BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 9207444)

  • 21. Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype.
    Kalb R; Neveling K; Hoehn H; Schneider H; Linka Y; Batish SD; Hunt C; Berwick M; Callen E; Surralles J; Casado JA; Bueren J; Dasi A; Soulier J; Gluckman E; Zwaan CM; van Spaendonk R; Pals G; de Winter JP; Joenje H; Grompe M; Auerbach AD; Hanenberg H; Schindler D
    Am J Hum Genet; 2007 May; 80(5):895-910. PubMed ID: 17436244
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Sequence variation in the Fanconi anemia gene FAA.
    Levran O; Erlich T; Magdalena N; Gregory JJ; Batish SD; Verlander PC; Auerbach AD
    Proc Natl Acad Sci U S A; 1997 Nov; 94(24):13051-6. PubMed ID: 9371798
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report].
    Puchmajerová A; Švojgr K; Novotná D; Macháčková E; Sumerauer D; Smíšek P; Kodet R; Kynčl M; Křepelová A; Foretová L
    Klin Onkol; 2016; 29 Suppl 1():S89-92. PubMed ID: 26691948
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.
    Tamary H; Dgany O; Toledano H; Shalev Z; Krasnov T; Shalmon L; Schechter T; Bercovich D; Attias D; Laor R; Koren A; Yaniv I
    Eur J Haematol; 2004 May; 72(5):330-5. PubMed ID: 15059067
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel homozygous FANCL mutation and somatic heterozygous SETBP1 mutation in a Chinese girl with Fanconi Anemia.
    Wu W; Liu Y; Zhou Q; Wang Q; Luo F; Xu Z; Geng Q; Li P; Zhang HZ; Xie J
    Eur J Med Genet; 2017 Jul; 60(7):369-373. PubMed ID: 28419882
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Frequency of Fanconi anemia in Brazil and efficacy of screening for the FANCA 3788-3790del mutation.
    Magdalena N; Pilonetto DV; Bitencourt MA; Pereira NF; Ribeiro RC; Jeng M; Pasquini R
    Braz J Med Biol Res; 2005 May; 38(5):669-73. PubMed ID: 15917947
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations.
    Dokal I; Chase A; Morgan NV; Coulthard S; Hall G; Mathew CG; Roberts I
    Br J Haematol; 1996 Jun; 93(4):813-6. PubMed ID: 8703809
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Intermediate DNA repair activity associated with the 322delG allele of the fanconi anemia complementation group C gene.
    Donahue SL; Lundberg R; Campbell C
    J Mol Biol; 2004 Oct; 342(5):1443-55. PubMed ID: 15364573
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Inactivation of the Fanconi anemia group C gene augments interferon-gamma-induced apoptotic responses in hematopoietic cells.
    Rathbun RK; Faulkner GR; Ostroski MH; Christianson TA; Hughes G; Jones G; Cahn R; Maziarz R; Royle G; Keeble W; Heinrich MC; Grompe M; Tower PA; Bagby GC
    Blood; 1997 Aug; 90(3):974-85. PubMed ID: 9242526
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes.
    Yamashita T; Nakahata T
    Int J Hematol; 2001 Jul; 74(1):33-41. PubMed ID: 11530803
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Fanconi anemia and leukemia: tracking the genes.
    Auerbach AD
    Leukemia; 1992; 6 Suppl 1():1-4. PubMed ID: 1548931
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The Fanconi anemia complementation group C gene (FAC) suppresses transformation of mutant fibroblasts by the SV40 virus.
    Liu JM; Poiley J; Devetten M; Kajigaya S; Walsh CE
    Biochem Biophys Res Commun; 1996 Jun; 223(3):685-90. PubMed ID: 8687457
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fanconi anemia: causes and consequences of genetic instability.
    Kalb R; Neveling K; Nanda I; Schindler D; Hoehn H
    Genome Dyn; 2006; 1():218-242. PubMed ID: 18724063
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Complementation group assignments in Fanconi anemia fibroblast cell lines from North America.
    Jakobs PM; Fiddler-Odell E; Reifsteck C; Olson S; Moses RE; Grompe M
    Somat Cell Mol Genet; 1997 Jan; 23(1):1-7. PubMed ID: 9217996
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Developmental expression of the Fac gene correlates with congenital defects in Fanconi anemia patients.
    Krasnoshtein F; Buchwald M
    Hum Mol Genet; 1996 Jan; 5(1):85-93. PubMed ID: 8789444
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Fanconi anemia group A and C double-mutant mice: functional evidence for a multi-protein Fanconi anemia complex.
    Noll M; Battaile KP; Bateman R; Lax TP; Rathbun K; Reifsteck C; Bagby G; Finegold M; Olson S; Grompe M
    Exp Hematol; 2002 Jul; 30(7):679-88. PubMed ID: 12135664
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Retroviral gene transfer for the assignment of Fanconi anemia (FA) patients to a FA complementation group.
    Fu KL; Thuss PC; Fujino T; Digweed M; Liu JM; Walsh CE
    Hum Genet; 1998 Feb; 102(2):166-9. PubMed ID: 9521584
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel mutations of the FANCG gene causing alternative splicing in Japanese Fanconi anemia.
    Yamada T; Tachibana A; Shimizu T; Mugishima H; Okubo M; Sasaki MS
    J Hum Genet; 2000; 45(3):159-66. PubMed ID: 10807541
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2.
    Kupfer GM; Yamashita T; Naf D; Suliman A; Asano S; D'Andrea AD
    Blood; 1997 Aug; 90(3):1047-54. PubMed ID: 9242535
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.