UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 996

Sortiert nach

Correlating Multiallelic Copy Number Polymorphisms with Disease Susceptibility

Human mutation, 2013-01, Vol.34 (1), p.1-13

2013

Link zum Volltext

Verfügbarkeit prüfen

Flexible and Scalable Full-Length CYP2D6 Long Amplicon PacBio Sequencing

Human mutation, 2017-03, Vol.38 (3), p.310-316

2017

Link zum Volltext

Verfügbarkeit prüfen

Targeted Locus Amplification and Next-Generation Sequencing

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1492, p.185

2017

Link zum Volltext

Verfügbarkeit prüfen

Molecular methods for genotyping complex copy number polymorphisms

Genomics (San Diego, Calif.), 2013-02, Vol.101 (2), p.86-93

2013

Link zum Volltext

Verfügbarkeit prüfen

Identification of SOX3 as an XX male sex reversal gene in mice and humans

The Journal of clinical investigation, 2011-01, Vol.121 (1), p.328-341

2011

Link zum Volltext

Verfügbarkeit prüfen

Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication

BMC genomics, 2014-05, Vol.15 (1), p.329-329

2014

Link zum Volltext

Verfügbarkeit prüfen

Seminoma and embryonal carcinoma footprints identified by analysis of integrated genome-wide epigenetic and expression profiles of germ cell cancer cell lines

PloS one, 2014-06, Vol.9 (6), p.e98330-e98330

2014

Link zum Volltext

Verfügbarkeit prüfen

Glucocorticoid-induced leucine zipper (GILZ) inhibits B cell activation in systemic lupus erythematosus

Annals of the rheumatic diseases, 2016-04, Vol.75 (4), p.739-747

2016

Link zum Volltext

Verfügbarkeit prüfen

Flexible and Scalable Full‐Length CYP2D6 Long Amplicon PacBio Sequencing

Human mutation, 2017-03, Vol.38 (3), p.310-316

2017

Link zum Volltext

Verfügbarkeit prüfen

BTB-ZF transcriptional regulator PLZF modifies chromatin to restrain inflammatory signaling programs

Proceedings of the National Academy of Sciences - PNAS, 2015-02, Vol.112 (5), p.1535-1540

2015

Link zum Volltext

Verfügbarkeit prüfen

Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance

BMC biology, 2018-09, Vol.16 (1), p.104-104, Article 104

2018

Link zum Volltext

Verfügbarkeit prüfen

Copy number variation associated with meiotic arrest in idiopathic male infertility

Fertility and sterility, 2015, Vol.103 (1), p.214-219

2015

Link zum Volltext

Verfügbarkeit prüfen

Genotyping Multiallelic Copy Number Variation with Multiplex Ligation-Dependent Probe Amplification (MLPA)

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1492, p.147

2017

Link zum Volltext

Verfügbarkeit prüfen

Mutations in MAP3K1 Cause 46,XY Disorders of Sex Development and Implicate a Common Signal Transduction Pathway in Human Testis Determination

American journal of human genetics, 2010-12, Vol.87 (6), p.898-904

2010

Link zum Volltext

Verfügbarkeit prüfen

Rare variants in non-coding regulatory regions of the genome that affect gene expression in systemic lupus erythematosus

Scientific reports, 2019-10, Vol.9 (1), p.15433-9, Article 15433

2019

Link zum Volltext

Verfügbarkeit prüfen

Loss of maternal EED results in postnatal overgrowth

Clinical epigenetics, 2018-07, Vol.10 (1), p.95-95, Article 95

2018

Link zum Volltext

Verfügbarkeit prüfen

Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration

PloS one, 2012-04, Vol.7 (4), p.e35255-e35255

2012

Link zum Volltext

Verfügbarkeit prüfen

Quantitative DNA Analysis Using Droplet Digital PCR

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1492, p.167

2017

Link zum Volltext

Verfügbarkeit prüfen

GILZ overexpression inhibits endothelial cell adhesive function through regulation of NF-κB and MAPK activity

