130 related articles for article (PubMed ID: 8199593)
1. Exhaustive analysis of the P53 gene coding sequence by denaturing gradient gel electrophoresis: application to the detection of point mutations in acute leukemias.
Pignon JM; Vinatier I; Fanen P; Jonveaux P; Tournilhac O; Imbert M; Rochant H; Goossens M
Hum Mutat; 1994; 3(2):126-32. PubMed ID: 8199593
[TBL] [Abstract][Full Text] [Related]
2. Mechanisms of relapse in acute leukaemia: involvement of p53 mutated subclones in disease progression in acute lymphoblastic leukaemia.
Zhu YM; Foroni L; McQuaker IG; Papaioannou M; Haynes A; Russell HH
Br J Cancer; 1999 Mar; 79(7-8):1151-7. PubMed ID: 10098750
[TBL] [Abstract][Full Text] [Related]
3. Single-step DGGE-based mutation scanning of the p53 gene: application to genetic diagnosis of colorectal cancer.
Guldberg P; Nedergaard T; Nielsen HJ; Olsen AC; Ahrenkiel V; Zeuthen J
Hum Mutat; 1997; 9(4):348-55. PubMed ID: 9101296
[TBL] [Abstract][Full Text] [Related]
4. Efficient screening of p53 mutations by denaturing gradient gel electrophoresis in colorectal tumors.
Hamelin R; Jego N; Laurent-Puig P; Vidaud M; Thomas G
Oncogene; 1993 Aug; 8(8):2213-20. PubMed ID: 8336944
[TBL] [Abstract][Full Text] [Related]
5. Relative efficiency of denaturing gradient gel electrophoresis and single strand conformation polymorphism in the detection of mutations in exons 5 to 8 of the p53 gene.
Moyret C; Theillet C; Puig PL; Molés JP; Thomas G; Hamelin R
Oncogene; 1994 Jun; 9(6):1739-43. PubMed ID: 8183571
[TBL] [Abstract][Full Text] [Related]
6. Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene.
Laprise SL; Mak EK; Killoran KA; Layman LC; Gray MR
Hum Mutat; 1998; 12(6):393-402. PubMed ID: 9829908
[TBL] [Abstract][Full Text] [Related]
7. Detection of p53 mutations in hematological malignancies: comparison between immunocytochemistry and DNA analysis.
Lepelley P; Preudhomme C; Vanrumbeke M; Quesnel B; Cosson A; Fenaux P
Leukemia; 1994 Aug; 8(8):1342-9. PubMed ID: 8057671
[TBL] [Abstract][Full Text] [Related]
8. Incidence of p53 and ras gene mutations in DMBA-induced rat leukemias.
Wei S; Kito K; Miyoshi A; Matsumoto S; Kauzi A; Aramoto T; Abe Y; Ueda N
J Exp Clin Cancer Res; 2002 Sep; 21(3):389-96. PubMed ID: 12385583
[TBL] [Abstract][Full Text] [Related]
9. A directed search for mutations in hemophilia A using restriction enzyme analysis and denaturing gradient gel electrophoresis. A study of seven exons in the factor VIII gene of 170 cases.
Lavergne JM; Bahnak BR; Vidaud M; Laurian Y; Meyer D
Nouv Rev Fr Hematol (1978); 1992; 34(1):85-91. PubMed ID: 1523102
[TBL] [Abstract][Full Text] [Related]
10. p53 gene mutations and loss of a chromosome 17p in Philadelphia chromosome (Ph1)-positive acute leukemia.
Nakai H; Misawa S; Tanaka S; Nishigaki H; Taniwaki M; Yokota S; Horiike S; Takashima T; Seriu T; Nakagawa H
Leukemia; 1993 Oct; 7(10):1547-51. PubMed ID: 8412316
[TBL] [Abstract][Full Text] [Related]
11. Detection of p53 point mutations in primary human vulvar cancer by PCR and temperature gradient gel electrophoresis.
Sliutz G; Schmidt W; Tempfer C; Speiser P; Gitsch G; Eder S; Schneeberger C; Kainz C; Zeillinger R
Gynecol Oncol; 1997 Jan; 64(1):93-8. PubMed ID: 8995554
[TBL] [Abstract][Full Text] [Related]
12. Mutation detection by denaturing gradient gel electrophoresis (DGGE).
Fodde R; Losekoot M
Hum Mutat; 1994; 3(2):83-94. PubMed ID: 8199599
[TBL] [Abstract][Full Text] [Related]
13. Analysis of mutations of neurofibromatosis type 1 gene and N-ras gene in acute myelogenous leukemia.
Lee YY; Kim WS; Bang YJ; Jung CW; Park S; Yoon WJ; Cho KS; Kim IS; Jung TJ; Choi IY
Stem Cells; 1995 Sep; 13(5):556-63. PubMed ID: 8528106
[TBL] [Abstract][Full Text] [Related]
14. Development of standard reference materials for diagnosis of p53 mutations: analysis by slab gel single strand conformation polymorphism.
O'Connell CD; Tian J; Juhasz A; Wenz HM; Atha DH
Electrophoresis; 1998 Feb; 19(2):164-71. PubMed ID: 9548275
[TBL] [Abstract][Full Text] [Related]
15. Detection of p53 gene mutations in human leukemia by PCR-SSCP analysis and direct nucleotide sequencing.
Wang R; Yu Z; Gu J; Li D; Wang M; Cao Y
Chin Med J (Engl); 1998 Apr; 111(4):339-42. PubMed ID: 10374399
[TBL] [Abstract][Full Text] [Related]
16. Abnormalities of the P53, MDM2, BCL2 and BAX genes in acute leukemias.
Wojcik I; Szybka M; Golanska E; Rieske P; Blonski JZ; Robak T; Bartkowiak J
Neoplasma; 2005; 52(4):318-24. PubMed ID: 16059649
[TBL] [Abstract][Full Text] [Related]
17. Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemia.
Felix CA; Nau MM; Takahashi T; Mitsudomi T; Chiba I; Poplack DG; Reaman GH; Cole DE; Letterio JJ; Whang-Peng J
J Clin Invest; 1992 Feb; 89(2):640-7. PubMed ID: 1737852
[TBL] [Abstract][Full Text] [Related]
18. Infrequent mutations in the P53 gene in primary human T-cell acute lymphoblastic leukemia.
Jonveaux P; Berger R
Leukemia; 1991 Oct; 5(10):839-40. PubMed ID: 1961018
[TBL] [Abstract][Full Text] [Related]
19. Scanning method to establish the molecular basis of protein C deficiencies.
Gandrille S; Goossens M; Aiach M
Hum Mutat; 1994; 4(1):20-30. PubMed ID: 7951255
[TBL] [Abstract][Full Text] [Related]
20. [Alterations of the p53 gene and clinical features in childhood acute lymphoblastic leukemia].
Kawamua M; Hayashi Y; Bessho F; Yanagisawa M; Hanada R; Yamamoto K; Horibe K; Hongo T; Ueda K
Rinsho Ketsueki; 1997 Sep; 38(9):719-26. PubMed ID: 9364861
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
