BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

356 related articles for article (PubMed ID: 24006476)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. Pathogenic role of Fgf23 in Dmp1-null mice.
    Liu S; Zhou J; Tang W; Menard R; Feng JQ; Quarles LD
    Am J Physiol Endocrinol Metab; 2008 Aug; 295(2):E254-61. PubMed ID: 18559986
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Serum FGF23 levels in normal and disordered phosphorus homeostasis.
    Weber TJ; Liu S; Indridason OS; Quarles LD
    J Bone Miner Res; 2003 Jul; 18(7):1227-34. PubMed ID: 12854832
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A case report to assess the safety and efficacy of Burosumab, an investigational antibody to FGF23, in a single pediatric patient with Epidermal Nevus Syndrome and associated hypophosphatemic rickets.
    Huynh C; Gillis A; Fazendin J; Abdullatif H
    Bone Rep; 2022 Dec; 17():101605. PubMed ID: 35899095
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Schimmelpenning-Feuerstein-Mims syndrome induced by HRAS Gly12Ser somatic mosaic mutation: Case report and literature review.
    Ono H; Yamaguchi R; Arai M; Togi S; Ura H; Niida Y; Shimizu A
    J Dermatol; 2023 Sep; 50(9):1213-1215. PubMed ID: 37170693
    [TBL] [Abstract][Full Text] [Related]  

  • 29. An update on congenital melanocytic nevus syndrome: A case report and literature review.
    Abdulmajid L; Bosisio FM; Brems H; De Vlieger G; Garmyn M; Segers H; Demaerel P; Segers K; Jansen K; Lagae L; Verheecke M
    J Cutan Pathol; 2021 Dec; 48(12):1497-1503. PubMed ID: 34255877
    [TBL] [Abstract][Full Text] [Related]  

  • 30. BRAF mutations are also associated with neurocutaneous melanocytosis and large/giant congenital melanocytic nevi.
    Salgado CM; Basu D; Nikiforova M; Bauer BS; Johnson D; Rundell V; Grunwaldt LJ; Reyes-Múgica M
    Pediatr Dev Pathol; 2015; 18(1):1-9. PubMed ID: 25490715
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS.
    Kinsler VA; Thomas AC; Ishida M; Bulstrode NW; Loughlin S; Hing S; Chalker J; McKenzie K; Abu-Amero S; Slater O; Chanudet E; Palmer R; Morrogh D; Stanier P; Healy E; Sebire NJ; Moore GE
    J Invest Dermatol; 2013 Sep; 133(9):2229-36. PubMed ID: 23392294
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. A Symmetric Eczematous Eruption Harboring Thousands of Melanocytic Lesions.
    Ratushny V; Kraft S; Moschella SL; Duncan LM; Lawrence DP; Tsao H
    JAMA Dermatol; 2016 Sep; 152(9):1021-4. PubMed ID: 27192392
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Combined melanocytic and sweat gland neoplasm: cell subsets harbor an identical HRAS mutation in phacomatosis pigmentokeratotica.
    Li JY; Berger MF; Marghoob A; Bhanot UK; Toyohara JP; Pulitzer MP
    J Cutan Pathol; 2014 Aug; 41(8):663-71. PubMed ID: 24628623
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Hereditary spastic paraplegia masqueraded by congenital melanocytic nevus syndrome: Dual pathogenesis of germline non-mosaicism and somatic mosaicism.
    Sakaguchi Y; Uehara T; Sasaki M; Fujimura K; Kishi K; Kosaki K; Takenouchi T
    Eur J Med Genet; 2020 Apr; 63(4):103803. PubMed ID: 31698101
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Lack of BRAF(V600E) mutations in giant congenital melanocytic nevi in a Chinese population.
    Wu D; Wang M; Wang X; Yin N; Song T; Li H; Yu J; Wang DM; Zhao Z
    Am J Dermatopathol; 2011 Jun; 33(4):341-4. PubMed ID: 21430505
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Proliferative nodules arising within congenital melanocytic nevi: a histologic, immunohistochemical, and molecular analyses of 43 cases.
    Phadke PA; Rakheja D; Le LP; Selim MA; Kapur P; Davis A; Mihm MC; Hoang MP
    Am J Surg Pathol; 2011 May; 35(5):656-69. PubMed ID: 21436676
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spatiotemporal expression of NRAS and occurrence of giant congenital melanocytic nevi.
    Aimaier R; Chung M; Zhu H; Yu Q
    Exp Dermatol; 2022 Apr; 31(4):582-585. PubMed ID: 35020224
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Tumor-induced osteomalacia with elevated fibroblast growth factor 23: a case of phosphaturic mesenchymal tumor mixed with connective tissue variants and review of the literature.
    Hu FK; Yuan F; Jiang CY; Lv DW; Mao BB; Zhang Q; Yuan ZQ; Wang Y
    Chin J Cancer; 2011 Nov; 30(11):794-804. PubMed ID: 22035861
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.