These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 25219651)

  • 1. Epidermal, sebaceous, and melanocytic nevoid proliferations are spectrums of mosaic RASopathies.
    Luo S; Tsao H
    J Invest Dermatol; 2014 Oct; 134(10):2493-2496. PubMed ID: 25219651
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Making a mountain out of a molehill: NRAS, mosaicism, and large congenital nevi.
    Gerami P; Paller AS
    J Invest Dermatol; 2013 Sep; 133(9):2127-30. PubMed ID: 23949765
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Next-generation sequencing of nevus spilus-type congenital melanocytic nevus: exquisite genotype-phenotype correlation in mosaic RASopathies.
    Kinsler VA; Krengel S; Riviere JB; Waelchli R; Chapusot C; Al-Olabi L; Faivre L; Haenssle HA; Weibel L; Jeudy G; Vabres P
    J Invest Dermatol; 2014 Oct; 134(10):2658-2660. PubMed ID: 24751729
    [No Abstract]   [Full Text] [Related]  

  • 4. Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia.
    Lim YH; Ovejero D; Sugarman JS; Deklotz CM; Maruri A; Eichenfield LF; Kelley PK; Jüppner H; Gottschalk M; Tifft CJ; Gafni RI; Boyce AM; Cowen EW; Bhattacharyya N; Guthrie LC; Gahl WA; Golas G; Loring EC; Overton JD; Mane SM; Lifton RP; Levy ML; Collins MT; Choate KA
    Hum Mol Genet; 2014 Jan; 23(2):397-407. PubMed ID: 24006476
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mosaic NRAS Q61R mutation in a child with giant congenital melanocytic naevus, epidermal naevus syndrome and hypophosphataemic rickets.
    Ramesh R; Shaw N; Miles EK; Richard B; Colmenero I; Moss C
    Clin Exp Dermatol; 2017 Jan; 42(1):75-79. PubMed ID: 27900779
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mosaic NRASopathy n a child with giant melanocytic congenital naevus, epidermal hamartoma and bilateral nephroblastomatosis: clinical implication for follow-up.
    Maridet C; Morice-Picard F; Gros A; Crivelli L; de la Fouchardière A; Vergier B; Taïeb A
    J Eur Acad Dermatol Venereol; 2018 Jul; 32(7):e258-e260. PubMed ID: 29314428
    [No Abstract]   [Full Text] [Related]  

  • 7. Large-Giant Congenital Melanocytic Nevi: Moving Beyond NRAS Mutations.
    Stark MS
    J Invest Dermatol; 2019 Apr; 139(4):756-759. PubMed ID: 30904080
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic analyses of mosaic neurofibromatosis type 1 with giant café-au-lait macule, plexiform neurofibroma and multiple melanocytic nevi.
    Hida T; Idogawa M; Okura M; Sugita S; Sugawara T; Sasaki Y; Tokino T; Yamashita T; Uhara H
    J Dermatol; 2020 Jun; 47(6):658-662. PubMed ID: 32246533
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular Genomic Profiling of Melanocytic Nevi.
    Colebatch AJ; Ferguson P; Newell F; Kazakoff SH; Witkowski T; Dobrovic A; Johansson PA; Saw RPM; Stretch JR; McArthur GA; Long GV; Thompson JF; Pearson JV; Mann GJ; Hayward NK; Waddell N; Scolyer RA; Wilmott JS
    J Invest Dermatol; 2019 Aug; 139(8):1762-1768. PubMed ID: 30772300
    [TBL] [Abstract][Full Text] [Related]  

  • 10. BRAF, NRAS, and GNAQ Mutations in Conjunctival Melanocytic Nevi.
    Francis JH; Grossniklaus HE; Habib LA; Marr B; Abramson DH; Busam KJ
    Invest Ophthalmol Vis Sci; 2018 Jan; 59(1):117-121. PubMed ID: 29332123
    [TBL] [Abstract][Full Text] [Related]  

