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...

Identifying patient-specific flow of signal transduction perturbed by multiple single-nucleotide alterations

Quantitative biology, 2020-12, Vol.8 (4), p.336-346

2020

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)

Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein

Stem cell reports, 2021-04, Vol.16 (4), p.985-996

2021

Volltextzugriff (PDF)

Concomitant inhibition of B7-H3 and PD-L1 expression by a novel and synthetic microRNA delivers potent antitumor activities in colorectal tumor models

Investigational new drugs, 2021-10, Vol.39 (5), p.1267-1274

2021

Volltextzugriff (PDF)

Single nucleotide alterations in MicroRNAs and human cancer-A not fully explored field

Non-coding RNA research, 2020-03, Vol.5 (1), p.27-31

Zhao, Dan

2020

Volltextzugriff (PDF)

Low-density lipoprotein receptor variants are associated with spontaneous and treatment-induced recovery from hepatitis C virus infection

Infection, genetics and evolution, 2009-09, Vol.9 (5), p.847-852

2009

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)

Evaluation of cell-free DNA approaches for multi-cancer early detection

Cancer cell, 2022-12, Vol.40 (12), p.1537-1549.e12

2022

Volltextzugriff (PDF)

Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data

Annals of oncology, 2015-01, Vol.26 (1), p.64-70

2015

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)

Single-cell Sequencing Reveals Variants in ARID1A , GPRC5A and MLL2 Driving Self-renewal of Human Bladder Cancer Stem Cells

European urology, 2017-01, Vol.71 (1), p.8-12

2017

Volltextzugriff (PDF)

Precision Nutrition

2023

Volltextzugriff (PDF)

Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis

Leukemia, 2010-02, Vol.24 (2), p.438-449

2010

Volltextzugriff (PDF)

A genome‐wide study of the relationship between chromosomal abnormalities and gene expression in colorectal tumors

Genes chromosomes & cancer, 2021-04, Vol.60 (4), p.250-262

2021

Volltextzugriff (PDF)

Genomic analysis reveals few genetic alterations in pediatric acute myeloid leukemia

Proceedings of the National Academy of Sciences - PNAS, 2009-08, Vol.106 (31), p.12944-12949

2009

Volltextzugriff (PDF)

Molecular alterations in colorectal adenomas and intramucosal adenocarcinomas defined by high-density single-nucleotide polymorphism arrays

Journal of gastroenterology, 2017-11, Vol.52 (11), p.1158-1168

2017

Volltextzugriff (PDF)

Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population

Nutrients, 2020-11, Vol.12 (11), p.3389

2020

Volltextzugriff (PDF)

Detection of DNA copy number alterations by matrix-assisted laser desorption/ionization time-of-flight mass spectrometric analysis of single nucleotide polymorphisms

Clinical chemistry and laboratory medicine, 2022-09, Vol.60 (10), p.1543-1550

2022

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)

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)

Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer

The Journal of pathology, 2022-05, Vol.257 (1), p.68-81

2022

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)

Genetic alterations in hepatocellular carcinoma: An update

World journal of gastroenterology : WJG, 2016-11, Vol.22 (41), p.9069-9095

2016

Volltextzugriff (PDF)

1 – 25 von 165

Suche als RSS-Feed

Aktive Filter

Nur zeigenMit Volltextzugriff

SpracheEnglisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(149)

Publikationsform

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Identifying patient-specific flow of signal transduction perturbed by multiple single-nucleotide alterations

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

Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein

Concomitant inhibition of B7-H3 and PD-L1 expression by a novel and synthetic microRNA delivers potent antitumor activities in colorectal tumor models

Single nucleotide alterations in MicroRNAs and human cancer-A not fully explored field

Low-density lipoprotein receptor variants are associated with spontaneous and treatment-induced recovery from hepatitis C virus infection

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

Evaluation of cell-free DNA approaches for multi-cancer early detection

Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data

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

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

Single-cell Sequencing Reveals Variants in ARID1A , GPRC5A and MLL2 Driving Self-renewal of Human Bladder Cancer Stem Cells

Precision Nutrition

Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis

A genome‐wide study of the relationship between chromosomal abnormalities and gene expression in colorectal tumors

Genomic analysis reveals few genetic alterations in pediatric acute myeloid leukemia

Molecular alterations in colorectal adenomas and intramucosal adenocarcinomas defined by high-density single-nucleotide polymorphism arrays

A comprehensive survey of genomic alterations in gastric cancer reveals systematic patterns of molecular exclusivity and co-occurrence among distinct therapeutic targets

Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population

Detection of DNA copy number alterations by matrix-assisted laser desorption/ionization time-of-flight mass spectrometric analysis of single nucleotide polymorphisms

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

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

Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer

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

Genetic alterations in hepatocellular carcinoma: An update

Aktive Filter

Suchergebnisse filtern