Lista de obras - Aaron Pollett - Dominio Público Uruguay

A descriptive analysis of gastric cancer specimen processing techniques ⬇️

artículo científico publicado el 1 de marzo de 2011

A histology-based model for predicting microsatellite instability in colorectal cancers

artículo científico publicado en 2010

A human colon cancer cell capable of initiating tumour growth in immunodeficient mice

artículo científico publicado en 2007

A novel and rapid method of determining the effect of unclassified MLH1 genetic variants on differential allelic expression

artículo científico publicado en 2010

A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome

artículo científico publicado en 2009

ARID1A loss correlates with mismatch repair deficiency and intact p53 expression in high-grade endometrial carcinomas

artículo científico publicado en 2013

Café-au-lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2.

artículo científico publicado en 2008

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

artículo científico publicado en 2015

Comparison of clinical schemas and morphologic features in predicting Lynch syndrome in mutation-positive patients with endometrial cancer encountered in the context of familial gastrointestinal cancer registries.

artículo científico publicado en 2011

Controlled Attenuation Parameter (CAP): a noninvasive method for the detection of hepatic steatosis based on transient elastography

article

Correlation of p53 Mutations in ThinPrep-Processed Fine Needle Breast Aspirates with Surgically Resected Breast Cancers

artículo científico publicado en 2000

Digital pathology: Attitudes and practices in the Canadian pathology community

artículo científico publicado en 2013

Discordance in fibrosis staging between liver biopsy and transient elastography using the FibroScan XL probe

artículo científico publicado en 2011

Exacerbated tissue destruction in DSS-induced acute colitis of OPN-null mice is associated with downregulation of TNF-alpha expression and non-programmed cell death

artículo científico publicado en 2006

Feasibility and diagnostic performance of the FibroScan XL probe for liver stiffness measurement in overweight and obese patients

article

Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation

article

Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium.

artículo científico publicado en 2014

Genetic testing for Lynch syndrome in the province of Ontario.

artículo científico publicado en 2016

Germline BRCA1 mutations predispose to pancreatic adenocarcinoma

artículo científico publicado en 2008

Hepatic Adenomas Caused by Somatic HNF1A Mutations in Children With Biallelic Mismatch Repair Gene Mutations ⬇️

artículo científico publicado el 21 de diciembre de 2010

Hereditary nonpolyposis colorectal cancer--molecular basis

artículo científico publicado en 2003

High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.

artículo científico publicado en 2005

High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry

artículo científico publicado en 2014

High-grade papillary cystadenocarcinoma of the tongue.

artículo científico publicado en 1997

Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing.

artículo científico publicado en 2015

Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variants

artículo científico publicado en 2014

Improving the quality of processing gastric cancer specimens: The pathologist's perspective

artículo científico publicado en 2010

Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation

article

Lynch syndrome in a predominantly Afrocentric population: a clinicopathological and genetic study.

artículo científico publicado en 2012

Mucinous tumor of the appendix with limited peritoneal spread: is there a role for expectant observation?

artículo científico publicado en 2013

Mule Regulates the Intestinal Stem Cell Niche via the Wnt Pathway and Targets EphB3 for Proteasomal and Lysosomal Degradation

artículo científico publicado en 2016

Pathological features of colorectal carcinomas in MYH-associated polyposis

artículo científico publicado en 2008

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study

artículo científico publicado en 2007

Patients with Lynch syndrome mismatch repair gene mutations are at higher risk for not only upper tract urothelial cancer but also bladder cancer.

artículo científico publicado en 2012

Performance characteristics of a brief Family History Questionnaire to screen for Lynch syndrome in women with newly diagnosed endometrial cancer.

artículo científico publicado en 2014

Performance characteristics of screening strategies for Lynch syndrome in unselected women with newly diagnosed endometrial cancer who have undergone universal germline mutation testing.

artículo científico publicado en 2014

Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome

artículo científico

Plk4 haploinsufficiency causes mitotic infidelity and carcinogenesis.

artículo científico publicado en 2005

Plk4 is required for cytokinesis and maintenance of chromosomal stability

artículo científico publicado en 2010

Prevalence of loss of expression of DNA mismatch repair proteins in primary epithelial ovarian tumors.

artículo científico publicado en 2012

Prognostic significance of mesenteric tumor nodules in patients with stage III colorectal cancer

artículo científico publicado en 2008

Progression and Management of Duodenal Neoplasia in Familial Adenomatous Polyposis

article

Promoter methylation of Wnt antagonistsDKK1andSFRP1is associated with opposing tumor subtypes in two large populations of colorectal cancer patients ⬇️

artículo científico publicado el 8 de febrero de 2011

Review of findings in prophylactic gynaecological specimens in Lynch syndrome with literature review and recommendations for grossing

artículo científico

Sclerosing pancreatitis presenting as a periampullary tumour

artículo científico publicado en 2003

Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer

artículo científico publicado en 2010

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease

artículo científico publicado en 2010

The histomorphology of Lynch syndrome-associated ovarian carcinomas: toward a subtype-specific screening strategy

artículo científico

The microenvironment-specific transformation of adult stem cells models malignant triton tumors

artículo científico publicado en 2013

Tumor microsatellite instability in early onset gastric cancer

artículo científico publicado en 2005

Unifying diagnosis for adenomatous polyps, café-au-lait macules, and a brain mass?

