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Wyszukujesz frazę ""T cell receptor"" wg kryterium: Temat


Tytuł :
TCR Vβ Usage of Peripheral Blood and Liver Infiltrating Lymphocytes in Patients with Chronic Hepatitis B.
Autorzy :
Zhou J; Affiliated Hospital of Jining Medical University, China. Clinical Laboratory.
Kong C; Affiliated Hospital of Jining Medical University, China. Nursing Department.
Ban B; Affiliated Hospital of Jining Medical University, China. Endocrinology Department.
Dong H; Affiliated Hospital of Jining Medical University, China. Clinical Laboratory.
Jin C; Affiliated Hospital of Jining Medical University, China. Clinical Laboratory.
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Źródło :
Annals of hepatology [Ann Hepatol] 2018 Mar 01; Vol. 17 (2), pp. 214-222.
Typ publikacji :
Journal Article
MeSH Terms :
Genes, T-Cell Receptor beta*
Hepatitis B, Chronic/*genetics
Hepatitis B, Chronic/*immunology
Immunoglobulin Variable Region/*genetics
Liver/*immunology
Lymphocytes/*immunology
Receptors, Antigen, T-Cell, alpha-beta/*genetics
Adult ; Case-Control Studies ; Complementarity Determining Regions/genetics ; Complementarity Determining Regions/immunology ; Female ; HLA-DR Serological Subtypes/genetics ; HLA-DR Serological Subtypes/immunology ; Hepatitis B, Chronic/diagnosis ; Hepatitis B, Chronic/virology ; Host-Pathogen Interactions ; Humans ; Immunoglobulin Variable Region/immunology ; Liver/virology ; Lymphocytes/virology ; Male ; Middle Aged ; Receptors, Antigen, T-Cell, alpha-beta/immunology
Czasopismo naukowe
Tytuł :
The deterministic role of 5-mers in microRNA-gene targeting.
Autorzy :
Hart M; a Institute of Human Genetics, Saarland University , Homburg , Germany.
Kern F; b Chair for Clinical Bioinformatics, Saarland University , Saarbrücken , Germany.
Backes C; b Chair for Clinical Bioinformatics, Saarland University , Saarbrücken , Germany.
Rheinheimer S; a Institute of Human Genetics, Saarland University , Homburg , Germany.
Fehlmann T; b Chair for Clinical Bioinformatics, Saarland University , Saarbrücken , Germany.
Keller A; b Chair for Clinical Bioinformatics, Saarland University , Saarbrücken , Germany.
Meese E; a Institute of Human Genetics, Saarland University , Homburg , Germany.
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Źródło :
RNA biology [RNA Biol] 2018; Vol. 15 (6), pp. 819-825. Date of Electronic Publication: 2018 May 11.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
3' Untranslated Regions*
Genes, T-Cell Receptor alpha*
MicroRNAs*/genetics
MicroRNAs*/metabolism
Computer Simulation ; HEK293 Cells ; Humans
Czasopismo naukowe
Tytuł :
T cell receptor (TCR) genes in circulating cells of patients with systemic lupus erythematosus and their healthy relatives
Autorzy :
Jakez-Ocampo J; Departamento de Inmunología y Reumatología, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México. México.
Paulín-Vera CM; Departamento de Inmunología y Reumatología, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México. México.
Rivadeneyra-Espinoza L; Laboratorios Clínicos de Puebla, Puebla, Pue. México.
Gómez-Martín D; Departamento de Inmunología y Reumatología, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México. México.
Carrillo-Maravilla E; Departamento de Medicina Interna, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México. México.
Lima G; Departamento de Inmunología y Reumatología, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México. México.
Vargas-Rojas MI; Departamento de Inmunología y Reumatología, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México. México.
Pérez-Romano B; Laboratorios Clínicos de Puebla, Puebla, Pue. México.
Calva-Cevenini G; Laboratorios Clínicos de Puebla, Puebla, Pue. México.
García-Carrasco M; Escuela de Medicina, Benemérita Universidad Autónoma de Puebla, Puebla, Pue. México.
Ruiz-Argüelles A; Laboratorios Clínicos de Puebla, Puebla, Pue. México.
Llorente L; Departamento de Inmunología y Reumatología, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México. México.
