UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 226

Sortiert nach

Update on Lynch syndrome genomics

Familial cancer, 2016-07, Vol.15 (3), p.385-393

Peltomaeki, Paeivi

2016

Link zum Volltext

Verfügbarkeit prüfen

Role of DNA Mismatch Repair Defects in the Pathogenesis of Human Cancer

Journal of clinical oncology, 2003-03, Vol.21 (6), p.1174-1179

Päivi Peltomäki

2003

Link zum Volltext

Verfügbarkeit prüfen

Mutations and epimutations in the origin of cancer

Experimental cell research, 2012-02, Vol.318 (4), p.299-310

Peltomaeki, Paeivi

2012

Link zum Volltext

Verfügbarkeit prüfen

Germline Mutation of RPS20 , Encoding a Ribosomal Protein, Causes Predisposition to Hereditary Nonpolyposis Colorectal Carcinoma Without DNA Mismatch Repair Deficiency

Gastroenterology (New York, N.Y. 1943), 2014-09, Vol.147 (3), p.595-598.e5

2014

Link zum Volltext

Verfügbarkeit prüfen

Epidemiological, clinical and molecular characterization of Lynch‐like syndrome: A population‐based study

International journal of cancer, 2019-07, Vol.145 (1), p.87-98

2019

Link zum Volltext

Verfügbarkeit prüfen

Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

Journal of clinical oncology, 2009-10, Vol.27 (28), p.4793-4797

2009

Link zum Volltext

Verfügbarkeit prüfen

Somatic mutation profiles as molecular classifiers of ulcerative colitis‐associated colorectal cancer

International journal of cancer, 2021-06, Vol.148 (12), p.2997-3007

2021

Link zum Volltext

Verfügbarkeit prüfen

Gene fusions and oncogenic mutations in MLH1 deficient and BRAFV600E wild-type colorectal cancers

Virchows Archiv : an international journal of pathology, 2022-04, Vol.480 (4), p.807-817

2022

Link zum Volltext

Verfügbarkeit prüfen

Oncogenic Potential of Bisphenol A and Common Environmental Contaminants in Human Mammary Epithelial Cells

International journal of molecular sciences, 2020-05, Vol.21 (10), p.3735

2020

Link zum Volltext

Verfügbarkeit prüfen

Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Journal of surgical oncology, 2016-02, Vol.113 (2), p.209-212

2016

Link zum Volltext

Verfügbarkeit prüfen

Novel insights into tumorigenesis revealed by molecular analysis of Lynch syndrome cases with multiple colorectal tumors

Frontiers in oncology, 2024, Vol.14, p.1378392-1378392

2024

Link zum Volltext

Verfügbarkeit prüfen

Epigenetic signatures of familial cancer are characteristic of tumor type and family category

Cancer research (Chicago, Ill.), 2008-06, Vol.68 (12), p.4597-4605

2008

Link zum Volltext

Verfügbarkeit prüfen

Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis

Genes chromosomes & cancer, 2014-10, Vol.53 (10), p.857-864

2014

Link zum Volltext

Verfügbarkeit prüfen

BRAF mutation in sporadic colorectal cancer and Lynch syndrome

Virchows Archiv : an international journal of pathology, 2013-11, Vol.463 (5), p.613-621

2013

Link zum Volltext

Verfügbarkeit prüfen

Molecular changes preceding endometrial and ovarian cancer: a study of consecutive endometrial specimens from Lynch syndrome surveillance

Modern pathology, 2018-08, Vol.31 (8), p.1291-1301

2018

Link zum Volltext

Verfügbarkeit prüfen

Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

Genes chromosomes & cancer, 2015-12, Vol.54 (12), p.776-787

2015

Link zum Volltext

Verfügbarkeit prüfen

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Genetics in medicine, 2019-08, Vol.21 (8), p.1868-1873

2019

Link zum Volltext

Verfügbarkeit prüfen

Converging endometrial and ovarian tumorigenesis in Lynch syndrome: Shared origin of synchronous carcinomas

