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 *

95 related articles for article (PubMed ID: 15680406)

  • 41. Recurrent germline mutation in MSH2 arises frequently de novo.
    Desai DC; Lockman JC; Chadwick RB; Gao X; Percesepe A; Evans DG; Miyaki M; Yuen ST; Radice P; Maher ER; Wright FA; de La Chapelle A
    J Med Genet; 2000 Sep; 37(9):646-52. PubMed ID: 10978353
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Suppression of intestinal and mammary neoplasia by lifetime administration of aspirin in Apc(Min/+) and Apc(Min/+), Msh2(-/-) mice.
    Sansom OJ; Stark LA; Dunlop MG; Clarke AR
    Cancer Res; 2001 Oct; 61(19):7060-4. PubMed ID: 11585736
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A novel in frame deletion of codons 188-190 in the hMSH2 gene of a slovenian patient with hereditary non-polyposis colorectal cancer.
    Ravnik-Glavac M; Potocnik U; Kozelj M; Krizman I; Glavac D
    Hum Hered; 1998; 48(5):285-7. PubMed ID: 9748699
    [No Abstract]   [Full Text] [Related]  

  • 44. Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage.
    Nyström-Lahti M; Parsons R; Sistonen P; Pylkkänen L; Aaltonen LA; Leach FS; Hamilton SR; Watson P; Bronson E; Fusaro R
    Am J Hum Genet; 1994 Oct; 55(4):659-65. PubMed ID: 7942843
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Role of tumor marker in the presymptomatic diagnosis of hereditary malignant tumors].
    Baba S; Ando H
    Nihon Rinsho; 1996 Jun; 54(6):1597-603. PubMed ID: 8691615
    [TBL] [Abstract][Full Text] [Related]  

  • 46. New EPCAM founder deletion in Polish population.
    Dymerska D; Gołębiewska K; Kuświk M; Rudnicka H; Scott RJ; Billings R; Pławski A; Boruń P; Siołek M; Kozak-Klonowska B; Szwiec M; Kilar E; Huzarski T; Byrski T; Lubiński J; Kurzawski G
    Clin Genet; 2017 Dec; 92(6):649-653. PubMed ID: 28369810
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The nonsense mutation MSH2 c.2152C>T shows a founder effect in Portuguese Lynch syndrome families.
    Pinheiro M; Francisco I; Pinto C; Peixoto A; Veiga I; Filipe B; Santos C; Maia S; Silva J; Pinto P; Santos R; Claro I; Lage P; Lopes P; Ferreira S; Rosa I; Fonseca R; Rodrigues P; Henrique R; Chaves P; Pereira AD; Brandão C; Albuquerque C; Teixeira MR
    Genes Chromosomes Cancer; 2019 Sep; 58(9):657-664. PubMed ID: 30968502
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Founding mutations and Alu-mediated recombination in hereditary colon cancer.
    Nyström-Lahti M; Kristo P; Nicolaides NC; Chang SY; Aaltonen LA; Moisio AL; Järvinen HJ; Mecklin JP; Kinzler KW; Vogelstein B
    Nat Med; 1995 Nov; 1(11):1203-6. PubMed ID: 7584997
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Direct mutational analysis in a family with hereditary non-polyposis colorectal cancer.
    Van de Water NS; Jeevaratnam P; Browett PJ; Stewart SM; Lane MR; Jass JR
    Aust N Z J Med; 1994 Dec; 24(6):682-6. PubMed ID: 7717919
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Gene symbol: hMSH. Disease: Hereditary nonpolyposis colorectal cancer.
    Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D
    Hum Genet; 2004 Mar; 114(4):409. PubMed ID: 15046092
    [No Abstract]   [Full Text] [Related]  

  • 51. Met688Ile and Leu390Phe of the MSH2 gene are not functional mutations, but polymorphisms in Japanese individuals.
    Banno K; Susumu N; Nozawa S; Sugano K
    Cancer Genet Cytogenet; 2004 Nov; 155(1):92. PubMed ID: 15527911
    [No Abstract]   [Full Text] [Related]  

  • 52. A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer.
    Lucci-Cordisco E; Zollino M; Baglioni S; Mancuso I; Lecce R; Gurrieri F; Crucitti A; Papi L; Neri G; Genuardi M
    Clin Genet; 2005 Feb; 67(2):178-82. PubMed ID: 15679831
    [TBL] [Abstract][Full Text] [Related]  

  • 53. An Msh2 point mutation uncouples DNA mismatch repair and apoptosis.
    Lin DP; Wang Y; Scherer SJ; Clark AB; Yang K; Avdievich E; Jin B; Werling U; Parris T; Kurihara N; Umar A; Kucherlapati R; Lipkin M; Kunkel TA; Edelmann W
    Cancer Res; 2004 Jan; 64(2):517-22. PubMed ID: 14744764
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2.
    Pyatt RE; Nakagawa H; Hampel H; Sedra M; Fuchik MB; Comeras I; de la Chapelle A; Prior TW
    Clin Genet; 2003 Mar; 63(3):215-8. PubMed ID: 12694232
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Gene symbol: msh2. Disease: MSH2.
    Colombino M
    Hum Genet; 2004 Jul; 115(2):173. PubMed ID: 15300982
    [No Abstract]   [Full Text] [Related]  

  • 56. Somatic deletion events occur during early embryonic development and modify the extent of CAG expansion in subsequent generations.
    Kovtun IV; Thornhill AR; McMurray CT
    Hum Mol Genet; 2004 Dec; 13(24):3057-68. PubMed ID: 15496421
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Development of a Premature Stop Codon-detection method based on a bacterial two-hybrid system.
    Real SM; Marzese DM; Gomez LC; Mayorga LS; Roqué M
    BMC Biotechnol; 2006 Sep; 6():38. PubMed ID: 16948859
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer.
    Fishel R; Lescoe MK; Rao MR; Copeland NG; Jenkins NA; Garber J; Kane M; Kolodner R
    Cell; 1994 Apr; 77(1):1 p following 166. PubMed ID: 8156592
    [No Abstract]   [Full Text] [Related]  

  • 59. Gene symbol: msh2. Disease: MSH2.
    Colombino M
    Hum Genet; 2004 Jul; 115(2):171. PubMed ID: 15300972
    [No Abstract]   [Full Text] [Related]  

  • 60. Gene symbol: msh2. Disease: MSH2.
    Colombino M
    Hum Genet; 2004 Jul; 115(2):170. PubMed ID: 15300970
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.