  • 11. NRAS mutation is the sole recurrent somatic mutation in large congenital melanocytic nevi.
    Charbel C; Fontaine RH; Malouf GG; Picard A; Kadlub N; El-Murr N; How-Kit A; Su X; Coulomb-L'Hermine A; Tost J; Mourah S; Aractingi S; Guégan S
    J Invest Dermatol; 2014 Apr; 134(4):1067-1074. PubMed ID: 24129063
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cutaneous Melanocytic Tumors With Concomitant NRASQ61R and IDH1R132C Mutations: A Report of 6 Cases.
    Macagno N; Pissaloux D; Etchevers H; Haddad V; Vergier B; Sierra-Fortuny S; Tirode F; de la Fouchardière A
    Am J Surg Pathol; 2020 Oct; 44(10):1398-1405. PubMed ID: 32732488
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Melanoma arising in a giant congenital melanocytic nevus with neuroblastoma RAS mutation.
    Dudani P; Senthilnathan G; Wajid MA; Gupta AK; Kaushal S; Arora S; Shamim SA; Bhari N
    Indian J Dermatol Venereol Leprol; 2021; 87(3):416-420. PubMed ID: 33871206
    [No Abstract]   [Full Text] [Related]  

  • 14. The Distinctive Genomic Landscape of Giant Congenital Melanocytic Nevi.
    Stark MS; Tell-Martí G; Martins da Silva V; Martinez-Barrios E; Calbet-Llopart N; Vicente A; Sturm RA; Soyer HP; Puig S; Malvehy J; Carrera C; Puig-Butillé JA
    J Invest Dermatol; 2021 Mar; 141(3):692-695.e2. PubMed ID: 32800874
    [No Abstract]   [Full Text] [Related]  

  • 15. Hiding in plain sight: molecular genetics applied to giant congenital melanocytic nevi.
    Etchevers HC
    J Invest Dermatol; 2014 Apr; 134(4):879-882. PubMed ID: 24646799
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genomic analysis of adult case of ocular surface giant congenital melanocytic nevus and associated clinicopathological findings.
    McGrath LA; Palmer JM; Stark A; Glasson W; Warrier SK; Whitehead K; Hamilton H; Brooks K; Johansson PA; Hayward NK
    Ophthalmic Genet; 2020 Dec; 41(6):616-620. PubMed ID: 32814477
    [TBL] [Abstract][Full Text] [Related]  

  • 17. SCALP syndrome with a germline heterozygous DOCK6 mutation and somatic mosaic NRAS Q61R mutation.
    Meyer SN; Simmons EM; McPherson JD; Awasthi S; Kiuru M
    Pediatr Dermatol; 2023; 40(3):523-527. PubMed ID: 36456540
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Aggressive melanoma in an infant with congenital melanocytic nevus syndrome and multiple, NRAS and BRAF mutation-negative nodules.
    de la Rosa Carrillo D; Vindenes H; Kinsler VA; Rønnestad A; Ringstad G; Müller LO; Tafjord S; Tønseth KA; Kvamme B; Clausen OPF
    Pediatr Dermatol; 2018 Sep; 35(5):e281-e285. PubMed ID: 29999207
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Naevus spilus-type congenital melanocytic naevus associated with a novel NRAS codon 61 mutation.
    Krengel S; Widmer DS; Kerl K; Levesque MP; Schiestl C; Weibel L
    Br J Dermatol; 2016 Mar; 174(3):642-4. PubMed ID: 26302237
    [No Abstract]   [Full Text] [Related]  

  • 20. Successful treatment with MEK-inhibitor in a patient with NRAS-related cutaneous skeletal hypophosphatemia syndrome.
    Carli D; Cardaropoli S; Tessaris D; Coppo P; La Selva R; Cesario C; Lepri FR; Pullano V; Palumbo M; Ramenghi U; Brusco A; Medico E; De Sanctis L; Ferrero GB; Mussa A
    Genes Chromosomes Cancer; 2022 Dec; 61(12):740-746. PubMed ID: 35999193
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.