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Transliterated Title :
Genes del receptor variable beta de células T en células circulantes de pacientes con lupus eritematoso generalizado y sus familiares sanos.
Źródło :
Gaceta medica de Mexico [Gac Med Mex] 2018; Vol. 154 (1), pp. 74-79.
Typ publikacji :
Journal Article
MeSH Terms :
Genes, T-Cell Receptor beta*/genetics
T-Lymphocytes*
Lupus Erythematosus, Systemic/*blood
Case-Control Studies ; Female ; Humans ; Lupus Erythematosus, Systemic/genetics ; Male
Czasopismo naukowe
Tytuł :
High-throughput sequencing of the T cell receptor β gene identifies aggressive early-stage mycosis fungoides.
Autorzy :
de Masson A; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
O'Malley JT; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
Elco CP; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
Garcia SS; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
Divito SJ; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
Lowry EL; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
Tawa M; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
Fisher DC; Center for Hematologic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
Devlin PM; Department of Radiation Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
Teague JE; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
Leboeuf NR; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA.
Kirsch IR; Adaptive Biotechnologies, Seattle, WA 98102, USA.
Robins H; Adaptive Biotechnologies, Seattle, WA 98102, USA.
Clark RA; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA. .
Kupper TS; Department of Dermatology, Brigham and Women's Hospital, and the Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, MA 02115, USA. .
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Źródło :
Science translational medicine [Sci Transl Med] 2018 May 09; Vol. 10 (440).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Genes, T-Cell Receptor beta*
High-Throughput Nucleotide Sequencing/*methods
Mycosis Fungoides/*genetics
Mycosis Fungoides/*immunology
Skin Neoplasms/*genetics
Skin Neoplasms/*immunology
Cellular Microenvironment ; Clone Cells ; Exome/genetics ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; Lymphoma, T-Cell, Cutaneous/genetics ; Lymphoma, T-Cell, Cutaneous/immunology ; Lymphoma, T-Cell, Cutaneous/pathology ; Male ; Middle Aged ; Multivariate Analysis ; Mycosis Fungoides/pathology ; Prognosis ; Progression-Free Survival ; Skin/pathology ; Skin Neoplasms/pathology
Czasopismo naukowe
Tytuł :
Adjustments of γδ T Cells in the Lung of Schistosoma japonicum -Infected C56BL/6 Mice.
Autorzy :
Cha H; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Xie H; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Jin C; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Feng Y; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Xie S; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Xie A; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Yang Q; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Qi Y; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Qiu H; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Wu Q; Department of Immunology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Yin Z; Biomedical Translational Research Institute, School of Pharmacy, Jinan University, Guangzhou, China.
Mu J; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
Huang J; Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
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Źródło :
Frontiers in immunology [Front Immunol] 2020 Jun 04; Vol. 11, pp. 1045. Date of Electronic Publication: 2020 Jun 04 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Intraepithelial Lymphocytes/*immunology
Intraepithelial Lymphocytes/*parasitology
Lung/*immunology
Lung/*parasitology
Schistosomiasis japonica/*immunology
Animals ; B-Lymphocytes/immunology ; Cytokines/metabolism ; Disease Models, Animal ; Female ; Genes, T-Cell Receptor delta ; Immunity, Innate ; Immunophenotyping ; Lung/pathology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Receptors, Antigen, T-Cell, gamma-delta/deficiency ; Receptors, Antigen, T-Cell, gamma-delta/genetics ; Receptors, Antigen, T-Cell, gamma-delta/immunology ; Schistosoma japonicum/immunology ; Schistosoma japonicum/pathogenicity ; Schistosomiasis japonica/parasitology ; Schistosomiasis japonica/pathology
Czasopismo naukowe
Tytuł :
Maternal T Cells in the Human Placental Villi Support an Allograft Response during Noninfectious Villitis.
Autorzy :
Enninga EAL; Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN 55905; .
Raber P; Adaptive Biotechnologies, Seattle, WA 98102.
Quinton RA; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905.
Ruano R; Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN 55905.
Ikumi N; Division of Immunology, Institute of Infectious Disease and Molecular Medicine, Department of Pathology, University of Cape Town, Cape Town, South Africa 7791.
Gray CM; Division of Immunology, Institute of Infectious Disease and Molecular Medicine, Department of Pathology, University of Cape Town, Cape Town, South Africa 7791.
