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...

13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia

Leukemia, 2011-03, Vol.25 (3), p.489-497

2011

Volltextzugriff (PDF)

Acute myeloid leukaemia

The Genetic Basis of Haematological Cancers, 2016, p.133-202

2016

Volltextzugriff (PDF)

AM22, a novel synthetic microRNA, inhibits the proliferation of colorectal cancer cells by targeting core binding factor subunit β (CBFB)

Investigational new drugs, 2022-06, Vol.40 (3), p.469-477

2022

Volltextzugriff (PDF)

Amplified genes may be overexpressed, unchanged, or downregulated in cervical cancer cell lines

PloS one, 2012-03, Vol.7 (3), p.e32667

2012

Volltextzugriff (PDF)

Analysis of genomic rearrangements by using the Burrows-Wheeler transform of short-read data

BMC bioinformatics, 2015-12, Vol.16 Suppl 18 (S18), p.S5-S5, Article S5

2015

Volltextzugriff (PDF)

Analysis of Germline Gene Copy Number Variants of Patients with Sporadic Pancreatic Adenocarcinoma Reveals Specific Variations

Oncology, 2013-11, Vol.85 (5), p.306-311

2013

Volltextzugriff (PDF)

Analysis of somatic copy number alterations in biliary tract carcinoma using a single nucleotide polymorphism array

Future science OA, 2022-01, Vol.8 (1), p.FSO766

2022

Volltextzugriff (PDF)

Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma

Proceedings of the National Academy of Sciences - PNAS, 2007-12, Vol.104 (50), p.20007-20012

2007

Volltextzugriff (PDF)

Association between DNA repair gene polymorphisms and p53 alterations in Japanese patients with muscle-invasive bladder cancer

Pathobiology (Basel), 2006-01, Vol.73 (6), p.295-303

2006

Volltextzugriff (PDF)

Atrial fibrillation and hypercoagulability: Dependent on clinical factors or/and on genetic alterations?

Journal of thrombosis and thrombolysis, 2003-12, Vol.16 (3), p.155-161

2003

Volltextzugriff (PDF)

BAK1 gene variation and abdominal aortic aneurysms

Human mutation, 2009-07, Vol.30 (7), p.1043-1047

2009

Volltextzugriff (PDF)

BCRgt: a Bayesian cluster regression-based genotyping algorithm for the samples with copy number alterations

BMC bioinformatics, 2014-03, Vol.15 (1), p.74-74, Article 74

2014

Volltextzugriff (PDF)

Catecholaminergic Gene Polymorphisms Are Associated with GI Symptoms and Morphological Brain Changes in Irritable Bowel Syndrome

PloS one, 2015-08, Vol.10 (8), p.e0135910-e0135910

2015

Volltextzugriff (PDF)

Chromosomal Aberrations in Canine Gliomas Define Candidate Genes and Common Pathways in Dogs and Humans

Journal of neuropathology and experimental neurology, 2016-07, Vol.75 (7), p.700-710

2016

Volltextzugriff (PDF)

Clinical Targeted Next-Generation Sequencing Shows Increased Mutational Load in Endometrioid-type Endometrial Adenocarcinoma With Deficient DNA Mismatch Repair

International journal of gynecological pathology, 2018-11, Vol.37 (6), p.581-589

2018

Volltextzugriff (PDF)

The Clinical Utility of Optical Genome Mapping for the Assessment of Genomic Aberrations in Acute Lymphoblastic Leukemia

Cancers, 2021-08, Vol.13 (17), p.4388

2021

Volltextzugriff (PDF)

A clinically applicable molecular classification of oncocytic cell thyroid nodules

Endocrine-related cancer, 2023-09, Vol.30 (9), p.1

2023

Volltextzugriff (PDF)

CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

BMC bioinformatics, 2016-08, Vol.17 (1), p.310-310, Article 310

2016

Volltextzugriff (PDF)

Combining targeted sequencing and ultra-low-pass whole-genome sequencing for accurate somatic copy number alteration detection

