Pages that link to "Q45374479"

The following pages link to Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. (Q45374479):

Displaying 33 items.

• Melanoma: from melanocyte to genetic alterations and clinical options (Q21284811) (← links)
• Update in genetic susceptibility in melanoma (Q26778756) (← links)
• The melanocyte lineage in development and disease (Q26853648) (← links)
• Sumoylation in gene regulation, human disease, and therapeutic action (Q27865271) (← links)
• A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma (Q28386783) (← links)
• Genetic profiling of a rare condition: co-occurrence of albinism and multiple primary melanoma in a Caucasian family (Q33728131) (← links)
• Melanoma genetics (Q34044830) (← links)
• MITF in melanoma: mechanisms behind its expression and activity. (Q35187734) (← links)
• Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition (Q35213835) (← links)
• Characterization of melanoma susceptibility genes in high-risk patients from Central Italy. (Q36266148) (← links)
• Identification, genetic testing, and management of hereditary melanoma. (Q36304955) (← links)
• Hereditary melanoma: Update on syndromes and management: Emerging melanoma cancer complexes and genetic counseling (Q36599690) (← links)
• Appearance of malignant melanoma after a non-cutaneous cancer diagnosis (Q36807224) (← links)
• The impact of MITF on melanoma development: news from bench and bedside (Q37507876) (← links)
• Heterogeneity and frequency of BRAF mutations in primary melanoma: Comparison between molecular methods and immunohistochemistry (Q37702662) (← links)
• MITF E318K's effect on melanoma risk independent of, but modified by, other risk factors (Q37705148) (← links)
• Desmoplastic melanoma: a challenge for the oncologist (Q38812696) (← links)
• Genetic predisposition to kidney cancer (Q39023793) (← links)
• Focus on cutaneous and uveal melanoma specificities. (Q39312161) (← links)
• The CDKN2A/p16(INK) (4a) 5'UTR sequence and translational regulation: impact of novel variants predisposing to melanoma (Q41115366) (← links)
• Updated field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma: the MelGene database (Q44716312) (← links)
• Functional analysis of a CDKN2A 5'UTR germline variant associated with pancreatic cancer development (Q47104868) (← links)
• Improvement of Genetic Testing for Cutaneous Melanoma in Countries With Low to Moderate Incidence: The Rule of 2 vs the Rule of 3. (Q47270996) (← links)
• Pathways from senescence to melanoma: focus on MITF sumoylation. (Q47927484) (← links)
• Combining molecular and immunohistochemical analyses of key drivers in primary melanomas: interplay between germline and somatic variations. (Q49787884) (← links)
• Phenotypic characterization of nevus and tumor patterns in MITF E318K mutation carrier melanoma patients (Q50489618) (← links)
• Malignant and benign tumors associated with multiple primary melanomas: just the starting block for the involvement of MITF, PTEN and CDKN2A in multiple cancerogenesis? (Q50876968) (← links)
• Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families (Q50905629) (← links)
• Prognostic and predictive values of oncogenic BRAF, NRAS, c-KIT and MITF in cutaneous and mucous melanoma. (Q55068437) (← links)
• Multi-gene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non-CDKN2A/CDK4 melanoma families (Q58556516) (← links)
• Epidemiological and genetic factors underlying melanoma development in Italy. (Q64975143) (← links)
• Clinical, pathological and dermoscopic phenotype of MITF p.E318K carrier cutaneous melanoma patients (Q89699834) (← links)
• Cancer risks associated with the germline MITF(E318K) variant (Q100533853) (← links)