BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 24384015)

  • 1. RAS in FGF23: another piece in the puzzle.
    Ovejero D; Collins MT
    J Clin Endocrinol Metab; 2014 Jan; 99(1):63-6. PubMed ID: 24384015
    [No Abstract]   [Full Text] [Related]  

  • 2. Postzygotic HRAS mutation causing both keratinocytic epidermal nevus and thymoma and associated with bone dysplasia and hypophosphatemia due to elevated FGF23.
    Avitan-Hersh E; Tatur S; Indelman M; Gepstein V; Shreter R; Hershkovitz D; Brick R; Bergman R; Tiosano D
    J Clin Endocrinol Metab; 2014 Jan; 99(1):E132-6. PubMed ID: 24243633
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Cutaneous skeletal hypophosphatemia syndrome (CSHS) is a multilineage somatic mosaic RASopathy.
    Lim YH; Ovejero D; Derrick KM; ; Collins MT; Choate KA
    J Am Acad Dermatol; 2016 Aug; 75(2):420-7. PubMed ID: 27444071
    [TBL] [Abstract][Full Text] [Related]  

  • 5. HRAS mutation mosaicism causing urothelial cancer and epidermal nevus.
    Hafner C; Toll A; Real FX
    N Engl J Med; 2011 Nov; 365(20):1940-2. PubMed ID: 22087699
    [No Abstract]   [Full Text] [Related]  

  • 6. [Neurocutaneous melanosis and multiple congenital melanocytic naevi are associated with post-zygotic N-ras mutations].
    Dereure O
    Ann Dermatol Venereol; 2014 Apr; 141(4):314-5. PubMed ID: 24703650
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. N-Ras mutation in vemurafenib-associated expanding melanocytic nevus.
    Harada K; Kato Y; Maeda T; Yoshida M; Irisawa R; Nagao T; Tsuboi R
    J Dermatol; 2017 May; 44(5):e101-e102. PubMed ID: 27790745
    [No Abstract]   [Full Text] [Related]  

  • 9. Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatment.
    Ovejero D; Lim YH; Boyce AM; Gafni RI; McCarthy E; Nguyen TA; Eichenfield LF; DeKlotz CM; Guthrie LC; Tosi LL; Thornton PS; Choate KA; Collins MT
    Osteoporos Int; 2016 Dec; 27(12):3615-3626. PubMed ID: 27497815
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inheritance of giant pigmented hairy nevus of the scalp.
    Hecht F; LaCanne KM; Carroll DB
    Am J Med Genet; 1981; 9(2):177-8. PubMed ID: 7258230
    [No Abstract]   [Full Text] [Related]  

  • 11. Elevated fibroblast growth factor-23 in hypophosphatemic linear nevus sebaceous syndrome.
    Hoffman WH; Jueppner HW; Deyoung BR; O'dorisio MS; Given KS
    Am J Med Genet A; 2005 Apr; 134(3):233-6. PubMed ID: 15742370
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phacomatosis pigmentokeratotica and precocious puberty associated with HRAS mutation.
    Martin RJ; Arefi M; Splitt M; Redford L; Moss C; Rajan N
    Br J Dermatol; 2018 Jan; 178(1):289-291. PubMed ID: 28489335
    [No Abstract]   [Full Text] [Related]  

  • 13. [Nevus-cell nevus, melanosis extensiva Hutchinson, Schwann-cell nevus (syn. juvenile melanoma). I. Nevus-cell nevi and the control of their development].
    Schreus HT
    Hautarzt; 1969 Nov; 20(11):490-1. PubMed ID: 4915766
    [No Abstract]   [Full Text] [Related]  

  • 14. Identification of somatic KRAS mutation in a Korean baby with nevus sebaceus syndrome.
    Kim SW; Song JS; Kang MS; Sin JB; Ki CS; Jeon GW
    Ann Lab Med; 2015 Jan; 35(1):178-80. PubMed ID: 25553307
    [No Abstract]   [Full Text] [Related]  

  • 15. The role of oncogenes and growth factors in progressive melanoma-genesis.
    Albino AP
    Pigment Cell Res; 1992; Suppl 2():199-218. PubMed ID: 1409423
    [No Abstract]   [Full Text] [Related]  

  • 16. HRAS mutation in phacomatosis pigmentokeratotica without extracutaneous disease.
    Jennings L; Cummins R; Murphy GM; Gulmann C; O'Kane M
    Clin Exp Dermatol; 2017 Oct; 42(7):791-792. PubMed ID: 28736904
    [No Abstract]   [Full Text] [Related]  

  • 17. Genomic analysis of a case of agminated Spitz nevi and congenital-pattern nevi arising in extensive nevus spilus.
    Porubsky C; Teer JK; Zhang Y; Deschaine M; Sondak VK; Messina JL
    J Cutan Pathol; 2018 Feb; 45(2):180-183. PubMed ID: 29210482
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hypophosphatemic rickets: A rare complication of congenital melanocytic nevus syndrome.
    Welfringer-Morin A; Pinto G; Baujat G; Vial Y; Hadj-Rabia S; Bodemer C; Boccara O
    Pediatr Dermatol; 2020 May; 37(3):541-544. PubMed ID: 32157705
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial nevus fusco-caeruleus zygomaticus.
    Yang B; Li L; Hu N; Li Y; Deng C
    Int J Dermatol; 2011 Jul; 50(7):858-9. PubMed ID: 21470213
    [No Abstract]   [Full Text] [Related]  

  • 20. Phacomatosis pigmentokeratotica is a "pseudodidymosis".
    Happle R
    J Invest Dermatol; 2013 Aug; 133(8):1923-5. PubMed ID: 23856930
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.