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Wyszukujesz frazę ""Antigens, CD -- metabolism"" wg kryterium: Temat


Tytuł :
Caveolin-1 opens endothelial cell junctions by targeting catenins.
Autorzy :
Kronstein, Romy
Seebach, Jochen
Großklaus, Sylvia
Minten, Carsten
Engelhardt, Britta
Drab, Marek
Liebner, Stefan
Arsenijevic, Yvan
Taha, Abdallah Abu
Afanasieva, Tatiana
Schnittler, Hans-Joachim
Pokaż więcej
Temat :
Animals
Antigens, CD/metabolism
Base Sequence
CHO Cells
Cadherins/metabolism
Catenins/metabolism
Caveolin 1/deficiency
Caveolin 1/genetics
Cell Line
Cricetinae
Cricetulus
DNA Primers/genetics
Endothelial Cells/drug effects
Endothelial Cells/metabolism
Human Umbilical Vein Endothelial Cells
Humans
Intercellular Junctions/drug effects
Intercellular Junctions/metabolism
Mice
Mice, Knockout
Multiprotein Complexes/metabolism
Mutant Proteins/genetics
Mutant Proteins/metabolism
Thrombin/pharmacology
Źródło :
Kronstein, Romy; Seebach, Jochen; Grossklaus, Sylvia; Minten, Carsten; Engelhardt, Britta; Drab, Marek; Liebner, Stefan; Arsenijevic, Yvan; Taha, Abdallah Abu; Afanasieva, Tatiana; Schnittler, Hans-Joachim (2012). Caveolin-1 opens endothelial cell junctions by targeting catenins. Cardiovascular research, 93(1), pp. 130-40. Oxford: Oxford University Press 10.1093/cvr/cvr256
Cardiovascular Research, vol. 93, no. 1, pp. 130-140
Opis pliku :
application/pdf
Tytuł :
Elucidation of altered pathways in tumor-initiating cells of triple-negative breast cancer:A useful cell model system for drug screening
Autorzy :
Christensen, Anne G
Ehmsen, Sidse
Terp, Mikkel G
Batra, Richa
Alcaraz, Nicolas
Baumbach, Jan
Noer, Julie Boertmann
Moreira, José M A
Leth-Larsen, Rikke
Larsen, Martin R
Ditzel, Henrik J
Pokaż więcej
Temat :
Journal Article
NF-κB
Targeted treatment
Cancer stem cells
Mammospheres
Apoptosis
Triple-negative breast cancer
Cell Proliferation
Antigens, CD/metabolism
Humans
Neoplastic Stem Cells/pathology
Protein Interaction Maps
Triple Negative Breast Neoplasms/drug therapy
Cell Shape
Mass Spectrometry
Epithelial-Mesenchymal Transition
Female
Drug Evaluation, Preclinical
Wnt Signaling Pathway
Spheroids, Cellular/pathology
Reproducibility of Results
Signal Transduction
Cell Survival
Carcinogenesis/metabolism
Animals
Models, Biological
Proteomics
Cell Line, Tumor
Mice
Biomarkers, Tumor/metabolism
Źródło :
Christensen, A G, Ehmsen, S, Terp, M G, Batra, R, Alcaraz, N, Baumbach, J, Noer, J B, Moreira, J M A, Leth-Larsen, R, Larsen, M R & Ditzel, H J 2017, ' Elucidation of altered pathways in tumor-initiating cells of triple-negative breast cancer : A useful cell model system for drug screening ', Stem Cells, vol. 35, no. 8, pp. 1898–1912 . https://doi.org/10.1002/stem.2654
Tytuł :
Soluble Siglec-5 associates to PSGL-1 and displays anti-inflammatory activity
Autorzy :
Pepin, Marion
Mezouar, Soraya
Pegon, Julie
Muczynski, Vincent
Adam, Frédéric
Bianchini, Elsa P.
Bazaa, Amine
Proulle, Valerie
Rupin, Alain
Paysant, Jerome
Panicot-Dubois, Laurence
Christophe, Olivier D.
Dubois, Christophe
Lenting, Peter J.
Denis, Cécile V.
