-03, Vol.93 (3), p.661-665

2008

Volltextzugriff (PDF)

TET3 controls the expression of the H3K27me3 demethylase Kdm6b during neural commitment

Cellular and molecular life sciences : CMLS, 2021-01, Vol.78 (2), p.757-768

2021

Volltextzugriff (PDF)

DNA methylation profiling reveals a pathological signature that contributes to transcriptional defects of CD34+CD15− cells in early chronic‐phase chronic myeloid leukemia

Molecular oncology, 2018-06, Vol.12 (6), p.814-829

2018

Volltextzugriff (PDF)

DNA methylation profiling reveals a pathological signature that contributes to transcriptional defects of CD 34 + CD 15 − cells in early chronic‐phase chronic myeloid leukemia

Molecular oncology, 2018-06, Vol.12 (6), p.814-829

2018

Volltextzugriff (PDF)

Simultaneous Hyper- and Hypomethylation at Imprinted Loci in a Subset of Patients with GNAS Epimutations Underlies a Complex and Different Mechanism of Multilocus Methylation Defect in Pseudohypoparathyroidism Type 1b

Human mutation, 2013-08, Vol.34 (8), p.1172-1180

2013

Volltextzugriff (PDF)

Imprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactive

Nucleic acids research, 2016-01, Vol.44 (2), p.621-635

2016

Volltextzugriff (PDF)

Biallelic non-productive enhancer-promoter interactions precede imprinted expression of Kcnk9 during mouse neural commitment

HGG advances, 2024-04, Vol.5 (2), p.100271-100271, Article 100271

2024

Volltextzugriff (PDF)

GNAS-Related Loss-of-Function Disorders and the Role of Imprinting

Hormone research in paediatrics, 2013-01, Vol.79 (3), p.119-129

2013

Volltextzugriff (PDF)

Methylation and Transcripts Expression at the Imprinted GNAS Locus in Human Embryonic and Induced Pluripotent Stem Cells and Their Derivatives

Stem cell reports, 2014-09, Vol.3 (3), p.432-443

2014

Volltextzugriff (PDF)

Loss of Methylation at GNAS Exon A/B Is Associated With Increased Intrauterine Growth

The journal of clinical endocrinology and metabolism, 2015-04, Vol.100 (4), p.E623-E631

2015

Volltextzugriff (PDF)

In Vitro Corticogenesis from Embryonic Stem Cells Recapitulates the In Vivo Epigenetic Control of Imprinted Gene Expression

Cerebral cortex (New York, N.Y. 1991), 2017-03, Vol.27 (3), p.2418-2433

2017

Volltextzugriff (PDF)

European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study

European journal of human genetics : EJHG, 2015-04, Vol.23 (4), p.438-444

2015

Volltextzugriff (PDF)

1 – 17 von 17

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(17)
Mit Volltextzugriff
(15)

Publikationsform

Artikel
(17)

Sprache

Englisch
(17)

Erscheinungsjahr

n.n

Thema

Science & Technology
(16)
Life Sciences & Biomedicine
(15)
Life Sciences
(11)
Dna Methylation
(10)
Humans
(9)
Chromogranins
(7)
Genomic Imprinting
(7)
Gtp-Binding Protein Alpha Subunits, Gs - Genetics
(7)
Biochemistry, Molecular Biology
(6)
Female
(6)
Animals
(5)
Epigenesis, Genetic
(5)
Epigenetics
(5)
Genetics & Heredity
(5)
Genomics
(5)
Pseudohypoparathyroidism
(5)
Pseudohypoparathyroidism - Genetics
(5)
Biochemistry & Molecular Biology
(4)
Genetics
(4)
Male
(4)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Transposon Reactivation in the Germline May Be Useful for Both Transposons and Their Host Genomes

Deep sequencing and de novo assembly of the mouse oocyte transcriptome define the contribution of transcription to the DNA methylation landscape

Reactivation of a somatic errantivirus and germline invasion in Drosophila ovaries

Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type Ib

The interplay between the Argonaute proteins Piwi and Aub within Drosophila germarium is critical for oogenesis, piRNA biogenesis and TE silencing

A Maternal Epimutation of GNAS Leads to Albright Osteodystrophy and Parathyroid Hormone Resistance

TET3 controls the expression of the H3K27me3 demethylase Kdm6b during neural commitment

DNA methylation profiling reveals a pathological signature that contributes to transcriptional defects of CD34+CD15− cells in early chronic‐phase chronic myeloid leukemia

DNA methylation profiling reveals a pathological signature that contributes to transcriptional defects of CD 34 + CD 15 − cells in early chronic‐phase chronic myeloid leukemia

Simultaneous Hyper- and Hypomethylation at Imprinted Loci in a Subset of Patients with GNAS Epimutations Underlies a Complex and Different Mechanism of Multilocus Methylation Defect in Pseudohypoparathyroidism Type 1b

Imprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactive

Biallelic non-productive enhancer-promoter interactions precede imprinted expression of Kcnk9 during mouse neural commitment

GNAS-Related Loss-of-Function Disorders and the Role of Imprinting

Methylation and Transcripts Expression at the Imprinted GNAS Locus in Human Embryonic and Induced Pluripotent Stem Cells and Their Derivatives

Loss of Methylation at GNAS Exon A/B Is Associated With Increased Intrauterine Growth

In Vitro Corticogenesis from Embryonic Stem Cells Recapitulates the In Vivo Epigenetic Control of Imprinted Gene Expression

European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study

Suchergebnisse filtern