Johnson EL; Division of Infectious Diseases, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322.
Chakraborty R; Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN 55905.; Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905.; Department of Immunology, Mayo Clinic, Rochester, MN 55905; and.
Kerr SE; Hospital Pathology Associates, Minneapolis, MN 55407.
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Źródło :
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2020 Jun 01; Vol. 204 (11), pp. 2931-2939. Date of Electronic Publication: 2020 Apr 22.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Chorionic Villi/*immunology
Genes, T-Cell Receptor beta/*genetics
Graft Rejection/*immunology
Inflammation/*immunology
Placenta Diseases/*immunology
Pregnancy/*immunology
T-Lymphocytes/*immunology
Adult ; Allografts/immunology ; Antigens, Viral/immunology ; Cell Movement ; Cohort Studies ; Epitopes, T-Lymphocyte/immunology ; Female ; Fetus ; HLA Antigens/immunology ; Humans ; Young Adult
Czasopismo naukowe
Tytuł :
Tumoral PD-1hiCD8+ T cells are partially exhausted and predict favorable outcome in triple-negative breast cancer.
Autorzy :
Guo L; Department of Breast Surgery, Key Laboratory of Breast Cancer in Shanghai, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China.; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, P.R. China.
Cao C; Department of Breast Surgery, Key Laboratory of Breast Cancer in Shanghai, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China.; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, P.R. China.
Goswami S; The Center for Microbes, Development and Health, Key Laboratory of Molecular Virology and Immunology, Institute Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, P.R. China.
Huang X; Department of Breast Surgery, Key Laboratory of Breast Cancer in Shanghai, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China.; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, P.R. China.
Ma L; Department of Breast Surgery, Key Laboratory of Breast Cancer in Shanghai, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China.; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, P.R. China.
Guo Y; Zuckerman Mind Brain Behavior Institute, Columbia University, New York, NY 10027, U.S.A.
Yang B; Department of Breast Surgery, Key Laboratory of Breast Cancer in Shanghai, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China.; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, P.R. China.
Li T; The Center for Microbes, Development and Health, Key Laboratory of Molecular Virology and Immunology, Institute Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, P.R. China.
Chi Y; Department of Breast Surgery, Key Laboratory of Breast Cancer in Shanghai, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China.; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, P.R. China.
Zhang X; The Center for Microbes, Development and Health, Key Laboratory of Molecular Virology and Immunology, Institute Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, P.R. China.
Wu J; Department of Breast Surgery, Key Laboratory of Breast Cancer in Shanghai, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China.; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, P.R. China.; Collaborative Innovation Center for Cancer Medicine, Shanghai 200032, P.R. China.
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Źródło :
Clinical science (London, England : 1979) [Clin Sci (Lond)] 2020 Apr 17; Vol. 134 (7), pp. 711-726.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Biomarkers, Tumor/*immunology
CD8-Positive T-Lymphocytes/*immunology
Lymphocytes, Tumor-Infiltrating/*immunology
Programmed Cell Death 1 Receptor/*immunology
Triple Negative Breast Neoplasms/*immunology
Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; CD8-Positive T-Lymphocytes/metabolism ; CD8-Positive T-Lymphocytes/pathology ; Disease-Free Survival ; Female ; Gene Expression Regulation, Neoplastic ; Genes, T-Cell Receptor ; Humans ; Immunologic Memory ; Lymphocytes, Tumor-Infiltrating/metabolism ; Lymphocytes, Tumor-Infiltrating/pathology ; Middle Aged ; Phenotype ; Programmed Cell Death 1 Receptor/genetics ; Programmed Cell Death 1 Receptor/metabolism ; Prospective Studies ; Risk Factors ; Time Factors ; Transcriptome ; Triple Negative Breast Neoplasms/metabolism ; Triple Negative Breast Neoplasms/mortality ; Triple Negative Breast Neoplasms/surgery ; Tumor Microenvironment
Czasopismo naukowe
Tytuł :
Identification of genes of prognostic value in the ccRCC microenvironment from TCGA database.
Autorzy :
Wan B; Department of Urology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, Haikou, Hainan, China.
Liu B; Laboratory of Developmental Cell Biology and Disease, School of Ophthalmology and Optometry and Eye Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Huang Y; Department of Neurology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, Haikou, Hainan, China.
Lv C; Department of Urology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, Haikou, Hainan, China.
