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Stuart Rudikoff

Researcher at National Institutes of Health

Publications -  98
Citations -  11270

Stuart Rudikoff is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Gene & Peptide sequence. The author has an hindex of 42, co-authored 98 publications receiving 11132 citations. Previous affiliations of Stuart Rudikoff include Yeshiva University & Laboratory of Molecular Biology.

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Single amino acid substitution altering antigen-binding specificity

TL;DR: Results suggest that small numbers of substitutions in antibodies, such as those presumably introduced by somatic mutation, may in some situations be effective in altering antigen-binding specificity.
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Immune system impairment and hepatic fibrosis in mice lacking the dioxin-binding Ah receptor

TL;DR: The aryl hydrocarbon (Ah) receptor (AHR) mediates many carcinogenic and teratogenic effects of environmentally toxic chemicals such as dioxin and plays an important role in the development of the liver and the immune system.
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Purification and characterization of a newly identified growth factor specific for epithelial cells

TL;DR: The release of this growth factor by human embryonic fibroblasts raises the possibility that KGF may play a role in mesenchymal stimulation of normal epithelial cell proliferation, and Lack of mitogenic activity on either fibro Blasts or endothelial cells indicated that K GF possessed a target cell specificity distinct from any previously characterized growth factor.
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Aryl-hydrocarbon receptor-deficient mice are resistant to 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced toxicity

TL;DR: Results suggest that the pathological changes induced by TCDD in the liver and thymus are mediated entirely by the AHR, however, it is important to note that at high doses of T CDD, AHR-deficient mice displayed limited vasculitis and scattered single cell necrosis in their lungs and livers, respectively.
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Molecular cloning and expression of cDNAs for the human interleukin-2 receptor

TL;DR: The human T-cell growth factor (interleukin-2) receptor is purified and cloned, sequenced and expressed cDNAs corresponding to this receptor and one gene, but two interleukIn-2 receptor mRNAs which differ in their polyadenylation signals are identified.