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1. Full Text Active chronic sarcoidosis is characterized by increased transitional blood B cells, increased IL-10-producing regulatory B cells and high BAFF levels
by Saussine, Anne and Tazi, Abdellatif and Feuillet, Séverine and Rybojad, Michel and Juillard, Caroline and Bergeron, Anne and Dessirier, Valérie and Bouhidel, Fatiha and Janin, Anne and Bensussan, Armand and Bagot, Martine and Bouaziz, Jean-David
PLoS ONE, ISSN 1932-6203, 08/2012, Volume 7, Issue 8, p. e43588
Background: Sarcoidosis is a multisystemic disease of unknown etiology characterized by a disproportionate Th1 granulomatous immune response in the organs... 
DISEASES | RITUXIMAB | MULTIDISCIPLINARY SCIENCES | SCLEROSIS | CD4(+) | LYMPHOCYTE STIMULATOR | PULMONARY SARCOIDOSIS | MICE | T-CELLS | B-Lymphocytes, Regulatory - metabolism | Cell Count | Humans | Middle Aged | Male | Sarcoidosis - blood | Case-Control Studies | Granuloma - complications | Young Adult | Sarcoidosis - complications | Phenotype | Time Factors | Sarcoidosis - immunology | Adolescent | B-Lymphocytes, Regulatory - cytology | Adult | Female | Granuloma - blood | Hypergammaglobulinemia - complications | Interleukin-10 - biosynthesis | Aged | B-Cell Activating Factor - blood | Chronic Disease | Interleukin-10 | Sarcoidosis | Physiological aspects | Development and progression | Genetic aspects | Research | Diagnosis | B cells | Lymphocyte receptors | Drugs | Flow cytometry | Disease | Laboratories | Pathogenesis | Homeostasis | Oncology | Lymphocytes T | Blood | Inflammatory diseases | Immunosuppressive agents | Immunology | Etiology | Peptidyl-dipeptidase A | Lymphocytes | Tumor necrosis factor-TNF | Lesions | Immune system | Lupus | Immunological memory | Memory cells | Immune response | Cytokines | Dermatology | Medical treatment | Organs | Patients | Immune response (humoral) | Serum levels | Lymphocytes B | BLyS protein | Hypergammaglobulinemia | Interleukin 10 | Angiotensin
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2. Full Text TWEAK affects keratinocyte G2/M growth arrest and induces apoptosis through the translocation of the AIF protein to the nucleus
by Sabour Alaoui, Sanaa and Dessirier, Valérie and de Araujo, Elisabeth and Alexaki, Vassilia-Ismini and Pelekanou, Vassiliki and Lkhider, Mustapha and Stathopoulos, Efstathios N and Castanas, Elias and Bagot, Martine and Bensussan, Armand and Tsapis, Andreas
PLoS ONE, ISSN 1932-6203, 03/2012, Volume 7, Issue 3, p. e33609
The soluble TNF-like weak inducer of apoptosis (TWEAK, TNFSF12) binds to the fibroblast growth factor-inducible 14 receptor (FN14, TNFRSF12A) on the cell... 
