119 related articles for article (PubMed ID: 7510955)
21. 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]
22. An inactive X specific replication origin associated with a matrix attachment region in the human X linked HPRT gene.
Koina E; Piper A
J Cell Biochem; 2005 May; 95(2):391-402. PubMed ID: 15779006
[TBL] [Abstract][Full Text] [Related]
23. Clonal composition of pituitary adenomas in patients with Cushing's disease: determination by X-chromosome inactivation analysis.
Schulte HM; Oldfield EH; Allolio B; Katz DA; Berkman RA; Ali IU
J Clin Endocrinol Metab; 1991 Dec; 73(6):1302-8. PubMed ID: 1720126
[TBL] [Abstract][Full Text] [Related]
24. Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred.
Belsham DD; Pereira F; Greenberg CR; Liao S; Wrogemann K
Hum Mutat; 1995; 5(1):28-33. PubMed ID: 7537149
[TBL] [Abstract][Full Text] [Related]
25. Clonality analysis of defined cell populations in paraffin-embedded tissue sections by RT-PCR amplification of X-linked G6PD gene.
Peng H; R Lakhani S; Lee C; Zheng Q; Chaggar RK; Wright NA; Pan L; Isaacson PG
J Pathol; 2000 Jul; 191(3):313-7. PubMed ID: 10878554
[TBL] [Abstract][Full Text] [Related]
26. Sex determination of dried blood stains using the polymerase chain reaction (PCR) with homologous X-Y primers of the zinc finger protein gene.
Stacks B; Witte MM
J Forensic Sci; 1996 Mar; 41(2):287-90. PubMed ID: 8871389
[TBL] [Abstract][Full Text] [Related]
27. Clonal involvement of granulocytes and monocytes, but not of T and B lymphocytes and natural killer cells in patients with myelodysplasia: analysis by X-linked restriction fragment length polymorphisms and polymerase chain reaction of the phosphoglycerate kinase gene.
van Kamp H; Fibbe WE; Jansen RP; van der Keur M; de Graaff E; Willemze R; Landegent JE
Blood; 1992 Oct; 80(7):1774-80. PubMed ID: 1356510
[TBL] [Abstract][Full Text] [Related]
28. Clonal determination by the fragile X (FMR1) and phosphoglycerate kinase (PGK) genes in hematological malignancies.
Lee ST; McGlennen RC; Litz CE
Cancer Res; 1994 Oct; 54(19):5212-6. PubMed ID: 7923142
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status.
Mansfield ES; Blasband A; Kronick MN; Wrabetz L; Kaplan P; Rappaport E; Sartore M; Parrella T; Surrey S; Fortina P
Mol Cell Probes; 1993 Aug; 7(4):311-24. PubMed ID: 8232348
[TBL] [Abstract][Full Text] [Related]
31. Monoclonal origins of malignant mixed tumors (carcinosarcomas). Evidence for a divergent histogenesis.
Thompson L; Chang B; Barsky SH
Am J Surg Pathol; 1996 Mar; 20(3):277-85. PubMed ID: 8772780
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. X-Inactivation and histone H4 acetylation in embryonic stem cells.
Keohane AM; O'neill LP; Belyaev ND; Lavender JS; Turner BM
Dev Biol; 1996 Dec; 180(2):618-30. PubMed ID: 8954732
[TBL] [Abstract][Full Text] [Related]
34. [Clonality of the peripheral papilloma and cancerous cells of breast].
Niu Y; Yu Q; Yu Y; Ding XM; Shi YR
Zhonghua Yi Xue Za Zhi; 2007 Feb; 87(8):542-5. PubMed ID: 17459204
[TBL] [Abstract][Full Text] [Related]
35. Clonal X-inactivation analysis of human tumours using the human androgen receptor gene (HUMARA) polymorphism: a non-radioactive and semiquantitative strategy applicable to fresh and archival tissue.
Kopp P; Jaggi R; Tobler A; Borisch B; Oestreicher M; Sabacan L; Jameson JL; Fey MF
Mol Cell Probes; 1997 Jun; 11(3):217-28. PubMed ID: 9232621
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Clonal analysis of focal nodular hyperplasia of the liver.
Gaffey MJ; Iezzoni JC; Weiss LM
Am J Pathol; 1996 Apr; 148(4):1089-96. PubMed ID: 8644851
[TBL] [Abstract][Full Text] [Related]
38. Clonal analysis of a solitary follicular nodule of the thyroid with the polymerase chain reaction method.
Chung DH; Kang GH; Kim WH; Ro JY
Mod Pathol; 1999 Mar; 12(3):265-71. PubMed ID: 10102611
[TBL] [Abstract][Full Text] [Related]
39. The effects of hypoxia and cysteamine on X-ray mutagenesis in human cells. II. hprt mRNA expression and cDNA sequence analysis of induced mutants.
Denault CM; Skopek TR; Liber HL
Radiat Res; 1993 Nov; 136(2):271-9. PubMed ID: 8248485
[TBL] [Abstract][Full Text] [Related]
40. Clonal studies in the myelodysplastic syndrome using X-linked restriction fragment length polymorphisms.
Tefferi A; Thibodeau SN; Solberg LA
Blood; 1990 May; 75(9):1770-3. PubMed ID: 1970487
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