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Źródło :
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2020 Apr; Vol. 8 (4), pp. e1159. Date of Electronic Publication: 2020 Feb 03.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Biomarkers, Tumor/*genetics
Carcinoma, Renal Cell/*genetics
Kidney Neoplasms/*genetics
Tumor Microenvironment/*genetics
Carcinoma, Renal Cell/pathology ; Cytokines/genetics ; Cytokines/metabolism ; Databases, Genetic ; Genes, T-Cell Receptor ; Humans ; Kidney Neoplasms/pathology ; Protein Interaction Maps ; Transcriptome
Czasopismo naukowe
Tytuł :
A Subset of Human Autoreactive CD1c-Restricted T Cells Preferentially Expresses TRBV4-1 TCRs.
Autorzy :
Guo T; Tumor Immunotherapy Program, Campbell Family Institute for Breast Cancer Research, Campbell Family Cancer Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 2M9, Canada.; Department of Immunology, University of Toronto, Toronto, Ontario M5S 1A8, Canada; and.
Koo MY; Tumor Immunotherapy Program, Campbell Family Institute for Breast Cancer Research, Campbell Family Cancer Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 2M9, Canada.; Department of Immunology, University of Toronto, Toronto, Ontario M5S 1A8, Canada; and.
Kagoya Y; Tumor Immunotherapy Program, Campbell Family Institute for Breast Cancer Research, Campbell Family Cancer Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 2M9, Canada.
Anczurowski M; Tumor Immunotherapy Program, Campbell Family Institute for Breast Cancer Research, Campbell Family Cancer Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 2M9, Canada.; Department of Immunology, University of Toronto, Toronto, Ontario M5S 1A8, Canada; and.
Wang CH; Tumor Immunotherapy Program, Campbell Family Institute for Breast Cancer Research, Campbell Family Cancer Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 2M9, Canada.; Department of Immunology, University of Toronto, Toronto, Ontario M5S 1A8, Canada; and.
Saso K; Tumor Immunotherapy Program, Campbell Family Institute for Breast Cancer Research, Campbell Family Cancer Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 2M9, Canada.
Butler MO; Tumor Immunotherapy Program, Campbell Family Institute for Breast Cancer Research, Campbell Family Cancer Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 2M9, Canada.; Department of Immunology, University of Toronto, Toronto, Ontario M5S 1A8, Canada; and.; Department of Medicine, University of Toronto, Toronto, Ontario M5S 1A8, Canada.
Hirano N; Tumor Immunotherapy Program, Campbell Family Institute for Breast Cancer Research, Campbell Family Cancer Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 2M9, Canada; .; Department of Immunology, University of Toronto, Toronto, Ontario M5S 1A8, Canada; and.
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Źródło :
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2018 Jan 15; Vol. 200 (2), pp. 500-511. Date of Electronic Publication: 2017 Dec 13.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Autoimmunity*
Gene Expression*
Genes, T-Cell Receptor beta*
Antigens, CD1/*immunology
Antigens, CD1/*metabolism
T-Lymphocyte Subsets/*immunology
T-Lymphocyte Subsets/*metabolism
Antigen Presentation/immunology ; Antigen-Presenting Cells/immunology ; Antigen-Presenting Cells/metabolism ; Arginine/genetics ; Biomarkers ; CD4-Positive T-Lymphocytes/immunology ; CD4-Positive T-Lymphocytes/metabolism ; Cell Line ; Clonal Evolution/genetics ; Clonal Evolution/immunology ; Codon ; Complementarity Determining Regions/genetics ; Humans ; Immunophenotyping ; Lymphocyte Activation ; Phenotype ; Tyrosine/genetics
Czasopismo naukowe
Tytuł :
Inverse correlation of Vδ2 T-cell recovery with EBV reactivation after haematopoietic stem cell transplantation.
Autorzy :
Liu J; Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Bian Z; Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Wang X; Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Xu LP; Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Fu Q; Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Wang C; State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Peking University, Beijing, China.
Chang YJ; Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Wang Y; Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Zhang XH; Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Jiang Z; State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Peking University, Beijing, China.