WEAK INDUCER | ACTIVATION | NECROSIS | GENOTOXIC STRESS | FACTOR RECEPTOR FAMILY | ENDOTHELIAL-CELLS | BIOLOGY | EPIDERMAL-KERATINOCYTES | TNF-ALPHA | KAPPA-B | CELL-DEATH | CDC2 Protein Kinase | G2 Phase Cell Cycle Checkpoints - physiology | Inflammation - pathology | Skin - cytology | Skin - metabolism | Humans | Cyclin B1 - metabolism | TWEAK Receptor | Inflammation - metabolism | Caspases - metabolism | TNF-Related Apoptosis-Inducing Ligand - biosynthesis | Psoriasis - pathology | Psoriasis - metabolism | Active Transport, Cell Nucleus | Cyclin-Dependent Kinases | Apoptosis Inducing Factor - metabolism | Receptors, Tumor Necrosis Factor - metabolism | Skin Neoplasms - pathology | Cell Line | Tumor Necrosis Factors - metabolism | Cathepsin B - metabolism | Keratinocytes - cytology | Skin Neoplasms - metabolism | Cytokine TWEAK | Keratinocytes - metabolism | Cyclin B - metabolism | Apoptosis - physiology | Tumor Necrosis Factor-alpha - biosynthesis | Squamous cell carcinoma | Psoriasis | Tumor necrosis factor | Growth | Physiological aspects | Cathepsins | Fibroblast growth factors | Skin | Apoptosis | Cdc2 protein | Flow cytometry | Fibroblast growth factor | Phosphorylation | Leukocyte migration | Laboratories | Homeostasis | Confocal microscopy | Confocal | Caspase-3 | Nuclei | Proteins | Angiogenesis | Mitochondria | Cell growth | Cell cycle | Cathepsin B | Cleavage | Membrane potential | Protein transport | FOXO3 protein | Translocation | Antigens | Free radicals | Secretion | Apoptosis-inducing factor | Neutrophils | Keratinocytes | Caspase | Epidermis | Inflammation | Tumor cell lines | Gene expression | Medicine | Pathology | Microscopy | Ligands | GADD45 protein | Cell migration | Endocrinology
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3. Full Text HACE1 , a Potential Tumor Suppressor Gene on 6q21, Is Not Involved in Extranodal Natural Killer/T-Cell Lymphoma Pathophysiology
by Sako, Nouhoum and Dessirier, Valérie and Bagot, Martine and Bensussan, Armand and Schmitt, Christian
American Journal of Pathology, The, ISSN 0002-9440, 2014, Volume 184, Issue 11, pp. 2899 - 2907
Extranodal natural killer–T-cell lymphoma (NKTCL) of nasal type is a malignant disorder of cytotoxic lymphocytes of natural killer or more rarely T cells,... 
Pathology | MIGRATION | METHYLATION | MESSENGER-RNA | NASAL-TYPE | LYMPHOPROLIFERATIVE DISEASE | COLORECTAL-CANCER | PATHOLOGY | LIGASE HACE1 | EXPRESSION | PERIPHERAL T-CELL | Cell Cycle - genetics | Cell Proliferation - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Gene Expression Regulation, Neoplastic | Ubiquitin-Protein Ligases - metabolism | Apoptosis - genetics | Gene Expression Profiling | Lymphoma, Extranodal NK-T-Cell - genetics | DNA Methylation | CpG Islands | Ubiquitin-Protein Ligases - genetics | Lymphoma, Extranodal NK-T-Cell - metabolism
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4. Full Text CD24hiCD27+ and plasmablast-like regulatory B cells in human chronic graft-versus-host disease
by de Masson, Adèle and De Masson, Adèle and Bouaziz, Jean-David and Bouaziz, Jean-David and Le Buanec, Hélène and Le Buanec, Hélène and Robin, Marie and Robin, Marie and O'Meara, Alix and O'Meara, Alix and Parquet, Nathalie and Parquet, Nathalie and Rybojad, Michel and Rybojad, Michel and Hau, Estelle and Hau, Estelle and Monfort, Jean-Benoît and Monfort, Jean-Benoît and Branchtein, Mylène and Branchtein, Mylène and Michonneau, David and Michonneau, David and Dessirier, Valérie and Dessirier, Valérie and De Fontbrune, Flore Sicre and Sicre de Fontbrune, Flore and Bergeron, Anne and Bergeron, Anne and Itzykson, Raphaël and Itzykson, Raphaël and Dhédin, Nathalie and Dhédin, Nathalie and Bengoufa, Djaouida and Bengoufa, Djaouida and Peffault de Latour, Régis and De Latour, Régis Peffault and Xhaard, Aliénor and Xhaard, Aliénor and Bagot, Martine and Bagot, Martine and Bensussan, Armand and Bensussan, Armand and Socié, Gérard and Socié, Gérard
Blood, ISSN 0006-4971, 03/2015, Volume 125, Issue 11, pp. 1830 - 1839
Key Points Chronic graft-versus-host disease is associated with a global Breg defect. This defect is particularly accentuated in the CD24hiCD27+ Breg... 
