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1. Full Text Functional heterogeneity and antimycobacterial effects of mouse mucosal-associated invariant T cells specific for riboflavin metabolites
by Sakala, Isaac G and Kjer-Nielsen, Lars and Eickhoff, Christopher S and Wang, Xiaoli and Blazevic, Azra and Liu, Ligong and Fairlie, David P and Rossjohn, Jamie and McCluskey, James and Fremont, Daved H and Hansen, Ted H and Hoft, Daniel F
Journal of Immunology, ISSN 0022-1767, 07/2015, Volume 195, Issue 2, pp. 587 - 601
Mucosal-associated invariant T (MAIT) cells have a semi-invariant TCR V alpha-chain, and their optimal development is dependent upon commensal flora and... 
MYCOBACTERIUM-TUBERCULOSIS | ANTIGEN RECEPTOR RECOGNITION | IMMUNE-RESPONSE | NATURAL-KILLER-CELLS | MAIT CELLS | NK CELLS | MULTIPLE-SCLEROSIS | VITAMIN-B METABOLITES | TCR ALPHA-CHAIN | BACTERIAL-INFECTION | IMMUNOLOGY | Lung - microbiology | Interleukin-18 - immunology | Mycobacterium bovis - immunology | Immunity, Mucosal | Receptors, Antigen, T-Cell, alpha-beta - immunology | Antigens, CD - genetics | Riboflavin - analogs & derivatives | CD4-Positive T-Lymphocytes - immunology | Tuberculosis - pathology | CD4-Positive T-Lymphocytes - microbiology | Signal Transduction | Riboflavin - immunology | Genetic Heterogeneity | Mice, Knockout | Integrin alpha4beta1 - immunology | Lung - drug effects | Receptors, CXCR3 - genetics | Interleukin-12 - immunology | Receptors, CXCR3 - immunology | Hyaluronan Receptors - immunology | Mice | CD8-Positive T-Lymphocytes - immunology | Interleukin-18 - genetics | Antigens, CD - immunology | CD8-Positive T-Lymphocytes - pathology | Interleukin-12 - genetics | Minor Histocompatibility Antigens | Protein Multimerization | Antigens, Ly - genetics | Lectins, C-Type - immunology | Tuberculosis - microbiology | Riboflavin - pharmacology | CD4-Positive T-Lymphocytes - pathology | Lectins, C-Type - genetics | Gene Expression Regulation, Developmental | CD8-Positive T-Lymphocytes - microbiology | Antigens, Differentiation, T-Lymphocyte - immunology | Mice, Inbred C57BL | Cells, Cultured | Histocompatibility Antigens Class I - immunology | Integrin alpha4beta1 - genetics | Histocompatibility Antigens Class I - genetics | Tuberculosis - veterinary | Hyaluronan Receptors - genetics | NK Cell Lectin-Like Receptor Subfamily B - immunology | Receptors, Antigen, T-Cell, alpha-beta - genetics | Tuberculosis - immunology | Animals | Antigens, Ly - immunology | NK Cell Lectin-Like Receptor Subfamily B - genetics | CD8-Positive T-Lymphocytes - drug effects | Antigens, Differentiation, T-Lymphocyte - genetics | Immunologic Memory | CD4-Positive T-Lymphocytes - drug effects | Lung - immunology | Index Medicus | Abridged Index Medicus
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2. Full Text CD44 antibody inhibition of macrophage phagocytosis targets Fcγ receptor-and complement receptor 3-dependent mechanisms
by Amash, Alaa and Wang, Lin and Wang, Yawen and Bhakta, Varsha and Fairn, Gregory D and Hou, Ming and Peng, Jun and Sheffield, William P and Lazarus, Alan H
Journal of Immunology, ISSN 0022-1767, 04/2016, Volume 196, Issue 8, pp. 3331 - 3340
Targeting CD44, a major leukocyte adhesion molecule, using specific Abs has been shown beneficial in several models of autoimmune and inflammatory diseases.... 
