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...

Gene copy-number polymorphism caused by retrotransposition in humans

PLoS genetics, 2013-01, Vol.9 (1), p.e1003242

2013

Volltextzugriff (PDF)

Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families

PloS one, 2022-01, Vol.17 (1), p.e0262419-e0262419

2022

Volltextzugriff (PDF)

A genetic network that suppresses genome rearrangements in Saccharomyces cerevisiae and contains defects in cancers

Nature communications, 2016-04, Vol.7 (1), p.11256-11256, Article 11256

2016

Volltextzugriff (PDF)

The role of exon shuffling in shaping protein-protein interaction networks

BMC genomics, 2010-12, Vol.11 Suppl 5 (Suppl 5), p.S11-S11

2010

Volltextzugriff (PDF)

Exome Sequencing of Native Populations From the Amazon Reveals Patterns on the Peopling of South America

Frontiers in genetics, 2020-10, Vol.11, p.548507-548507

2020

Volltextzugriff (PDF)

The Shared Use of Extended Phenotypes Increases the Fitness of Simulated Populations

Frontiers in genetics, 2021-02, Vol.12, p.617915-617915

2021

Volltextzugriff (PDF)

Assessment of somatic mutations in urine and plasma of Wilms tumor patients

Cancer medicine (Malden, MA), 2020-08, Vol.9 (16), p.5948-5959

2020

Volltextzugriff (PDF)

Domain shuffling and the increasing complexity of biological networks

BioEssays, 2012-08, Vol.34 (8), p.655-657

de Souza, Sandro J.

2012

Volltextzugriff (PDF)

Transcriptome-guided characterization of genomic rearrangements in a breast cancer cell line

Proceedings of the National Academy of Sciences - PNAS, 2009-02, Vol.106 (6), p.1886-1891

2009

Volltextzugriff (PDF)

neoANT-HILL: an integrated tool for identification of potential neoantigens

BMC medical genomics, 2020-02, Vol.13 (1), p.30-30, Article 30

2020

Volltextzugriff (PDF)

Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer

Frontiers in genetics, 2018-05, Vol.9, p.161-161

2018

Volltextzugriff (PDF)

S-score: a scoring system for the identification and prioritization of predicted cancer genes

PloS one, 2014-04, Vol.9 (4), p.e94147-e94147

2014

Volltextzugriff (PDF)

An Anatomy of Normal and Malignant Gene Expression

Proceedings of the National Academy of Sciences - PNAS, 2002-08, Vol.99 (17), p.11287-11292

2002

Volltextzugriff (PDF)

Mutation Detection in Tumor-Derived Cell Free DNA Anticipates Progression in a Patient With Metastatic Colorectal Cancer

Frontiers in oncology, 2018-08, Vol.8, p.306

2018

Volltextzugriff (PDF)

High-throughput sequencing of a South American Amerindian

PloS one, 2013-12, Vol.8 (12), p.e83340

2013

Volltextzugriff (PDF)

Splicing Express: a software suite for alternative splicing analysis using next-generation sequencing data

PeerJ (San Francisco, CA), 2015-11, Vol.3, p.e1419-e1419, Article e1419

2015

Volltextzugriff (PDF)

Identification of rare alternative splicing events in MS/MS data reveals a significant fraction of alternative translation initiation sites

PeerJ (San Francisco, CA), 2014-11, Vol.2, p.e673-e673

2014

Volltextzugriff (PDF)

Origin of Genes

Proceedings of the National Academy of Sciences - PNAS, 1997-07, Vol.94 (15), p.7698-7703

1997

Volltextzugriff (PDF)

Alternative splicing enriched cDNA libraries identify breast cancer-associated transcripts

BMC genomics, 2010-12, Vol.11 Suppl 5 (Suppl 5), p.S4-S4, Article S4

2010

Volltextzugriff (PDF)

Toward a Resolution of the Introns Early/Late Debate: Only Phase Zero Introns are Correlated with the Structure of Ancient Proteins

Proceedings of the National Academy of Sciences - PNAS, 1998-04, Vol.95 (9), p.5094-5099

1998

Volltextzugriff (PDF)

Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types

International journal of genomics, 2016-01, Vol.2016 (2016), p.1-7

2016

Volltextzugriff (PDF)

Essential Saccharomyces cerevisiae genome instability suppressing genes identify potential human tumor suppressors

Proceedings of the National Academy of Sciences - PNAS, 2019-08, Vol.116 (35), p.17377-17382

2019

Volltextzugriff (PDF)

A New Approach for Identification of Cancer-related Pathways using Protein Networks and Genomic Data

Cancer informatics, 2015-01, Vol.2015 (Suppl. 5), p.139-149

2015

Volltextzugriff (PDF)

1 – 25 von 160

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(145)
Mit Volltextzugriff
(143)

Publikationsform

Sprache

Englisch
(158)
Portugiesisch
(3)

Erscheinungsjahr

n.n

Thema

Science & Technology
(123)
Life Sciences & Biomedicine
(88)
Humans
(73)
Animals
(35)
Biochemistry & Molecular Biology
(32)
Genetics & Heredity
(32)
Genes
(27)
Multidisciplinary Sciences
(23)
Science & Technology - Other Topics
(23)
Genomics
(22)
Biotechnology & Applied Microbiology
(20)
Exons
(20)
Genomes
(20)
Introns
(20)
Proteins
(18)
Biological And Medical Sciences
(17)
Alternative Splicing
(16)
Female
(16)
Molecular Sequence Data
(16)
Evolution, Molecular
(15)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Gene copy-number polymorphism caused by retrotransposition in humans

Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families

A genetic network that suppresses genome rearrangements in Saccharomyces cerevisiae and contains defects in cancers

The role of exon shuffling in shaping protein-protein interaction networks

Exome Sequencing of Native Populations From the Amazon Reveals Patterns on the Peopling of South America

The Shared Use of Extended Phenotypes Increases the Fitness of Simulated Populations

Assessment of somatic mutations in urine and plasma of Wilms tumor patients

Domain shuffling and the increasing complexity of biological networks

Transcriptome-guided characterization of genomic rearrangements in a breast cancer cell line

The Complete Mitogenome of Amazonian Hyphessobrycon heterorhabdus (Characiformes: Characidae) as a Valuable Resource for Phylogenetic Analyses of Characidae

neoANT-HILL: an integrated tool for identification of potential neoantigens

Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer

S-score: a scoring system for the identification and prioritization of predicted cancer genes

An Anatomy of Normal and Malignant Gene Expression

Mutation Detection in Tumor-Derived Cell Free DNA Anticipates Progression in a Patient With Metastatic Colorectal Cancer

High-throughput sequencing of a South American Amerindian

Splicing Express: a software suite for alternative splicing analysis using next-generation sequencing data

Identification of rare alternative splicing events in MS/MS data reveals a significant fraction of alternative translation initiation sites

Origin of Genes

Analysis of the microarray gene expression for breast cancer progression after the application modified logistic regression

Alternative splicing enriched cDNA libraries identify breast cancer-associated transcripts

Toward a Resolution of the Introns Early/Late Debate: Only Phase Zero Introns are Correlated with the Structure of Ancient Proteins

Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types

Essential Saccharomyces cerevisiae genome instability suppressing genes identify potential human tumor suppressors

A New Approach for Identification of Cancer-related Pathways using Protein Networks and Genomic Data

Suchergebnisse filtern