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5. Full Text CD24(hi)CD27(+) and plasmablast-like regulatory B cells in human chronic graft-versus-host disease
by de Masson, A and Bouaziz, JD and Le Buanec, H and Robin, M and O'Meara, A and Parquet, N and Rybojad, M and Hau, E and Monfort, JB and Branchtein, M and Michonneau, D and Dessirier, V and de Fontbrune, FS and Bergeron, A and Itzykson, R and Dhedin, N and Bengoufa, D and de Latour, RP and Xhaard, A and Bagot, M and Bensussan, A and Socie, G
BLOOD, ISSN 0006-4971, 03/2015, Volume 125, Issue 11, pp. 1830 - 1839
Interleukin 10 (IL-10)-producing B cells (regulatory B cells [Bregs]) regulate autoimmunity in mice and humans, and a regulatory role of IL-10-producing plasma... 
BRONCHIOLITIS OBLITERANS | SURVIVAL | MEMORY | CHRONIC GVHD | B10 CELLS | STAT3 | DIFFERENTIATION | HEMATOLOGY | ACTIVATING FACTOR | IL-21 | TRANSPLANTATION | Prospective Studies | Membrane Glycoproteins - metabolism | CD24 Antigen - metabolism | Humans | Middle Aged | Male | Graft vs Host Disease - immunology | B-Lymphocytes, Regulatory - pathology | MAP Kinase Signaling System | Plasma Cells - pathology | Young Adult | Hematopoietic Stem Cell Transplantation - adverse effects | Adult | Female | Plasma Cells - metabolism | Cell Differentiation | Graft vs Host Disease - etiology | STAT3 Transcription Factor - metabolism | B-Lymphocytes, Regulatory - metabolism | Signal Transduction | B-Lymphocytes, Regulatory - immunology | Graft vs Host Disease - pathology | Animals | Tumor Necrosis Factor Receptor Superfamily, Member 7 - metabolism | ADP-ribosyl Cyclase 1 - metabolism | Interleukin-10 - biosynthesis | Aged | Mice | Chronic Disease | Plasma Cells - immunology
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6. Full Text Membrane expression of NK receptors CD160 and CD158k contributes to delineate a unique CD4+T-lymphocyte subset in normal and mycosis fungoides skin
: CD160 and CD158k on CD4+Skin T-Lymphocytes
by Sako, Nouhoum and Schiavon, Valérie and Bounfour, Touda and Dessirier, Valérie and Ortonne, Nicolas and Olive, Daniel and Ram-Wolff, Caroline and Michel, Laurence and Sicard, Hélène and Marie-Cardine, Anne and Bagot, Martine and Bensussan, Armand and Schmitt, Christian
Cytometry Part A, ISSN 1552-4922, 10/2014, Volume 85, Issue 10, pp. 869 - 882
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7. Full Text Membrane expression of NK receptors CD160 and CD158k contributes to delineate a unique CD4+ T‐lymphocyte subset in normal and mycosis fungoides skin
by Sako, Nouhoum and Schiavon, Valérie and Bounfour, Touda and Dessirier, Valérie and Ortonne, Nicolas and Olive, Daniel and Ram‐Wolff, Caroline and Michel, Laurence and Sicard, Hélène and Marie‐Cardine, Anne and Bagot, Martine and Bensussan, Armand and Schmitt, Christian
Cytometry Part A, ISSN 1552-4922, 10/2014, Volume 85, Issue 10, pp. 869 - 882
CD160 is a GPI‐anchored Ig‐like receptor identified by the BY55 mAb on human circulating CD56dim+ NK cells and TCRγδ lymphocytes. In addition, while most... 