Huang XJ; Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
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Źródło :
British journal of haematology [Br J Haematol] 2018 Jan; Vol. 180 (2), pp. 276-285. Date of Electronic Publication: 2017 Dec 21.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Genes, T-Cell Receptor delta*
Hematopoietic Stem Cell Transplantation*/adverse effects
Virus Activation*
Epstein-Barr Virus Infections/*etiology
Herpesvirus 4, Human/*physiology
T-Lymphocytes/*metabolism
Adolescent ; Adult ; Apoptosis/genetics ; Apoptosis/immunology ; Cytotoxicity, Immunologic ; Epstein-Barr Virus Infections/diagnosis ; Female ; Graft vs Host Disease/etiology ; Graft vs Host Disease/prevention & control ; HLA Antigens/genetics ; HLA Antigens/immunology ; Haplotypes ; Humans ; Incidence ; Lymphocyte Activation/immunology ; Male ; Middle Aged ; T-Lymphocytes/immunology ; Transplantation, Homologous ; Young Adult
Czasopismo naukowe
Tytuł :
PD-1 Imposes Qualitative Control of Cellular Transcriptomes in Response to T Cell Activation.
Autorzy :
Shimizu K; Laboratory of Molecular Immunology, Institute for Quantitative Biosciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-0032, Japan; Division of Immune Regulation, Institute of Advanced Medical Sciences, Tokushima University, Tokushima 770-8503, Japan.
Sugiura D; Laboratory of Molecular Immunology, Institute for Quantitative Biosciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-0032, Japan; Division of Immune Regulation, Institute of Advanced Medical Sciences, Tokushima University, Tokushima 770-8503, Japan.
Okazaki IM; Laboratory of Molecular Immunology, Institute for Quantitative Biosciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-0032, Japan; Division of Immune Regulation, Institute of Advanced Medical Sciences, Tokushima University, Tokushima 770-8503, Japan.
Maruhashi T; Laboratory of Molecular Immunology, Institute for Quantitative Biosciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-0032, Japan; Division of Immune Regulation, Institute of Advanced Medical Sciences, Tokushima University, Tokushima 770-8503, Japan.
Takegami Y; K.K. DNAFORM, Yokohama, Kanagawa 230-0046, Japan.
Cheng C; K.K. DNAFORM, Yokohama, Kanagawa 230-0046, Japan.
Ozaki S; K.K. DNAFORM, Yokohama, Kanagawa 230-0046, Japan.
Okazaki T; Laboratory of Molecular Immunology, Institute for Quantitative Biosciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-0032, Japan; Division of Immune Regulation, Institute of Advanced Medical Sciences, Tokushima University, Tokushima 770-8503, Japan. Electronic address: .
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Źródło :
Molecular cell [Mol Cell] 2020 Mar 05; Vol. 77 (5), pp. 937-950.e6. Date of Electronic Publication: 2020 Jan 08.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Lymphocyte Activation*
Transcriptome*
Lymphocytes, Tumor-Infiltrating/*metabolism
Neoplasms/*metabolism
Programmed Cell Death 1 Receptor/*metabolism
T-Lymphocytes/*metabolism
Animals ; Apoptosis ; Binding Sites ; Cell Proliferation ; Coculture Techniques ; CpG Islands ; Cytokines/genetics ; Cytokines/metabolism ; Gene Expression Regulation, Neoplastic ; Genes, T-Cell Receptor ; HEK293 Cells ; Humans ; Jurkat Cells ; Lymphocytes, Tumor-Infiltrating/immunology ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Knockout ; Neoplasms/genetics ; Neoplasms/immunology ; Neoplasms/pathology ; Programmed Cell Death 1 Receptor/deficiency ; Programmed Cell Death 1 Receptor/genetics ; Promoter Regions, Genetic ; Signal Transduction ; T-Lymphocytes/immunology ; Transcription Factors/genetics ; Transcription Factors/metabolism ; Transcriptional Activation
Czasopismo naukowe
Tytuł :
Alterations in T and B Cell Receptor Repertoires Patterns in Patients With IL10 Signaling Defects and History of Infantile-Onset IBD.
Autorzy :
Werner L; Pediatric Gastroenterology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Lee YN; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.; Pediatric Department A, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Immunology Service, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Jeffrey Modell Foundation Center, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.
Rechavi E; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.; Pediatric Department A, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Immunology Service, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Jeffrey Modell Foundation Center, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.
Lev A; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.; Pediatric Department A, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Immunology Service, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Jeffrey Modell Foundation Center, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.
