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...

Alignment of roles of near-peer mentors for medical students underrepresented in medicine with medical education competencies: a qualitative study

BMC medical education, 2019-11, Vol.19 (1), p.417-417, Article 417

2019

Volltextzugriff (PDF)

Development of an interdisciplinary pre-matriculation program designed to promote medical students' self efficacy

Medical education online, 2017-01, Vol.22 (1), p.1272835-1272835

2017

Volltextzugriff (PDF)

Imagination, the first virtual meeting

Journal of regional medical campuses, 2020-11, Vol.3 (3)

2020

Volltextzugriff (PDF)

The Difference a Mission Driven Campus Can Make: Serving American Indian/Alaska Native Communities

Journal of regional medical campuses, 2019-09, Vol.2 (3)

2019

Volltextzugriff (PDF)

The Impact of COVID-19 on American Indian and Alaska Native Communities: A Call for Better Relational Models

American journal of public health (1971), 2021-05, Vol.111 (5), p.801-803

2021

Volltextzugriff (PDF)

Staying connected: Native American women faculty members on experiencing success

Academic medicine, 2010-04, Vol.85 (4), p.675-679

2010

Volltextzugriff (PDF)

The Experiences of Native American Women Physician Faculty in U.S. Medical Schools: Culture, Diversity, and Retention

Wirta Kosobuski, Anna

2013

Volltextzugriff (PDF)

Genetic and Epigenetic Characteristics of Inflammatory Bowel Disease–Associated Colorectal Cancer

Gastroenterology (New York, N.Y. 1943), 2021-08, Vol.161 (2), p.592-607

2021

Volltextzugriff (PDF)

NGS method for parallel processing of high quality, damaged or fragmented input material using target enrichment

PloS one, 2024-05, Vol.19 (5), p.e0304411-e0304411

2024

Volltextzugriff (PDF)

Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

Genome medicine, 2021-03, Vol.13 (1), p.40-40, Article 40

2021

Volltextzugriff (PDF)

Precision medicine in rare diseases: What is next?

Journal of internal medicine, 2023-10, Vol.294 (4), p.397-412

2023

Volltextzugriff (PDF)

Loqusdb: added value of an observations database of local genomic variation

BMC bioinformatics, 2020-07, Vol.21 (1), p.1-273, Article 273

2020

Volltextzugriff (PDF)

Exome and immune cell score analyses reveal great variation within synchronous primary colorectal cancers

British journal of cancer, 2019-04, Vol.120 (9), p.922-930

2019

Volltextzugriff (PDF)

Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization

PLoS genetics, 2018-11, Vol.14 (11), p.e1007780-e1007780

2018

Volltextzugriff (PDF)

Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism

BMC genomics, 2014-12, Vol.15 (1), p.1090-1090

2014

Volltextzugriff (PDF)

Trailblazing precision medicine in Europe: A joint view by Genomic Medicine Sweden and the Centers for Personalized Medicine, ZPM, in Germany

Seminars in cancer biology, 2022-09, Vol.84, p.242-254

2022

Volltextzugriff (PDF)

Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel

Genes chromosomes & cancer, 2024-07, Vol.63 (7), p.e23257-n/a

2024

Volltextzugriff (PDF)

Altered Methylation of IGF2 Locus 20 Years after Preterm Birth at Very Low Birth Weight

PloS one, 2013-06, Vol.8 (6), p.e67379-e67379

2013

Volltextzugriff (PDF)

PatientMatcher: A customizable Python‐based open‐source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network

Human mutation, 2022-06, Vol.43 (6), p.708-716

2022

Volltextzugriff (PDF)

Epidemiology of heart failure and trends in diagnostic work-up: a retrospective, population-based cohort study in Sweden

Clinical epidemiology, 2019-01, Vol.11, p.231-244

2019

Volltextzugriff (PDF)

Immunoprofiles and DNA Methylation of Inflammatory Marker Genes in Ulcerative Colitis-Associated Colorectal Tumorigenesis

Biomolecules (Basel, Switzerland), 2021-09, Vol.11 (10), p.1440

2021

Volltextzugriff (PDF)

1 – 25 von 37

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(36)
Mit Volltextzugriff
(33)

Publikationsform

Sprache

Englisch
(37)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Plos One
(3)
Genome Medicine
(2)
Human Mutation
(2)
Journal Of Regional Medical Campuses
(2)
Academic Medicine
(1)
American Journal Of Public Health
(1)
Biomolecules
(1)
Bmc Bioinformatics
(1)
Bmc Genomics
(1)
Bmc Medical Education
(1)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Alignment of roles of near-peer mentors for medical students underrepresented in medicine with medical education competencies: a qualitative study

Development of an interdisciplinary pre-matriculation program designed to promote medical students' self efficacy

Imagination, the first virtual meeting

The Difference a Mission Driven Campus Can Make: Serving American Indian/Alaska Native Communities

The Impact of COVID-19 on American Indian and Alaska Native Communities: A Call for Better Relational Models

Staying connected: Native American women faculty members on experiencing success

The Experiences of Native American Women Physician Faculty in U.S. Medical Schools: Culture, Diversity, and Retention

Genetic and Epigenetic Characteristics of Inflammatory Bowel Disease–Associated Colorectal Cancer

NGS method for parallel processing of high quality, damaged or fragmented input material using target enrichment

Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses

Precision medicine in rare diseases: What is next?

Loqusdb: added value of an observations database of local genomic variation

Whole‐Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation

Exome and immune cell score analyses reveal great variation within synchronous primary colorectal cancers

Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia

Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization

Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism

Trailblazing precision medicine in Europe: A joint view by Genomic Medicine Sweden and the Centers for Personalized Medicine, ZPM, in Germany

Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel

Altered Methylation of IGF2 Locus 20 Years after Preterm Birth at Very Low Birth Weight

PatientMatcher: A customizable Python‐based open‐source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network

Epidemiology of heart failure and trends in diagnostic work-up: a retrospective, population-based cohort study in Sweden

Immunoprofiles and DNA Methylation of Inflammatory Marker Genes in Ulcerative Colitis-Associated Colorectal Tumorigenesis

Suchergebnisse filtern