UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 124

Sortiert nach

Predicting Pancreatic Cancer in the UK Biobank Cohort Using Polygenic Risk Scores and Diabetes Mellitus

Gastroenterology (New York, N.Y. 1943), 2022-05, Vol.162 (6), p.1665-1674.e2

2022

Volltextzugriff (PDF)

Clonal myelopoiesis in the UK Biobank cohort: ASXL1 mutations are strongly associated with smoking

Leukemia, 2020-10, Vol.34 (10), p.2660-2672

2020

Volltextzugriff (PDF)

Clonal myelopoiesis promotes adverse outcomes in chronic kidney disease

Leukemia, 2022-02, Vol.36 (2), p.507-515

2022

Volltextzugriff (PDF)

The genomic landscape and clonal evolutionary trajectory of classical hairy cell leukemia

Leukemia, 2023-04, Vol.37 (4), p.929-933

2023

Volltextzugriff (PDF)

Therapeutic targeting of integrin αvβ6 in breast cancer

JNCI : Journal of the National Cancer Institute, 2014-08, Vol.106 (8)

2014

Volltextzugriff (PDF)

Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

Journal of clinical oncology, 2015-02, Vol.33 (4), p.304-311

2015

Volltextzugriff (PDF)

Development of childhood asthma prediction models using machine learning approaches

Clinical and translational allergy, 2021-11, Vol.11 (9), p.e12076-n/a

2021

Volltextzugriff (PDF)

Exome sequence read depth methods for identifying copy number changes

Briefings in bioinformatics, 2015-05, Vol.16 (3), p.380-392

2015

Volltextzugriff (PDF)

Megalencephaly syndromes: exome pipeline strategies for detecting low-level mosaic mutations

PloS one, 2014-01, Vol.9 (1), p.e86940-e86940

2014

Volltextzugriff (PDF)

A CRISPR and high-content imaging assay compliant with ACMG/AMP guidelines for clinical variant interpretation in ciliopathies

Human genetics, 2021-04, Vol.140 (4), p.593-607

2021

Volltextzugriff (PDF)

Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women

Nature communications, 2017-11, Vol.8 (1), p.1632-12, Article 1632

2017

Volltextzugriff (PDF)

PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia

Leukemia, 2019-05, Vol.33 (5), p.1184-1194

2019

Volltextzugriff (PDF)

Nonlinear effects of environment on childhood asthma susceptibility

Pediatric allergy and immunology, 2022-04, Vol.33 (4), p.e13777-n/a

2022

Volltextzugriff (PDF)

The Application of Radiomics and AI to Molecular Imaging for Prostate Cancer

Journal of personalized medicine, 2024-03, Vol.14 (3), p.287

2024

Volltextzugriff (PDF)

A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis

PloS one, 2014-12, Vol.9 (12), p.e101488-e101488

2014

Volltextzugriff (PDF)

Integration of Genomic Risk Scores to Improve the Prediction of Childhood Asthma Diagnosis

Journal of personalized medicine, 2022-01, Vol.12 (1), p.75

2022

Volltextzugriff (PDF)

Identification of Inherited Genetic Variations Influencing Prognosis in Early-Onset Breast Cancer

Cancer research (Chicago, Ill.), 2013-03, Vol.73 (6), p.1883-1891

2013

Volltextzugriff (PDF)

Age-related loss of chromosome Y is associated with levels of sex hormone binding globulin and clonal hematopoiesis defined by TET2 , TP53 , and CBL mutations

Science advances, 2023-04, Vol.9 (16), p.eade9746-eade9746

2023

Volltextzugriff (PDF)

Pharmacological EZH2 inhibition combined with retinoic acid treatment promotes differentiation and apoptosis in rhabdomyosarcoma cells

Clinical epigenetics, 2023-10, Vol.15 (1), p.1-167, Article 167

2023

Volltextzugriff (PDF)

The clinical impact and molecular biology of del(17p) in multiple myeloma treated with conventional or thalidomide-based therapy

Genes chromosomes & cancer, 2011-10, Vol.50 (10), p.765-774

2011

Volltextzugriff (PDF)

The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms

Blood, 2010-06, Vol.115 (22), p.4517-4523

2010

Volltextzugriff (PDF)

Gender Disparities in the Tumor Genetics and Clinical Outcome of Multiple Myeloma

Cancer epidemiology, biomarkers & prevention, 2011-08, Vol.20 (8), p.1703-1707

2011

Volltextzugriff (PDF)

1 – 25 von 124

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(116)
Mit Volltextzugriff
(111)

Publikationsform

Sprache

Englisch
(124)
Japanisch
(15)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Predicting Pancreatic Cancer in the UK Biobank Cohort Using Polygenic Risk Scores and Diabetes Mellitus

Clonal myelopoiesis in the UK Biobank cohort: ASXL1 mutations are strongly associated with smoking

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

Clonal myelopoiesis promotes adverse outcomes in chronic kidney disease

The genomic landscape and clonal evolutionary trajectory of classical hairy cell leukemia

Recurrent activating STAT5B N642H mutation in myeloid neoplasms with eosinophilia

Therapeutic targeting of integrin αvβ6 in breast cancer

Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

Development of childhood asthma prediction models using machine learning approaches

Exome sequence read depth methods for identifying copy number changes

Megalencephaly syndromes: exome pipeline strategies for detecting low-level mosaic mutations

Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis

A CRISPR and high-content imaging assay compliant with ACMG/AMP guidelines for clinical variant interpretation in ciliopathies

Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women

PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia

Nonlinear effects of environment on childhood asthma susceptibility

The Application of Radiomics and AI to Molecular Imaging for Prostate Cancer

A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis

Integration of Genomic Risk Scores to Improve the Prediction of Childhood Asthma Diagnosis

Identification of Inherited Genetic Variations Influencing Prognosis in Early-Onset Breast Cancer

Age-related loss of chromosome Y is associated with levels of sex hormone binding globulin and clonal hematopoiesis defined by TET2 , TP53 , and CBL mutations

Pharmacological EZH2 inhibition combined with retinoic acid treatment promotes differentiation and apoptosis in rhabdomyosarcoma cells

The clinical impact and molecular biology of del(17p) in multiple myeloma treated with conventional or thalidomide-based therapy

The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms

Gender Disparities in the Tumor Genetics and Clinical Outcome of Multiple Myeloma

Suchergebnisse filtern