Yerushalmi B; Pediatric Gastroenterology Unit, Soroka University Medical Center, Ben Gurion University of the Negev, Be'er Sheva, Israel.
Ling G; Pediatric Gastroenterology Unit, Soroka University Medical Center, Ben Gurion University of the Negev, Be'er Sheva, Israel.
Shah N; Department of Gastroenterology, Great Ormond Street Hospital, London, United Kingdom.
Uhlig HH; Translational Gastroenterology Unit, Nuffield Department of Experimental Medicine, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.; Department of Pediatrics, University of Oxford, Oxford, United Kingdom.; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, United Kingdom.
Weiss B; Pediatric Gastroenterology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Somech R; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.; Pediatric Department A, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Immunology Service, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Jeffrey Modell Foundation Center, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.
Snapper SB; Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA, United States.; Harvard Medical School, Boston, MA, United States.
Shouval DS; Pediatric Gastroenterology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Centre, Ramat Gan, Israel.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
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Źródło :
Frontiers in immunology [Front Immunol] 2020 Feb 06; Vol. 11, pp. 109. Date of Electronic Publication: 2020 Feb 06 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Inflammatory Bowel Diseases/*immunology
Interleukin-10/*genetics
Receptors, Antigen, B-Cell/*genetics
Receptors, Antigen, T-Cell/*genetics
Receptors, Interleukin-10/*genetics
Adaptive Immunity ; B-Lymphocytes ; Child, Preschool ; Female ; Genes, T-Cell Receptor beta ; High-Throughput Nucleotide Sequencing ; Humans ; Infant ; Infant, Newborn ; Interleukin-10/deficiency ; Lymphocytes/immunology ; Male ; Mutation ; Receptors, Interleukin-10/deficiency ; Signal Transduction ; T-Lymphocytes
Czasopismo naukowe
Tytuł :
Simultaneous Deletion of Endogenous TCRαβ for TCR Gene Therapy Creates an Improved and Safe Cellular Therapeutic.
Autorzy :
Morton LT; Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: l.t..
Reijmers RM; Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands.
Wouters AK; Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands.
Kweekel C; Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands.
Remst DFG; Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands.
Pothast CR; Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands.
Falkenburg JHF; Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands.
Heemskerk MHM; Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: .
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Źródło :
Molecular therapy : the journal of the American Society of Gene Therapy [Mol Ther] 2020 Jan 08; Vol. 28 (1), pp. 64-74. Date of Electronic Publication: 2019 Oct 04.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
CRISPR-Cas Systems*
Adoptive Transfer/*methods
Gene Editing/*methods
Genetic Therapy/*methods
Multiple Myeloma/*therapy
Receptors, Antigen, T-Cell, alpha-beta/*genetics
Adoptive Transfer/adverse effects ; Animals ; Antigens, Neoplasm/immunology ; CD8-Positive T-Lymphocytes ; Female ; Genes, T-Cell Receptor ; Genetic Therapy/adverse effects ; Healthy Volunteers ; Humans ; K562 Cells ; Male ; Mice ; Mice, Inbred NOD ; Multiple Myeloma/pathology ; Receptors, Antigen, T-Cell, alpha-beta/immunology ; Transduction, Genetic ; Treatment Outcome ; Xenograft Model Antitumor Assays
Czasopismo naukowe
Tytuł :
Characterization of the diversity of T cell receptor γδ complementary determinant region 3 in human peripheral blood by Immune Repertoire Sequencing.
Autorzy :
Chen H; Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medicine, Peking Union Medical College, State Key Laboratory of Medical Molecular Biology, Beijing 100005, China.
Zou M; Department of Clinical Laboratory, Qilu Hospital of Shandong University, 107 Wenhua Xi Road, Jinan 250012, China.
Teng D; Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medicine, Peking Union Medical College, State Key Laboratory of Medical Molecular Biology, Beijing 100005, China.
Zhang J; Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medicine, Peking Union Medical College, State Key Laboratory of Medical Molecular Biology, Beijing 100005, China. Electronic address: .
He W; Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medicine, Peking Union Medical College, State Key Laboratory of Medical Molecular Biology, Beijing 100005, China. Electronic address: .
