UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Hereditary Predisposition to Prostate Cancer: From Genetics to Clinical Implications

International journal of molecular sciences, 2020-07, Vol.21 (14), p.5036

2020

Link zum Volltext

Verfügbarkeit prüfen

Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer

PLoS genetics, 2018-04, Vol.14 (4), p.e1007355-e1007355

2018

Link zum Volltext

Verfügbarkeit prüfen

Genetic basis of PD-L1 overexpression in diffuse large B-cell lymphomas

Blood, 2016-06, Vol.127 (24), p.3026-3034

2016

Link zum Volltext

Verfügbarkeit prüfen

Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients

PloS one, 2015-07, Vol.10 (7), p.e0132728

2015

Link zum Volltext

Verfügbarkeit prüfen

Exome sequencing reveals novel mutation targets in diffuse large B-cell lymphomas derived from Chinese patients

Blood, 2014-10, Vol.124 (16), p.2544-2553

2014

Link zum Volltext

Verfügbarkeit prüfen

Portuguese Consensus Recommendations for Next-Generation Sequencing of Lung Cancer, Rare Tumors, and Cancers of Unknown Primary Origin in Clinical Practice

Acta médica portuguesa, 2022-09, Vol.35 (9), p.677-690

2022

Link zum Volltext

Verfügbarkeit prüfen

SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas

Cancer research (Chicago, Ill.), 2005-05, Vol.65 (10), p.4012-4019

2005

Link zum Volltext

Verfügbarkeit prüfen

Truncating and missense PPM1D mutations in early-onset and/or familial/hereditary prostate cancer patients

Genes chromosomes & cancer, 2016-12, Vol.55 (12), p.954-961

2016

Link zum Volltext

Verfügbarkeit prüfen

TMPRSS2-ERG Gene Fusion Causing ERG Overexpression Precedes Chromosome Copy Number Changes in Prostate Carcinomas, Paired HGPIN Lesions

Neoplasia (New York, N.Y.), 2006-10, Vol.8 (10), p.826-832

2006

Link zum Volltext

Verfügbarkeit prüfen

MLL-SEPTIN gene fusions in hematological malignancies

Biological chemistry, 2011-08, Vol.392 (8-9), p.713-724

2011

Link zum Volltext

Verfügbarkeit prüfen

DNA repair genes are selectively mutated in diffuse large B cell lymphomas

The Journal of experimental medicine, 2013-08, Vol.210 (9), p.1729-1742

2013

Link zum Volltext

Verfügbarkeit prüfen

Combined germline and tumor mutation signature testing identifies new families with NTHL1 tumor syndrome

Frontiers in genetics, 2023-08, Vol.14, p.1254908-1254908

2023

Link zum Volltext

Verfügbarkeit prüfen

Multi-Gene Panel Testing in Gastroenterology: Are We Ready for the Results?

GE Portuguese journal of gastroenterology, 2021-11, Vol.28 (6), p.403-409

2021

Link zum Volltext

Verfügbarkeit prüfen

Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas

PloS one, 2016-08, Vol.11 (8), p.e0161438-e0161438

2016

Link zum Volltext

Verfügbarkeit prüfen

Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity

Breast cancer research and treatment, 2016-09, Vol.159 (2), p.245-256

2016

Link zum Volltext

Verfügbarkeit prüfen

Next Generation Sequencing of Tumor and Matched Plasma Samples: Identification of Somatic Variants in ctDNA From Ovarian Cancer Patients

Frontiers in oncology, 2021-09, Vol.11, p.754094-754094

2021

Link zum Volltext

Verfügbarkeit prüfen

Altered expression of MGMT in high-grade gliomas results from the combined effect of epigenetic and genetic aberrations

PloS one, 2013-03, Vol.8 (3), p.e58206-e58206

2013

Link zum Volltext

Verfügbarkeit prüfen

Molecular circuit involving KLK4 integrates androgen and mTOR signaling in prostate cancer

Proceedings of the National Academy of Sciences - PNAS, 2013-07, Vol.110 (28), p.E2572-E2581

2013

Link zum Volltext

Verfügbarkeit prüfen

Frequency of CDH1, CTNNA1 and CTNND1 Germline Variants in Families with Diffuse and Mixed Gastric Cancer