MURINE MODEL | CELLS | MOLECULE | INFLAMMATION | IN-VIVO | INVOLVEMENT | LEUKOCYTE EXTRAVASATION | IMMUNOLOGY | MONOCLONAL-ANTIBODIES | ARTHRITIS | MEDIATED PHAGOCYTOSIS | Erythrocytes - immunology | Cell Line | Anti-Inflammatory Agents - pharmacology | Antibodies, Monoclonal - pharmacology | Mice, Inbred C57BL | Lectins, C-Type - immunology | Phagocytosis - immunology | Anti-Inflammatory Agents - immunology | Antibodies, Blocking - pharmacology | Inflammation - immunology | Receptors, IgG - immunology | Mice, Knockout | Zymosan - immunology | Animals | Receptors, Complement - immunology | Immunoglobulin G - immunology | Antibodies, Blocking - immunology | Hyaluronan Receptors - immunology | Inflammation - prevention & control | Mice | Antibodies, Monoclonal - immunology | Macrophages - immunology | Index Medicus | Abridged Index Medicus
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3. Full Text Galectin-9-CD44 Interaction Enhances Stability and Function of Adaptive Regulatory T Cells
by Wu, Chuan and Thalhamer, Theresa and Franca, Rafael F and Xiao, Sheng and Wang, Chao and Hotta, Chie and Zhu, Chen and Hirashima, Mitsuomi and Anderson, Ana C and Kuchroo, Vijay K
Immunity, ISSN 1074-7613, 08/2014, Volume 41, Issue 2, pp. 270 - 282
The β-galactoside-binding protein galectin-9 is critical in regulating the immune response, but the mechanism by which it functions remains unclear. We have... 
SIGNAL-TRANSDUCTION | FOXP3 EXPRESSION | GROWTH-FACTOR-BETA | TGF-BETA | DENDRITIC CELLS | IFN-GAMMA | INFLAMMATION | IN-VIVO | RETINOIC-ACID | REG-CELLS | IMMUNOLOGY | Transforming Growth Factor beta - immunology | Forkhead Transcription Factors - biosynthesis | Receptors, Transforming Growth Factor beta - immunology | Colitis - genetics | Mice, Inbred C57BL | Smad3 Protein - immunology | Hepatitis A Virus Cellular Receptor 2 | Mice, Knockout | T-Lymphocytes, Regulatory - immunology | Cell Differentiation - immunology | Signal Transduction - immunology | Lymphocyte Activation - immunology | Animals | Galectins - immunology | Receptors, Virus - immunology | Protein-Serine-Threonine Kinases - immunology | Hyaluronan Receptors - immunology | Mice | Colitis - immunology | Galectins - genetics | Bone morphogenetic proteins | T cells | Transforming growth factors | Cell differentiation | Protein binding | Software | Statistical analysis | Lymphocytes | Experiments | Rodents | Index Medicus
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4. Full Text γδ T Cells Exhibit Multifunctional and Protective Memory in Intestinal Tissues
by Sheridan, Brian S and Romagnoli, Pablo A and Pham, Quynh-Mai and Fu, Han-Hsuan and Alonzo, Francis and Schubert, Wolf-Dieter and Freitag, Nancy E and Lefrançois, Leo
Immunity, ISSN 1074-7613, 07/2013, Volume 39, Issue 1, pp. 184 - 195
The study of T cell memory and the target of vaccine design have focused on memory subsumed by T cells bearing the αβ T cell receptor. Alternatively, γδ... 