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Źródło :
Journal of immunological methods [J Immunol Methods] 2017 Apr; Vol. 443, pp. 9-17. Date of Electronic Publication: 2017 Jan 31.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Genes, T-Cell Receptor delta*
Genes, T-Cell Receptor gamma*
Complementarity Determining Regions/*genetics
Receptors, Antigen, T-Cell, gamma-delta/*genetics
Sequence Analysis, DNA/*methods
T-Lymphocytes/*immunology
Adult ; Aged ; Complementarity Determining Regions/immunology ; Female ; Gene Rearrangement, delta-Chain T-Cell Antigen Receptor ; Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor ; Genotype ; Healthy Volunteers ; Humans ; Male ; Middle Aged ; Phenotype ; Receptors, Antigen, T-Cell, gamma-delta/immunology ; Reverse Transcriptase Polymerase Chain Reaction
Czasopismo naukowe
Tytuł :
High frequency of clonal IG and T-cell receptor gene rearrangements in histiocytic and dendritic cell neoplasms.
Autorzy :
Huang W; Department of Pathology, National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Qiu T; Department of Pathology, National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Zeng L; Department of Pathology, National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Zheng B; Department of Pathology, National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Ying J; Department of Pathology, National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Feng X; Department of Pathology, National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
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Źródło :
Oncotarget [Oncotarget] 2016 Nov 29; Vol. 7 (48), pp. 78355-78362.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Rearrangement, beta-Chain T-Cell Antigen Receptor*
Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor*
Genes, Immunoglobulin Heavy Chain*
Genes, T-Cell Receptor beta*
Genes, T-Cell Receptor gamma*
Biomarkers, Tumor/*genetics
Histiocytic Disorders, Malignant/*genetics
Histiocytosis, Langerhans-Cell/*genetics
Immunoglobulin kappa-Chains/*genetics
Adolescent ; Adult ; Aged ; Child ; Dendritic Cell Sarcoma, Follicular/genetics ; Dendritic Cell Sarcoma, Follicular/immunology ; Dendritic Cell Sarcoma, Follicular/pathology ; Dendritic Cell Sarcoma, Interdigitating/genetics ; Dendritic Cell Sarcoma, Interdigitating/immunology ; Dendritic Cell Sarcoma, Interdigitating/pathology ; Female ; Genetic Predisposition to Disease ; Histiocytic Disorders, Malignant/immunology ; Histiocytic Disorders, Malignant/pathology ; Histiocytic Sarcoma/genetics ; Histiocytic Sarcoma/immunology ; Histiocytic Sarcoma/pathology ; Histiocytosis, Langerhans-Cell/immunology ; Histiocytosis, Langerhans-Cell/pathology ; Humans ; Langerhans Cell Sarcoma/genetics ; Langerhans Cell Sarcoma/immunology ; Langerhans Cell Sarcoma/pathology ; Male ; Middle Aged ; Phenotype ; Young Adult
Czasopismo naukowe
Tytuł :
Prospects for chimeric antigen receptor (CAR) γδ T cells: A potential game changer for adoptive T cell cancer immunotherapy.
Autorzy :
Mirzaei HR; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Mirzaei H; Department of Medical Biotechnology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Lee SY; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Hadjati J; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Cancer Biology Research Center, Tehran University of Medical Sciences, Tehran, Iran. Electronic address: .
Till BG; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. Electronic address: .
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Źródło :
Cancer letters [Cancer Lett] 2016 Oct 01; Vol. 380 (2), pp. 413-423. Date of Electronic Publication: 2016 Jul 05.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Genes, T-Cell Receptor delta*
Genes, T-Cell Receptor gamma*
Genetic Therapy/*methods
Immunotherapy, Adoptive/*methods
Lymphocytes, Tumor-Infiltrating/*transplantation
Neoplasms/*therapy
Receptors, Antigen, T-Cell, gamma-delta/*genetics
T-Lymphocytes/*transplantation
Animals ; Humans ; Lymphocytes, Tumor-Infiltrating/immunology ; Lymphocytes, Tumor-Infiltrating/metabolism ; Neoplasms/genetics ; Neoplasms/metabolism ; Neoplasms/pathology ; Phenotype ; Receptors, Antigen, T-Cell, gamma-delta/biosynthesis ; Receptors, Antigen, T-Cell, gamma-delta/immunology ; Recombinant Fusion Proteins/biosynthesis ; Recombinant Fusion Proteins/immunology ; T-Lymphocytes/immunology ; T-Lymphocytes/metabolism ; Tumor Microenvironment
Czasopismo naukowe
Tytuł :
High-throughput single-cell sequencing of paired TCRα and TCRβ genes for the direct expression-cloning and functional analysis of murine T-cell receptors.
