BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 24584348)

  • 1. Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.
    De Rocco D; Bottega R; Cappelli E; Cavani S; Criscuolo M; Nicchia E; Corsolini F; Greco C; Borriello A; Svahn J; Pillon M; Mecucci C; Casazza G; Verzegnassi F; Cugno C; Locasciulli A; Farruggia P; Longoni D; Ramenghi U; Barberi W; Tucci F; Perrotta S; Grammatico P; Hanenberg H; Della Ragione F; Dufour C; Savoia A;
    Haematologica; 2014 Jun; 99(6):1022-31. PubMed ID: 24584348
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients.
    Mori M; Hira A; Yoshida K; Muramatsu H; Okuno Y; Shiraishi Y; Anmae M; Yasuda J; Tadaka S; Kinoshita K; Osumi T; Noguchi Y; Adachi S; Kobayashi R; Kawabata H; Imai K; Morio T; Tamura K; Takaori-Kondo A; Yamamoto M; Miyano S; Kojima S; Ito E; Ogawa S; Matsuo K; Yabe H; Yabe M; Takata M
    Haematologica; 2019 Oct; 104(10):1962-1973. PubMed ID: 30792206
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
    Chandrasekharappa SC; Lach FP; Kimble DC; Kamat A; Teer JK; Donovan FX; Flynn E; Sen SK; Thongthip S; Sanborn E; Smogorzewska A; Auerbach AD; Ostrander EA;
    Blood; 2013 May; 121(22):e138-48. PubMed ID: 23613520
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comprehensive analysis of pathogenic deletion variants in Fanconi anemia genes.
    Flynn EK; Kamat A; Lach FP; Donovan FX; Kimble DC; Narisu N; Sanborn E; Boulad F; Davies SM; Gillio AP; Harris RE; MacMillan ML; Wagner JE; Smogorzewska A; Auerbach AD; Ostrander EA; Chandrasekharappa SC
    Hum Mutat; 2014 Nov; 35(11):1342-53. PubMed ID: 25168418
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evaluation of Fanconi Anemia genes in familial breast cancer predisposition.
    Seal S; Barfoot R; Jayatilake H; Smith P; Renwick A; Bascombe L; McGuffog L; Evans DG; Eccles D; Easton DF; Stratton MR; Rahman N;
    Cancer Res; 2003 Dec; 63(24):8596-9. PubMed ID: 14695169
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects.
    George M; Solanki A; Chavan N; Rajendran A; Raj R; Mohan S; Nemani S; Kanvinde S; Munirathnam D; Rao S; Radhakrishnan N; Lashkari HP; Ghildhiyal RG; Manglani M; Shanmukhaiah C; Bhat S; Ramesh S; Cherian A; Junagade P; Vundinti BR
    Hum Mutat; 2021 Dec; 42(12):1648-1665. PubMed ID: 34585473
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of clinical severity with FANCB variant type in Fanconi anemia.
    Jung M; Ramanagoudr-Bhojappa R; van Twest S; Rosti RO; Murphy V; Tan W; Donovan FX; Lach FP; Kimble DC; Jiang CS; Vaughan R; Mehta PA; Pierri F; Dufour C; Auerbach AD; Deans AJ; Smogorzewska A; Chandrasekharappa SC
    Blood; 2020 Apr; 135(18):1588-1602. PubMed ID: 32106311
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence for subcomplexes in the Fanconi anemia pathway.
    Medhurst AL; Laghmani el H; Steltenpool J; Ferrer M; Fontaine C; de Groot J; Rooimans MA; Scheper RJ; Meetei AR; Wang W; Joenje H; de Winter JP
    Blood; 2006 Sep; 108(6):2072-80. PubMed ID: 16720839
    [TBL] [Abstract][Full Text] [Related]  

  • 9. In silico study of missense variants of FANCA, FANCC and FANCG genes reveals high risk deleterious alleles predisposing to Fanconi anemia pathogenesis.
    Shahid M; Azfaralariff A; Zubair M; Abdulkareem Najm A; Khalili N; Law D; Firasat S; Fazry S
    Gene; 2022 Feb; 812():146104. PubMed ID: 34864095
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant.
    Savino M; Borriello A; D'Apolito M; Criscuolo M; Del Vecchio M; Bianco AM; Di Perna M; Calzone R; Nobili B; Zatterale A; Zelante L; Joenje H; Della Ragione F; Savoia A
    Hum Mutat; 2003 Oct; 22(4):338-9. PubMed ID: 12955722
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
    Ameziane N; Errami A; Léveillé F; Fontaine C; de Vries Y; van Spaendonk RM; de Winter JP; Pals G; Joenje H
    Hum Mutat; 2008 Jan; 29(1):159-66. PubMed ID: 17924555
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.
    Bouchlaka C; Abdelhak S; Amouri A; Ben Abid H; Hadiji S; Frikha M; Ben Othman T; Amri F; Ayadi H; Hachicha M; Rebaï A; Saad A; Dellagi K;
    J Hum Genet; 2003; 48(7):352-61. PubMed ID: 12827451
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype.
    Asur RS; Kimble DC; Lach FP; Jung M; Donovan FX; Kamat A; Noonan RJ; Thomas JW; Park M; Chines P; Vlachos A; Auerbach AD; Smogorzewska A; Chandrasekharappa SC
    Mol Genet Genomic Med; 2018 Jan; 6(1):77-91. PubMed ID: 29193904
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems.
    Gordon SM; Buchwald M
    Blood; 2003 Jul; 102(1):136-41. PubMed ID: 12649160
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia.
    Doubaj Y; Zrhidri A; Elalaoui SC; Lyahyai J; El Kadiri Y; Elkassimi N; Sbiti A; El Kababri M; Hessissen L; Sefiani A
    Pan Afr Med J; 2021; 39():72. PubMed ID: 34422195
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
    Levran O; Diotti R; Pujara K; Batish SD; Hanenberg H; Auerbach AD
    Hum Mutat; 2005 Feb; 25(2):142-9. PubMed ID: 15643609
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The molecular biology of Fanconi anemia.
    Tamary H; Bar-Yam R; Zemach M; Dgany O; Shalmon L; Yaniv I
    Isr Med Assoc J; 2002 Oct; 4(10):819-23. PubMed ID: 12389351
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Profiling Fanconi Anemia Gene Mutations among Iranian Patients.
    Esmail Nia G; Fadaee M; Royer R; Najmabadi H; Akbari MR
    Arch Iran Med; 2016 Apr; 19(4):236-40. PubMed ID: 27041517
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.