Pokaż więcej
Temat :
IN-VIVO
MESH: Animals
MESH: Disease Models, Animal
MESH: Antigens, CD/pharmacology
MESH: Inflammation/drug therapy
MESH: Antigens, Differentiation, Myelomonocytic/metabolism
VON-WILLEBRAND-FACTOR
MESH: Lectins/pharmacology
MESH: Leukocyte Rolling/physiology
CD33-RELATED SIGLECS
MESH: Mice, Inbred C57BL
MESH: Antigens, Differentiation, Myelomonocytic/pharmacology
MESH: Female
MESH: Antigens, CD/metabolism
IMMUNE-SYSTEM
MESH: Inflammation/pathology
NEUTROPHILS
MESH: E-Selectin/metabolism
MESH: Tumor Necrosis Factor-alpha/toxicity
MESH: Protein Interaction Domains and Motifs
SIALIC-ACID
MESH: Antigens, Differentiation, Myelomonocytic/genetics
MYELOID CELLS
MESH: Membrane Glycoproteins/metabolism
GLYCOPROTEIN LIGAND
MESH: Inflammation/chemically induced
MESH: Lectins/metabolism
MESH: Humans
MESH: Antigens, CD/genetics
MESH: Lectins/genetics
Article
E-SELECTIN LIGAND-1
P-SELECTIN
MESH: P-Selectin/metabolism
MESH: Solubility
MESH: Leukocytes, Mononuclear/drug effects
MESH: Leukocytes, Mononuclear/metabolism
MESH: Membrane Glycoproteins/genetics
[SDV]Life Sciences [q-bio]
MESH: Anti-Inflammatory Agents/pharmacology
Źródło :
Scientific Reports, Nature Publishing Group, 2016, 6 (1), pp.37953. ⟨10.1038/srep37953⟩
Tytuł :
pMHC affinity controls duration of CD8+ T cell-DC interactions and imprints timing of effector differentiation versus expansion.
Autorzy :
Ozga, Aleksandra J.
Moalli, Federica
Abe, Jun
Swoger, Jim
Merkler, Doron
Ripoll, Jorge
Sharpe, James
Zehn, Dietmar
Kreutzfeldt, Mario
Stein, Jens V.
Pokaż więcej
Temat :
610 Medicine & health
Research Articles
Animals
Antigens, CD/metabolism
Antigens, Differentiation, T-Lymphocyte/metabolism
CD8-Positive T-Lymphocytes/cytology
CD8-Positive T-Lymphocytes/immunology
Cell Communication/immunology
Cell Differentiation/immunology
Cell Proliferation
Cross-Priming/immunology
Cytotoxicity, Immunologic
Dendritic Cells/cytology
Dendritic Cells/immunology
Gene Expression Regulation
Granzymes/metabolism
Image Processing, Computer-Assisted
Lectins, C-Type/metabolism
Lymph Nodes/immunology
Lymphatic Vessels/metabolism
Major Histocompatibility Complex/immunology
Mice, Inbred C57BL
Peptides/immunology
Receptors, Antigen, T-Cell/metabolism
Signal Transduction
Virus Diseases/immunology
Article
Źródło :
The Journal of Experimental Medicine
Ozga, Aleksandra J; Moalli, Federica; Abe, Jun; Swoger, Jim; Sharpe, James; Zehn, Dietmar; Kreutzfeldt, Mario; Merkler, Doron; Ripoll, Jorge; Stein, Jens Volker (2016). pMHC affinity controls duration of CD8+ T cell-DC interactions and imprints timing of effector differentiation versus expansion. The Journal of experimental medicine, 213(12), pp. 2811-2829. Rockefeller Univ. Press 10.1084/jem.20160206
The Journal of experimental medicine, vol. 213, no. 12, pp. 2811-2829
Opis pliku :
application/pdf
Tytuł :
Intramembrane binding of VE-cadherin to VEGFR2 and VEGFR3 assembles the endothelial mechanosensory complex.
Autorzy :
Coon, Brian G.
Baeyens, Nicolas
Han, Jinah
Budatha, Madhusudhan
Ross, Tyler D.
Fang, Jennifer S.
Yun, Sanguk
Thomas, Jeon-Leon
Schwartz, Martin A.
