195 related articles for article (PubMed ID: 6840756)
1. Basic defect in the expression of adenosine deaminase in ADA-SCID disease. II. Deficiency of ADA-CRM detected in heterozygote human-Chinese hamster cell hybrids.
Herbschleb-Voogt E; Scholten JW; Meera Khan P
Hum Genet; 1983; 63(2):121-5. PubMed ID: 6840756
[TBL] [Abstract][Full Text] [Related]
2. Basic defect in the expression of adenosine deaminase in ADA- SCID disease investigated through the cells of an obligate heterozygote.
Herbschleb-Voogt E; Pearson PL; Vossen JM; Meera Khan P
Hum Genet; 1981; 56(3):379-86. PubMed ID: 7239521
[TBL] [Abstract][Full Text] [Related]
3. Basic molecular defect in ADA-SCID.
Herbschleb-Voogt E; Scholten JW; Vossen JM; Pearson PL; Meera Khan P
Adv Exp Med Biol; 1984; 165 Pt A():381-4. PubMed ID: 6720406
[No Abstract] [Full Text] [Related]
4. Somatic cell genetics of adenosine deaminase expression and severe combined immunodeficiency disease in humans.
Koch G; Shows TB
Proc Natl Acad Sci U S A; 1980 Jul; 77(7):4211-5. PubMed ID: 6933468
[TBL] [Abstract][Full Text] [Related]
5. Adenosine deaminase (ADA) deficiency in cells derived from humans with severe combined immunodeficiency is due to an aberration of the ADA protein.
Valerio D; Duyvesteyn MG; van Ormondt H; Meera Khan P; van der Eb AJ
Nucleic Acids Res; 1984 Jan; 12(2):1015-24. PubMed ID: 6198631
[TBL] [Abstract][Full Text] [Related]
6. Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybrids.
Hopkinson DA; Povey S; Solomon E; Bobrow M; Gormley IP
Cytogenet Cell Genet; 1976; 16(1-5):159-60. PubMed ID: 185012
[No Abstract] [Full Text] [Related]
7. A gene on human chromosome 6 functions in assembly of tissue-specific adenosine deaminase isozymes.
Koch G; Shows TB
Proc Natl Acad Sci U S A; 1978 Aug; 75(8):3876-80. PubMed ID: 279003
[TBL] [Abstract][Full Text] [Related]
8. Regional assignment of ADA and ITPA to mouse chromosome 2 (C1----ter). A demonstration of the conserved linkage of enzyme and proto-oncogene loci.
Siciliano MJ; Fournier RE; Stallings RL
J Hered; 1984; 75(3):175-80. PubMed ID: 6145740
[TBL] [Abstract][Full Text] [Related]
9. Radioimmunochemical quantitation of human adenosine deaminase.
Daddona PE; Frohman MA; Kelley WN
J Clin Invest; 1979 Sep; 64(3):798-803. PubMed ID: 468994
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the human adenosine deaminase gene that affect protein structure and RNA splicing.
Akeson AL; Wiginton DA; States JC; Perme CM; Dusing MR; Hutton JJ
Proc Natl Acad Sci U S A; 1987 Aug; 84(16):5947-51. PubMed ID: 3475710
[TBL] [Abstract][Full Text] [Related]
11. Establishment and characterization of adenosine deaminase-deficient human T cell lines.
Kohn DB; Mitsuya H; Ballow M; Selegue JE; Barankiewicz J; Cohen A; Gelfand E; Anderson WF; Blaese RM
J Immunol; 1989 Jun; 142(11):3971-7. PubMed ID: 2497184
[TBL] [Abstract][Full Text] [Related]
12. Transfer of the adenosine deaminase (ADA) gene of a B-lymphoblastoid cell line (LCL) to an ADA-deficient LCL by a microcell-mediated chromosome transfer technique.
Sawami H; Ito K; Norioka M; Monden S; Fujita M; Uchino H
Nihon Ketsueki Gakkai Zasshi; 1989 Sep; 52(6):1033-44. PubMed ID: 2588953
[TBL] [Abstract][Full Text] [Related]
13. Correction of adenosine deaminase deficiency in cultured human T and B cells by retrovirus-mediated gene transfer.
Kantoff PW; Kohn DB; Mitsuya H; Armentano D; Sieberg M; Zwiebel JA; Eglitis MA; McLachlin JR; Wiginton DA; Hutton JJ
Proc Natl Acad Sci U S A; 1986 Sep; 83(17):6563-7. PubMed ID: 3489233
[TBL] [Abstract][Full Text] [Related]
14. Adenosine deaminase deficiency: another family with "silent" ADA allele and normal ADA activity in two heterozygotes.
Chen SH; Scott CR; Giblett ER; Levin AS
Am J Hum Genet; 1977 Nov; 29(6):642-4. PubMed ID: 930931
[No Abstract] [Full Text] [Related]
15. Confirmation of the regional localization of the genes for human acid alpha-glucosidase (GAA) and adenosine deaminase (ADA) by somatic cell hybridization.
Honig J; Martiniuk F; D'Eustachio P; Zamfirescu C; Desnick R; Hirschhorn K; Hirschhorn LR; Hirschhorn R
Ann Hum Genet; 1984 Jan; 48(1):49-56. PubMed ID: 6370091
[TBL] [Abstract][Full Text] [Related]
16. Comparative characterization of B-lymphoblastoid cell lines in adenosine deaminase deficiency and its heterozygote.
Sawami H; Toyokawa Y; Ito K; Uchino H
Nihon Ketsueki Gakkai Zasshi; 1989 Jul; 52(4):721-9. PubMed ID: 2618547
[TBL] [Abstract][Full Text] [Related]
17. Identical 3250-bp deletion between two AluI repeats in the ADA genes of unrelated ADA-SCID patients.
Berkvens TM; van Ormondt H; Gerritsen EJ; Khan PM; van der Eb AJ
Genomics; 1990 Aug; 7(4):486-90. PubMed ID: 1696926
[TBL] [Abstract][Full Text] [Related]
18. Genetic heterogeneity in adenosine deaminase (ADA) deficiency: five different mutations in five new patients with partial ADA deficiency.
Hirschhorn R; Ellenbogen A
Am J Hum Genet; 1986 Jan; 38(1):13-25. PubMed ID: 3946419
[TBL] [Abstract][Full Text] [Related]
19. Localization of human adenosine deaminase (ADA) gene sequences to the q12----q13.11 region of chromosome 20 by in situ hybridization.
Jhanwar SC; Berkvens TM; Breukel C; van Ormondt H; van der Eb AJ; Meera Khan P
Cytogenet Cell Genet; 1989; 50(2-3):168-71. PubMed ID: 2776485
[TBL] [Abstract][Full Text] [Related]
20. Isolation of cDNA clones for human adenosine deaminase.
Valerio D; Duyvesteyn MG; Meera Khan P; Geurts van Kessel A; de Waard A; van der Eb AJ
Gene; 1983 Nov; 25(2-3):231-40. PubMed ID: 6198240
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