The Journal of immunology (1950), 2013-07, Vol.191 (1), p.424-433

2013

Link zum Volltext

Verfügbarkeit prüfen

Breakpoint characterization of a rare alpha0‐thalassemia deletion using targeted locus amplification on genomic DNA

International journal of laboratory hematology, 2021-12, Vol.43 (6), p.1628-1634

2021

Link zum Volltext

Verfügbarkeit prüfen

Breakpoint characterization of a rare alpha 0 -thalassemia deletion using targeted locus amplification on genomic DNA

International journal of laboratory hematology, 2021-12, Vol.43 (6), p.1628-1634

2021

Link zum Volltext

Verfügbarkeit prüfen

Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease

American journal of human genetics, 2005-04, Vol.76 (4), p.572-580

2005

Link zum Volltext

Verfügbarkeit prüfen

Spinoza's Philosophy of Ratio

Beth Lord

2018

Link zum Volltext

Verfügbarkeit prüfen

Identification of Streptococcus parasanguinis DNA contamination in human buccal DNA samples

BMC research notes, 2013-11, Vol.6 (1), p.481-481, Article 481

2013

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 996

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(849)
Mit Volltextzugriff
(905)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(633)
Life Sciences & Biomedicine
(477)
Humans
(404)
Female
(205)
Male
(200)
Middle Aged
(130)
Adult
(110)
Aged
(109)
Animals
(96)
Biological And Medical Sciences
(93)
Medical Sciences
(76)
Physical Sciences
(75)
Science & Technology - Other Topics
(74)
Biochemistry & Molecular Biology
(71)
Genetics & Heredity
(71)
Multidisciplinary Sciences
(70)
Cardiovascular System & Cardiology
(65)
Risk Factors
(63)
Cardiac & Cardiovascular Systems
(60)
Mutation
(59)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(4)
... seit 90 Tagen
(21)

Menü

Weitere Dienste

Einstellungen

Correlating Multiallelic Copy Number Polymorphisms with Disease Susceptibility

Flexible and Scalable Full-Length CYP2D6 Long Amplicon PacBio Sequencing

Targeted Locus Amplification and Next-Generation Sequencing

Molecular methods for genotyping complex copy number polymorphisms

Identification of SOX3 as an XX male sex reversal gene in mice and humans

Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication

Seminoma and embryonal carcinoma footprints identified by analysis of integrated genome-wide epigenetic and expression profiles of germ cell cancer cell lines

Glucocorticoid-induced leucine zipper (GILZ) inhibits B cell activation in systemic lupus erythematosus

Flexible and Scalable Full‐Length CYP2D6 Long Amplicon PacBio Sequencing

BTB-ZF transcriptional regulator PLZF modifies chromatin to restrain inflammatory signaling programs

Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance

Copy number variation associated with meiotic arrest in idiopathic male infertility

Genotyping Multiallelic Copy Number Variation with Multiplex Ligation-Dependent Probe Amplification (MLPA)

Mutations in MAP3K1 Cause 46,XY Disorders of Sex Development and Implicate a Common Signal Transduction Pathway in Human Testis Determination

Rare variants in non-coding regulatory regions of the genome that affect gene expression in systemic lupus erythematosus

Loss of maternal EED results in postnatal overgrowth

Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration

Quantitative DNA Analysis Using Droplet Digital PCR

GILZ overexpression inhibits endothelial cell adhesive function through regulation of NF-κB and MAPK activity

Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis

Breakpoint characterization of a rare alpha0‐thalassemia deletion using targeted locus amplification on genomic DNA

Breakpoint characterization of a rare alpha 0 -thalassemia deletion using targeted locus amplification on genomic DNA

Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease

Spinoza's Philosophy of Ratio

Identification of Streptococcus parasanguinis DNA contamination in human buccal DNA samples

Suchergebnisse filtern