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Germline BAP1 alterations in familial uveal melanoma

Genes chromosomes & cancer, 2017-02, Vol.56 (2), p.168-174

2017

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

Genes chromosomes & cancer, 2014-02, Vol.53 (2), p.177-182

2014

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

Genes chromosomes & cancer, 2019-09, Vol.58 (9), p.650-656

2019

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

Genes chromosomes & cancer, 2018-09, Vol.57 (9), p.478-481

2018

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Effect of the COVID-19 Pandemic on the Rate of Interventional Pain Management Therapies. Could the Application of Personal Protective Equipment Help?

Pain physician, 2022-12, Vol.25 (9), p.E1405-E1413

2022

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

Journal of cancer research and clinical oncology, 2021, Vol.147 (1), p.167-175

2021

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

Annals of human genetics, 2017-09, Vol.81 (5), p.177-183

2017

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

Scientific reports, 2017-10, Vol.7 (1), p.14336-15, Article 14336

2017

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KIR Genotypes Impact Progression to Hepatocellular Carcinoma in Patients with Chronic Hepatitis C Infection

Livers, 2023-09, Vol.3 (3), p.354-368

2023

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

Cancer genetics, 2018-08, Vol.224-225, p.21-28

2018

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A Mathematical Model of Breast Tumor Progression Based on Immune Infiltration

Journal of personalized medicine, 2021-10, Vol.11 (10), p.1031

2021

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Uveal melanoma

Nature reviews. Disease primers, 2020-04, Vol.6 (1), p.24, Article 24

2020

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

Journal of medical genetics, 2011-12, Vol.48 (12), p.856-859

2011

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Uveal melanoma-associated cancers revisited

ESMO open, 2020-11, Vol.5 (6), p.e000990-e000990, Article e000990

2020

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High Frequency of Submicroscopic Hemizygous Deletion Is a Major Mechanism of Loss of Expression of PTEN in Uveal Melanoma

Journal of clinical oncology, 2006-01, Vol.24 (2), p.288-295

2006

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Uveal Melanoma in BAP1 Tumor Predisposition Syndrome: Estimation of Risk

American journal of ophthalmology, 2021-04, Vol.224, p.172-177

2021

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Transcriptionally Active Androgen Receptor Splice Variants Promote Hepatocellular Carcinoma Progression

Cancer research (Chicago, Ill.), 2020-02, Vol.80 (3), p.561-575

2020

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

International journal of dermatology, 2014-06, Vol.53 (6), p.657-663

2014

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

Progress in retinal and eye research, 2017-11, Vol.61, p.72-97

2017

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Low Frequency of Aflatoxin Induced TP53 Gene Codon 249 Mutation in Hepatocellular Carcinoma from Egyptian Patients Living in the Nile Delta Region

Asian Pacific Journal of Cancer Prevention, 2023-09, Vol.24 (9), p.3165-3168

2023

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Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma

Cancer cell, 2018-01, Vol.33 (1), p.151-151

2018

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

Investigative ophthalmology & visual science, 2019-06, Vol.60 (7), p.2474-2480

2019

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Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma

Ophthalmology (Rochester, Minn.), 2020-05, Vol.127 (5), p.668-678

2020

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Lymphoepithelioma-like Hepatocellular Carcinoma: a Case Report and Review of Literature

Journal of gastrointestinal cancer, 2023-03, Vol.54 (1), p.275-281

2023

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Presumed spinocerebellar ataxia 7: challenges without molecular diagnosis

Clinical and experimental optometry, 2021-05, Vol.104 (4), p.547-549

2021

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Germline BAP1 alterations in familial uveal melanoma

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

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

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

Effect of the COVID-19 Pandemic on the Rate of Interventional Pain Management Therapies. Could the Application of Personal Protective Equipment Help?

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

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

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

KIR Genotypes Impact Progression to Hepatocellular Carcinoma in Patients with Chronic Hepatitis C Infection

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

A Mathematical Model of Breast Tumor Progression Based on Immune Infiltration

Uveal melanoma

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

Uveal melanoma-associated cancers revisited

High Frequency of Submicroscopic Hemizygous Deletion Is a Major Mechanism of Loss of Expression of PTEN in Uveal Melanoma

Uveal Melanoma in BAP1 Tumor Predisposition Syndrome: Estimation of Risk

Transcriptionally Active Androgen Receptor Splice Variants Promote Hepatocellular Carcinoma Progression

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

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

Low Frequency of Aflatoxin Induced TP53 Gene Codon 249 Mutation in Hepatocellular Carcinoma from Egyptian Patients Living in the Nile Delta Region

Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma

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

Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma

Lymphoepithelioma-like Hepatocellular Carcinoma: a Case Report and Review of Literature

Presumed spinocerebellar ataxia 7: challenges without molecular diagnosis

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