BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 37799138)

  • 1. Erratum: A self-repair history: compensatory effect of a
    Frontiers Production Office
    Front Genet; 2023; 14():1293778. PubMed ID: 37799138
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A self-repair history: compensatory effect of a
    Persico I; Fontana G; Faleschini M; Zanchetta ME; Ammeti D; Cappelli E; Corsolini F; Mosa C; Guarina A; Bogliolo M; Surrallés J; Dufour C; Farruggia P; Savoia A; Bottega R
    Front Genet; 2023; 14():1209138. PubMed ID: 37547463
    [No Abstract]   [Full Text] [Related]  

  • 3. Corrigendum: Parental Somatic Mosaicism Uncovers Inheritance of an Apparently De Novo GFAP Mutation.
    Grossi A; Morelli F; Di Duca M; Caroli F; Moroni I; Tonduti D; Bachetti T; Ceccherini I
    Front Genet; 2022; 13():877443. PubMed ID: 35386286
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Natural gene therapy in monozygotic twins with Fanconi anemia.
    Mankad A; Taniguchi T; Cox B; Akkari Y; Rathbun RK; Lucas L; Bagby G; Olson S; D'Andrea A; Grompe M
    Blood; 2006 Apr; 107(8):3084-90. PubMed ID: 16397136
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.
    Waisfisz Q; Morgan NV; Savino M; de Winter JP; van Berkel CG; Hoatlin ME; Ianzano L; Gibson RA; Arwert F; Savoia A; Mathew CG; Pronk JC; Joenje H
    Nat Genet; 1999 Aug; 22(4):379-83. PubMed ID: 10431244
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.
    Gross M; Hanenberg H; Lobitz S; Friedl R; Herterich S; Dietrich R; Gruhn B; Schindler D; Hoehn H
    Cytogenet Genome Res; 2002; 98(2-3):126-35. PubMed ID: 12697994
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Phenotype reversion as "natural gene therapy" in Fanconi anemia by a gene conversion event.
    Persico I; Fiscarelli I; Pelle A; Faleschini M; Pasini B; Savoia A; Bottega R
    Front Genet; 2023; 14():1240758. PubMed ID: 37790699
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Somatic mosaicism in Fanconi anemia: evidence of genotypic reversion in lymphohematopoietic stem cells.
    Gregory JJ; Wagner JE; Verlander PC; Levran O; Batish SD; Eide CR; Steffenhagen A; Hirsch B; Auerbach AD
    Proc Natl Acad Sci U S A; 2001 Feb; 98(5):2532-7. PubMed ID: 11226273
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. 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]  

  • 15. Novel Variations of FANCA Gene Provokes Fanconi Anemia: Molecular Diagnosis in a Special Chinese Family.
    Li N; Song A; Ding L; Zhu H; Li G; Miao Y; Wang J; Li B; Chen J
    J Pediatr Hematol Oncol; 2018 Jul; 40(5):e299-e304. PubMed ID: 29702541
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of rare heterozygous missense mutations in FANCA in esophageal atresia patients using next-generation sequencing.
    Feng Y; Chen R; Da M; Qian B; Mo X
    Gene; 2018 Jun; 661():182-188. PubMed ID: 29621589
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A synonymous variant contributes to a rare Wiedemann-Rautenstrauch syndrome complicated with mild anemia
    Peng Q; Zhang Y; Xian B; Wu L; Ding J; Ding W; Zhang X; Ding B; Li D; Wu J; Hu X; Lu G
    Front Mol Neurosci; 2022; 15():1026530. PubMed ID: 36385762
    [TBL] [Abstract][Full Text] [Related]  

  • 18. De novo pathogenic germline variant in PALB2 in a patient with pancreatic cancer.
    Bernstein Molho R; Zalmanoviz S; Laitman Y; Friedman E
    Fam Cancer; 2020 Apr; 19(2):193-196. PubMed ID: 31858328
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey.
    Toksoy G; Uludağ Alkaya D; Bagirova G; Avcı Ş; Aghayev A; Günes N; Altunoğlu U; Alanay Y; Başaran S; Berkay EG; Karaman B; Celkan TT; Apak H; Kayserili H; Tüysüz B; Uyguner ZO
    Mol Syndromol; 2020 Nov; 11(4):183-196. PubMed ID: 33224012
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.