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Journal Abstract Search

728 related items for PubMed ID: 29371009

  • 1.
    ; . PubMed ID:
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  • 2. Frequent GNAQ, GNA11, and EIF1AX Mutations in Iris Melanoma.
    Scholz SL, Möller I, Reis H, Süßkind D, van de Nes JAP, Leonardelli S, Schilling B, Livingstone E, Schimming T, Paschen A, Sucker A, Murali R, Steuhl KP, Schadendorf D, Westekemper H, Griewank KG.
    Invest Ophthalmol Vis Sci; 2017 Jul 01; 58(9):3464-3470. PubMed ID: 28700778
    [Abstract] [Full Text] [Related]

  • 3. 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 01; 127(3):435-44. PubMed ID: 26744134
    [Abstract] [Full Text] [Related]

  • 4. 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 26; 55(8):5160-7. PubMed ID: 24970262
    [Abstract] [Full Text] [Related]

  • 5. Driver Mutations in Uveal Melanoma: Associations With Gene Expression Profile and Patient Outcomes.
    Decatur CL, Ong E, Garg N, Anbunathan H, Bowcock AM, Field MG, Harbour JW.
    JAMA Ophthalmol; 2016 Jul 01; 134(7):728-33. PubMed ID: 27123562
    [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 01; 40(3):368-77. PubMed ID: 26645730
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 30(7):928-939. PubMed ID: 28409567
    [Abstract] [Full Text] [Related]

  • 8. Uveal Melanomas with SF3B1 Mutations: A Distinct Subclass Associated with Late-Onset Metastases.
    Yavuzyigitoglu S, Koopmans AE, Verdijk RM, Vaarwater J, Eussen B, van Bodegom A, Paridaens D, Kiliç E, de Klein A, Rotterdam Ocular Melanoma Study Group.
    Ophthalmology; 2016 May 01; 123(5):1118-28. PubMed ID: 26923342
    [Abstract] [Full Text] [Related]

  • 9. SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas.
    Küsters-Vandevelde HV, Creytens D, van Engen-van Grunsven AC, Jeunink M, Winnepenninckx V, Groenen PJ, Küsters B, Wesseling P, Blokx WA, Prinsen CF.
    Acta Neuropathol Commun; 2016 Jan 15; 4():5. PubMed ID: 26769193
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 96(1):31-38. PubMed ID: 28444874
    [Abstract] [Full Text] [Related]

  • 11. Metastatic Disease in Polyploid Uveal Melanoma Patients Is Associated With BAP1 Mutations.
    Yavuzyigitoglu S, Mensink HW, Smit KN, Vaarwater J, Verdijk RM, Beverloo B, Brüggenwirth HT, van Marion R, Dubbink HJ, Paridaens D, Naus NC, de Klein A, Kiliç E, Rotterdam Ocular Melanoma Study Group (ROMS).
    Invest Ophthalmol Vis Sci; 2016 Apr 01; 57(4):2232-9. PubMed ID: 27116551
    [Abstract] [Full Text] [Related]

  • 12. Chromosomal rearrangements in uveal melanoma: Chromothripsis.
    van Poppelen NM, Yavuzyigitoglu S, Smit KN, Vaarwater J, Eussen B, Brands T, Paridaens D, Kiliç E, de Klein A.
    Genes Chromosomes Cancer; 2018 Sep 01; 57(9):452-458. PubMed ID: 29726589
    [Abstract] [Full Text] [Related]

  • 13. Genetic Profiling of Primary Orbital Melanoma: An Analysis of 6 Cases with Clinicopathologic Correlation.
    Mudhar HS, Doherty RE, Salvi SM, Currie ZI, Tan JH, Sisley K.
    Ophthalmology; 2019 Jul 01; 126(7):1045-1052. PubMed ID: 30605742
    [Abstract] [Full Text] [Related]

  • 14. Bioinformatics analysis of GNAQ, GNA11, BAP1, SF3B1,SRSF2, EIF1AX, PLCB4, and CYSLTR2 genes and their role in the pathogenesis of Uveal Melanoma.
    Akin-Bali DF.
    Ophthalmic Genet; 2021 Dec 01; 42(6):732-743. PubMed ID: 34353217
    [Abstract] [Full Text] [Related]

  • 15. Iris and Ciliary Body Melanocytomas Are Defined by Solitary GNAQ Mutation Without Additional Oncogenic Alterations.
    Solomon DA, Ramani B, Eiger-Moscovich M, Milman T, Uludag G, Crawford JB, Phan I, Char DH, Shields CL, Eagle RC, Bastian BC, Bloomer MM, Pekmezci M.
    Ophthalmology; 2022 Dec 01; 129(12):1429-1439. PubMed ID: 35835335
    [Abstract] [Full Text] [Related]

  • 16. Oncogenic mutations in melanomas and benign melanocytic nevi of the female genital tract.
    Tseng D, Kim J, Warrick A, Nelson D, Pukay M, Beadling C, Heinrich M, Selim MA, Corless CL, Nelson K.
    J Am Acad Dermatol; 2014 Aug 01; 71(2):229-36. PubMed ID: 24842760
    [Abstract] [Full Text] [Related]

  • 17. GNAQ and GNA11 mutant nonuveal melanoma: a subtype distinct from both cutaneous and uveal melanoma.
    Livingstone E, Zaremba A, Horn S, Ugurel S, Casalini B, Schlaak M, Hassel JC, Herbst R, Utikal JS, Weide B, Gutzmer R, Meier F, Koelsche C, Hadaschik E, Sucker A, Reis H, Merkelbach-Bruse S, Siewert M, Sahm F, von Deimling A, Cosgarea I, Zimmer L, Schadendorf D, Schilling B, Griewank KG.
    Br J Dermatol; 2020 Nov 01; 183(5):928-939. PubMed ID: 32064597
    [Abstract] [Full Text] [Related]

  • 18. Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma.
    Patrone S, Maric I, Rutigliani M, Lanza F, Puntoni M, Banelli B, Rancati S, Angelini G, Amaro A, Ligorio P, Defferrari C, Castagnetta M, Bandelloni R, Mosci C, DeCensi A, Romani M, Pfeffer U, Viaggi S, Coviello DA.
    Genes Chromosomes Cancer; 2018 Aug 01; 57(8):387-400. PubMed ID: 29689622
    [Abstract] [Full Text] [Related]

  • 19. BAP1 and BRAFV600E expression in benign and malignant melanocytic proliferations.
    Piris A, Mihm MC, Hoang MP.
    Hum Pathol; 2015 Feb 01; 46(2):239-45. PubMed ID: 25479927
    [Abstract] [Full Text] [Related]

  • 20. Genomic Profiling of Metastatic Uveal Melanoma Shows Frequent Coexisting BAP1 or SF3B1 and GNAQ/GNA11 Mutations and Correlation With Prognosis.
    Isaacson AL, Sompallae RR, Guseva NV, Bellizzi AM, Bossler AD, Ma D.
    Am J Clin Pathol; 2022 Aug 04; 158(2):177-186. PubMed ID: 35212356
    [Abstract] [Full Text] [Related]

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