artículo científico publicado en 2013

Use of mismatch repair immunohistochemistry and microsatellite instability testing: exploring Canadian practices.

artículo científico publicado en 2012

Variable clonal repopulation dynamics influence chemotherapy response in colorectal cancer

artículo científico publicado en 2012

Venous invasion in colorectal cancer: impact of an elastin stain on detection and interobserver agreement among gastrointestinal and nongastrointestinal pathologists.

artículo científico publicado en 2013

Lista de obras de Aaron Pollett

A descriptive analysis of gastric cancer specimen processing techniques ⬇️

A histology-based model for predicting microsatellite instability in colorectal cancers

A human colon cancer cell capable of initiating tumour growth in immunodeficient mice

A novel and rapid method of determining the effect of unclassified MLH1 genetic variants on differential allelic expression

A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome

ARID1A loss correlates with mismatch repair deficiency and intact p53 expression in high-grade endometrial carcinomas

Café-au-lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2.

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Comparison of clinical schemas and morphologic features in predicting Lynch syndrome in mutation-positive patients with endometrial cancer encountered in the context of familial gastrointestinal cancer registries.

Controlled Attenuation Parameter (CAP): a noninvasive method for the detection of hepatic steatosis based on transient elastography

Correlation of p53 Mutations in ThinPrep-Processed Fine Needle Breast Aspirates with Surgically Resected Breast Cancers

Digital pathology: Attitudes and practices in the Canadian pathology community

Discordance in fibrosis staging between liver biopsy and transient elastography using the FibroScan XL probe

Exacerbated tissue destruction in DSS-induced acute colitis of OPN-null mice is associated with downregulation of TNF-alpha expression and non-programmed cell death

Feasibility and diagnostic performance of the FibroScan XL probe for liver stiffness measurement in overweight and obese patients

Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation

Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium.

Genetic testing for Lynch syndrome in the province of Ontario.

Germline BRCA1 mutations predispose to pancreatic adenocarcinoma

Hepatic Adenomas Caused by Somatic HNF1A Mutations in Children With Biallelic Mismatch Repair Gene Mutations ⬇️

Hereditary nonpolyposis colorectal cancer--molecular basis

High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.

High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry

High-grade papillary cystadenocarcinoma of the tongue.

Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing.

Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variants

Improving the quality of processing gastric cancer specimens: The pathologist's perspective

Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation

Lynch syndrome in a predominantly Afrocentric population: a clinicopathological and genetic study.

Mucinous tumor of the appendix with limited peritoneal spread: is there a role for expectant observation?

Mule Regulates the Intestinal Stem Cell Niche via the Wnt Pathway and Targets EphB3 for Proteasomal and Lysosomal Degradation

Pathological features of colorectal carcinomas in MYH-associated polyposis

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study

Patients with Lynch syndrome mismatch repair gene mutations are at higher risk for not only upper tract urothelial cancer but also bladder cancer.

Performance characteristics of a brief Family History Questionnaire to screen for Lynch syndrome in women with newly diagnosed endometrial cancer.

Performance characteristics of screening strategies for Lynch syndrome in unselected women with newly diagnosed endometrial cancer who have undergone universal germline mutation testing.

Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome

Plk4 haploinsufficiency causes mitotic infidelity and carcinogenesis.

Plk4 is required for cytokinesis and maintenance of chromosomal stability

Prevalence of loss of expression of DNA mismatch repair proteins in primary epithelial ovarian tumors.

Prognostic significance of mesenteric tumor nodules in patients with stage III colorectal cancer

Progression and Management of Duodenal Neoplasia in Familial Adenomatous Polyposis

Promoter methylation of Wnt antagonistsDKK1andSFRP1is associated with opposing tumor subtypes in two large populations of colorectal cancer patients ⬇️

Review of findings in prophylactic gynaecological specimens in Lynch syndrome with literature review and recommendations for grossing

Sclerosing pancreatitis presenting as a periampullary tumour

Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease

The histomorphology of Lynch syndrome-associated ovarian carcinomas: toward a subtype-specific screening strategy

The microenvironment-specific transformation of adult stem cells models malignant triton tumors

Tumor microsatellite instability in early onset gastric cancer

Unifying diagnosis for adenomatous polyps, café-au-lait macules, and a brain mass?

Use of mismatch repair immunohistochemistry and microsatellite instability testing: exploring Canadian practices.

Variable clonal repopulation dynamics influence chemotherapy response in colorectal cancer

Venous invasion in colorectal cancer: impact of an elastin stain on detection and interobserver agreement among gastrointestinal and nongastrointestinal pathologists.