Markert ML - Search Results

1

Successful formation of a chimeric human thymus allograft following transplantation of cultured postnatal human thymus.

Markert ML, Kostyu DD, Ward FE, McLaughlin TM, Watson TJ, Buckley RH, Schiff SE, Ungerleider RM, Gaynor JW, Oldham KT, Mahaffey SM, Ballow M, Driscoll DA, Hale LP, Haynes BF. Markert ML, et al. J Immunol. 1997 Jan 15;158(2):998-1005. J Immunol. 1997. PMID: 8993022

2

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

Markert ML, Norby-Slycord C, Ward FE. Markert ML, et al. Am J Hum Genet. 1989 Sep;45(3):354-61. Am J Hum Genet. 1989. PMID: 2773932 Free PMC article.

3

Development of immunity in human severe primary T cell deficiency following haploidentical bone marrow stem cell transplantation.

Buckley RH, Schiff SE, Sampson HA, Schiff RI, Markert ML, Knutsen AP, Hershfield MS, Huang AT, Mickey GH, Ward FE. Buckley RH, et al. Among authors: markert ml. J Immunol. 1986 Apr 1;136(7):2398-407. J Immunol. 1986. PMID: 2869085

4

Adenosine deaminase and purine nucleoside phosphorylase deficiencies: evaluation of therapeutic interventions in eight patients.

Markert ML, Hershfield MS, Schiff RI, Buckley RH. Markert ML, et al. J Clin Immunol. 1987 Sep;7(5):389-99. doi: 10.1007/BF00917017. J Clin Immunol. 1987. PMID: 3116034

5

Natural-killer-cell function and bone marrow transplantation.

Markert ML, Buckley RH. Markert ML, et al. N Engl J Med. 1986 Nov 27;315(22):1418-9. doi: 10.1056/NEJM198611273152216. N Engl J Med. 1986. PMID: 3534572 No abstract available.

6

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. Markert ML, et al. J Immunol. 1987 May 15;138(10):3203-6. J Immunol. 1987. PMID: 3571974

7

Haploidentical bone marrow stem cell transplantation in human severe combined immunodeficiency.

Buckley RH, Schiff SE, Schiff RI, Roberts JL, Markert ML, Peters W, Williams LW, Ward FE. Buckley RH, et al. Among authors: markert ml. Semin Hematol. 1993 Oct;30(4 Suppl 4):92-101; discussion 102-4. Semin Hematol. 1993. PMID: 7905667 Review.

8

The human thymic microenvironment during organ culture.

Markert ML, Watson TJ, Kaplan I, Hale LP, Haynes BF. Markert ML, et al. Clin Immunol Immunopathol. 1997 Jan;82(1):26-36. doi: 10.1006/clin.1996.4266. Clin Immunol Immunopathol. 1997. PMID: 9000039

9

Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants.

Buckley RH, Schiff RI, Schiff SE, Markert ML, Williams LW, Harville TO, Roberts JL, Puck JM. Buckley RH, et al. Among authors: markert ml. J Pediatr. 1997 Mar;130(3):378-87. doi: 10.1016/s0022-3476(97)70199-9. J Pediatr. 1997. PMID: 9063412

10

Mutations in purine nucleoside phosphorylase deficiency.

Markert ML, Finkel BD, McLaughlin TM, Watson TJ, Collard HR, McMahon CP, Andrews LG, Barrett MJ, Ward FE. Markert ML, et al. Hum Mutat. 1997;9(2):118-21. doi: 10.1002/(SICI)1098-1004(1997)9:2<118::AID-HUMU3>3.0.CO;2-5. Hum Mutat. 1997. PMID: 9067751

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