BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

257 related articles for article (PubMed ID: 24356203)

  • 1. Fanconi anemia founder mutation in Macedonian patients.
    Madjunkova S; Kocheva SA; Plaseska-Karanfilska D
    Acta Haematol; 2014; 132(1):15-21. PubMed ID: 24356203
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. [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]  

  • 6. A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain.
    Callén E; Casado JA; Tischkowitz MD; Bueren JA; Creus A; Marcos R; Dasí A; Estella JM; Muñoz A; Ortega JJ; de Winter J; Joenje H; Schindler D; Hanenberg H; Hodgson SV; Mathew CG; Surrallés J
    Blood; 2005 Mar; 105(5):1946-9. PubMed ID: 15522956
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Investigation of FANCA mutations in Greek patients.
    Selenti N; Sofocleous C; Kattamis A; Kolialexi A; Kitsiou S; Fryssira E; Polychronopoulou S; Kanavakis E; Mavrou A
    Anticancer Res; 2013 Aug; 33(8):3369-74. PubMed ID: 23898106
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Quantitative PCR analysis reveals a high incidence of large intragenic deletions in the FANCA gene in Spanish Fanconi anemia patients.
    Callén E; Tischkowitz MD; Creus A; Marcos R; Bueren JA; Casado JA; Mathew CG; Surrallés J
    Cytogenet Genome Res; 2004; 104(1-4):341-5. PubMed ID: 15162062
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Construction of FANCA mutant protein from Fanconi anemia patient and analysis of its function].
    Chen F; Zhang KJ; Zuo XL; Zeng XC
    Zhonghua Xue Ye Xue Za Zhi; 2007 Nov; 28(11):741-4. PubMed ID: 18457264
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Screening of the FANCA gene mutational hotspots in the Pakistani fanconi anemia patients revealed 19 sequence variations.
    Shahid M; Firasat S; Satti HS; Satti TM; Ghafoor T; Sharif I; Afshan K
    Congenit Anom (Kyoto); 2020 Jan; 60(1):32-39. PubMed ID: 30809872
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Identification of a novel large intragenic deletion in a family with Fanconi anemia: first molecular report from India and review of literature.
    Shukla P; Rao A; Ghosh K; Vundinti BR
    Gene; 2013 Apr; 518(2):470-5. PubMed ID: 23370339
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence for complete epistasis of null mutations in murine Fanconi anemia genes Fanca and Fancg.
    van de Vrugt HJ; Koomen M; Bakker S; Berns MA; Cheng NC; van der Valk MA; de Vries Y; Rooimans MA; Oostra AB; Hoatlin ME; Te Riele H; Joenje H; Arwert F
    DNA Repair (Amst); 2011 Dec; 10(12):1252-61. PubMed ID: 22036606
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The FANCA gene in Japanese Fanconi anemia: reports of eight novel mutations and analysis of sequence variability.
    Tachibana A; Kato T; Ejima Y; Yamada T; Shimizu T; Yang L; Tsunematsu Y; Sasaki MS
    Hum Mutat; 1999; 13(3):237-44. PubMed ID: 10090479
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Molecular defects identified by whole exome sequencing in a child with Fanconi anemia.
    Zheng Z; Geng J; Yao RE; Li C; Ying D; Shen Y; Ying L; Yu Y; Fu Q
    Gene; 2013 Nov; 530(2):295-300. PubMed ID: 23973728
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case report and literature review of Fanconi Anemia (FA) diagnosed by genetic testing.
    Solomon PJ; Margaret P; Rajendran R; Ramalingam R; Menezes GA; Shirley AS; Lee SJ; Seong MW; Park SS; Seol D; Seo SH
    Ital J Pediatr; 2015 May; 41():38. PubMed ID: 25953249
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.