Functional & integrative genomics, 2021-03, Vol.21 (2), p.161-169

2021

Volltextzugriff (PDF)

Common Polymorphisms in the MDM2 and TP53 Genes and the Relationship between TP53 Mutations and Patient Outcomes in Glioblastomas

Brain pathology (Zurich, Switzerland), 2009-04, Vol.19 (2), p.188-194

2009

Volltextzugriff (PDF)

Comparative analysis of methods for identifying somatic copy number alterations from deep sequencing data

Briefings in bioinformatics, 2015-03, Vol.16 (2), p.242-254

2015

Volltextzugriff (PDF)

Comparative Cytogenetic Analysis of Dog and Human Choroid Plexus Tumors Defines Syntenic Regions of Genomic Loss

Journal of neuropathology and experimental neurology, 2018-05, Vol.77 (5), p.413-419

2018

Volltextzugriff (PDF)

Comparative genetic analysis of a rare synchronous collision tumor composed of malignant pleural mesothelioma and primary pulmonary adenocarcinoma

Diagnostic pathology, 2016-04, Vol.11 (38), p.38, Article 38

2016

Volltextzugriff (PDF)

Comprehensive Analyses of Somatic Copy Number Alterations and Mutations Based on the Adenoma–Carcinoma Sequence

Genes chromosomes & cancer, 2024-09, Vol.63 (9), p.e23267-n/a

2024

Volltextzugriff (PDF)

1 – 25 von 163

Suche als RSS-Feed

Aktive Filter

SpracheEnglisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(148)
Mit Volltextzugriff
(144)

Publikationsform

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia

Acute myeloid leukaemia

AM22, a novel synthetic microRNA, inhibits the proliferation of colorectal cancer cells by targeting core binding factor subunit β (CBFB)

Amplified genes may be overexpressed, unchanged, or downregulated in cervical cancer cell lines

Analysis of genomic rearrangements by using the Burrows-Wheeler transform of short-read data

Analysis of Germline Gene Copy Number Variants of Patients with Sporadic Pancreatic Adenocarcinoma Reveals Specific Variations

Analysis of somatic copy number alterations in biliary tract carcinoma using a single nucleotide polymorphism array

Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma

Association between DNA repair gene polymorphisms and p53 alterations in Japanese patients with muscle-invasive bladder cancer

Atrial fibrillation and hypercoagulability: Dependent on clinical factors or/and on genetic alterations?

BAK1 gene variation and abdominal aortic aneurysms

BCRgt: a Bayesian cluster regression-based genotyping algorithm for the samples with copy number alterations

Catecholaminergic Gene Polymorphisms Are Associated with GI Symptoms and Morphological Brain Changes in Irritable Bowel Syndrome

Chromosomal Aberrations in Canine Gliomas Define Candidate Genes and Common Pathways in Dogs and Humans

Clinical Targeted Next-Generation Sequencing Shows Increased Mutational Load in Endometrioid-type Endometrial Adenocarcinoma With Deficient DNA Mismatch Repair

The Clinical Utility of Optical Genome Mapping for the Assessment of Genomic Aberrations in Acute Lymphoblastic Leukemia

Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project

A clinically applicable molecular classification of oncocytic cell thyroid nodules

CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

Combining targeted sequencing and ultra-low-pass whole-genome sequencing for accurate somatic copy number alteration detection

Common Polymorphisms in the MDM2 and TP53 Genes and the Relationship between TP53 Mutations and Patient Outcomes in Glioblastomas

Comparative analysis of methods for identifying somatic copy number alterations from deep sequencing data

Comparative Cytogenetic Analysis of Dog and Human Choroid Plexus Tumors Defines Syntenic Regions of Genomic Loss

Comparative genetic analysis of a rare synchronous collision tumor composed of malignant pleural mesothelioma and primary pulmonary adenocarcinoma

Comprehensive Analyses of Somatic Copy Number Alterations and Mutations Based on the Adenoma–Carcinoma Sequence

Aktive Filter

Suchergebnisse filtern