BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

53 related articles for article (PubMed ID: 18273873)

  • 1. Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome.
    Ingham D; Diggle CP; Berry I; Bristow CA; Hayward BE; Rahman N; Markham AF; Sheridan EG; Bonthron DT; Carr IM
    Hum Mutat; 2013 Jun; 34(6):847-52. PubMed ID: 23483711
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Constitutional Mismatch Repair Deficiency Syndromes, a Neurofibromatosis 1 Mimicker That Hinders Timely Management.
    Mir A; AlMudhry M; AlOtaibi W; AlHazmi R; AlBaradie R; AlHarbi Q; Bashir S; Chamdine O; Housawi Y
    J Pediatr Hematol Oncol; 2023 Jul; 45(5):e613-e620. PubMed ID: 36897649
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2.
    Narayanan L; Fritzell JA; Baker SM; Liskay RM; Glazer PM
    Proc Natl Acad Sci U S A; 1997 Apr; 94(7):3122-7. PubMed ID: 9096356
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA mismatch repair: molecular mechanism, cancer, and ageing.
    Hsieh P; Yamane K
    Mech Ageing Dev; 2008; 129(7-8):391-407. PubMed ID: 18406444
    [TBL] [Abstract][Full Text] [Related]  

  • 5.
    Budair FM
    Clin Cosmet Investig Dermatol; 2024; 17():713-716. PubMed ID: 38524391
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Integrated analysis of unclassified variants in mismatch repair genes.
    Pastrello C; Pin E; Marroni F; Bedin C; Fornasarig M; Tibiletti MG; Oliani C; Ponz de Leon M; Urso ED; Della Puppa L; Agostini M; Viel A
    Genet Med; 2011 Feb; 13(2):115-24. PubMed ID: 21239990
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pitfalls in molecular analysis for mismatch repair deficiency in a family with biallelic pms2 germline mutations.
    Leenen CH; Geurts-Giele WR; Dubbink HJ; Reddingius R; van den Ouweland AM; Tops CM; van de Klift HM; Kuipers EJ; van Leerdam ME; Dinjens WN; Wagner A
    Clin Genet; 2011 Dec; 80(6):558-65. PubMed ID: 21204794
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium.
    Aronson M; Gallinger S; Cohen Z; Cohen S; Dvir R; Elhasid R; Baris HN; Kariv R; Druker H; Chan H; Ling SC; Kortan P; Holter S; Semotiuk K; Malkin D; Farah R; Sayad A; Heald B; Kalady MF; Penney LS; Rideout AL; Rashid M; Hasadsri L; Pichurin P; Riegert-Johnson D; Campbell B; Bakry D; Al-Rimawi H; Alharbi QK; Alharbi M; Shamvil A; Tabori U; Durno C
    Am J Gastroenterol; 2016 Feb; 111(2):275-84. PubMed ID: 26729549
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PMS2 monoallelic mutation carriers: the known unknown.
    Goodenberger ML; Thomas BC; Riegert-Johnson D; Boland CR; Plon SE; Clendenning M; Win AK; Senter L; Lipkin SM; Stadler ZK; Macrae FA; Lynch HT; Weitzel JN; de la Chapelle A; Syngal S; Lynch P; Parry S; Jenkins MA; Gallinger S; Holter S; Aronson M; Newcomb PA; Burnett T; Le Marchand L; Pichurin P; Hampel H; Terdiman JP; Lu KH; Thibodeau S; Lindor NM
    Genet Med; 2016 Jan; 18(1):13-9. PubMed ID: 25856668
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recurrent and founder mutations in the PMS2 gene.
    Tomsic J; Senter L; Liyanarachchi S; Clendenning M; Vaughn CP; Jenkins MA; Hopper JL; Young J; Samowitz W; de la Chapelle A
    Clin Genet; 2013 Mar; 83(3):238-43. PubMed ID: 22577899
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome.
    Giunti L; Cetica V; Ricci U; Giglio S; Sardi I; Paglierani M; Andreucci E; Sanzo M; Forni M; Buccoliero AM; Genitori L; Genuardi M
    Eur J Hum Genet; 2009 Jul; 17(7):919-27. PubMed ID: 19156169
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?
    Wimmer K; Etzler J
    Hum Genet; 2008 Sep; 124(2):105-22. PubMed ID: 18709565
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
    Senter L; Clendenning M; Sotamaa K; Hampel H; Green J; Potter JD; Lindblom A; Lagerstedt K; Thibodeau SN; Lindor NM; Young J; Winship I; Dowty JG; White DM; Hopper JL; Baglietto L; Jenkins MA; de la Chapelle A
    Gastroenterology; 2008 Aug; 135(2):419-28. PubMed ID: 18602922
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Café-au-lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2.
    Jackson CC; Holter S; Pollett A; Clendenning M; Chou S; Senter L; Ramphal R; Gallinger S; Boycott K
    Pediatr Blood Cancer; 2008 Jun; 50(6):1268-70. PubMed ID: 18273873
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity.
    Baris HN; Barnes-Kedar I; Toledano H; Halpern M; Hershkovitz D; Lossos A; Lerer I; Peretz T; Kariv R; Cohen S; Half EE; Magal N; Drasinover V; Wimmer K; Goldberg Y; Bercovich D; Levi Z
    Pediatr Blood Cancer; 2016 Mar; 63(3):418-27. PubMed ID: 26544533
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1.
    Krüger S; Kinzel M; Walldorf C; Gottschling S; Bier A; Tinschert S; von Stackelberg A; Henn W; Görgens H; Boue S; Kölble K; Büttner R; Schackert HK
    Eur J Hum Genet; 2008 Jan; 16(1):62-72. PubMed ID: 17851451
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotype associated with recessively inherited mutations in DNA mismatch repair (MMR) genes.
    de Vos M; Hayward B; Bonthron DT; Sheridan E
    Biochem Soc Trans; 2005 Aug; 33(Pt 4):718-20. PubMed ID: 16042583
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Biallelic PMS2 mutations and a distinctive childhood cancer syndrome.
    Tan TY; Orme LM; Lynch E; Croxford MA; Dow C; Dewan PA; Lipton L
    J Pediatr Hematol Oncol; 2008 Mar; 30(3):254-7. PubMed ID: 18376293
    [TBL] [Abstract][Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.