Pokaż więcej
Temat :
Sciences bio-médicales et agricoles
Stress, Physiological
Antigens, CD31 -- metabolism
Vascular Endothelial Growth Factor Receptor-3
Cadherins
Vascular Endothelial Growth Factor Receptor-2
Plaque, Atherosclerotic
Mice
Antigens, CD -- metabolism
Mechanotransduction, Cellular
Mice, Inbred C57BL
Cells, Cultured
Animals
Antigens, CD31
HEK293 Cells
Stress, Mechanical
Cadherins -- metabolism
Endothelium, Vascular -- metabolism
cardiovascular system
Antigens, CD
Neovascularization, Physiologic -- physiology
Plaque, Atherosclerotic -- pathology
Protein Structure, Tertiary
Mechanotransduction, Cellular -- physiology
Article
Neovascularization, Physiologic
Vascular Endothelial Growth Factor Receptor-3 -- genetics -- metabolism
Endothelium, Vascular
Cell Movement
Human Umbilical Vein Endothelial Cells
Research Articles
Humans
RNA Interference
Vascular Endothelial Growth Factor Receptor-2 -- genetics -- metabolism
RNA, Small Interfering
Źródło :
Coon, B G, Baeyens, N, Han, J, Budatha, M, Ross, T D, Fang, J S, Yun, S, Thomas, J-L & Schwartz, M A 2015, ' Intramembrane binding of VE-cadherin to VEGFR2 and VEGFR3 assembles the endothelial mechanosensory complex ', The Journal of cell biology, vol. 208, no. 7, pp. 975-86 . https://doi.org/10.1083/jcb.201408103
The Journal of Cell Biology
The Journal of cell biology, 208 (7
Opis pliku :
1 full-text file(s): application/pdf
Tytuł :
Loss of prolyl hydroxylase-2 in myeloid cells and T-lymphocytes impairs tumor development
Autorzy :
Mamlouk, Soulafa
Kalucka, Joanna
Singh, Rashim Pal
Franke, Kristin
Muschter, Antje
Langer, Anika
Jakob, Christiane
Gassmann, Max
Baretton, Gustavo B
Wielockx, Ben
Pokaż więcej
Temat :
610 Medicine & health
Antigens, Differentiation, Myelomonocytic/metabolism
Bone Marrow/metabolism
RNA, Messenger/genetics
Apoptosis
Disease Progression
Carcinoma, Lewis Lung/genetics
Mice
Mice, Knockout
Myeloid Cells/immunology
T-Lymphocytes/immunology
Mice, Inbred C57BL
Institute of Veterinary Physiology
Oligonucleotide Array Sequence Analysis
Reverse Transcriptase Polymerase Chain Reaction
Flow Cytometry
Animals
Melanoma, Experimental/genetics
Antigens, CD/metabolism
Hypoxia-Inducible Factor-Proline Dioxygenases/physiology
Cell Proliferation
Real-Time Polymerase Chain Reaction
Biomarkers, Tumor/genetics
Immunoenzyme Techniques
Center for Integrative Human Physiology
Blotting, Western
Cell Movement
Hypoxia-Inducible Factor 1, alpha Subunit/physiology
Cytokines/genetics
570 Life sciences
biology
Gene Expression Profiling
Integrases/metabolism
Źródło :
Mamlouk, S, Kalucka, J, Singh, R P, Franke, K, Muschter, A, Langer, A, Jakob, C, Gassmann, M, Baretton, G B & Wielockx, B 2014, ' Loss of prolyl hydroxylase-2 in myeloid cells and T-lymphocytes impairs tumor development ', International Journal of Cancer, vol. 134, no. 4, pp. 849-58 . https://doi.org/10.1002/ijc.28409
Mamlouk, Soulafa; Kalucka, Joanna; Singh, Rashim Pal; Franke, Kristin; Muschter, Antje; Langer, Anika; Jakob, Christiane; Gassmann, Max; Baretton, Gustavo B; Wielockx, Ben (2014). Loss of prolyl hydroxylase-2 in myeloid cells and T-lymphocytes impairs tumor development. International Journal of Cancer, 134(4):849-858.
Opis pliku :
application/pdf

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