يعرض 1 - 10 نتائج من 22 نتيجة بحث عن '"CD40 Antigen"', وقت الاستعلام: 2.02s تنقيح النتائج
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    دورية أكاديمية
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    المساهمون: Franco, G, Guarnotta, C, Frossi, Piccaluga, PP, Boveri, E, Gulino, A, Fuligni, F, Rigoni, A, Porcasi, R, Buffa, S, Betto, E, Florena, AM, Franco, V, Iannitto, E, Arcaini, L, Pileri, SA, Pucillo, C, Colombo, MP, Sangaletti, S, Tripodo, C, Franco, Giovanni, Guarnotta, Carla, Frossi, Barbara, Piccaluga, Pier Paolo, Boveri, Emanuela, Gulino, Alessandro, Fuligni, Fabio, Rigoni, Alice, Porcasi, Rossana, Buffa, Salvatore, Betto, Elena, Florena, Ada Maria, Franco, Vito, Iannitto, Emilio, Arcaini, Luca, Pileri, Stefano Aldo, Pucillo, Carlo, Colombo, Mario Paolo, Sangaletti, Sabina, Tripodo, Claudio

    المصدر: Blood. 123:1836-1849

    وصف الملف: STAMPA

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    دورية أكاديمية

    المصدر: Human Molecular Genetics

    العلاقة: Gandhi, Kaushal, McKay, Fiona, Cox, Mathew, Riveros, Carlos, Armstrong, Nicola, Heard, Robert, Vucic, Stephen, Williams, David, Stankovich, Jim, Brown, Matthew, Danoy, Patrick, Stewart, Graeme, Broadley, Simon, Moscato, Pablo, Lechner-Scott, Jeannette, Scott, Rodney, & Booth, David (2010) The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis. Human Molecular Genetics, 19(11), pp. 2134-2143.; https://eprints.qut.edu.au/218071Test/; Faculty of Health; Institute of Health and Biomedical Innovation

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    المصدر: Repositorio EdocUR-U. Rosario
    Universidad del Rosario
    instacron:Universidad del Rosario

    وصف الملف: application/pdf

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    دورية أكاديمية
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    المساهمون: Uludağ Üniversitesi/ Tıp Fakültesi/ Pediatri Anabilim Dalı., Kılı., Sara Şebnem

    مصطلحات موضوعية: Amino acid substitution, Bone marrow cell, Disease gene sh2d1a, Major histocompatibility complex, B lymphocyte receptor, Immune deficiency, Antigens, CD79, Autoimmunity, Review, Bruton tyrosine kinase, Antibody-deficiency syndrome, CD40 antigen, Genetic heterogeneity, Opportunistic infection, Agammaglobulinemia, Immunoglobulin A deficiency, Pre B lymphocyte, Symptomatology, Scaffold protein, Priority journal, B-Lymphocytes, Adaptor proteins, signal transducing, Antigens, differentiation, T-Lymphocyte, Protein-tyrosine kinases, Cellular immunity, Immunologic deficiency syndromes, Amino acid, Bruton Tyrosine Kinase, Bruton Type Agammaglobulinemia, Ibrutinib, Btk, CD79b antigen, Hyper IgM syndrome, CD27 antigen, Dysgammaglobulinemia, CD40 ligand, Human, Precursor cells, B-Lymphoid, Neutropenia, X-linked agammaglobulinemia, Antigens, CD19, Immunology, X linked agammaglobulinemia, Patient care, Beta 2 microglobulin, Common variable immunodeficiency, Sepsis, Autosomal recessive form, Immunoglobulin, Animals, Humans, Genotype phenotype correlation, Meningitis, Gene mutation, Empyema, Hyper-igm syndrome, lymphocyte activation, Autosomal recessive disorder, B lymphocyte, TACI, CD19 antigen, Pneumonia, Transmembrane activator and CAML interactor protein, Immunoglobulin E, Nonhuman, Induced cytidine deaminase, Environmental factor, Immunoglobulin A, Immunoglobulin M, Immunoglobulin G, Immunoglobulin G1, Brutons tyrosine kinase, Mutation, Genetic association, Transmembrane activator and CAML interactor, Genetic variability, Cell maturation, Class-switch recombination, Macroglobulin