BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 28493158)

  • 21. 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]  

  • 22. Alpha-fetoprotein and Fanconi Anemia: Relevance to DNA Repair and Breast Cancer Susceptibility.
    Lakhi NA; Mizejewski GJ
    Fetal Pediatr Pathol; 2017 Feb; 36(1):49-61. PubMed ID: 27690720
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Analysis of a FANCE Splice Isoform in Regard to DNA Repair.
    Bouffard F; Plourde K; Bélanger S; Ouellette G; Labrie Y; Durocher F
    J Mol Biol; 2015 Sep; 427(19):3056-73. PubMed ID: 26277624
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study.
    Yaz I; Ozbek B; Ng YY; Cetinkaya PG; Halacli SO; Tan C; Kasikci M; Kosukcu C; Tezcan I; Cagdas D
    J Clin Immunol; 2020 Apr; 40(3):494-502. PubMed ID: 32056073
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mechanism of Ubiquitination and Deubiquitination in the Fanconi Anemia Pathway.
    van Twest S; Murphy VJ; Hodson C; Tan W; Swuec P; O'Rourke JJ; Heierhorst J; Crismani W; Deans AJ
    Mol Cell; 2017 Jan; 65(2):247-259. PubMed ID: 27986371
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The Fanconi anemia ID2 complex: dueling saxes at the crossroads.
    Boisvert RA; Howlett NG
    Cell Cycle; 2014; 13(19):2999-3015. PubMed ID: 25486561
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Thymic and bone marrow output in patients with common variable immunodeficiency.
    Serana F; Airò P; Chiarini M; Zanotti C; Scarsi M; Frassi M; Lougaris V; Plebani A; Caimi L; Imberti L
    J Clin Immunol; 2011 Aug; 31(4):540-9. PubMed ID: 21491094
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Variation in cisplatinum sensitivity is not associated with Fanconi Anemia/BRCA pathway inactivation in head and neck squamous cell carcinoma cell lines.
    Snyder ER; Ricker JL; Chen Z; Waes CV
    Cancer Lett; 2007 Jan; 245(1-2):75-80. PubMed ID: 16466850
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Update of the human and mouse Fanconi anemia genes.
    Dong H; Nebert DW; Bruford EA; Thompson DC; Joenje H; Vasiliou V
    Hum Genomics; 2015 Nov; 9():32. PubMed ID: 26596371
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A new frontier in Fanconi anemia: From DNA repair to ribosome biogenesis.
    Gueiderikh A; Maczkowiak-Chartois F; Rosselli F
    Blood Rev; 2022 Mar; 52():100904. PubMed ID: 34750031
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insights.
    Thompson LH; Hinz JM
    Mutat Res; 2009 Jul; 668(1-2):54-72. PubMed ID: 19622404
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The Fanconi anemia proteins FANCD2 and FANCJ interact and regulate each other's chromatin localization.
    Chen X; Wilson JB; McChesney P; Williams SA; Kwon Y; Longerich S; Marriott AS; Sung P; Jones NJ; Kupfer GM
    J Biol Chem; 2014 Sep; 289(37):25774-82. PubMed ID: 25070891
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [The role of the Fanconi anemia pathway in DNA repair and maintenance of genome stability].
    Koczorowska AM; Białkowska A; Kluzek K; Zdzienicka MZ
    Postepy Hig Med Dosw (Online); 2014 May; 68():459-72. PubMed ID: 24864098
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication.
    Shen X; Do H; Li Y; Chung WH; Tomasz M; de Winter JP; Xia B; Elledge SJ; Wang W; Li L
    Mol Cell; 2009 Sep; 35(5):716-23. PubMed ID: 19748364
    [TBL] [Abstract][Full Text] [Related]  

  • 36. FANCI is a second monoubiquitinated member of the Fanconi anemia pathway.
    Sims AE; Spiteri E; Sims RJ; Arita AG; Lach FP; Landers T; Wurm M; Freund M; Neveling K; Hanenberg H; Auerbach AD; Huang TT
    Nat Struct Mol Biol; 2007 Jun; 14(6):564-7. PubMed ID: 17460694
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Whole-exome sequencing identifies FANC heterozygous germline mutation as an adverse factor for immunosuppressive therapy in Chinese aplastic anemia patients aged 40 or younger: a single-center retrospective study.
    Shen Y; Liu Q; Li H; Liu W; Hu H; Zhao Y; Li Y; Chen Y; Liu S; Yu Q; Zhuang H; Wu L; Hu Z; Zheng Z; Shen J; Lin S; Shen Y; Zhou Y; Ye B; Wu D
    Ann Hematol; 2023 Mar; 102(3):503-517. PubMed ID: 36622392
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Common variable immunodeficiency classification by quantifying T-cell receptor and immunoglobulin κ-deleting recombination excision circles.
    Kamae C; Nakagawa N; Sato H; Honma K; Mitsuiki N; Ohara O; Kanegane H; Pasic S; Pan-Hammarström Q; van Zelm MC; Morio T; Imai K; Nonoyama S
    J Allergy Clin Immunol; 2013 May; 131(5):1437-40.e5. PubMed ID: 23273952
    [No Abstract]   [Full Text] [Related]  

  • 40. Genotyping of fanconi anemia patients by whole exome sequencing: advantages and challenges.
    Knies K; Schuster B; Ameziane N; Rooimans M; Bettecken T; de Winter J; Schindler D
    PLoS One; 2012; 7(12):e52648. PubMed ID: 23285130
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.