Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 284

Similar articles for PubMed (Select 6198631)

1.

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 25;12(2):1015-24.

3.

Severe combined immune deficiency due to a homozygous 3.2-kb deletion spanning the promoter and first exon of the adenosine deaminase gene.

Berkvens TM, Gerritsen EJ, Oldenburg M, Breukel C, Wijnen JT, van Ormondt H, Vossen JM, van der Eb AJ, Meera Khan P.

Nucleic Acids Res. 1987 Nov 25;15(22):9365-78.

4.

Identification of a deletion in the adenosine deaminase gene in a child with severe combined immunodeficiency.

Markert ML, Hershfield MS, Wiginton DA, States JC, Ward FE, Bigner SH, Buckley RH, Kaufman RE, Hutton JJ.

J Immunol. 1987 May 15;138(10):3203-6.

PMID:
3571974
5.
6.

Cloning of cDNA sequences of human adenosine deaminase.

Wiginton DA, Adrian GS, Friedman RL, Suttle DP, Hutton JJ.

Proc Natl Acad Sci U S A. 1983 Dec;80(24):7481-5.

7.

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.

8.

Normal and mutant human adenosine deaminase genes.

Akeson AL, Wiginton DA, Hutton JJ.

J Cell Biochem. 1989 Mar;39(3):217-28. Review.

PMID:
2651461
9.

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 1;142(11):3971-7.

PMID:
2497184
10.
11.

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.

PMID:
7239521
12.

Paradoxical expression of adenosine deaminase in T cells cultured from a patient with adenosine deaminase deficiency and combine immunodeficiency.

Arredondo-Vega FX, Kurtzberg J, Chaffee S, Santisteban I, Reisner E, Povey MS, Hershfield MS.

J Clin Invest. 1990 Aug;86(2):444-52.

13.

One adenosine deaminase allele in a patient with severe combined immunodeficiency contains a point mutation abolishing enzyme activity.

Valerio D, Dekker BM, Duyvesteyn MG, van der Voorn L, Berkvens TM, van Ormondt H, van der Eb AJ.

EMBO J. 1986 Jan;5(1):113-9.

15.

Erythrocyte adenosine deaminase deficiency without immunodeficiency. Evidence for an unstable mutant enzyme.

Hirschhorn R, Roegner V, Jenkins T, Seaman C, Piomelli S, Borkowsky W.

J Clin Invest. 1979 Oct;64(4):1130-9.

16.

Molecular biology of the adenosine deaminase gene and messenger RNA.

Hutton JJ, Wiginton DA.

Ann N Y Acad Sci. 1985;451:227-37.

PMID:
3865573
17.

Adenosine deaminase deficiency in combined immunologic deficiency disease.

Meuwissen HJ, Pickering RJ, Pollara B.

Birth Defects Orig Artic Ser. 1975;11(1):117-9.

PMID:
1148375
18.

Abnormal platelet aggregation in severe combined immunodeficiency disease with adenosine deaminase deficiency.

Schwartz AL, Polmar SH, Stern RC, Cowan DH.

Br J Haematol. 1978 Jun;39(2):189-94.

PMID:
678472
19.

A high proportion of ADA point mutations associated with a specific alanine-to-valine substitution.

Markert ML, Norby-Slycord C, Ward FE.

Am J Hum Genet. 1989 Sep;45(3):354-61.

20.

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.

PMID:
1696926
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk