UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 84

Sortiert nach

Novel germline BRCA1 and BRCA2 mutations in breast and breast/ovarian cancer families from the Czech Republic

Human mutation, 2001-12, Vol.18 (6), p.545-545

2001

Link zum Volltext

Verfügbarkeit prüfen

GAPPS - Gastric Adenocarcinoma and Proximal Polyposis of the Stomach Syndrome in 8 Families Tested at Masaryk Memorial Cancer Institute - Prevention and Prophylactic Gastrectomies

Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti, 2019, Vol.32 (Supplementum2), p.109

2019

Link zum Volltext

Verfügbarkeit prüfen

Differentiating pathogenic mutations from polymorphic alterations in the splice sites of BRCA1 and BRCA2

Genes chromosomes & cancer, 2003-07, Vol.37 (3), p.314-320

2003

Link zum Volltext

Verfügbarkeit prüfen

Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. Online

Human mutation, 1999, Vol.13 (3), p.256-256

1999

Link zum Volltext

Verfügbarkeit prüfen

The Czech Republic: Genetic Counseling in High-Risk Breast/Ovarian Cancer Families

Disease markers, 1999-01, Vol.15 (1-3), p.50-50

1999

Link zum Volltext

Verfügbarkeit prüfen

Classification of germline variants identified in cancer predisposition genetic testing - consensus of the CZECANCA consortium

Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti, 2023, Vol.37 (6), p.431

2023

Link zum Volltext

Verfügbarkeit prüfen

Hereditary breast cancer – a spectrum of pathogenic mutations and unknown variants of BRCA1 and BRCA2 genes in the Czech Republic: efficiency of testing and clinical follow-up

Breast cancer research : BCR, 2005-01, Vol.7 (S2), p.P1-P1, Article P1.06

2005

Link zum Volltext

Verfügbarkeit prüfen

Effect of salivary gland extract from Ixodes ricinus ticks on the proliferation of Borrelia burgdorferi sensu stricto in vivo

Folia parasitologica, 2006-06, Vol.53 (2), p.153-158

2006

Link zum Volltext

Verfügbarkeit prüfen

Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5+3A>G

Disease markers, 1999-10, Vol.15 (1-3), p.69-73

1999

Link zum Volltext

Verfügbarkeit prüfen

Recommended Extension of Indication Criteria for Genetic Testing of BRCA1 and BRCA2 Mutations in Hereditary Breast and Ovarian Cancer Syndrome

Klinická onkologie, 2016, Vol.29 Suppl 1 (Suppl 1), p.S9-S13

2016

Link zum Volltext

Verfügbarkeit prüfen

Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute

Klinická onkologie, 2016-01, Vol.29 Suppl 1 (Suppl 1), p.S35-S45

2016

Link zum Volltext

Verfügbarkeit prüfen

Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report

Klinická onkologie, 2016-01, Vol.29 Suppl 1 (Suppl 1), p.S89-S92

2016

Link zum Volltext

Verfügbarkeit prüfen

Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report

Klinická onkologie, 2016-01, Vol.29 Suppl 1, p.S89-S92

2016

Link zum Volltext

Verfügbarkeit prüfen

Breast cancer in monozygotic twins

Klinická onkologie, 2013, Vol.26 (3), p.213-217

2013

Link zum Volltext

Verfügbarkeit prüfen

Disease-causing mutations versus neutral polymorphism: use of bioinformatics and DNA diagnosis

Časopis lékařů českých, 2003-03, Vol.142 (3), p.150

Machácková, E

2003

Link zum Volltext

Verfügbarkeit prüfen

A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer families

Časopis lékařů českých, 2000-10, Vol.139 (20), p.635

2000

Link zum Volltext

Verfügbarkeit prüfen

Hereditary diffuse gastric cancer

Klinická onkologie, 2012, Vol.25 Suppl, p.S30-S33

2012

Link zum Volltext

Verfügbarkeit prüfen

Evaluation of variants of unknown significance in the BRCA2 gene

Klinická onkologie, 2012, Vol.25 Suppl, p.S87-S95

2012

Link zum Volltext

Verfügbarkeit prüfen

Limitations of genetic testing in oncology

Klinická onkologie, 2009, Vol.22 Suppl, p.S65-S68

2009

Link zum Volltext

Verfügbarkeit prüfen

The clinical importance of a genetic analysis of moderate-risk cancer susceptibility genes in breast and other cancer patients from the Czech Republic