T-Lymphocyte Subsets - immunology | Intestinal Mucosa - metabolism | Interleukin-17 - immunology | Receptors, Antigen, T-Cell, gamma-delta - genetics | Intestines - metabolism | Interferon-gamma - metabolism | Listeria monocytogenes - immunology | Intestines - immunology | Host-Pathogen Interactions - immunology | Flow Cytometry | T-Lymphocytes - metabolism | Intestinal Mucosa - immunology | Hyaluronan Receptors - metabolism | Listeriosis - immunology | Female | Listeria monocytogenes - physiology | Adaptive Immunity - immunology | Immunologic Memory - immunology | Tumor Necrosis Factor Receptor Superfamily, Member 7 - immunology | Amino Acid Sequence | Listeriosis - metabolism | Receptors, Antigen, T-Cell, gamma-delta - metabolism | Cells, Cultured | Receptors, Antigen, T-Cell, gamma-delta - immunology | Interleukin-17 - metabolism | Animals | T-Lymphocyte Subsets - metabolism | Tumor Necrosis Factor Receptor Superfamily, Member 7 - metabolism | Interferon-gamma - immunology | T-Lymphocytes - immunology | Hyaluronan Receptors - immunology | Mice | Mice, Congenic | Mice, Inbred BALB C | Index Medicus
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5. Full Text CD44v6-targeted T cells mediate potent antitumor effects against acute myeloid leukemia and multiple myeloma
by Casucci, Monica and Casucci, Monica and Nicolis di Robilant, Benedetta and Di Robilant, Benedetta Nicolis and Falcone, Laura and Falcone, Laura and Camisa, Barbara and Camisa, Barbara and Norelli, Margherita and Norelli, Margherita and Genovese, Pietro and Genovese, Pietro and Gentner, Bernhard and Gentner, Bernhard and Gullotta, Fabiana and Gullotta, Fabiana and Ponzoni, Maurilio and Ponzoni, Maurilio and Bernardi, Massimo and Bernardi, Massimo and Marcatti, Magda and Marcatti, Magda and Saudemont, Aurore and Saudemont, Aurore and Bordignon, Claudio and Bordignon, Claudio and Savoldo, Barbara and Savoldo, Barbara and Ciceri, Fabio and Ciceri, Fabio and Naldini, Luigi and Naldini, Luigi and Dotti, Gianpietro and Dotti, Gianpietro and Bonini, Chiara and Bonini, Chiara and Bondanza, Attilio and Bondanza, Attilio
Blood, ISSN 0006-4971, 2013, Volume 122, Issue 20, pp. 3461 - 3472
Genetically targeted T cells promise to solve the feasibility and efficacy hurdles of adoptive T-cell therapy for cancer. Selecting a target expressed in... 
STEM-CELLS | ADVERSE EVENT | CLINICAL-TRIAL | GRAFT-VERSUS-LEUKEMIA | CHIMERIC-ANTIGEN-RECEPTOR | BONE-MARROW | GENE-THERAPY | HEMATOLOGY | PHASE-I | ADOPTIVE IMMUNOTHERAPY | DONOR LYMPHOCYTES | Graft vs Host Disease - therapy | Recombinant Fusion Proteins - immunology | T-Lymphocyte Subsets - immunology | Neoplasm Transplantation | Humans | Interleukin-7 - pharmacology | Multiple Myeloma - immunology | Cell Line, Tumor - transplantation | Leukemia, Myeloid, Acute - immunology | Molecular Targeted Therapy | Interleukin-15 - immunology | Multiple Myeloma - therapy | Leukemia, Myelomonocytic, Acute - therapy | Leukemia, Myeloid, Acute - therapy | Protein Structure, Tertiary | Antigens, Neoplasm - genetics | Genes, Transgenic, Suicide | Immunotherapy, Adoptive | Antigens, Neoplasm - immunology | Leukemia, Myeloid, Acute - pathology | Lymphocyte Activation | RNA, Small Interfering - pharmacology | CD28 Antigens - immunology | Hyaluronan Receptors - genetics | Xenograft Model Antitumor Assays | Interleukin-15 - pharmacology | Multiple Myeloma - pathology | Animals | Interleukin-7 - immunology | Leukemia, Myelomonocytic, Acute - pathology | Cell Line, Tumor - immunology | CD3 Complex - immunology | Leukemia, Myelomonocytic, Acute - immunology | T-Cell Antigen Receptor Specificity | Hyaluronan Receptors - immunology | Mice | Cytotoxicity, Immunologic | Index Medicus | Abridged Index Medicus
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6. Full Text Actively targeted in vivo multiplex detection of intrinsic cancer biomarkers using biocompatible SERS nanotags
by Dinish, U.S and Balasundaram, Ghayathri and Chang, Young-Tae and Olivo, Malini
Scientific Reports, ISSN 2045-2322, 02/2014, Volume 4, Issue 1, pp. 4075 - 4075
Surface-enhanced Raman scattering (SERS) technique is becoming highly popular for multiplex biosensing due to the 'fingerprint' Raman spectra from every... 
