These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 27041517)

  • 21. 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]  

  • 22. Loss-of-Function FANCL Mutations Associate with Severe Fanconi Anemia Overlapping the VACTERL Association.
    Vetro A; Iascone M; Limongelli I; Ameziane N; Gana S; Della Mina E; Giussani U; Ciccone R; Forlino A; Pezzoli L; Rooimans MA; van Essen AJ; Messa J; Rizzuti T; Bianchi P; Dorsman J; de Winter JP; Lalatta F; Zuffardi O
    Hum Mutat; 2015 May; 36(5):562-8. PubMed ID: 25754594
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Whole exome sequencing reveals concomitant mutations of multiple FA genes in individual Fanconi anemia patients.
    Chang L; Yuan W; Zeng H; Zhou Q; Wei W; Zhou J; Li M; Wang X; Xu M; Yang F; Yang Y; Cheng T; Zhu X
    BMC Med Genomics; 2014 May; 7():24. PubMed ID: 24885126
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Characterization of two novel FANCG mutations in Indian Fanconi anemia patients.
    Solanki A; Kumar Selvaa C; Sheth F; Radhakrishnan N; Kalra M; Vundinti BR
    Leuk Res; 2017 Feb; 53():50-56. PubMed ID: 28024295
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Severe telomere shortening in Fanconi anemia complementation group L.
    Shah A; George M; Dhangar S; Rajendran A; Mohan S; Vundinti BR
    Mol Biol Rep; 2021 Jan; 48(1):585-593. PubMed ID: 33394227
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer.
    Mantere T; Haanpää M; Hanenberg H; Schleutker J; Kallioniemi A; Kähkönen M; Parto K; Avela K; Aittomäki K; von Koskull H; Hartikainen JM; Kosma VM; Laasanen SL; Mannermaa A; Pylkäs K; Winqvist R
    Clin Genet; 2015 Jul; 88(1):68-73. PubMed ID: 24989076
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. 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]  

  • 32. Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study.
    Auerbach AD; Greenbaum J; Pujara K; Batish SD; Bitencourt MA; Kokemohr I; Schneider H; Lobitzc S; Pasquini R; Giampietro PF; Hanenberg H; Levran O;
    Hum Mutat; 2003 Feb; 21(2):158-68. PubMed ID: 12552564
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia.
    Behera CK; Gyandeep G; Mishra R; Mohanty RP; Pal A; Behera J; Samal S; Das B
    Mol Biol Rep; 2023 Jan; 50(1):931-936. PubMed ID: 36369330
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. [Molecular basis of Fanconi's anemia].
    Digweed M
    Klin Padiatr; 1999; 211(4):192-7. PubMed ID: 10472548
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. [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]  

  • 39. Two common founder mutations of the fanconi anemia group G gene FANCG/XRCC9 in the Japanese population.
    Yagasaki H; Oda T; Adachi D; Nakajima T; Nakahata T; Asano S; Yamashita T
    Hum Mutat; 2003 May; 21(5):555. PubMed ID: 12673805
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 12.