Lista de obras - Gemma Tell-Martí - Dominio Público Uruguay

A Common Variant in the MC1R Gene (p.V92M) is associated with Alzheimer's Disease Risk

artículo científico publicado en 2017

AURKA Overexpression Is Driven by FOXM1 and MAPK/ERK Activation in Melanoma Cells Harboring BRAF or NRAS Mutations: Impact on Melanoma Prognosis and Therapy

artículo científico publicado en 2017

Amelanotic melanoma in oculocutaneous albinism: a genetic, dermoscopic and reflectance confocal microscopy study.

artículo científico publicado en 2017

Capturing the biological impact of CDKN2A and MC1R genes as an early predisposing event in melanoma and non melanoma skin cancer

artículo científico publicado en 2014

Detection of cell-free circulating BRAFV 600E by droplet digital polymerase chain reaction in patients with and without melanoma under dermatological surveillance

artículo científico publicado en 2019

Discrepant mutational status between naevi and melanomas in naevus-associated melanomas: about mutation-specific immunohistochemistry: reply from the authors

artículo científico publicado en 2016

Genetic Abnormalities in Large to Giant Congenital Nevi: Beyond NRAS mutations

article

Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

article

Genomic analysis and clinical management of adolescent cutaneous melanoma

artículo científico publicado en 2017

Genomic expression differences between cutaneous cells from red hair color individuals and black hair color individuals based on bioinformatic analysis ⬇️

artículo científico publicado en 2016

IRF4 rs12203592 functional variant and melanoma survival.

artículo científico publicado en 2017

Inherited functional variants of the lymphocyte receptor CD5 influence melanoma survival

artículo científico publicado en 2016

KIT Mutations and CD117 Overexpression Are Markers of Better Progression-Free Survival in Vulvar Melanomas.

artículo científico publicado en 2017

Melanocortin 1 receptor (MC1R) polymorphisms' influence on size and dermoscopic features of nevi.

artículo científico publicado en 2017

Multiple BRAF Wild-Type Melanomas During Dabrafenib Treatment for Metastatic BRAF-Mutant Melanoma.

artículo científico publicado en 2015

Mutational status of naevus-associated melanomas.

artículo científico publicado en 2015

Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations

artículo científico publicado en 2015

Prognostic Role of Tumoral PDL1 Expression and Peritumoral FoxP3+ Lymphocytes in Vulvar Melanomas.

artículo científico publicado en 2018

Reply

artículo científico publicado en 2015

The MC1R melanoma risk variant p.R160W is associated with Parkinson disease.

artículo científico publicado en 2015

The p. R151C Polymorphism in MC1R Gene Modifies the Age of Onset in Spanish Huntington's Disease Patients.

artículo científico publicado en 2016

Time and tumor type (primary or metastatic) do not influence the detection of BRAF/NRAS mutations in formalin fixed paraffin embedded samples from melanomas.

artículo científico publicado en 2016

Lista de obras de Gemma Tell-Martí

A Common Variant in the MC1R Gene (p.V92M) is associated with Alzheimer's Disease Risk

AURKA Overexpression Is Driven by FOXM1 and MAPK/ERK Activation in Melanoma Cells Harboring BRAF or NRAS Mutations: Impact on Melanoma Prognosis and Therapy

Amelanotic melanoma in oculocutaneous albinism: a genetic, dermoscopic and reflectance confocal microscopy study.

Capturing the biological impact of CDKN2A and MC1R genes as an early predisposing event in melanoma and non melanoma skin cancer

Detection of cell-free circulating BRAFV 600E by droplet digital polymerase chain reaction in patients with and without melanoma under dermatological surveillance

Discrepant mutational status between naevi and melanomas in naevus-associated melanomas: about mutation-specific immunohistochemistry: reply from the authors

Genetic Abnormalities in Large to Giant Congenital Nevi: Beyond NRAS mutations

Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

Genomic analysis and clinical management of adolescent cutaneous melanoma

Genomic expression differences between cutaneous cells from red hair color individuals and black hair color individuals based on bioinformatic analysis ⬇️

IRF4 rs12203592 functional variant and melanoma survival.

Inherited functional variants of the lymphocyte receptor CD5 influence melanoma survival

KIT Mutations and CD117 Overexpression Are Markers of Better Progression-Free Survival in Vulvar Melanomas.

Melanocortin 1 receptor (MC1R) polymorphisms' influence on size and dermoscopic features of nevi.

Multiple BRAF Wild-Type Melanomas During Dabrafenib Treatment for Metastatic BRAF-Mutant Melanoma.

Mutational status of naevus-associated melanomas.

Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations

Prognostic Role of Tumoral PDL1 Expression and Peritumoral FoxP3+ Lymphocytes in Vulvar Melanomas.

Reply

The MC1R melanoma risk variant p.R160W is associated with Parkinson disease.

The p. R151C Polymorphism in MC1R Gene Modifies the Age of Onset in Spanish Huntington's Disease Patients.

Time and tumor type (primary or metastatic) do not influence the detection of BRAF/NRAS mutations in formalin fixed paraffin embedded samples from melanomas.