Gynecologic oncology, 2018-07, Vol.150 (1), p.92-98

2018

Link zum Volltext

Verfügbarkeit prüfen

Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

JNCI : Journal of the National Cancer Institute, 2007-02, Vol.99 (4), p.291-299

2007

Link zum Volltext

Verfügbarkeit prüfen

LINE-1 hypomethylation in familial and sporadic cancer

Journal of molecular medicine (Berlin, Germany), 2012-07, Vol.90 (7), p.827-835

2012

Link zum Volltext

Verfügbarkeit prüfen

Body Weight, Physical Activity, and Risk of Cancer in Lynch Syndrome

Cancers, 2021-04, Vol.13 (8), p.1849

2021

Link zum Volltext

Verfügbarkeit prüfen

MicroRNA Methylation in Colorectal Cancer

Advances in experimental medicine and biology, 2016, Vol.937, p.109-122

2016

Link zum Volltext

Verfügbarkeit prüfen

Molecular Basis of Mismatch Repair Protein Deficiency in Tumors from Lynch Suspected Cases with Negative Germline Test Results

Cancers, 2020-07, Vol.12 (7), p.1853

2020

Link zum Volltext

Verfügbarkeit prüfen

p53 Codon 72 and MDM2 SNP309 Polymorphisms and Age of Colorectal Cancer Onset in Lynch Syndrome

Clinical cancer research, 2005-10, Vol.11 (19), p.6840-6844

2005

Link zum Volltext

Verfügbarkeit prüfen

Altered methylation at microRNA-associated CpG islands in hereditary and sporadic carcinomas: a methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA)-based approach

Molecular medicine (Cambridge, Mass.), 2011-07, Vol.17 (7-8), p.726-735

2011

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 226

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(208)
Mit Volltextzugriff
(204)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(161)
Science & Technology
(158)
Life Sciences & Biomedicine
(149)
Colorectal Neoplasms, Hereditary Nonpolyposis - Genetics
(85)
Biological And Medical Sciences
(83)
Oncology
(78)
Tumors
(78)
Female
(77)
Medical Sciences
(73)
Male
(71)
Middle Aged
(63)
Mutation
(63)
Adult
(52)
Gastroenterology. Liver. Pancreas. Abdomen
(51)
Stomach. Duodenum. Small Intestine. Colon. Rectum. Anus
(51)
Genetics & Heredity
(48)
Colorectal Neoplasms - Genetics
(47)
Aged
(43)
Colorectal Cancer
(41)
Mutl Protein Homolog 1
(40)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Update on Lynch syndrome genomics

Role of DNA Mismatch Repair Defects in the Pathogenesis of Human Cancer

Mutations and epimutations in the origin of cancer

Germline Mutation of RPS20 , Encoding a Ribosomal Protein, Causes Predisposition to Hereditary Nonpolyposis Colorectal Carcinoma Without DNA Mismatch Repair Deficiency

Epidemiological, clinical and molecular characterization of Lynch‐like syndrome: A population‐based study

Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

Somatic mutation profiles as molecular classifiers of ulcerative colitis‐associated colorectal cancer

Gene fusions and oncogenic mutations in MLH1 deficient and BRAFV600E wild-type colorectal cancers

Oncogenic Potential of Bisphenol A and Common Environmental Contaminants in Human Mammary Epithelial Cells

Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Novel insights into tumorigenesis revealed by molecular analysis of Lynch syndrome cases with multiple colorectal tumors

Epigenetic signatures of familial cancer are characteristic of tumor type and family category

Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis

BRAF mutation in sporadic colorectal cancer and Lynch syndrome

Molecular changes preceding endometrial and ovarian cancer: a study of consecutive endometrial specimens from Lynch syndrome surveillance

Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Converging endometrial and ovarian tumorigenesis in Lynch syndrome: Shared origin of synchronous carcinomas

Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

LINE-1 hypomethylation in familial and sporadic cancer

Body Weight, Physical Activity, and Risk of Cancer in Lynch Syndrome

MicroRNA Methylation in Colorectal Cancer

Molecular Basis of Mismatch Repair Protein Deficiency in Tumors from Lynch Suspected Cases with Negative Germline Test Results

p53 Codon 72 and MDM2 SNP309 Polymorphisms and Age of Colorectal Cancer Onset in Lynch Syndrome

Altered methylation at microRNA-associated CpG islands in hereditary and sporadic carcinomas: a methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA)-based approach

Suchergebnisse filtern