Autorzy :
Ludwig J; Department of B Cell Immunology, German Cancer Research Center, Heidelberg, Germany.
Huber AK; Department of B Cell Immunology, German Cancer Research Center, Heidelberg, Germany.
Bartsch I; Department of B Cell Immunology, German Cancer Research Center, Heidelberg, Germany.
Busse CE; Department of B Cell Immunology, German Cancer Research Center, Heidelberg, Germany.
Wardemann H; Department of B Cell Immunology, German Cancer Research Center, Heidelberg, Germany.
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Źródło :
European journal of immunology [Eur J Immunol] 2019 Aug; Vol. 49 (8), pp. 1269-1277. Date of Electronic Publication: 2019 May 02.
Typ publikacji :
Journal Article
MeSH Terms :
Genes, T-Cell Receptor alpha/*genetics
Genes, T-Cell Receptor beta/*genetics
High-Throughput Nucleotide Sequencing/*methods
Receptors, Antigen, T-Cell, alpha-beta/*genetics
T-Lymphocytes/*physiology
Animals ; Clone Cells ; Mice ; Phenotype ; Single-Cell Analysis
Czasopismo naukowe
Tytuł :
Safety and persistence of WT1-specific T-cell receptor gene-transduced lymphocytes in patients with AML and MDS.
Autorzy :
Tawara I; Department of Hematology and Oncology and.
Kageyama S; Department of Immuno-Gene Therapy, Mie University Graduate School of Medicine, Mie, Japan.
Miyahara Y; Department of Immuno-Gene Therapy, Mie University Graduate School of Medicine, Mie, Japan.
Fujiwara H; Department of Hematology, Clinical Immunology and Infectious Diseases, Graduate School of Medicine, Ehime University, Ehime, Japan.
Nishida T; Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Aichi, Japan.
Akatsuka Y; Department of Hematology, Fujita Health University School of Medicine, Aichi, Japan.
Ikeda H; Department of Oncology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; and.
Tanimoto K; Department of Hematology, Clinical Immunology and Infectious Diseases, Graduate School of Medicine, Ehime University, Ehime, Japan.
Terakura S; Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Aichi, Japan.
Murata M; Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Aichi, Japan.
Inaguma Y; Department of Hematology, Fujita Health University School of Medicine, Aichi, Japan.
Masuya M; Department of Hematology and Oncology and.
Inoue N; Takara Bio Inc., Shiga, Japan.
Kidokoro T; Takara Bio Inc., Shiga, Japan.
Okamoto S; Takara Bio Inc., Shiga, Japan.
Tomura D; Takara Bio Inc., Shiga, Japan.
Chono H; Takara Bio Inc., Shiga, Japan.
Nukaya I; Takara Bio Inc., Shiga, Japan.
Mineno J; Takara Bio Inc., Shiga, Japan.
Naoe T; Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Aichi, Japan.
Emi N; Department of Hematology, Fujita Health University School of Medicine, Aichi, Japan.
Yasukawa M; Department of Hematology, Clinical Immunology and Infectious Diseases, Graduate School of Medicine, Ehime University, Ehime, Japan.
Katayama N; Department of Hematology and Oncology and.
Shiku H; Department of Immuno-Gene Therapy, Mie University Graduate School of Medicine, Mie, Japan.
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Źródło :
Blood [Blood] 2017 Nov 02; Vol. 130 (18), pp. 1985-1994. Date of Electronic Publication: 2017 Aug 31.
Typ publikacji :
Clinical Trial, Phase I; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Genes, T-Cell Receptor*
Transduction, Genetic*
Leukemia, Myeloid, Acute/*therapy
Myelodysplastic Syndromes/*therapy
T-Lymphocytes/*metabolism
WT1 Proteins/*genetics
Adoptive Transfer ; Aged ; Bone Marrow/pathology ; Female ; Humans ; Kinetics ; Leukemia, Myeloid, Acute/genetics ; Male ; Middle Aged ; Myelodysplastic Syndromes/genetics ; Peptides/pharmacology
Czasopismo naukowe

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