UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 94

Sortiert nach

Emerging patterns of somatic mutations in cancer

Nature reviews. Genetics, 2013-10, Vol.14 (10), p.703

2013

Volltextzugriff (PDF)

Cancer genomics: from discovery science to personalized medicine

Nature medicine, 2011-03, Vol.17 (3), p.297-303

2011

Volltextzugriff (PDF)

Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing

Nature genetics, 2014-03, Vol.46 (3), p.225-233

2014

Volltextzugriff (PDF)

Preleukaemic clonal haemopoiesis and risk of therapy-related myeloid neoplasms: a case-control study

The lancet oncology, 2017, Vol.18 (1), p.100-111

2017

Volltextzugriff (PDF)

Somatic mutation distributions in cancer genomes vary with three-dimensional chromatin structure

Nature genetics, 2020-11, Vol.52 (11), p.1178-1188

2020

Volltextzugriff (PDF)

MuSE: accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data

Genome Biology, 2016-08, Vol.17 (1), p.178-178, Article 178

2016

Volltextzugriff (PDF)

Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone

Nature genetics, 2013-12, Vol.45 (12), p.1479-1482

2013

Volltextzugriff (PDF)

Mutations in the SWI/SNF complex induce a targetable dependence on oxidative phosphorylation in lung cancer

Nature medicine, 2018-07, Vol.24 (7), p.1047-1057

2018

Volltextzugriff (PDF)

A survey of RNA editing in human brain

Genome research, 2004-12, Vol.14 (12), p.2379

2004

Volltextzugriff (PDF)

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

Nature genetics, 2008-06, Vol.40 (6), p.722-729

2008

Volltextzugriff (PDF)

Immunogenomic profiling of lung adenocarcinoma reveals poorly differentiated tumors are associated with an immunogenic tumor microenvironment

Lung cancer (Amsterdam, Netherlands), 2022-10, Vol.172, p.19-28

2022

Volltextzugriff (PDF)

Estimation of rearrangement phylogeny for cancer genomes

Genome research, 2012-02, Vol.22 (2), p.346

2012

Volltextzugriff (PDF)

Learning to distinguish progressive and non-progressive ductal carcinoma in situ

Nature reviews. Cancer, 2022-12, Vol.22 (12), p.663

2022

Volltextzugriff (PDF)

Mutations in UPF3B , a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

Nature genetics, 2007-09, Vol.39 (9), p.1127-1133

2007

Volltextzugriff (PDF)

Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability

Nature genetics, 2010-06, Vol.42 (6), p.486-488

2010

Volltextzugriff (PDF)

High-resolution analysis of DNA copy number using oligonucleotide microarrays

Genome research, 2004-02, Vol.14 (2), p.287

2004

Volltextzugriff (PDF)

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Nature genetics, 2015-03, Vol.47 (3), p.257-262

2015

Volltextzugriff (PDF)

Gene mutations in primary tumors and corresponding patient-derived xenografts derived from non-small cell lung cancer

Cancer letters, 2015-02, Vol.357 (1), p.179-185

2015

Volltextzugriff (PDF)

Recurrent PTPRB and PLCG1 mutations in angiosarcoma

Nature genetics, 2014-04, Vol.46 (4), p.376-379

2014

Volltextzugriff (PDF)

High-throughput single-cell DNA sequencing of acute myeloid leukemia tumors with droplet microfluidics

Genome research, 2018-09, Vol.28 (9), p.1345

2018

Volltextzugriff (PDF)

Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

Nature genetics, 2009-05, Vol.41 (5), p.521-523

2009

Volltextzugriff (PDF)

Author Correction: Mutations in the SWI/SNF complex induce a targetable dependence on oxidative phosphorylation in lung cancer

Nature medicine, 2018-10, Vol.24 (10), p.1627-1627

2018

Volltextzugriff (PDF)

1 – 25 von 94

Suche als RSS-Feed

Aktive Filter

KollektionElectronic Journals Library

KollektionWK Lippincott Williams & Wilkins–Connect here FIRST to enable access

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(89)
Mit Volltextzugriff
(49)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Emerging patterns of somatic mutations in cancer

Cancer genomics: from discovery science to personalized medicine

Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing

Preleukaemic clonal haemopoiesis and risk of therapy-related myeloid neoplasms: a case-control study

Somatic mutation distributions in cancer genomes vary with three-dimensional chromatin structure

Exome sequencing of liver fluke―associated cholangiocarcinoma

MuSE: accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data

Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone

Mutations in the SWI/SNF complex induce a targetable dependence on oxidative phosphorylation in lung cancer

A survey of RNA editing in human brain

Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

Immunogenomic profiling of lung adenocarcinoma reveals poorly differentiated tumors are associated with an immunogenic tumor microenvironment

Estimation of rearrangement phylogeny for cancer genomes

Learning to distinguish progressive and non-progressive ductal carcinoma in situ

Mutations in UPF3B , a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability

High-resolution analysis of DNA copy number using oligonucleotide microarrays

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Gene mutations in primary tumors and corresponding patient-derived xenografts derived from non-small cell lung cancer

Recurrent PTPRB and PLCG1 mutations in angiosarcoma

Clonal Hematopoiesis Is Associated with Increased Risk of Severe Neurotoxicity in Axicabtagene Ciloleucel Therapy of Large B-Cell Lymphoma

High-throughput single-cell DNA sequencing of acute myeloid leukemia tumors with droplet microfluidics

Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

Author Correction: Mutations in the SWI/SNF complex induce a targetable dependence on oxidative phosphorylation in lung cancer

Aktive Filter

Suchergebnisse filtern