GROWTH-FACTOR RECEPTOR | NANOPARTICLES | CELLS | DIAGNOSIS | SPECTROSCOPY | DRUG-DELIVERY | MULTIDISCIPLINARY SCIENCES | BIODISTRIBUTION | ENHANCED RAMAN-SCATTERING | IMMUNOASSAY | CHEMOTHERAPY | Protein-Serine-Threonine Kinases - analysis | Biocompatible Materials - metabolism | Receptor, Epidermal Growth Factor - immunology | Antibodies, Immobilized - immunology | Receptors, Transforming Growth Factor beta - analysis | Receptors, Transforming Growth Factor beta - immunology | Nanoparticles - chemistry | Biomarkers, Tumor - analysis | Biocompatible Materials - chemistry | Humans | Transplantation, Heterologous | Neoplasms - diagnosis | Receptor, Epidermal Growth Factor - analysis | Hyaluronan Receptors - analysis | Animals | Mice, Nude | Cell Line, Tumor | Female | Protein-Serine-Threonine Kinases - immunology | Spectrum Analysis, Raman | Hyaluronan Receptors - immunology | Mice | Mice, Inbred BALB C | Biomarkers, Tumor - immunology | Nanoparticles | Epidermal growth factor receptors | CD44 antigen | Biomarkers | Antibodies | Breast cancer | Biosensors | Raman spectroscopy | Cell surface | Cancer | Index Medicus
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7. Full Text Tumour-derived microvesicles carry several surface determinants and mRNA of tumour cells and transfer some of these determinants to monocytes
by Baj-Krzyworzeka, Monika and Szatanek, Rafał and Węglarczyk, Kazimierz and Baran, Jarosław and Urbanowicz, Barbara and Brański, Piotr and Ratajczak, Mariusz Z and Zembala, Marek
Cancer Immunology, Immunotherapy, ISSN 0340-7004, 7/2006, Volume 55, Issue 7, pp. 808 - 818
This study was designed to determine the characteristics of tumour cell-derived microvesicles (TMV) and their interactions with human monocytes. TMV were shed... 
Monocytes | Biomedicine | Immunology | Transfer | Oncology | Cancer Research | mRNA | CCR6 | Tumour-derived microvesicles | CANCER-CELLS | monocytes | ACTIVATION | POLYMORPHONUCLEAR LEUKOCYTES | ADHESION MOLECULES | IMMUNOLOGY | IN-VITRO | transfer | PLATELET MICROPARTICLES | ONCOLOGY | MEMBRANE-VESICLES | GENE-EXPRESSION | MELANOMA-CELLS | ENDOTHELIAL MICROPARTICLES | tumour-derived microvesicles | RNA, Messenger - immunology | Adenocarcinoma - ultrastructure | Tetradecanoylphorbol Acetate - pharmacology | Humans | Neoplasm Proteins - immunology | RNA, Messenger - analysis | Cell Line, Tumor - drug effects | Gene Expression Profiling | Monocytes - immunology | Membrane Proteins - analysis | Basigin - genetics | Basigin - immunology | Antigens, Neoplasm - analysis | Neoplasm Proteins - genetics | Receptors, Chemokine | Receptors, Cytokine - genetics | Antigens, Neoplasm - immunology | Cell Survival | Adenocarcinoma - immunology | RNA, Messenger - genetics | HLA Antigens - immunology | Pancreatic Neoplasms - ultrastructure | Immunophenotyping | Membrane Proteins - immunology | Cell Membrane - ultrastructure | Neoplasms - ultrastructure | Chemotaxis | Hyaluronan Receptors - genetics | Particle Size | Cell Line, Tumor - ultrastructure | Lung Neoplasms - immunology | Colorectal Neoplasms - immunology | Neoplasms - immunology | Cell Line, Tumor - immunology | Pancreatic Neoplasms - immunology | Colorectal Neoplasms - ultrastructure | Lung Neoplasms - ultrastructure | Neoplasm Proteins - analysis | Receptors, Cytokine - immunology | Cell Membrane - immunology | Genes, MHC Class I | Hyaluronan Receptors - immunology | Apoptosis | Growth factors | Messenger RNA | Tumors | Index Medicus
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8. Full Text Inhibition of follicular T-helper cells by CD8 + regulatory T cells is essential for self tolerance
by Cantor, Harvey and Tang, Xiaolei and Kim, Hye-Jung and Verbinnen, Bert and Lu, Linrong
Nature, ISSN 0028-0836, 09/2010, Volume 467, Issue 7313, pp. 328 - 332
The ability to produce vigorous immune responses that spare self tissues and organs depends on the elimination of autoreactive T and B cells. However, purging... 
