BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 26701415)

  • 1. Genetic evolution of nevus of Ota reveals clonal heterogeneity acquiring BAP1 and TP53 mutations.
    Vivancos A; Caratú G; Matito J; Muñoz E; Ferrer B; Hernández-Losa J; Bodet D; Pérez-Alea M; Cortés J; Garcia-Patos V; Recio JA
    Pigment Cell Melanoma Res; 2016 Mar; 29(2):247-53. PubMed ID: 26701415
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nevus of Ota associated with a primary uveal melanoma and intracranial melanoma metastasis.
    Konstantinov NK; Berry TM; Elwood HR; Zlotoff BJ
    Cutis; 2018 Sep; 102(3):E2-E4. PubMed ID: 30372724
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SF3B1 and BAP1 mutations in blue nevus-like melanoma.
    Griewank KG; Müller H; Jackett LA; Emberger M; Möller I; van de Nes JA; Zimmer L; Livingstone E; Wiesner T; Scholz SL; Cosgarea I; Sucker A; Schimming T; Hillen U; Schilling B; Paschen A; Reis H; Mentzel T; Kutzner H; Rütten A; Murali R; Scolyer RA; Schadendorf D
    Mod Pathol; 2017 Jul; 30(7):928-939. PubMed ID: 28409567
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Melanoma arising in a nevus of Ito: novel genetic mutations and a review of the literature on cutaneous malignant transformation of dermal melanocytosis.
    Tse JY; Walls BE; Pomerantz H; Yoon CH; Buchbinder EI; Werchniak AE; Dong F; Lian CG; Granter SR
    J Cutan Pathol; 2016 Jan; 43(1):57-63. PubMed ID: 26260725
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Primary Melanoma of the Leptomeninges with BAP1 Expression-Loss in the Setting of a Nevus of Ota: A Clinical, Morphological and Genetic Study of 2 Cases.
    Goldman-Lévy G; Rigau V; Bléchet C; Bens G; Muckensturm B; Delage M; Labrousse F; Haddad V; Attignon V; Pissaloux D; de la Fouchardière A
    Brain Pathol; 2016 Jul; 26(4):547-50. PubMed ID: 26834043
    [No Abstract]   [Full Text] [Related]  

  • 6. Melanomas Associated With Blue Nevi or Mimicking Cellular Blue Nevi: Clinical, Pathologic, and Molecular Study of 11 Cases Displaying a High Frequency of GNA11 Mutations, BAP1 Expression Loss, and a Predilection for the Scalp.
    Costa S; Byrne M; Pissaloux D; Haddad V; Paindavoine S; Thomas L; Aubin F; Lesimple T; Grange F; Bonniaud B; Mortier L; Mateus C; Dreno B; Balme B; Vergier B; de la Fouchardiere A
    Am J Surg Pathol; 2016 Mar; 40(3):368-77. PubMed ID: 26645730
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fatal GNAQ-mutated CNS melanoma in an adolescent with nevus of Ota.
    Blundell AR; Moustafa D; Samore WR; Hawryluk EB
    Pediatr Dermatol; 2021 Mar; 38(2):497-499. PubMed ID: 33421174
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prognostic impact of chromosomal aberrations and GNAQ, GNA11 and BAP1 mutations in uveal melanoma.
    Staby KM; Gravdal K; Mørk SJ; Heegaard S; Vintermyr OK; Krohn J
    Acta Ophthalmol; 2018 Feb; 96(1):31-38. PubMed ID: 28444874
    [TBL] [Abstract][Full Text] [Related]  

  • 9. GNAQ-mutated primary subcutaneous blue melanoma arising in naevus of Ota presenting as a skin-coloured forehead mass.
    Santiago S; Roy SF; Tran TT; Bosenberg M; Weston GK
    Pathology; 2024 Apr; 56(3):426-428. PubMed ID: 37872018
    [No Abstract]   [Full Text] [Related]  

