Lista de obras - Jon T Bergthorsson - Dominio Público Uruguay

A common variant associated with prostate cancer in European and African populations

artículo científico publicado en 2006

A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes

artículo científico publicado en 2001

A population-based analysis of increased incidence and improved survival of testicular cancer patients in Iceland.

artículo científico publicado en 2003

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

artículo científico publicado en 2008

Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer

article

BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age.

artículo científico publicado en 2001

Chromosome imbalance at the 3p14 region in human breast tumours: high frequency in patients with inherited predisposition due to BRCA2.

artículo científico publicado en 1998

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

scientific journal article

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

artículo científico publicado en 2008

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

artículo científico publicado en 2009

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

artículo científico publicado en 2007

Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13

artículo científico publicado en 1995

Endothelial-rich microenvironment supports growth and branching morphogenesis of prostate epithelial cells.

artículo científico publicado en 2012

Epithelial Plasticity During Human Breast Morphogenesis and Cancer Progression.

artículo científico publicado en 2016

Functional Role of the microRNA-200 Family in Breast Morphogenesis and Neoplasia

artículo científico publicado en 2014

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

artículo científico publicado en 2007

High frequency of LOH, MSI and abnormal expression of FHIT in gastric cancer.

artículo científico publicado en 2002

High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients

scientific article published on 01 August 1996

Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non-polyposis colon cancer trait

artículo científico publicado en 1995

Identification of a novel splice-site mutation of the BRCA1 gene in two breast cancer families: screening reveals low frequency in Icelandic breast cancer patients

article

Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3

article

Loss of heterozygosity on chromosome 9 in human breast cancer: Association with clinical variables and genetic changes at other chromosome regions

artículo científico publicado en 1995

Mapping of chromosome-3 alterations in human breast-cancer using microsatellite PCR markers - correlation with clinical-variables

artículo científico publicado en 1995

MicroRNA-200c-141 and ∆Np63 are required for breast epithelial differentiation and branching morphogenesis

artículo científico publicado en 2015

Mutation analysis of the CHK2 gene in breast carcinoma and other cancers

artículo científico publicado en 2002

Mutations of the BRCA1 and BRCA2 Genes in Danish Patients Diagnosed at Young Age with Multi-Centric or Bilateral Breast Cancer.

artículo científico publicado en 1999

Replication error in colorectal carcinoma: association with loss of heterozygosity at mismatch repair loci and clinicopathological variables

article

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

artículo científico publicado en 2008

Testicular germ cell tumours in Iceland

artículo científico publicado en 2006

The BARD1 Cys557Ser variant and breast cancer risk in Iceland

artículo científico publicado en 2006

The effect of mismatch repair deficiency on tumourigenesis; microsatellite instability affecting genes containing short repeated sequences

article

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

article

deltaNp63 has a role in maintaining epithelial integrity in airway epithelium

artículo científico publicado en 2014

Lista de obras de Jon T Bergthorsson

A common variant associated with prostate cancer in European and African populations

A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes

A population-based analysis of increased incidence and improved survival of testicular cancer patients in Iceland.

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer

BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age.

Chromosome imbalance at the 3p14 region in human breast tumours: high frequency in patients with inherited predisposition due to BRCA2.

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13

Endothelial-rich microenvironment supports growth and branching morphogenesis of prostate epithelial cells.

Epithelial Plasticity During Human Breast Morphogenesis and Cancer Progression.

Functional Role of the microRNA-200 Family in Breast Morphogenesis and Neoplasia

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

High frequency of LOH, MSI and abnormal expression of FHIT in gastric cancer.

High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients

Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non-polyposis colon cancer trait

Identification of a novel splice-site mutation of the BRCA1 gene in two breast cancer families: screening reveals low frequency in Icelandic breast cancer patients

Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3

Loss of heterozygosity on chromosome 9 in human breast cancer: Association with clinical variables and genetic changes at other chromosome regions

Mapping of chromosome-3 alterations in human breast-cancer using microsatellite PCR markers - correlation with clinical-variables

MicroRNA-200c-141 and ∆Np63 are required for breast epithelial differentiation and branching morphogenesis

Mutation analysis of the CHK2 gene in breast carcinoma and other cancers

Mutations of the BRCA1 and BRCA2 Genes in Danish Patients Diagnosed at Young Age with Multi-Centric or Bilateral Breast Cancer.

Replication error in colorectal carcinoma: association with loss of heterozygosity at mismatch repair loci and clinicopathological variables

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

Testicular germ cell tumours in Iceland

The BARD1 Cys557Ser variant and breast cancer risk in Iceland

The effect of mismatch repair deficiency on tumourigenesis; microsatellite instability affecting genes containing short repeated sequences

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

deltaNp63 has a role in maintaining epithelial integrity in airway epithelium