B-CELLS | SYSTEMIC-LUPUS-ERYTHEMATOSUS | MULTIDISCIPLINARY SCIENCES | T-HELPER-2 | EXPANSION | IL-15 | GENERATION | MICE | SUPPRESSION | AUTOIMMUNE-DISEASE | IL-21 | CD8-Positive T-Lymphocytes - cytology | Immunoglobulin G - blood | Self Tolerance - immunology | Germinal Center - immunology | Antibody Affinity - immunology | Autoantibodies - biosynthesis | T-Lymphocytes, Regulatory - immunology | Histocompatibility Antigens Class I - metabolism | T-Lymphocytes, Helper-Inducer - immunology | Hyaluronan Receptors - metabolism | Lupus Erythematosus, Systemic - immunology | T-Lymphocytes, Helper-Inducer - cytology | T-Lymphocytes, Regulatory - cytology | Antibodies - immunology | Germinal Center - cytology | T-Lymphocytes, Helper-Inducer - metabolism | Histocompatibility Antigens Class I - immunology | Histocompatibility Antigens Class I - genetics | Cell Lineage | Autoantibodies - immunology | Models, Immunological | Animals | Antigens - immunology | Hyaluronan Receptors - immunology | Mice | Mutation | CD8-Positive T-Lymphocytes - immunology | Index Medicus
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9. Full Text CD4 effector T cell subsets in the response to influenza: Heterogeneity, migration, and function
by Román, Eulogia and Miller, Ellen and Harmsen, Allen and Wiley, James and Von Andrian, Ulrich H and Huston, Gail and Swain, Susan L
Journal of Experimental Medicine, ISSN 0022-1007, 10/2002, Volume 196, Issue 7, pp. 957 - 968
The immune response of naive CD4 T cells to influenza virus is initiated in the draining lymph nodes and spleen, and only after effectors are generated do... 
Inflammation | Cytokines | Memory | Migration | Chemokine receptors | MEDICINE, RESEARCH & EXPERIMENTAL | chemokine receptors | memory | HEMAGGLUTININ | LYMPH-NODES | IMMUNOLOGY | MEMORY CELLS | CUTTING EDGE | inflammation | IN-VIVO | migration | cytokines | DIFFERENTIATION | HIGH ENDOTHELIAL VENULES | RESPIRATORY VIRUS-INFECTIONS | ANTIGEN | LYMPHOCYTES | T-Lymphocyte Subsets - immunology | Spleen - immunology | Bronchoalveolar Lavage Fluid - immunology | T-Lymphocyte Subsets - physiology | CD4-Positive T-Lymphocytes - physiology | CD4-Positive T-Lymphocytes - immunology | L-Selectin - immunology | Influenza A virus - immunology | Receptors, Antigen, T-Cell - immunology | CD4-Positive T-Lymphocytes - virology | Lymphocyte Activation | Receptors, CCR7 | Immunophenotyping | Mice, Transgenic | Receptors, Chemokine - immunology | Receptors, Interleukin-2 - immunology | T-Lymphocyte Subsets - virology | Animals | Hyaluronan Receptors - immunology | Mice | Mice, Inbred BALB C | Receptors, Antigen, T-Cell - genetics | Receptors, CCR3 | Lung - immunology | Orthomyxoviridae Infections - immunology | Index Medicus
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10. Full Text Increased Osteopontin Expression in Dendritic Cells Amplifies IL-17 Production by CD4+ T Cells in Experimental Autoimmune Encephalomyelitis and in Multiple Sclerosis
by Murugaiyan, Gopal and Mittal, Akanksha and Weiner, Howard L
The Journal of Immunology, ISSN 0022-1767, 12/2008, Volume 181, Issue 11, pp. 7480 - 7488
Osteopontin (Opn) is a broadly expressed pleiotropic cytokine, and has been shown to play an important role in various autoimmune diseases, including multiple... 
