BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 27241746)

  • 1. Myelodysplastic Syndrome Occurring in a Patient with Gorlin Syndrome.
    Mull JL; Madden LM; Bayliss SJ
    Pediatr Dermatol; 2016 Jul; 33(4):e256-7. PubMed ID: 27241746
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gorlin syndrome and desmoplastic medulloblastoma: Report of 3 cases with unfavorable clinical course and novel mutations.
    Gururangan S; Robinson G; Ellison DW; Wu G; He X; Lu QR; McLendon R; Grant G; Driscoll T; Neuberg R
    Pediatr Blood Cancer; 2015 Oct; 62(10):1855-8. PubMed ID: 25940061
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SHH desmoplastic/nodular medulloblastoma and Gorlin syndrome in the setting of Down syndrome: case report, molecular profiling, and review of the literature.
    Mangum R; Varga E; Boué DR; Capper D; Benesch M; Leonard J; Osorio DS; Pierson CR; Zumberge N; Sahm F; Schrimpf D; Pfister SM; Finlay JL
    Childs Nerv Syst; 2016 Dec; 32(12):2439-2446. PubMed ID: 27444290
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gorlin syndrome-induced pluripotent stem cells form medulloblastoma with loss of heterozygosity in
    Ikemoto Y; Miyashita T; Nasu M; Hatsuse H; Kajiwara K; Fujii K; Motojima T; Kokido I; Toyoda M; Umezawa A
    Aging (Albany NY); 2020 May; 12(10):9935-9947. PubMed ID: 32436863
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long-lasting pemphigus vulgaris.
    Goetze S; Raessler F; Hipler UC; Schulz S; Kohlhase J; Elsner P
    J Eur Acad Dermatol Venereol; 2016 Mar; 30(3):493-4. PubMed ID: 25600101
    [No Abstract]   [Full Text] [Related]  

  • 6. Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.
    Musani V; Ozretić P; Trnski D; Sabol M; Poduje S; Tošić M; Šitum M; Levanat S
    Croat Med J; 2018 Feb; 59(1):20-24. PubMed ID: 29498494
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations.
    Smith MJ; Beetz C; Williams SG; Bhaskar SS; O'Sullivan J; Anderson B; Daly SB; Urquhart JE; Bholah Z; Oudit D; Cheesman E; Kelsey A; McCabe MG; Newman WG; Evans DG
    J Clin Oncol; 2014 Dec; 32(36):4155-61. PubMed ID: 25403219
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Myelodysplastic syndrome as a late complication following autologous bone marrow transplantation for non-Hodgkin's lymphoma.
    Stone RM; Neuberg D; Soiffer R; Takvorian T; Whelan M; Rabinowe SN; Aster JC; Leavitt P; Mauch P; Freedman AS
    J Clin Oncol; 1994 Dec; 12(12):2535-42. PubMed ID: 7989927
    [TBL] [Abstract][Full Text] [Related]  

  • 9. First evidence of genotype-phenotype correlations in Gorlin syndrome.
    Evans DG; Oudit D; Smith MJ; Rutkowski D; Allan E; Newman WG; Lear JT
    J Med Genet; 2017 Aug; 54(8):530-536. PubMed ID: 28596197
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Myelodysplastic syndrome in a child with a history of medulloblastoma.
    Akyüz C; Emir S; Güler N; Tüker A; Büyükpamukçu M
    Turk J Pediatr; 1998; 40(1):131-4. PubMed ID: 9673540
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome.
    Durmaz CD; Evans G; Smith MJ; Ertop P; Akay BN; Tuncalı T
    Cytogenet Genome Res; 2018; 154(2):57-61. PubMed ID: 29544218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gorlin syndrome with an ovarian leiomyoma associated with a PTCH1 second hit.
    Akizawa Y; Miyashita T; Sasaki R; Nagata R; Aoki R; Ishitani K; Nagashima Y; Matsui H; Saito K
    Am J Med Genet A; 2016 Apr; 170A(4):1029-34. PubMed ID: 26782978
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gorlin Syndrome Associated With a Solitary Circumscribed Retinal Astrocytic Proliferation in a Pediatric Patient.
    Lopez-Cañizares A; Al-Khersan H; Carletti P; Shields CL; Berrocal AM
    Ophthalmic Surg Lasers Imaging Retina; 2022 Sep; 53(9):514-516. PubMed ID: 36107625
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel PTCH1 Mutation in a Young Child With Gorlin Syndrome and Medulloblastoma.
    Gloude NJ; Yoon JM; Crawford JR
    Pediatr Blood Cancer; 2016 Jun; 63(6):1128-9. PubMed ID: 26840755
    [No Abstract]   [Full Text] [Related]  

  • 15. Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.
    Garavelli L; Piemontese MR; Cavazza A; Rosato S; Wischmeijer A; Gelmini C; Albertini E; Albertini G; Forzano F; Franchi F; Carella M; Zelante L; Superti-Furga A
    Am J Med Genet A; 2013 Nov; 161A(11):2894-901. PubMed ID: 24124115
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Therapy-related myelodysplastic syndrome as a late adverse event of definitive chemoradiotherapy for esophageal and oropharyngeal cancer].
    Kamihara Y; Sato Y; Takada K; Okagawa Y; Iyama S; Sato T; Miyanishi K; Takimoto R; Kobune M; Kato J
    Nihon Shokakibyo Gakkai Zasshi; 2015; 112(9):1664-73. PubMed ID: 26346357
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spontaneous recovery from a medulloblastoma by a female with Gorlin-Goltz syndrome.
    Su CW; Lin KL; Hou JW; Jung SM; Zen EC
    Pediatr Neurol; 2003 Mar; 28(3):231-4. PubMed ID: 12770681
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Severe PATCHED1 Deficiency in Cancer-Prone Gorlin Patient Cells Results in Intrinsic Radiosensitivity.
    Vulin A; Sedkaoui M; Moratille S; Sevenet N; Soularue P; Rigaud O; Guibbal L; Dulong J; Jeggo P; Deleuze JF; Lamartine J; Martin MT
    Int J Radiat Oncol Biol Phys; 2018 Oct; 102(2):417-425. PubMed ID: 30191873
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Incidence and characterization of secondary myelodysplastic syndrome and acute myelogenous leukemia following high-dose chemoradiotherapy and autologous stem-cell transplantation for lymphoid malignancies.
    Darrington DL; Vose JM; Anderson JR; Bierman PJ; Bishop MR; Chan WC; Morris ME; Reed EC; Sanger WG; Tarantolo SR
    J Clin Oncol; 1994 Dec; 12(12):2527-34. PubMed ID: 7989926
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin-Goltz syndrome.
    Ozcan G; Balta B; Sekerci AE; Etoz OA; Martinuzzi C; Kara O; Pastorino L; Kocoglu F; Ulker O; Erdogan M
    Indian J Pathol Microbiol; 2016; 59(3):335-8. PubMed ID: 27510672
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.