Cancers, 2023-08, Vol.15 (17), p.4313

2023

Link zum Volltext

Verfügbarkeit prüfen

POLE somatic mutations in advanced colorectal cancer

Cancer medicine (Malden, MA), 2017-12, Vol.6 (12), p.2966-2971

2017

Link zum Volltext

Verfügbarkeit prüfen

Ponatinib induces a sustained deep molecular response in a chronic myeloid leukaemia patient with an early relapse with a T315I mutation following allogeneic hematopoietic stem cell transplantation: a case report

BMC cancer, 2018-12, Vol.18 (1), p.1229-1229, Article 1229

2018

Link zum Volltext

Verfügbarkeit prüfen

A Quantitative Promoter Methylation Profile of Prostate Cancer

Clinical cancer research, 2004-12, Vol.10 (24), p.8472-8478

2004

Link zum Volltext

Verfügbarkeit prüfen

Discontinuation of tyrosine kinase inhibitors in CML patients in real-world clinical practice at a single institution

BMC cancer, 2018-12, Vol.18 (1), p.1245-1245, Article 1245

2018

Link zum Volltext

Verfügbarkeit prüfen

Tumor Testing for Somatic and Germline BRCA1/BRCA2 Variants in Ovarian Cancer Patients in the Context of Strong Founder Effects

Frontiers in oncology, 2020-07, Vol.10, p.1318-1318

2020

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 402

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(344)
Mit Volltextzugriff
(383)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Genes Chromosomes & Cancer
(23)
Cancer Genetics And Cytogenetics
(19)
Bmc Cancer
(14)
Breast Cancer Research And Treatment
(13)
Nature Communications
(12)
British Journal Of Cancer
(9)
Neoplasia
(9)
Familial Cancer
(8)
International Journal Of Cancer
(8)
Plos One
(8)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Hereditary Predisposition to Prostate Cancer: From Genetics to Clinical Implications

Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer

Genetic basis of PD-L1 overexpression in diffuse large B-cell lymphomas

Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients

Exome sequencing reveals novel mutation targets in diffuse large B-cell lymphomas derived from Chinese patients

Portuguese Consensus Recommendations for Next-Generation Sequencing of Lung Cancer, Rare Tumors, and Cancers of Unknown Primary Origin in Clinical Practice

SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas

Truncating and missense PPM1D mutations in early-onset and/or familial/hereditary prostate cancer patients

TMPRSS2-ERG Gene Fusion Causing ERG Overexpression Precedes Chromosome Copy Number Changes in Prostate Carcinomas, Paired HGPIN Lesions

MLL-SEPTIN gene fusions in hematological malignancies

DNA repair genes are selectively mutated in diffuse large B cell lymphomas

Combined germline and tumor mutation signature testing identifies new families with NTHL1 tumor syndrome

Multi-Gene Panel Testing in Gastroenterology: Are We Ready for the Results?

Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas

Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity

Haplotype analysis of the internationally distributed BRCA1 c.3331_3334delCAAG founder mutation reveals a common ancestral origin in Iberia

Next Generation Sequencing of Tumor and Matched Plasma Samples: Identification of Somatic Variants in ctDNA From Ovarian Cancer Patients

Altered expression of MGMT in high-grade gliomas results from the combined effect of epigenetic and genetic aberrations

Molecular circuit involving KLK4 integrates androgen and mTOR signaling in prostate cancer

Frequency of CDH1, CTNNA1 and CTNND1 Germline Variants in Families with Diffuse and Mixed Gastric Cancer

POLE somatic mutations in advanced colorectal cancer

Ponatinib induces a sustained deep molecular response in a chronic myeloid leukaemia patient with an early relapse with a T315I mutation following allogeneic hematopoietic stem cell transplantation: a case report

A Quantitative Promoter Methylation Profile of Prostate Cancer

Discontinuation of tyrosine kinase inhibitors in CML patients in real-world clinical practice at a single institution

Tumor Testing for Somatic and Germline BRCA1/BRCA2 Variants in Ovarian Cancer Patients in the Context of Strong Founder Effects

Suchergebnisse filtern