Leucine-rich repeat containing 8A (LRRC8A)–dependent volume-regulated anion channel activity is dispensable for T-cell development and function
Craig D. PlattDivision of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MassJanet ChouDivision of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MassPatrick R. HoulihanDepartment of Cardiology, Boston Children's Hospital, Boston, MassYousef R. BadranDivision of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MassLalit KumarDivision of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MassWayne BainterDivision of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MassPietro Luigi PolianiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, ItalyCarlos J. PérezDepartment of Epigenetics and Molecular Carcinogenesis, University of Texas M. D. Anderson Cancer Center, Smithville, and the Graduate School of Biomedical Sciences at Houston, Houston, TexSharon DentDepartment of Epigenetics and Molecular Carcinogenesis, University of Texas M. D. Anderson Cancer Center, Smithville, and the Graduate School of Biomedical Sciences at Houston, Houston, TexDavid E. ClaphamDepartment of Cardiology, Boston Children's Hospital, Boston, Mass; Howard Hughes Medical Institute, Chevy Chase, MdFernando BenavidesDepartment of Epigenetics and Molecular Carcinogenesis, University of Texas M. D. Anderson Cancer Center, Smithville, and the Graduate School of Biomedical Sciences at Houston, Houston, TexRaif S. GehaDivision of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, Mass. Electronic address: [email protected]
2017en
ABI
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