BY55 | skin lymphocytes | CD158k | KIR3DL2 | CD160 | mycosis fungoides | Mycosis fungoides | Skin lymphocytes | RHEUMATOID-ARTHRITIS | VIRUS-INFECTION | BIOCHEMICAL RESEARCH METHODS | PERIPHERAL-BLOOD | SEZARY-SYNDROME | CUTTING EDGE | CELL BIOLOGY | HERPESVIRUS ENTRY MEDIATOR | CELL SUBSETS | INTESTINAL INTRAEPITHELIAL LYMPHOCYTES | CUTANEOUS LYMPHOMAS | FLOW-CYTOMETRY | Flow Cytometry - methods | Antigens, CD - biosynthesis | Humans | CD4-Positive T-Lymphocytes - metabolism | Gene Expression Regulation, Neoplastic | GPI-Linked Proteins - biosynthesis | Male | Skin Neoplasms - metabolism | Mycosis Fungoides - metabolism | Receptors, Immunologic - biosynthesis | T-Lymphocyte Subsets - metabolism | Skin Neoplasms - diagnosis | Receptors, KIR2DL2 - biosynthesis | Female | Cell Membrane - metabolism | Killer Cells, Natural - metabolism | Mycosis Fungoides - diagnosis | Mycoses | Skin | Non-Hodgkin's lymphomas | T cells | Integrins
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8. Full Text APRIL binding to BCMA activates a JNK2-FOXO3-GADD45 pathway and induces a G2/M cell growth arrest in liver cells
by Notas, George and Alexaki, Vassilia-Ismini and Kampa, Marilena and Pelekanou, Vassiliki and Charalampopoulos, Ioannis and Sabour-Alaoui, Sanaa and Pediaditakis, Iosif and Dessirier, Valérie and Gravanis, Achille and Stathopoulos, Efstathios N and Tsapis, Andreas and Castanas, Elias
Journal of Immunology, ISSN 0022-1767, 11/2012, Volume 189, Issue 10, pp. 4748 - 4758
The TNF superfamily ligands APRIL and BAFF bind with different affinity to two receptors, BCMA and TACI, and induce cell survival and/or proliferation, whereas... 
Forkhead Transcription Factors - immunology | MAP Kinase Kinase 7 - genetics | G2 Phase Cell Cycle Checkpoints - immunology | Humans | M Phase Cell Cycle Checkpoints - genetics | MAP Kinase Kinase 7 - immunology | DNA-Binding Proteins - metabolism | MAP Kinase Kinase 7 - metabolism | Cell Cycle Proteins - immunology | Liver - immunology | Phosphorylation - genetics | Proliferating Cell Nuclear Antigen - genetics | Forkhead Transcription Factors - metabolism | Cell Cycle Proteins - genetics | B-Cell Activating Factor - immunology | Proliferating Cell Nuclear Antigen - immunology | Phosphorylation - immunology | Nuclear Proteins - genetics | Transcription Factors - immunology | B-Cell Maturation Antigen - immunology | DNA-Binding Proteins - immunology | Cell Cycle Proteins - metabolism | M Phase Cell Cycle Checkpoints - immunology | Nuclear Proteins - metabolism | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Forkhead Transcription Factors - genetics | Nuclear Proteins - immunology | Hep G2 Cells | Transcription Factors - metabolism | G2 Phase Cell Cycle Checkpoints - genetics | B-Cell Activating Factor - metabolism | B-Cell Maturation Antigen - metabolism | B-Cell Activating Factor - genetics | Protein Binding | Transcription, Genetic - immunology | Liver - cytology | B-Cell Maturation Antigen - genetics | Transcription, Genetic - genetics | Forkhead Box Protein O3 | Proliferating Cell Nuclear Antigen - metabolism
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9. Full Text BAFF enhances chemotaxis of primary human B cells: A particular synergy between BAFF and CXCL13 on memory B cells
by Badr, Gamal and Borhis, Gwenoline and Lefevre, Eric A and Chaoul, Nada and Deshayes, Frederique and Dessirier, Valérie and Lapree, Genevieve and Tsapis, Andreas and Richard, Yolande
Blood, ISSN 0006-4971, 03/2008, Volume 111, Issue 5, pp. 2744 - 2754
B-cell-activating factor of the TNF family, (BAFF), and a proliferation-inducing ligand (APRIL) regulate B-lymphocyte survival and activation. We report that... 
