126 related articles for article (PubMed ID: 1427881)
1. Mapping of the X-linked form of hyper-IgM syndrome (HIGM1) to Xq26 by close linkage to HPRT.
Padayachee M; Feighery C; Finn A; McKeown C; Levinsky RJ; Kinnon C; Malcolm S
Genomics; 1992 Oct; 14(2):551-3. PubMed ID: 1427881
[No Abstract] [Full Text] [Related]
2. Mapping of the X linked form of hyper IgM syndrome (HIGM1).
Padayachee M; Levinsky RJ; Kinnon C; Finn A; McKeown C; Feighery C; Notarangelo LD; Hendriks RW; Read AP; Malcolm S
J Med Genet; 1993 Mar; 30(3):202-5. PubMed ID: 8097258
[TBL] [Abstract][Full Text] [Related]
3. Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26).
Huang TH; Hejtmancik JF; Edwards A; Pettigrew AL; Herrera CA; Hammond HA; Caskey CT; Zoghbi HY; Ledbetter DH
Am J Hum Genet; 1991 Dec; 49(6):1312-9. PubMed ID: 1746558
[TBL] [Abstract][Full Text] [Related]
4. Gene for Simpson-Golabi-Behmel syndrome is linked to HPRT in Xq26 in two European families.
Orth U; Gurrieri F; Behmel A; Genuardi M; Cremer M; Gal A; Neri G
Am J Med Genet; 1994 May; 50(4):388-90. PubMed ID: 8209924
[TBL] [Abstract][Full Text] [Related]
5. Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA).
Malcolm S; de Saint Basile G; Arveiler B; Lau YL; Szabo P; Fischer A; Griscelli C; Debre M; Mandel JL; Callard RE
Hum Genet; 1987 Oct; 77(2):172-4. PubMed ID: 2888720
[TBL] [Abstract][Full Text] [Related]
6. Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages.
Notarangelo LD; Parolini O; Albertini A; Duse M; Mazzolari E; Plebani A; Camerino G; Ugazio AG
Hum Genet; 1991 Dec; 88(2):130-4. PubMed ID: 1757090
[TBL] [Abstract][Full Text] [Related]
7. Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27.
Xuan JY; Besner A; Ireland M; Hughes-Benzie RM; MacKenzie AE
Hum Mol Genet; 1994 Jan; 3(1):133-7. PubMed ID: 7909248
[TBL] [Abstract][Full Text] [Related]
8. Fine structure mapping of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene region of the human X chromosome (Xq26).
Nicklas JA; Hunter TC; O'Neill JP; Albertini RJ
Am J Hum Genet; 1991 Aug; 49(2):267-78. PubMed ID: 1678246
[TBL] [Abstract][Full Text] [Related]
9. Analysis of human HPRT deletion mutations with X-linked probes and pulsed field gel electrophoresis.
Nicklas JA; Lippert MJ; Hunter TC; O'Neill JP; Albertini RJ
Environ Mol Mutagen; 1991; 18(4):270-3. PubMed ID: 1748089
[TBL] [Abstract][Full Text] [Related]
10. Physical mapping of the human hprt chromosomal region (Xq26).
Lippert MJ; Albertini RJ; Nicklas JA
Mutat Res; 1995 Jan; 326(1):39-49. PubMed ID: 7528884
[TBL] [Abstract][Full Text] [Related]
11. X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked.
Mensink EJ; Schot JD; Tippett P; Ott J; Schuurman RK
Hum Genet; 1984; 68(4):303-9. PubMed ID: 6595200
[TBL] [Abstract][Full Text] [Related]
12. Disseminated lymphonodular cryptococcosis in a child with X-linked hyper-IgM immunodeficiency.
Tabone MD; Leverger G; Landman J; Aznar C; Boccon-Gibod L; Lasfargues G
Pediatr Infect Dis J; 1994 Jan; 13(1):77-9. PubMed ID: 8170740
[No Abstract] [Full Text] [Related]
13. Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity.
Mensink EJ; Thompson A; Schot JD; van de Greef WM; Sandkuyl LA; Schuurman RK
Hum Genet; 1986 Aug; 73(4):327-32. PubMed ID: 3502688
[TBL] [Abstract][Full Text] [Related]
14. X-linked polymorphism of hypoxanthine phosphoribosyl transferase gene (HPRT) in Chinese females.
Chan LC; Tse E; Pittaluga S
Cancer Genet Cytogenet; 1992 Dec; 64(2):192. PubMed ID: 1362524
[No Abstract] [Full Text] [Related]
15. The molecular basis of X-linked agammaglobulinemia, hyper-IgM syndrome, and severe combined immunodeficiency in humans.
Aruffo A; Hollenbaugh D; Wu LH; Ochs HD
Curr Opin Hematol; 1994 Jan; 1(1):12-8. PubMed ID: 9371254
[TBL] [Abstract][Full Text] [Related]
16. CD40 ligand (CD40L) expression and B cell function in agammaglobulinemia with normal or elevated levels of IgM (HIM). Comparison of X-linked, autosomal recessive, and non-X-linked forms of the disease, and obligate carriers.
Callard RE; Smith SH; Herbert J; Morgan G; Padayachee M; Lederman S; Chess L; Kroczek RA; Fanslow WC; Armitage RJ
J Immunol; 1994 Oct; 153(7):3295-306. PubMed ID: 7916370
[TBL] [Abstract][Full Text] [Related]
17. The fragile X mutation does not have any major effect on the expression of the hypoxanthine phosphoribosyltransferase (HPRT) locus in human fibroblasts.
Steen AM; Marcus S; Sahlén S; Nielsen KB; Lambert B
Hum Genet; 1991 Aug; 87(4):503-5. PubMed ID: 1715310
[TBL] [Abstract][Full Text] [Related]
18. Localization of MIC5 to the region between HPRT and G6PD on the human X chromosome.
Hope R; Goss S; Solomon E; Ropers HH; Banting G; Goodfellow PN
Ann Hum Genet; 1987 Jan; 51(1):1-7. PubMed ID: 3674747
[TBL] [Abstract][Full Text] [Related]
19. The random inactivation of the X chromosome carrying the defective gene responsible for X-linked hyper IgM syndrome (X-HIM) in female carriers of HIGM1.
Hollenbaugh D; Wu LH; Ochs HD; Nonoyama S; Grosmaire LS; Ledbetter JA; Noelle RJ; Hill H; Aruffo A
J Clin Invest; 1994 Aug; 94(2):616-22. PubMed ID: 7518839
[TBL] [Abstract][Full Text] [Related]
20. Electrophoretic variation for X chromosome-linked hypoxanthine phosphoribosyl transferase (HPRT) in wild-derived mice.
Chapman VM; Kratzer PG; Quarantillo BA
Genetics; 1983 Apr; 103(4):785-95. PubMed ID: 6852525
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]