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Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations.
Orange JS, Brodeur SR, Jain A, Bonilla FA, Schneider LC, Kretschmer R, Nurko S, Rasmussen WL, Köhler JR, Gellis SE, Ferguson BM, Strominger JL, Zonana J, Ramesh N, Ballas ZK, Geha RS. Orange JS, et al. Among authors: jain a. J Clin Invest. 2002 Jun;109(11):1501-9. doi: 10.1172/JCI14858. J Clin Invest. 2002. PMID: 12045264 Free PMC article.
Mechanisms of genotype-phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency.
Petersheim D, Massaad MJ, Lee S, Scarselli A, Cancrini C, Moriya K, Sasahara Y, Lankester AC, Dorsey M, Di Giovanni D, Bezrodnik L, Ohnishi H, Nishikomori R, Tanita K, Kanegane H, Morio T, Gelfand EW, Jain A, Secord E, Picard C, Casanova JL, Albert MH, Torgerson TR, Geha RS. Petersheim D, et al. Among authors: jain a. J Allergy Clin Immunol. 2018 Mar;141(3):1060-1073.e3. doi: 10.1016/j.jaci.2017.05.030. Epub 2017 Jun 17. J Allergy Clin Immunol. 2018. PMID: 28629746 Free PMC article.
Antibody deficiency associated with an inherited autosomal dominant mutation in TWEAK.
Wang HY, Ma CA, Zhao Y, Fan X, Zhou Q, Edmonds P, Uzel G, Oliveira JB, Orange J, Jain A. Wang HY, et al. Among authors: jain a. Proc Natl Acad Sci U S A. 2013 Mar 26;110(13):5127-32. doi: 10.1073/pnas.1221211110. Epub 2013 Mar 14. Proc Natl Acad Sci U S A. 2013. PMID: 23493554 Free PMC article. Clinical Trial.
A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiency.
Wang HY, Gopalan V, Aksentijevich I, Yeager M, Ma CA, Mohamoud YA, Quinones M, Matthews C, Boland J, Niemela JE, Torgerson TR, Giliani S, Uzel G, Orange JS, Shapiro R, Notarangelo L, Ochs HD, Fleisher T, Kastner D, Chanock SJ, Jain A. Wang HY, et al. Among authors: jain a. Hum Mutat. 2010 Sep;31(9):1080-8. doi: 10.1002/humu.21322. Hum Mutat. 2010. PMID: 20652909 Free PMC article.
8,701 results