117 related articles for article (PubMed ID: 2937302)
1. Variability of thymidylate synthase activity in whole blood cultures treated with FUdR.
Sklower SL; Jenkins EC; Anderson ML; Chan CB; Brown WT
Am J Med Genet; 1986; 23(1-2):483-90. PubMed ID: 2937302
[TBL] [Abstract][Full Text] [Related]
2. Fragile X expression increased by low cell-culture density.
Krawczun MS; Lele KP; Jenkins EC; Brown WT
Am J Med Genet; 1986; 23(1-2):467-73. PubMed ID: 2937301
[TBL] [Abstract][Full Text] [Related]
3. Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity.
Cantú ES; Nussbaum RL; Airhart SD; Ledbetter DH
Am J Hum Genet; 1985 Sep; 37(5):947-55. PubMed ID: 2931977
[TBL] [Abstract][Full Text] [Related]
4. Progress toward an internal control system for fragile-X induction by 5-fluorodeoxyuridine in whole-blood cultures.
Jenkins EC; Duncan CJ; Sanz MM; Genovese M; Gu H; Schwartz-Richstein C; Lele KP; Salandi ML; Krawczun MS
Pathobiology; 1990; 58(4):236-40. PubMed ID: 2147548
[TBL] [Abstract][Full Text] [Related]
5. The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes.
Brookwell R; Daniel A; Turner G; Fishburn J
Am J Med Genet; 1982 Oct; 13(2):139-48. PubMed ID: 6215863
[TBL] [Abstract][Full Text] [Related]
6. Frequency of tri- or multiradial configurations in fragile X identification.
Jenkins EC; Duncan CJ; Krawczun MS; Berns LM; Sanz MM; Brown WT
Am J Med Genet; 1986; 23(1-2):531-5. PubMed ID: 2937304
[TBL] [Abstract][Full Text] [Related]
7. FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition.
Glover TW
Am J Hum Genet; 1981 Mar; 33(2):234-42. PubMed ID: 6452060
[TBL] [Abstract][Full Text] [Related]
8. The effect of caffeine on fragile X expression.
Abruzzo MA; Pettay D; Mayer M; Jacobs PA
Hum Genet; 1986 May; 73(1):20-2. PubMed ID: 2940164
[TBL] [Abstract][Full Text] [Related]
9. Thymidylate synthetase inhibitors and fragile site expression in lymphocytes.
Jacky PB; Sutherland GR
Am J Hum Genet; 1983 Nov; 35(6):1276-83. PubMed ID: 6228136
[TBL] [Abstract][Full Text] [Related]
10. Caffeine enhances fragile (X) expression in somatic cell hybrids.
Ledbetter DH; Airhart SD; Nussbaum RL
Am J Med Genet; 1986; 23(1-2):445-55. PubMed ID: 2937299
[TBL] [Abstract][Full Text] [Related]
11. The combined effects of FUdR addition and methionine depletion on the X-chromosome fragile site.
Glover TW; Howard-Peebles PN
Am J Hum Genet; 1983 Jan; 35(1):117-22. PubMed ID: 6218753
[TBL] [Abstract][Full Text] [Related]
12. Fragile X expression in short-term whole blood cultures is affected by cell density.
Krawczun MS; Jenkins EC; Brown WT; Silverman WP
Am J Med Genet; 1988; 30(1-2):435-42. PubMed ID: 2972206
[TBL] [Abstract][Full Text] [Related]
13. Recent experience in prenatal fra(X) detection.
Jenkins EC; Brown WT; Krawczun MS; Duncan CJ; Lele KP; Cantu ES; Schonberg S; Golbus MS; Sekhon GS; Stark S
Am J Med Genet; 1988; 30(1-2):329-36. PubMed ID: 2972205
[TBL] [Abstract][Full Text] [Related]
14. Enhanced sensitivity of lymphoblastoid cells from individuals carrying the mutation for the fragile X syndrome to the clastogenic effects of FUdR.
Duncan AM
Mutat Res; 1986 Mar; 173(3):201-5. PubMed ID: 2936953
[TBL] [Abstract][Full Text] [Related]
15. Dialyzed fetal bovine serum increases cytogenetic fragile X expression.
Jenkins EC; Duncan CJ; Gu H; Genovese M; Krawczun MS
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):155-60. PubMed ID: 1534967
[TBL] [Abstract][Full Text] [Related]
16. Frequency of the common fragile site at Xq27.2 under conditions of thymidylate stress: implications for cytogenetic diagnosis of the fragile-X syndrome.
Ramos FJ; Emanuel BS; Spinner NB
Am J Med Genet; 1992 Apr; 42(6):835-8. PubMed ID: 1532475
[TBL] [Abstract][Full Text] [Related]
17. Distribution of diploidy, polyploidy, and endoreduplication in fra(X) positive and negative lymphocytes, amniocytes, and chorionic villi.
Jenkins EC; Sanz MM; Ray JH; Stark-Houck SL; Brown WT
Am J Med Genet; 1991; 38(2-3):434-6. PubMed ID: 1826811
[TBL] [Abstract][Full Text] [Related]
18. The prenatal detection of the fragile X chromosome: review of recent experience.
Jenkins EC; Brown WT; Wilson MG; Lin MS; Alfi OS; Wassman ER; Brooks J; Duncan CJ; Masia A; Krawczun MS
Am J Med Genet; 1986; 23(1-2):297-311. PubMed ID: 2937295
[TBL] [Abstract][Full Text] [Related]
19. Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures.
Jenkins EC; Krawczun MS; Stark-Houck SL; Duncan CJ; Kunaporn S; Gu H; Schwartz-Richstein C; Howard-Peebles PN; Gross A; Sherman SL
Am J Med Genet; 1991; 38(2-3):447-52. PubMed ID: 1826813
[TBL] [Abstract][Full Text] [Related]
20. Cytogenetic guidelines for fragile X studies tested in routine practice.
Dewald GW; Buckley DD; Spurbeck JL; Jalal SM
Am J Med Genet; 1992 Dec; 44(6):816-21. PubMed ID: 1481854
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
