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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2003 | 2 |
2004 | 1 |
2005 | 2 |
2024 | 0 |
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4 results
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Page 1
Molecular analysis of a large cohort of patients with the hyper immunoglobulin M (IgM) syndrome.
Blood. 2005 Mar 1;105(5):1881-90. doi: 10.1182/blood-2003-12-4420. Epub 2004 Sep 9.
Blood. 2005.
PMID: 15358621
Free article.
Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.
Imai K, Slupphaug G, Lee WI, Revy P, Nonoyama S, Catalan N, Yel L, Forveille M, Kavli B, Krokan HE, Ochs HD, Fischer A, Durandy A.
Imai K, et al.
Nat Immunol. 2003 Oct;4(10):1023-8. doi: 10.1038/ni974. Epub 2003 Sep 7.
Nat Immunol. 2003.
PMID: 12958596
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Inducible CO-stimulator molecule, a candidate gene for defective isotype switching, is normal in patients with hyper-IgM syndrome of unknown molecular diagnosis.
Lee WI, Zhu Q, Gambineri E, Jin Y, Welcher AA, Ochs HD.
Lee WI, et al.
J Allergy Clin Immunol. 2003 Nov;112(5):958-64. doi: 10.1016/s0091-6749(03)02021-9.
J Allergy Clin Immunol. 2003.
PMID: 14610488
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Rituximab inhibits the in vivo primary and secondary antibody response to a neoantigen, bacteriophage phiX174.
Bearden CM, Agarwal A, Book BK, Vieira CA, Sidner RA, Ochs HD, Young M, Pescovitz MD.
Bearden CM, et al.
Am J Transplant. 2005 Jan;5(1):50-7. doi: 10.1111/j.1600-6143.2003.00646.x.
Am J Transplant. 2005.
PMID: 15636611
Free article.
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