Lista de obras -

Analysis of the exome aggregation consortium (ExAC) database suggests that the BAP1-tumor predisposition syndrome is underreported in cancer patients

artículo científico publicado en 2018

Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma.

artículo científico publicado en 2010

Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide

artículo científico publicado en 2018

Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases.

artículo científico publicado en 2013

Frequency, molecular pathology and potential clinical significance of partial chromosome 3 aberrations in uveal melanoma.

artículo científico publicado en 2011

Genetic markers of pigmentation are novel risk loci for uveal melanoma

artículo científico publicado en 2016

Germline BAP1 alterations in familial uveal melanoma.

artículo científico publicado en 2016

Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

artículo científico publicado en 2011

Germline BAP1 mutations misreported as somatic based on tumor-only testing

artículo científico publicado en 2016

Germline large deletion of BAP1 and decreased expression in non-tumor choroid in uveal melanoma patients with high risk for inherited cancer

scientific article published on 23 April 2019

Heterogeneity in Mitogen-Activated Protein Kinase (MAPK) Pathway Activation in Uveal Melanoma With Somatic GNAQ and GNA11 Mutations.

artículo científico publicado en 2019

High frequency of submicroscopic hemizygous deletion is a major mechanism of loss of expression of PTEN in uveal melanoma

artículo científico publicado en 2005

In vitro anti-uveal melanoma activity of phenolic compounds from the Egyptian medicinal plant Acacia nilotica ⬇️

artículo científico publicado el 28 de agosto de 2011

Interleukin-10 promoter polymorphisms in hepatitis C patients with and without Schistosoma mansoni co-infection.

artículo científico publicado en 2009

Investigation of the potential utility of a linomide analogue for treatment of choroidal neovascularization.

artículo científico publicado en 2010

Lack of GNAQ germline mutations in uveal melanoma patients with high risk for hereditary cancer predisposition

artículo científico publicado en 2011

MET canonical transcript expression is a predictive biomarker for chemo-sensitivity to MET-inhibitors in hepatocellular carcinoma cell lines

scientific article published on 26 September 2020

MET oncogene inhibition as a potential target of therapy for uveal melanomas.

artículo científico publicado en 2010

MIF Inhibitor ISO-1 Protects Photoreceptors and Reduces Gliosis in Experimental Retinal Detachment

artículo científico publicado en 2017

MIF promoter polymorphisms are associated with epiretinal membrane but not retinal detachment with PVR in an american population

artículo científico publicado en 2019

Macrophage Migration Inhibitory Factor (MIF) Gene Promotor Polymorphism Is Associated with Increased Fibrosis in Biliary Atresia Patients, but Not with Disease Susceptibility.

artículo científico publicado en 2017

Melanoma candidate genes CDKN2A/p16/INK4A, p14ARF, and CDK4 sequencing in patients with uveal melanoma with relative high-risk for hereditary cancer predisposition ⬇️

artículo científico publicado el 1 de junio de 2011

Molecular genetic testing of uveal melanoma from routinely processed and stained cytology specimens

artículo científico publicado en 2011

Monosomy 3 status of uveal melanoma metastases is associated with rapidly progressive tumors and short survival

artículo científico publicado en 2012

Nuclear BAP1 loss is common in intrahepatic cholangiocarcinoma and a subtype of hepatocellular carcinoma but rare in pancreatic ductal adenocarcinoma

scientific article published on 09 April 2018

Ocular melanoma and the BAP1 hereditary cancer syndrome: implications for the dermatologist.

artículo científico

Oral Selumetinib Does Not Negatively Impact Photoreceptor Survival in Murine Experimental Retinal Detachment

artículo científico publicado en 2019

Patterns of BAP1 protein expression provide insights into prognostic significance and the biology of uveal melanoma

artículo científico publicado en 2017

Retinal MMP-12, MMP-13, TIMP-1, and TIMP-2 expression in murine experimental retinal detachment.

artículo científico publicado en 2014

The chick eye in vision research: An excellent model for the study of ocular disease.

artículo científico publicado en 2017

Transcriptionally Active Androgen Receptor Splice Variants Promote Hepatocellular Carcinoma Progression

scientific article published on 04 November 2019

Lista de obras de

Analysis of the exome aggregation consortium (ExAC) database suggests that the BAP1-tumor predisposition syndrome is underreported in cancer patients

Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma.

Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide

Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases.

Frequency, molecular pathology and potential clinical significance of partial chromosome 3 aberrations in uveal melanoma.

Genetic markers of pigmentation are novel risk loci for uveal melanoma

Germline BAP1 alterations in familial uveal melanoma.

Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

Germline BAP1 mutations misreported as somatic based on tumor-only testing

Germline large deletion of BAP1 and decreased expression in non-tumor choroid in uveal melanoma patients with high risk for inherited cancer

Heterogeneity in Mitogen-Activated Protein Kinase (MAPK) Pathway Activation in Uveal Melanoma With Somatic GNAQ and GNA11 Mutations.

High frequency of submicroscopic hemizygous deletion is a major mechanism of loss of expression of PTEN in uveal melanoma

In vitro anti-uveal melanoma activity of phenolic compounds from the Egyptian medicinal plant Acacia nilotica ⬇️

Interleukin-10 promoter polymorphisms in hepatitis C patients with and without Schistosoma mansoni co-infection.

Investigation of the potential utility of a linomide analogue for treatment of choroidal neovascularization.

Lack of GNAQ germline mutations in uveal melanoma patients with high risk for hereditary cancer predisposition

MET canonical transcript expression is a predictive biomarker for chemo-sensitivity to MET-inhibitors in hepatocellular carcinoma cell lines

MET oncogene inhibition as a potential target of therapy for uveal melanomas.

MIF Inhibitor ISO-1 Protects Photoreceptors and Reduces Gliosis in Experimental Retinal Detachment

MIF promoter polymorphisms are associated with epiretinal membrane but not retinal detachment with PVR in an american population

Macrophage Migration Inhibitory Factor (MIF) Gene Promotor Polymorphism Is Associated with Increased Fibrosis in Biliary Atresia Patients, but Not with Disease Susceptibility.

Melanoma candidate genes CDKN2A/p16/INK4A, p14ARF, and CDK4 sequencing in patients with uveal melanoma with relative high-risk for hereditary cancer predisposition ⬇️

Molecular genetic testing of uveal melanoma from routinely processed and stained cytology specimens

Monosomy 3 status of uveal melanoma metastases is associated with rapidly progressive tumors and short survival

Nuclear BAP1 loss is common in intrahepatic cholangiocarcinoma and a subtype of hepatocellular carcinoma but rare in pancreatic ductal adenocarcinoma

Ocular melanoma and the BAP1 hereditary cancer syndrome: implications for the dermatologist.

Oral Selumetinib Does Not Negatively Impact Photoreceptor Survival in Murine Experimental Retinal Detachment

Patterns of BAP1 protein expression provide insights into prognostic significance and the biology of uveal melanoma

Retinal MMP-12, MMP-13, TIMP-1, and TIMP-2 expression in murine experimental retinal detachment.

The chick eye in vision research: An excellent model for the study of ocular disease.

Transcriptionally Active Androgen Receptor Splice Variants Promote Hepatocellular Carcinoma Progression