120 related articles for article (PubMed ID: 2564852)
1. Nonrandom X chromosome DNA methylation patterns in hemophiliac females.
Nisen PD; Waber PG
J Clin Invest; 1989 Apr; 83(4):1400-3. PubMed ID: 2564852
[TBL] [Abstract][Full Text] [Related]
2. Clonal analysis using recombinant DNA probes from the X-chromosome.
Vogelstein B; Fearon ER; Hamilton SR; Preisinger AC; Willard HF; Michelson AM; Riggs AD; Orkin SH
Cancer Res; 1987 Sep; 47(18):4806-13. PubMed ID: 2887283
[TBL] [Abstract][Full Text] [Related]
3. Investigation of methylation at Hha I sites using the hypervariable probe M27 beta allows improved clonal analysis in myeloid leukaemia and demonstrates differences in methylation between leukaemic and remission samples.
Gale RE; Linch DC
Leukemia; 1994 Jan; 8(1):190-4. PubMed ID: 8289487
[TBL] [Abstract][Full Text] [Related]
4. The CpG island in intron 22 of the factor VIII gene is predominantly methylated on the X chromosome of human males.
De Brasi CD; Bowen DJ; Collins PW; Larripa IB
J Hum Genet; 2002; 47(5):239-42. PubMed ID: 12032591
[TBL] [Abstract][Full Text] [Related]
5. Molecular genetic approach to the analysis of clonal proliferation in hematologic disorders.
Morita K; Tsukamoto N; Karasawa M; Omine M
Nihon Ketsueki Gakkai Zasshi; 1989 Dec; 52(8):1414-22. PubMed ID: 2576494
[TBL] [Abstract][Full Text] [Related]
6. Clonal nature of Philadelphia chromosome-positive and -negative chronic myelogenous leukemia by DNA hybridization analyses.
Yoffe G; Chinault AC; Talpaz M; Blick MB; Kantarjian HM; Taylor K; Spitzer G
Exp Hematol; 1987 Aug; 15(7):725-8. PubMed ID: 2440709
[TBL] [Abstract][Full Text] [Related]
7. The utilization of the human phosphoglycerate kinase gene in the investigation of X-chromosome inactivation.
Goldman MA; Gartler SM; Keitges EA; Riley DE
Horiz Biochem Biophys; 1986; 8():169-205. PubMed ID: 2875931
[TBL] [Abstract][Full Text] [Related]
8. An unexpected affected female patient in a classical Lesch-Nyhan family.
De Gregorio L; Nyhan WL; Serafin E; Chamoles NA
Mol Genet Metab; 2000 Mar; 69(3):263-8. PubMed ID: 10767182
[TBL] [Abstract][Full Text] [Related]
9. X chromosome inactivation patterns in 45,X/46,XX mosaics.
Uehara S; Sato K; Hashiyada M; Obara Y; Matsuzaki S; Nata M; Okamura K
J Hum Genet; 2001; 46(3):126-31. PubMed ID: 11310579
[TBL] [Abstract][Full Text] [Related]
10. Assessment of X-chromosome inactivation patterns using the hypervariable probe M27 beta in normal hemopoietic cells and acute myeloid leukemic blasts.
Gale RE; Wheadon H; Linch DC
Leukemia; 1992 Jul; 6(7):649-55. PubMed ID: 1352560
[TBL] [Abstract][Full Text] [Related]
11. Myeloproliferative disorders: usefulness of X-linked probes in diagnosis.
Taylor KM; Shetta M; Talpaz M; Kantarjian HM; Hardikar S; Chinault AC; McCredie KB; Spitzer G
Leukemia; 1989 Jun; 3(6):419-22. PubMed ID: 2566725
[TBL] [Abstract][Full Text] [Related]
12. Methylation of HpaII site at the human DXS16 locus on Xp22 as an assay for abnormal patterns of X inactivation.
Khalifa MM; Struthers JL; Maurice S; Harrison K; Duncan AM
Am J Med Genet; 2001 Jan; 98(1):64-9. PubMed ID: 11426457
[TBL] [Abstract][Full Text] [Related]
13. Lesch-Nyhan disease in a female with a clinically normal monozygotic twin.
De Gregorio L; Jinnah HA; Harris JC; Nyhan WL; Schretlen DJ; Trombley LM; O'Neill JP
Mol Genet Metab; 2005 May; 85(1):70-7. PubMed ID: 15862283
[TBL] [Abstract][Full Text] [Related]
14. [Clonal analysis of hepatocellular carcinoma].
Ochiai T; Ueda K; Urata Y; Yamano T; Konishi E; Ogino A; Kawai K; Itoi H; Sonoyama T; Yamagishi H; Oka T; Ashihara T
Gan To Kagaku Ryoho; 1996 Jun; 23 Suppl 2():182-8. PubMed ID: 8678565
[TBL] [Abstract][Full Text] [Related]
15. Use of the X-chromosome linked hypoxanthine phosphoribosyl transferase gene as a marker of cell monoclonality in hemopoietic malignancies.
Browett PJ; Hoffbrand AV; Norton JD
Leuk Res; 1988; 12(4):321-6. PubMed ID: 2836664
[TBL] [Abstract][Full Text] [Related]
16. X-chromosome inactivation in the human trophoblast of early pregnancy.
Uehara S; Tamura M; Nata M; Ji G; Yaegashi N; Okamura K; Yajima A
J Hum Genet; 2000; 45(3):119-26. PubMed ID: 10807535
[TBL] [Abstract][Full Text] [Related]
17. A novel strategy for the investigation of clonality in precancerous disease states and early stages of tumor progression.
Sternlicht M; Mirell C; Safarians S; Barsky SH
Biochem Biophys Res Commun; 1994 Mar; 199(2):511-8. PubMed ID: 7510955
[TBL] [Abstract][Full Text] [Related]
18. Carrier detection of partial hypoxanthine-guanine phosphoribosyltransferase deficiency by analysis with BamHI restriction fragment length polymorphisms and oligonucleotide probes.
Igarashi T; Kamoshita S
Pediatr Res; 1990 Apr; 27(4 Pt 1):417-21. PubMed ID: 1971437
[TBL] [Abstract][Full Text] [Related]
19. A PCR based X-chromosome inactivation assay for carrier detection in X-linked immunodeficiencies using differential methylation of the androgen receptor gene.
Schmucker B; Meindl A; Achatz H; Mittermüller J; Krüger G; Hergersberg M; Spiegel R; Schinzel A; Belohradsky BH; Murken J
Immunodeficiency; 1995; 5(3):187-92. PubMed ID: 7749438
[TBL] [Abstract][Full Text] [Related]
20. The Wiskott-Aldrich syndrome.
Peacocke M; Siminovitch KA
Semin Dermatol; 1993 Sep; 12(3):247-54. PubMed ID: 8105860
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]