SURVIVAL | GROWTH-FACTOR-BETA | ROR-GAMMA-T | INFLAMMATION | HELPER-CELLS | TISSUE | DIFFERENTIATION | INDUCTION | IMMUNOLOGY | PROGRESSION | DISEASE-ACTIVITY | Osteopontin - genetics | Integrin beta3 - immunology | Integrin alphaV - immunology | Osteopontin - antagonists & inhibitors | Dendritic Cells - immunology | Humans | Interleukin-17 - immunology | Encephalomyelitis, Autoimmune, Experimental - immunology | Th1 Cells - immunology | Integrin beta3 - genetics | Encephalomyelitis, Autoimmune, Experimental - genetics | Interferon-gamma - genetics | Integrin alphaV - genetics | Gene Expression Regulation - immunology | Cells, Cultured | Interleukin-17 - genetics | Multiple Sclerosis - genetics | Hyaluronan Receptors - genetics | Mice, Knockout | Osteopontin - immunology | Antibodies - pharmacology | Gene Expression Regulation - drug effects | Cell Differentiation - immunology | Animals | Interferon-gamma - immunology | Interleukin-10 - genetics | Multiple Sclerosis - immunology | Hyaluronan Receptors - immunology | Mice | Interleukin-10 - immunology | Index Medicus | Abridged Index Medicus | EAE | Dendritic cells | T cells | MS and Osteopontin
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11. Full Text IL-21 Limits NK Cell Responses and Promotes Antigen-Specific T Cell Activation: A Mediator of the Transition from Innate to Adaptive Immunity
by Kasaian, Marion T and Whitters, Matthew J and Carter, Laura L and Lowe, Leslie D and Jussif, Jason M and Deng, Bijia and Johnson, Kaley A and Witek, JoAnn S and Senices, Mayra and Konz, Richard F and Wurster, Andrea L and Donaldson, Debra D and Collins, Mary and Young, Deborah A and Grusby, Michael J
Immunity, ISSN 1074-7613, 2002, Volume 16, Issue 4, pp. 559 - 569
IFNα/β, IL-12, and IL-15 regulate NK cell activation and expansion, but signals triggering resolution of the NK response upon induction of adaptive immunity... 
SURVIVAL | NATURAL-KILLER-CELLS | HOMEOSTASIS | HEMATOPOIETIC PROGENITOR CELLS | RECEPTOR-BETA CHAIN | INTERLEUKIN-15 | IN-VIVO | EXPANSION | PROLIFERATION | IMMUNOLOGY | MICE LACKING | Male | Interleukin-15 - immunology | Lymphocyte Activation - immunology | Interleukins - immunology | Isoantigens - immunology | Killer Cells, Natural - immunology | Female | Interleukins - pharmacology | Immunity, Active | Receptors, Interleukin-21 | Receptors, Interleukin - immunology | Receptors, Interleukin-2 - biosynthesis | Mice, Inbred C57BL | Immunity, Innate | Receptors, Interleukin - genetics | Mice, Knockout | Killer Cells, Natural - cytology | Animals | Apoptosis - immunology | Lymphocyte Count | Hyaluronan Receptors - immunology | Interleukin-21 Receptor alpha Subunit | Mice | Mice, Inbred BALB C | CD8-Positive T-Lymphocytes - immunology | Cytotoxicity, Immunologic | Spleen | Flow cytometry | Cell growth | Lymphocytes | Cytotoxicity | T cell receptors | Immune system | interleukin 12 receptors | g-Interferon | Index Medicus
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12. Full Text Brca1 breast tumors contain distinct CD44+/CD24- and CD133+ cells with cancer stem cell characteristics
by Wright, Mollie H and Calcagno, Anna M and Salcido, Crystal D and Carlson, Marisa D and Ambudkar, Suresh V and Varticovski, Lyuba
Breast Cancer Research, ISSN 1465-5411, 02/2008, Volume 10, Issue 1, pp. R10 - R10
Introduction Whether cancer stem cells occur in BRCA1-associated breast cancer and contribute to therapeutic response is not known. Methods We generated and... 
GENE | ONCOLOGY | SIGNALING PATHWAY | DNA-DAMAGE RESPONSE | INHIBITOR 17-(DIMETHYLAMINOETHYLAMINO)-17-DEMETHOXYGELDANAMYCIN | MAMMARY-GLAND CELLS | SPORADIC BREAST | OVARIAN-CANCER | MUTATIONS | IDENTIFICATION | MOUSE MODELS | Antigens, CD - immunology | Stem Cells - immunology | BRCA1 Protein - immunology | Breast Neoplasms - immunology | Peptides - immunology | AC133 Antigen | Glycoproteins - immunology | Animals | Cell Line, Tumor | Female | Hyaluronan Receptors - immunology | Mice | Biomarkers, Tumor - immunology | CD24 Antigen - immunology | Disease Models, Animal | Heat shock proteins | Breast cancer | Genetic aspects | Health aspects | Stem cells | Cancer | Index Medicus
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