BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

328 related articles for article (PubMed ID: 31033087)

  • 21. ATM: the protein encoded by the gene mutated in the radiosensitive syndrome ataxia-telangiectasia.
    Lavin MF; Khanna KK
    Int J Radiat Biol; 1999 Oct; 75(10):1201-14. PubMed ID: 10549596
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ataxia-telangiectasia: A review of clinical features and molecular pathology.
    Amirifar P; Ranjouri MR; Yazdani R; Abolhassani H; Aghamohammadi A
    Pediatr Allergy Immunol; 2019 May; 30(3):277-288. PubMed ID: 30685876
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A Rare Case of Ataxia-Telangiectasia-Like Disorder With
    Mahale RR; Reddy N; Mathuranth P; Mailankody P; Padmanabha H; Retnaswami CS
    J Pediatr Neurosci; 2020; 15(3):283-285. PubMed ID: 33531947
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template.
    Williams RS; Williams JS; Tainer JA
    Biochem Cell Biol; 2007 Aug; 85(4):509-20. PubMed ID: 17713585
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATM.
    Schröder S; Wieland B; Ohlenbusch A; Yigit G; Altmüller J; Boltshauser E; Dörk T; Brockmann K
    Am J Med Genet A; 2020 Dec; 182(12):2971-2975. PubMed ID: 32918381
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Severe reaction to radiotherapy provoked by hypomorphic germline mutations in ATM (ataxia-telangiectasia mutated gene).
    Asadollahi R; Britschgi C; Joset P; Oneda B; Schindler D; Meier UR; Rauch A
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1409. PubMed ID: 32748564
    [TBL] [Abstract][Full Text] [Related]  

  • 27. ATM and the Mre11 complex combine to recognize and signal DNA double-strand breaks.
    Lavin MF
    Oncogene; 2007 Dec; 26(56):7749-58. PubMed ID: 18066087
    [TBL] [Abstract][Full Text] [Related]  

  • 28. ATM directs DNA damage responses and proteostasis via genetically separable pathways.
    Lee JH; Mand MR; Kao CH; Zhou Y; Ryu SW; Richards AL; Coon JJ; Paull TT
    Sci Signal; 2018 Jan; 11(512):. PubMed ID: 29317520
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Double-strand breaks in ribosomal RNA genes activate a distinct signaling and chromatin response to facilitate nucleolar restructuring and repair.
    Korsholm LM; Gál Z; Lin L; Quevedo O; Ahmad DA; Dulina E; Luo Y; Bartek J; Larsen DH
    Nucleic Acids Res; 2019 Sep; 47(15):8019-8035. PubMed ID: 31184714
    [TBL] [Abstract][Full Text] [Related]  

  • 30. DNA repair functional analyses of NBN hypomorphic variants associated with NBN-related infertility.
    Fiévet A; Bellanger D; Zahed L; Burglen L; Derrien AC; Dubois d'Enghien C; Lespinasse J; Parfait B; Pedespan JM; Rieunier G; Stoppa-Lyonnet D; Stern MH
    Hum Mutat; 2020 Mar; 41(3):608-618. PubMed ID: 31729086
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The carboxy terminus of NBS1 is required for induction of apoptosis by the MRE11 complex.
    Stracker TH; Morales M; Couto SS; Hussein H; Petrini JH
    Nature; 2007 May; 447(7141):218-21. PubMed ID: 17429352
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The ATM signaling cascade promotes recombination-dependent pachytene arrest in mouse spermatocytes.
    Pacheco S; Marcet-Ortega M; Lange J; Jasin M; Keeney S; Roig I
    PLoS Genet; 2015 Mar; 11(3):e1005017. PubMed ID: 25768017
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genotype-phenotype correlations in ataxia telangiectasia patients with
    van Os NJH; Chessa L; Weemaes CMR; van Deuren M; Fiévet A; van Gaalen J; Mahlaoui N; Roeleveld N; Schrader C; Schindler D; Taylor AMR; Van de Warrenburg BPC; Dörk T; Willemsen MAAP
    J Med Genet; 2019 May; 56(5):308-316. PubMed ID: 30819809
    [TBL] [Abstract][Full Text] [Related]  

  • 34.
    Mi Y; Gurumurthy RK; Zadora PK; Meyer TF; Chumduri C
    mBio; 2018 Nov; 9(6):. PubMed ID: 30401777
    [TBL] [Abstract][Full Text] [Related]  

  • 35. FXR1 is a novel MRE11-binding partner and participates in oxidative stress responses.
    Qi F; Meng Q; Hayashi I; Kobayashi J
    J Radiat Res; 2020 May; 61(3):368-375. PubMed ID: 32211858
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Reduced levels of MRE11 cause disease phenotypes distinct from ataxia telangiectasia-like disorder.
    Hartlerode AJ; Mostafa AM; Orban SK; Benedeck R; Campbell K; Hoenerhoff MJ; Ferguson DO; Sekiguchi JM
    Hum Mol Genet; 2024 Jun; ():. PubMed ID: 38888340
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A murine model of Nijmegen breakage syndrome.
    Williams BR; Mirzoeva OK; Morgan WF; Lin J; Dunnick W; Petrini JH
    Curr Biol; 2002 Apr; 12(8):648-53. PubMed ID: 11967151
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mre11 assembles linear DNA fragments into DNA damage signaling complexes.
    Costanzo V; Paull T; Gottesman M; Gautier J
    PLoS Biol; 2004 May; 2(5):E110. PubMed ID: 15138496
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular basis of ataxia telangiectasia and related diseases.
    Ball LG; Xiao W
    Acta Pharmacol Sin; 2005 Aug; 26(8):897-907. PubMed ID: 16038621
    [TBL] [Abstract][Full Text] [Related]  

  • 40. An essential function for NBS1 in the prevention of ataxia and cerebellar defects.
    Frappart PO; Tong WM; Demuth I; Radovanovic I; Herceg Z; Aguzzi A; Digweed M; Wang ZQ
    Nat Med; 2005 May; 11(5):538-44. PubMed ID: 15821748
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.