BLYS RECEPTOR | MATURATION ANTIGEN | NECROSIS-FACTOR FAMILY | T-CELL | HEMATOLOGY | NF-KAPPA-B | ACTIVATING FACTOR | TNF FAMILY | CUTTING EDGE | MEMBER | APRIL | Tumor Necrosis Factor Ligand Superfamily Member 13 - immunology | B-Lymphocytes - cytology | B-Lymphocytes - enzymology | NF-KappaB Inhibitor alpha | Phosphorylation | Humans | Cells, Cultured | NF-kappa B - metabolism | Neutralization Tests | Phosphatidylinositol 3-Kinases - metabolism | I-kappa B Proteins - metabolism | Chemotaxis | NF-kappa B p52 Subunit - metabolism | B-Lymphocytes - immunology | Mitogen-Activated Protein Kinase 3 - metabolism | rho-Associated Kinases - metabolism | B-Cell Activating Factor - immunology | Immunologic Memory | p38 Mitogen-Activated Protein Kinases - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Chemokine CXCL13 - immunology | Protein-Serine-Threonine Kinases - metabolism | B-Cell Activation Factor Receptor - immunology | Mitogen-Activated Protein Kinase 1 - metabolism | Life Sciences | Adaptive immunology | Immunology
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10. Full Text B-Cell Maturation Antigen (BCMA) Activation Exerts Specific Proinflammatory Effects in Normal Human Keratinocytes and Is Preferentially Expressed in Inflammatory Skin Pathologies
by Alexaki, Vassilia-Ismini and Pelekanou, Vassiliki and Notas, George and Venihaki, Maria and Kampa, Marilena and Dessirier, Valérie and Sabour-Alaoui, Sanaa and Stathopoulos, Efstathios N and Tsapis, Andreas and Castanas, Elias
Endocrinology, ISSN 0013-7227, 02/2012, Volume 153, Issue 2, pp. 739 - 749
TNFα is known to be expressed in human skin, regulating immune-related responses. Here we report that human normal skin keratinocytes express the members of... 
TNF RECEPTOR | FACTOR FAMILY | TUMOR-NECROSIS-FACTOR | MEMBERS BAFF | ENDOCRINOLOGY & METABOLISM | HUMORAL IMMUNITY | LYMPHOCYTE STIMULATOR | PSORIATIC SKIN | NF-KAPPA-B | FACTOR-ALPHA | APRIL | Epidermis - metabolism | Epidermis - pathology | Interleukin-6 - genetics | Granulocyte-Macrophage Colony-Stimulating Factor - metabolism | Humans | Gene Expression Regulation - physiology | NF-kappa B - metabolism | Tumor Necrosis Factor Ligand Superfamily Member 13 - metabolism | Granulocyte-Macrophage Colony-Stimulating Factor - genetics | Transmembrane Activator and CAML Interactor Protein - metabolism | Dermatitis - pathology | Transmembrane Activator and CAML Interactor Protein - genetics | B-Cell Activating Factor - metabolism | B-Cell Maturation Antigen - metabolism | NF-kappa B - genetics | B-Cell Activating Factor - genetics | Keratinocytes - metabolism | Tumor Necrosis Factor Ligand Superfamily Member 13 - genetics | Interleukin-6 - metabolism | Dermatitis - metabolism
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11. Full Text Death ligand TRAIL, secreted by CD1a+ and CD14+ cells in blister fluids, is involved in killing keratinocytes in toxic epidermal necrolysis
: TRAIL in toxic epidermal necrolysis
by de Araujo, Elisabeth and Dessirier, Valérie and Laprée, Geneviève and Valeyrie-Allanore, Laurence and Ortonne, Nicolas and Stathopoulos, Efstathios N and Bagot, Martine and Bensussan, Armand and Mockenhaupt, Maja and Roujeau, Jean-Claude and Tsapis, Andreas
Experimental Dermatology, ISSN 0906-6705, 02/2011, Volume 20, Issue 2, pp. 107 - 112
Toxic epidermal necrolysis (TEN) is characterized by an acute detachment and destruction of keratinocytes, affecting large areas of the skin. It is often... 
Life Sciences | Biochemistry, Molecular Biology
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12. Full Text Hepatocyte growth factor induces colonic cancer cell invasiveness via enhanced motility and protease overproduction. Evidence for PI3 kinase and PKC involvement
by Kermorgant, S and Aparicio, T and Dessirier, V and Lewin, MJM and Lehy, T
CARCINOGENESIS, ISSN 0143-3334, 07/2001, Volume 22, Issue 7, pp. 1035 - 1042
Tumour progression to the metastatic phenotype is mainly dependent on tumour cell invasiveness, Cell migration is a crucial step in this process. Here we... 
