Mechanisms for Regulating Expression of Membrane Isoforms of FcγRIII (CD16)
Author:
Affiliation:
1. Center for Blood Research and Department of Pathology, Harvard Medical School, Boston, MA 02115.
2. Section on Clinical Immunology, National Institutes of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD 20892.
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference37 articles.
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2. ANEGON, I, INTERACTION OF FC-RECEPTOR (CD16) LIGANDS INDUCES TRANSCRIPTION OF INTERLEUKIN-2 RECEPTOR (CD25) AND LYMPHOKINE GENES AND EXPRESSION OF THEIR PRODUCTS IN HUMAN NATURAL-KILLER CELLS, JOURNAL OF EXPERIMENTAL MEDICINE 167: 452 (1988).
3. BARTHELS, D, ISOLATION AND NUCLEOTIDE-SEQUENCE OF MOUSE NCAM CDNA THAT CODES FOR A MR 79000 POLYPEPTIDE WITHOUT A MEMBRANE-SPANNING REGION, EMBO JOURNAL 6: 907 (1987).
4. BLANK, U, COMPLETE STRUCTURE AND EXPRESSION IN TRANSFECTED CELLS OF HIGH-AFFINITY IGE RECEPTOR, NATURE 337: 187 (1989).
5. BREITMEYER, J.B., LYMPHOCYTE-ACTIVATION - HOW T-CELLS COMMUNICATE, NATURE 329: 760 (1987).
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