  • 10. Chromosome 3 status combined with BAP1 and EIF1AX mutation profiles are associated with metastasis in uveal melanoma.
    Ewens KG; Kanetsky PA; Richards-Yutz J; Purrazzella J; Shields CL; Ganguly T; Ganguly A
    Invest Ophthalmol Vis Sci; 2014 Jun; 55(8):5160-7. PubMed ID: 24970262
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Histopathologic and mutational analysis of a case of blue nevus-like melanoma.
    Dai J; Tetzlaff MT; Schuchter LM; Elder DE; Elenitsas R
    J Cutan Pathol; 2016 Sep; 43(9):776-80. PubMed ID: 27152652
    [TBL] [Abstract][Full Text] [Related]  

  • 12. GNA11-mutated and BAP1-negative Melanomas Ex Blue Naevi: A Particularly Aggressive Entity.
    Uguen A; Guibourg B; Costa S; Marcorelles P
    Acta Derm Venereol; 2017 Jun; 97(6):743-744. PubMed ID: 27990554
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic profile of GNAQ-mutated blue melanocytic neoplasms reveals mutations in genes linked to genomic instability and the PI3K pathway.
    Pérez-Alea M; Vivancos A; Caratú G; Matito J; Ferrer B; Hernandez-Losa J; Cortés J; Muñoz E; Garcia-Patos V; Recio JA
    Oncotarget; 2016 May; 7(19):28086-95. PubMed ID: 27057633
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiple Cutaneous Melanomas and Clinically Atypical Moles in a Patient With a Novel Germline BAP1 Mutation.
    Gerami P; Yélamos O; Lee CY; Obregon R; Yazdan P; Sholl LM; Guitart GE; Njauw CN; Tsao H
    JAMA Dermatol; 2015 Nov; 151(11):1235-9. PubMed ID: 26154183
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular analysis of a case of nevus of ota showing progressive evolution to melanoma with intermediate stages resembling cellular blue nevus.
    Gerami P; Pouryazdanparast P; Vemula S; Bastian BC
    Am J Dermatopathol; 2010 May; 32(3):301-305. PubMed ID: 20110797
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic landscape of uveal melanoma.
    Rodrigues MJ; Stern MH
    J Fr Ophtalmol; 2015 Jun; 38(6):522-5. PubMed ID: 25976133
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tumours associated with BAP1 mutations.
    Murali R; Wiesner T; Scolyer RA
    Pathology; 2013 Feb; 45(2):116-26. PubMed ID: 23277170
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Targeted next generation sequencing reveals unique mutation profile of primary melanocytic tumors of the central nervous system.
    van de Nes J; Gessi M; Sucker A; Möller I; Stiller M; Horn S; Scholz SL; Pischler C; Stadtler N; Schilling B; Zimmer L; Hillen U; Scolyer RA; Buckland ME; Lauriola L; Pietsch T; Waha A; Schadendorf D; Murali R; Griewank KG
    J Neurooncol; 2016 May; 127(3):435-44. PubMed ID: 26744134
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Melanoma arising in plaque-type blue nevus and dermal melanocytosis: Diagnostic and prognostic value of BAP1.
    Requena C; Traves V; Ferrandis E; Antón Almero M; García-Casado Z; Manrique-Silva E; Santos Briz Á; Escalonilla P; Nagore E
    Actas Dermosifiliogr; 2023; 114(7):636-641. PubMed ID: 37088284
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of clinically relevant somatic mutations in high-risk head and neck cutaneous squamous cell carcinoma.
    Zilberg C; Lee MW; Yu B; Ashford B; Kraitsek S; Ranson M; Shannon K; Cowley M; Iyer NG; Palme CE; Ch'ng S; Low TH; O'Toole S; Clark JR; Gupta R
    Mod Pathol; 2018 Feb; 31(2):275-287. PubMed ID: 28984303
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.