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 *

132 related articles for article (PubMed ID: 38282294)

  • 1. Medulloblastoma and other neoplasms in patients with heterozygous germline SUFU variants: A scoping review.
    Lee SG; Evans G; Stephen M; Goren R; Bondy M; Goodman S
    Am J Med Genet A; 2024 Jun; 194(6):e63496. PubMed ID: 38282294
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Germline SUFU mutation carriers and medulloblastoma: clinical characteristics, cancer risk, and prognosis.
    Guerrini-Rousseau L; Dufour C; Varlet P; Masliah-Planchon J; Bourdeaut F; Guillaud-Bataille M; Abbas R; Bertozzi AI; Fouyssac F; Huybrechts S; Puget S; Bressac-De Paillerets B; Caron O; Sevenet N; Dimaria M; Villebasse S; Delattre O; Valteau-Couanet D; Grill J; Brugières L
    Neuro Oncol; 2018 Jul; 20(8):1122-1132. PubMed ID: 29186568
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation.
    Kijima C; Miyashita T; Suzuki M; Oka H; Fujii K
    Fam Cancer; 2012 Dec; 11(4):565-70. PubMed ID: 22829011
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SUFU-associated Gorlin syndrome: Expanding the spectrum between classic nevoid basal cell carcinoma syndrome and multiple hereditary infundibulocystic basal cell carcinoma.
    Álvarez-Salafranca M; García-García M; Montes-Torres A; Rivera-Fuertes I; López-Giménez MT; Ara M
    Australas J Dermatol; 2023 May; 64(2):249-254. PubMed ID: 36825822
    [TBL] [Abstract][Full Text] [Related]  

  • 7. High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age.
    Brugières L; Remenieras A; Pierron G; Varlet P; Forget S; Byrde V; Bombled J; Puget S; Caron O; Dufour C; Delattre O; Bressac-de Paillerets B; Grill J
    J Clin Oncol; 2012 Jun; 30(17):2087-93. PubMed ID: 22508808
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort.
    Waszak SM; Northcott PA; Buchhalter I; Robinson GW; Sutter C; Groebner S; Grund KB; Brugières L; Jones DTW; Pajtler KW; Morrissy AS; Kool M; Sturm D; Chavez L; Ernst A; Brabetz S; Hain M; Zichner T; Segura-Wang M; Weischenfeldt J; Rausch T; Mardin BR; Zhou X; Baciu C; Lawerenz C; Chan JA; Varlet P; Guerrini-Rousseau L; Fults DW; Grajkowska W; Hauser P; Jabado N; Ra YS; Zitterbart K; Shringarpure SS; De La Vega FM; Bustamante CD; Ng HK; Perry A; MacDonald TJ; Hernáiz Driever P; Bendel AE; Bowers DC; McCowage G; Chintagumpala MM; Cohn R; Hassall T; Fleischhack G; Eggen T; Wesenberg F; Feychting M; Lannering B; Schüz J; Johansen C; Andersen TV; Röösli M; Kuehni CE; Grotzer M; Kjaerheim K; Monoranu CM; Archer TC; Duke E; Pomeroy SL; Shelagh R; Frank S; Sumerauer D; Scheurlen W; Ryzhova MV; Milde T; Kratz CP; Samuel D; Zhang J; Solomon DA; Marra M; Eils R; Bartram CR; von Hoff K; Rutkowski S; Ramaswamy V; Gilbertson RJ; Korshunov A; Taylor MD; Lichter P; Malkin D; Gajjar A; Korbel JO; Pfister SM
    Lancet Oncol; 2018 Jun; 19(6):785-798. PubMed ID: 29753700
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Identification of a Family with SUFU Germline Deletion Based on a Case of Desmoplastic Medulloblastoma in an Infant].
    Šoukalová J; Vejmělková K; Cermanová T; Kašíková K; Mikulášová A; Janyšková H; Melichárková K; Pavelka Z; Ježová M; Pospíšilová Š; Kuglík P; Valášková I; Gaillyová R; Štěrba J; Zitterbart K
    Klin Onkol; 2016; 29 Suppl 1():S83-8. PubMed ID: 26691947
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome.
    Foulkes WD; Kamihara J; Evans DGR; Brugières L; Bourdeaut F; Molenaar JJ; Walsh MF; Brodeur GM; Diller L
    Clin Cancer Res; 2017 Jun; 23(12):e62-e67. PubMed ID: 28620006
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a SUFU germline mutation in a family with Gorlin syndrome.
    Pastorino L; Ghiorzo P; Nasti S; Battistuzzi L; Cusano R; Marzocchi C; Garrè ML; Clementi M; Scarrà GB
    Am J Med Genet A; 2009 Jul; 149A(7):1539-43. PubMed ID: 19533801
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cancer risk and tumour spectrum in 172 patients with a germline
    Guerrini-Rousseau L; Masliah-Planchon J; Waszak SM; Alhopuro P; Benusiglio PR; Bourdeaut F; Brecht IB; Del Baldo G; Dhanda SK; Garrè ML; Gidding CEM; Hirsch S; Hoarau P; Jorgensen M; Kratz C; Lafay-Cousin L; Mastronuzzi A; Pastorino L; Pfister SM; Schroeder C; Smith MJ; Vahteristo P; Vibert R; Vilain C; Waespe N; Winship IM; Evans DG; Brugieres L
    J Med Genet; 2022 Jun; 59(11):1123-32. PubMed ID: 35768194
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Leiomyomatosis in an Infant With a SUFU Splice Site Variant: Case Report.
    Rao RR; Dulken BW; Matalon DR; Borensztein M; McGuinness M; Cizek SM; Bruzoni M; Tan SY; Kreimer S
    J Pediatr Hematol Oncol; 2022 Jul; 44(5):e914-e917. PubMed ID: 35398865
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma.
    Cowan R; Hoban P; Kelsey A; Birch JM; Gattamaneni R; Evans DG
    Br J Cancer; 1997; 76(2):141-5. PubMed ID: 9231911
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Defining the Spectrum, Treatment and Outcome of Patients With Genetically Confirmed Gorlin Syndrome From the HIT-MED Cohort.
    Kloth K; Obrecht D; Sturm D; Pietsch T; Warmuth-Metz M; Bison B; Mynarek M; Rutkowski S
    Front Oncol; 2021; 11():756025. PubMed ID: 34888241
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same.
    Huq AJ; Walsh M; Rajagopalan B; Finlay M; Trainer AH; Bonnet F; Sevenet N; Winship IM
    Fam Cancer; 2018 Oct; 17(4):601-606. PubMed ID: 29356994
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular mechanism of extracutaneous tumours in patients with basal cell nevus syndrome.
    Verkouteren BJ; Roemen GM; Schuurs-Hoeijmakers JH; Abdul Hamid M; van Geel M; Speel EM; Mosterd K
    J Clin Pathol; 2023 May; 76(5):345-348. PubMed ID: 36002246
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Perspectives on the implications of carrying putative pathogenic variants in the medulloblastoma predisposition genes ELP1 and GPR161.
    Smith MJ; Woodward ER; Evans DG
    Fam Cancer; 2023 Jul; 22(3):341-344. PubMed ID: 36961676
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differences in RNA and microRNA Expression Between PTCH1- and SUFU-mutated Medulloblastoma.
    Gershanov S; Toledano H; Pernicone N; Fichman S; Michowiz S; Pinhasov A; Goldenberg-Cohen N; Listovsky T; Salmon-Divon M
    Cancer Genomics Proteomics; 2021; 18(3):335-347. PubMed ID: 33893086
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.