Klinická onkologie, 2012, Vol.25 Suppl, p.S59-S66

2012

Link zum Volltext

Verfügbarkeit prüfen

Li-Fraumeni syndrome - a proposal of complex prevention care for carriers of TP53 mutation with total-body MRI

Klinická onkologie, 2012, Vol.25 Suppl, p.S49-S54

2012

Link zum Volltext

Verfügbarkeit prüfen

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

JAMA : the journal of the American Medical Association, 2017-06, Vol.317 (23), p.2402

2017

Link zum Volltext

Verfügbarkeit prüfen

Sovetský príspevek k výzkumu recové cinnosti: Je. S. Kubrjakova, Nominativnyj aspekt recevoj dejatel'nosti

Slovo a slovesnost, 1987-01, Vol.48, p.246

Machácková, E

1987

Link zum Volltext

Verfügbarkeit prüfen

BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

Cancer research (Chicago, Ill.), 2017-06, Vol.77 (11), p.2789-2799

2017

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 84

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(81)
Mit Volltextzugriff
(65)

Publikationsform

Artikel
(84)

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Humans
(35)
Science & Technology
(35)
Life Sciences & Biomedicine
(31)
Female
(24)
Adult
(18)
Middle Aged
(16)
Mutation
(15)
Aged
(14)
Breast Neoplasms - Genetics
(13)
Male
(12)
Oncology
(11)
Biological And Medical Sciences
(10)
Ovarian Neoplasms - Genetics
(10)
Brca2 Protein
(9)
Genetic Predisposition To Disease
(9)
Plant Sciences
(9)
Risk Factors
(9)
Fundamental And Applied Biological Sciences. Psychology
(8)
Genetic Testing
(8)
Medicin Och Hälsovetenskap
(8)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Novel germline BRCA1 and BRCA2 mutations in breast and breast/ovarian cancer families from the Czech Republic

GAPPS - Gastric Adenocarcinoma and Proximal Polyposis of the Stomach Syndrome in 8 Families Tested at Masaryk Memorial Cancer Institute - Prevention and Prophylactic Gastrectomies

Differentiating pathogenic mutations from polymorphic alterations in the splice sites of BRCA1 and BRCA2

Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. Online

The Czech Republic: Genetic Counseling in High-Risk Breast/Ovarian Cancer Families

Classification of germline variants identified in cancer predisposition genetic testing - consensus of the CZECANCA consortium

Hereditary breast cancer – a spectrum of pathogenic mutations and unknown variants of BRCA1 and BRCA2 genes in the Czech Republic: efficiency of testing and clinical follow-up

Effect of salivary gland extract from Ixodes ricinus ticks on the proliferation of Borrelia burgdorferi sensu stricto in vivo

Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5+3A>G

Recommended Extension of Indication Criteria for Genetic Testing of BRCA1 and BRCA2 Mutations in Hereditary Breast and Ovarian Cancer Syndrome

Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute

Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report

Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report

Breast cancer in monozygotic twins

Disease-causing mutations versus neutral polymorphism: use of bioinformatics and DNA diagnosis

A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer families

Hereditary diffuse gastric cancer

Evaluation of variants of unknown significance in the BRCA2 gene

Limitations of genetic testing in oncology

The clinical importance of a genetic analysis of moderate-risk cancer susceptibility genes in breast and other cancer patients from the Czech Republic

Li-Fraumeni syndrome - a proposal of complex prevention care for carriers of TP53 mutation with total-body MRI

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

Sovetský príspevek k výzkumu recové cinnosti: Je. S. Kubrjakova, Nominativnyj aspekt recevoj dejatel'nosti

Prevalence of Propionibacterium acnes in Intervertebral Discs of Patients Undergoing Lumbar Microdiscectomy: A Prospective Cross-Sectional Study

BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

Suchergebnisse filtern