BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 37725782)

  • 1. Exceptional Response to Olaparib: A Case Report of Metastatic Esophageal Squamous Cell Carcinoma in a Patient With Fanconi Anemia, Germline
    Haggstrom LR; Tucker K; Williams R; Nelson A; Walsh R; Brungs D; Aghmesheh M
    JCO Precis Oncol; 2023 Sep; 7():e2300221. PubMed ID: 37725782
    [No Abstract]   [Full Text] [Related]  

  • 2. Esophageal cancer as initial presentation of Fanconi anemia in patients with a hypomorphic
    Lach FP; Singh S; Rickman KA; Ruiz PD; Noonan RJ; Hymes KB; DeLacure MD; Kennedy JA; Chandrasekharappa SC; Smogorzewska A
    Cold Spring Harb Mol Case Stud; 2020 Dec; 6(6):. PubMed ID: 33172906
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in Fanconi anemia genes and the risk of esophageal cancer.
    Akbari MR; Malekzadeh R; Lepage P; Roquis D; Sadjadi AR; Aghcheli K; Yazdanbod A; Shakeri R; Bashiri J; Sotoudeh M; Pourshams A; Ghadirian P; Narod SA
    Hum Genet; 2011 May; 129(5):573-82. PubMed ID: 21279724
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline BRCA2 Truncating Mutation in Familial Esophageal Squamous Cell Carcinoma: A Case Controlled Study in China.
    Liang Z; Hu W; Li S; Wei Z; Zhu Z
    Med Sci Monit; 2020 Jun; 26():e923926. PubMed ID: 32579544
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50.
    Chandrasekharappa SC; Chinn SB; Donovan FX; Chowdhury NI; Kamat A; Adeyemo AA; Thomas JW; Vemulapalli M; Hussey CS; Reid HH; Mullikin JC; Wei Q; Sturgis EM
    Cancer; 2017 Oct; 123(20):3943-3954. PubMed ID: 28678401
    [TBL] [Abstract][Full Text] [Related]  

  • 6. BRCA2 loss-of-function germline mutations are associated with esophageal squamous cell carcinoma risk in Chinese.
    Ko JM; Ning L; Zhao XK; Chai AWY; Lei LC; Choi SSA; Tao L; Law S; Kwong A; Lee NP; Chan KT; Lo A; Song X; Chen PN; Chang YL; Wang LD; Lung ML
    Int J Cancer; 2020 Feb; 146(4):1042-1051. PubMed ID: 31396961
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [FANCA gene mutation analysis in Fanconi anemia patients].
    Chen F; Peng GJ; Zhang K; Hu Q; Zhang LQ; Liu AG
    Zhonghua Xue Ye Xue Za Zhi; 2005 Oct; 26(10):616-8. PubMed ID: 16532972
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Recent progress in understanding molecular pathogenesis of Fanconi anemia].
    Yamashita T; Oda T; Sekimoto T
    Rinsho Ketsueki; 2009 Jul; 50(7):538-46. PubMed ID: 19638721
    [No Abstract]   [Full Text] [Related]  

  • 9. A germline FANCA alteration that is associated with increased sensitivity to DNA damaging agents.
    Wilkes DC; Sailer V; Xue H; Cheng H; Collins CC; Gleave M; Wang Y; Demichelis F; Beltran H; Rubin MA; Rickman DS
    Cold Spring Harb Mol Case Stud; 2017 Sep; 3(5):. PubMed ID: 28864460
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.
    Hussain S; Witt E; Huber PA; Medhurst AL; Ashworth A; Mathew CG
    Hum Mol Genet; 2003 Oct; 12(19):2503-10. PubMed ID: 12915460
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fanconi anemia and biallelic BRCA2 mutation diagnosed in a young child with an embryonal CNS tumor.
    Dewire MD; Ellison DW; Patay Z; McKinnon PJ; Sanders RP; Gajjar A
    Pediatr Blood Cancer; 2009 Dec; 53(6):1140-2. PubMed ID: 19530235
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Heterogeneous activation of the Fanconi anemia pathway by patient-derived FANCA mutants.
    Adachi D; Oda T; Yagasaki H; Nakasato K; Taniguchi T; D'Andrea AD; Asano S; Yamashita T
    Hum Mol Genet; 2002 Dec; 11(25):3125-34. PubMed ID: 12444097
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The role of Fanconi anemia/BRCA genes in zebrafish sex determination.
    Rodríguez-Marí A; Postlethwait JH
    Methods Cell Biol; 2011; 105():461-90. PubMed ID: 21951543
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Validation of Fanconi anemia complementation Group A assignment using molecular analysis.
    Moghrabi NN; Johnson MA; Yoshitomi MJ; Zhu X; Al-Dhalimy MJ; Olson SB; Grompe M; Richards CS
    Genet Med; 2009 Mar; 11(3):183-92. PubMed ID: 19367192
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Structural basis of the fanconi anemia-associated mutations within the FANCA and FANCG complex.
    Jeong E; Lee SG; Kim HS; Yang J; Shin J; Kim Y; Kim J; Schärer OD; Kim Y; Yeo JE; Kim HM; Cho Y
    Nucleic Acids Res; 2020 Apr; 48(6):3328-3342. PubMed ID: 32002546
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel Founder Mutation in
    Dimishkovska M; Kotori VM; Gucev Z; Kocheva S; Polenakovic M; Plaseska-Karanfilska D
    Balkan Med J; 2018 Jan; 35(1):108-111. PubMed ID: 29400309
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG.
    de Winter JP; van der Weel L; de Groot J; Stone S; Waisfisz Q; Arwert F; Scheper RJ; Kruyt FA; Hoatlin ME; Joenje H
    Hum Mol Genet; 2000 Nov; 9(18):2665-74. PubMed ID: 11063725
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Compromised repair of radiation-induced DNA double-strand breaks in Fanconi anemia fibroblasts in G2.
    Zahnreich S; Weber B; Rösch G; Schindler D; Schmidberger H
    DNA Repair (Amst); 2020 Dec; 96():102992. PubMed ID: 33069004
    [TBL] [Abstract][Full Text] [Related]  

  • 19. FANCA and FANCG are the major Fanconi anemia genes in the Korean population.
    Park J; Chung NG; Chae H; Kim M; Lee S; Kim Y; Lee JW; Cho B; Jeong DC; Park IY
    Clin Genet; 2013 Sep; 84(3):271-5. PubMed ID: 23067021
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.
    Faivre L; Guardiola P; Lewis C; Dokal I; Ebell W; Zatterale A; Altay C; Poole J; Stones D; Kwee ML; van Weel-Sipman M; Havenga C; Morgan N; de Winter J; Digweed M; Savoia A; Pronk J; de Ravel T; Jansen S; Joenje H; Gluckman E; Mathew CG
    Blood; 2000 Dec; 96(13):4064-70. PubMed ID: 11110674
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.