CARCINOMA-CELLS | IN-VITRO | INVASION | EPITHELIAL-CELLS | MESSENGER-RNA | ONCOLOGY | FACTOR SCATTER FACTOR | C-MET | DIGESTIVE TISSUES | FACTOR RECEPTOR | WOUND REPAIR | Caco-2 Cells | Proto-Oncogene Proteins c-met - metabolism | Neoplasm Metastasis | Hepatocyte Growth Factor - physiology | Neoplasm Invasiveness | Protein Kinase C - metabolism | Colonic Neoplasms - pathology | Humans | Colonic Neoplasms - enzymology | Phosphatidylinositol 3-Kinases - metabolism | Matrix Metalloproteinases - metabolism | Matrix Metalloproteinases - biosynthesis
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13. Full Text Localized edema with sclerodermatous evolution: a possible form of skin chronic graft-versus-host disease associated with endothelial activation
by Tardieu, Mathilde and Tardieu, Mathilde and Rybojad, Michel and Rybojad, Michel and Peffault De Latour, Régis and Peffault de Latour, Régis and Robin, Marie and Robin, Marie and De Masson, Adèle and de Masson, Adèle and Xhaard, Aliénor and Xhaard, Aliénor and Le Buanec, Hélène and Le Buanec, Hélène and Parquet, Nathalie and Parquet, Nathalie and De Fontbrune, Flore Sicre and Sicre de Fontbrune, Flore and Bergeron, Anne and Bergeron, Anne and Scieux, Catherine and Scieux, Catherine and Dessirier, Valérie and Dessirier, Valérie and Bensussan, Armand and Bensussan, Armand and Bagot, Martine and Bagot, Martine and Socié, Gérard and Socié, Gérard and Bouaziz, Jean-David and Bouaziz, Jean-David
Blood, ISSN 0006-4971, 07/2013, Volume 122, Issue 3, pp. 463 - 465
CELL-ADHESION MOLECULE-1 | EOSINOPHILIC FASCIITIS | HEMATOLOGY | SERUM-LEVELS | Edema - complications | Endothelium - pathology | Scleroderma, Localized - blood | Scleroderma, Localized - drug therapy | Sirolimus - therapeutic use | Graft vs Host Disease - complications | Scleroderma, Localized - complications | Humans | Scleroderma, Localized - pathology | Solubility | Edema - drug therapy | Graft vs Host Disease - blood | Graft vs Host Disease - pathology | Vascular Cell Adhesion Molecule-1 - blood | Edema - blood | Graft vs Host Disease - drug therapy | Chronic Disease | Edema - pathology | Skin - pathology
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14. Full Text Death ligand TRAIL, secreted by CD1a+ and CD14+ cells in blister fluids, is involved in killing keratinocytes in toxic epidermal necrolysis
by de Araujo, Elisabeth and Dessirier, Valérie and Laprée, Geneviève and Valeyrie‐Allanore, Laurence and Ortonne, Nicolas and Stathopoulos, Efstathios N and Bagot, Martine and Bensussan, Armand and Mockenhaupt, Maja and Roujeau, Jean‐Claude and Tsapis, Andreas
Experimental Dermatology, ISSN 0906-6705, 02/2011, Volume 20, Issue 2, pp. 107 - 112
:  Toxic epidermal necrolysis (TEN) is characterized by an acute detachment and destruction of keratinocytes, affecting large areas of the skin. It is often... 
skin | apoptosis | human | cytotoxicity | TNFSF superfamily | Human | Cytotoxicity | Skin | Apoptosis | MEDIATED CYTOTOXICITY | HUMAN NK CELLS | INTERLEUKIN-8 | FACTOR-ALPHA | DERMATOLOGY | CYTOTOXIC T-CELLS | TUMOR-NECROSIS-FACTOR | APOPTOSIS-INDUCING LIGAND | INTERFERON-GAMMA | STEVENS-JOHNSON-SYNDROME | SOLUBLE FAS LIGAND | T-Lymphocytes, Cytotoxic - immunology | Tumor Necrosis Factor-alpha - metabolism | Cell Line | Cell Proliferation | Humans | T-Lymphocytes, Cytotoxic - secretion | Tumor Necrosis Factors - metabolism | Interferon-gamma - metabolism | TNF-Related Apoptosis-Inducing Ligand - metabolism | Case-Control Studies | Lipopolysaccharide Receptors - metabolism | T-Lymphocytes, Cytotoxic - pathology | Cytokine TWEAK | Keratinocytes - pathology | Biopsy | Antigens, CD1 - metabolism | Stevens-Johnson Syndrome - metabolism | Blister - pathology | Stevens-Johnson Syndrome - pathology | Blister - metabolism | Biological response modifiers | T cells | Interferon gamma | Indexing in process | Index Medicus
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15. Full Text HGF upregulates and modifies subcellular distribution of proteins in colon cancer cell enterocytic differentiation
by Stéphanie Kermorgant and Valérie Dessirier and Miguel J. M. Lewin and Thérèse Lehy
American Journal of Physiology - Gastrointestinal and Liver Physiology, ISSN 0193-1857, 10/2001, Volume 281, Issue 4, pp. 1068 - 1080
Hepatocyte growth factor (HGF) and its receptor, c-Met, are involved in cell transformation. To study their role in intestinal cell differentiation, we used... 
