Lista de obras - Hans Konrad Schackert - Dominio Público Uruguay

Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2006

Age-dependent performance of BRAF mutation testing in Lynch syndrome diagnostics

artículo científico publicado en 2020

An Ambystoma mexicanum EST sequencing project: analysis of 17,352 expressed sequence tags from embryonic and regenerating blastema cDNA libraries

artículo científico publicado en 2004

Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study

artículo científico publicado en 2005

Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin

artículo científico publicado en 2011

Cancer Risks for PMS2-Associated Lynch Syndrome

artículo científico publicado en 2018

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

scientific article published on 24 July 2019

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

artículo científico publicado en 2020

Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2009

Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue

artículo científico publicado en 2004

Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families

article

Examination of apoptosis signaling in pancreatic cancer by computational signal transduction analysis

artículo científico publicado en 2010

Gene expression profiling of microdissected pancreatic ductal carcinomas using high-density DNA microarrays

artículo científico publicado en 2004

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.

artículo científico publicado en 2013

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

artículo científico publicado en 2010

Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium

artículo científico publicado en 2006

Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome

artículo científico publicado en 2013

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium

scientific article published on 13 October 2004

Meta-analysis of microarray data on pancreatic cancer defines a set of commonly dysregulated genes

artículo científico publicado en 2005

Microarray-based gene expression profiling in pancreatic ductal carcinoma: status quo and perspectives

artículo científico publicado en 2004

Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies

artículo científico publicado en 2011

N-acetyltransferase (NAT) 2 acetylator status and age of onset in patients with hereditary nonpolyposis colorectal cancer (HNPCC).

artículo científico publicado en 2005

No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies

artículo científico publicado en 2018

Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2006

Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study

artículo científico publicado en 2010

Risks of less common cancers in proven mutation carriers with lynch syndrome

artículo científico publicado en 2012

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2005

Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families

article

The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect

scientific article published on 01 March 2019

The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1

artículo científico publicado en 2007

Value of upper GI endoscopy for gastric cancer surveillance in patients with Lynch syndrome

scientific article published on 15 September 2020

Lista de obras de Hans Konrad Schackert

Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer

Age-dependent performance of BRAF mutation testing in Lynch syndrome diagnostics

An Ambystoma mexicanum EST sequencing project: analysis of 17,352 expressed sequence tags from embryonic and regenerating blastema cDNA libraries

Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study

Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin

Cancer Risks for PMS2-Associated Lynch Syndrome

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer

Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue

Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families

Examination of apoptosis signaling in pancreatic cancer by computational signal transduction analysis

Gene expression profiling of microdissected pancreatic ductal carcinomas using high-density DNA microarrays

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium

Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium

Meta-analysis of microarray data on pancreatic cancer defines a set of commonly dysregulated genes

Microarray-based gene expression profiling in pancreatic ductal carcinoma: status quo and perspectives

Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies

N-acetyltransferase (NAT) 2 acetylator status and age of onset in patients with hereditary nonpolyposis colorectal cancer (HNPCC).

No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies

Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer

Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study

Risks of less common cancers in proven mutation carriers with lynch syndrome

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer

Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families

The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect

The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1

Value of upper GI endoscopy for gastric cancer surveillance in patients with Lynch syndrome