Conley ME - Search Results

1

Brief report: a point mutation in the SH2 domain of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia.

Saffran DC, Parolini O, Fitch-Hilgenberg ME, Rawlings DJ, Afar DE, Witte ON, Conley ME. Saffran DC, et al. Among authors: conley me. N Engl J Med. 1994 May 26;330(21):1488-91. doi: 10.1056/NEJM199405263302104. N Engl J Med. 1994. PMID: 8164701 Free article. No abstract available.

2

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia. 1993.

Tsukada S, Saffran DC, Rawlings DJ, Parolini O, Allen RC, Klisak I, Sparkes RS, Kubagawa H, Mohandas T, Quan S, Belmont JW, Cooper MD, Conley ME, Witte ON. Tsukada S, et al. Among authors: conley me. J Immunol. 2012 Apr 1;188(7):2936-47. J Immunol. 2012. PMID: 22442491 No abstract available.

3

Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase.

Conley ME, Fitch-Hilgenberg ME, Cleveland JL, Parolini O, Rohrer J. Conley ME, et al. Hum Mol Genet. 1994 Oct;3(10):1751-6. doi: 10.1093/hmg/3.10.1751. Hum Mol Genet. 1994. PMID: 7849697

4

Additional polymorphisms useful in linkage analysis for X-linked agammaglobulinemia.

Parolini O, Conley ME. Parolini O, et al. Among authors: conley me. Immunodeficiency. 1993;4(1-4):217-9. Immunodeficiency. 1993. PMID: 8167704 No abstract available.

5

The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia.

Rohrer J, Parolini O, Belmont JW, Conley ME, Parolino O [corrected to Parolini O]. Rohrer J, et al. Among authors: conley me. Immunogenetics. 1994;40(5):319-24. doi: 10.1007/BF01246672. Immunogenetics. 1994. PMID: 7927535

6

X-linked agammaglobulinemia: new approaches to old questions based on the identification of the defective gene.

Conley ME, Parolini O, Rohrer J, Campana D. Conley ME, et al. Immunol Rev. 1994 Apr;138:5-21. doi: 10.1111/j.1600-065x.1994.tb00844.x. Immunol Rev. 1994. PMID: 8070817 Review.

7

B-cell-specific demethylation of BTK, the defective gene in X-linked agammaglobulinemia.

Parolini O, Rohrer J, Shapiro LH, Conley ME. Parolini O, et al. Among authors: conley me. Immunogenetics. 1995;42(2):129-35. doi: 10.1007/BF00178587. Immunogenetics. 1995. PMID: 7541776

8

Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22.

Parolini O, Hejtmancik JF, Allen RC, Belmont JW, Lassiter GL, Henry MJ, Barker DF, Conley ME. Parolini O, et al. Among authors: conley me. Genomics. 1993 Feb;15(2):342-9. doi: 10.1006/geno.1993.1066. Genomics. 1993. PMID: 8449500

9

Nonrandom X chromosome inactivation in natural killer cells from obligate carriers of X-linked severe combined immunodeficiency.

Wengler GS, Allen RC, Parolini O, Smith H, Conley ME. Wengler GS, et al. Among authors: conley me. J Immunol. 1993 Jan 15;150(2):700-4. J Immunol. 1993. PMID: 8093460

10

Expression of the gene defect in X-linked agammaglobulinemia.

Conley ME, Brown P, Pickard AR, Buckley RH, Miller DS, Raskind WH, Singer JW, Fialkow PJ. Conley ME, et al. N Engl J Med. 1986 Aug 28;315(9):564-7. doi: 10.1056/NEJM198608283150907. N Engl J Med. 1986. PMID: 3488506 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

181 results

Search Page

Filters