Protein kinase C | Gab-1 | Cell differentiation | Hepatocyte growth factor | C-Met | cell differentiation | PHYSIOLOGY | FACTOR SCATTER FACTOR | HEPATOCYTE GROWTH-FACTOR | C-MET RECEPTOR | COLORECTAL-CARCINOMA | DIGESTIVE TISSUES | FACTOR/SCATTER FACTOR | EPITHELIAL-CELLS | hepatocyte growth factor | c-Met | GRB2 BINDING-SITE | GASTROENTEROLOGY & HEPATOLOGY | protein kinase C | RECEPTOR TYROSINE KINASE | CACO-2 CELLS | Proto-Oncogene Proteins c-met - metabolism | Protein Kinase C - genetics | Phosphorylation | Cadherins - metabolism | Enterocytes - metabolism | Humans | Actins - metabolism | Alkaline Phosphatase - metabolism | Immunoblotting | Hepatocyte Growth Factor - pharmacology | Phosphoproteins - metabolism | Sucrase-Isomaltase Complex - metabolism | Time Factors | Isoenzymes - metabolism | Protein Kinase C - metabolism | Membrane Proteins - metabolism | Microfilament Proteins - metabolism | Protein Kinase C-alpha | Caco-2 Cells | Alkaline Phosphatase - genetics | Sucrase-Isomaltase Complex - genetics | Enterocytes - cytology | Isoenzymes - genetics | Protein Kinase C - antagonists & inhibitors | Phosphoproteins - genetics | Recombinant Proteins - pharmacology | Reverse Transcriptase Polymerase Chain Reaction | Adaptor Proteins, Signal Transducing | Carrier Proteins - metabolism | Zonula Occludens-1 Protein | Enterocytes - drug effects | Cell Differentiation - drug effects | Biomarkers | Colonic Neoplasms | Isoenzymes - antagonists & inhibitors | Microscopy, Fluorescence
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16. Full Text Matrix metalloproteinase inhibition prevents colon cancer peritoneal carcinomatosis development and prolongs survival in rats
by Aparicio, Thomas and Kermorgant, Stéphanie and Dessirier, Valérie and Lewin, Miguel J.M and Lehy, Thérèse
Carcinogenesis, ISSN 0143-3334, 1999, Volume 20, Issue 8, pp. 1445 - 1451
Matrix metalloproteinases (MMP) are enzymes responsible for extracellular matrix degradation which play a role in cancer progression and metastatic spreading.... 
NUDE-MICE | METASTASIS | MESSENGER-RNA | ONCOLOGY | IN-VIVO | BATIMASTAT BB-94 | TISSUE INHIBITOR | STROMAL CELLS | TUMOR-GROWTH | EXPRESSION | HUMAN COLORECTAL-CANCER | Phenylalanine - analogs & derivatives | Phenylalanine - pharmacology | Carcinoma - mortality | Male | Metalloendopeptidases - metabolism | Neoplasm Proteins - antagonists & inhibitors | Gelatinases - metabolism | Female | Antineoplastic Agents - pharmacology | Carcinoma - pathology | Metalloendopeptidases - antagonists & inhibitors | Peritoneal Neoplasms - pathology | Colonic Neoplasms - mortality | Neoplasm Invasiveness | Matrix Metalloproteinase 2 | Tumor Cells, Cultured - drug effects | Matrix Metalloproteinase 1 | Rats | Thiophenes - pharmacology | Carcinoma - prevention & control | Peritoneal Neoplasms - prevention & control | Peritoneal Neoplasms - mortality | Animals | Colonic Neoplasms - pathology | Colonic Neoplasms - enzymology | Collagenases - metabolism | Matrix Metalloproteinase 9
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