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Wyświetlanie 1-10 z 478
Tytuł:
Growth differentiation factor 7 autocrine signaling promotes hepatic progenitor cell expansion in liver fibrosis.
Autorzy:
Kong D; Department of Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands.
Mourtzinos A; Department of Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands.
Heegsma J; Department of Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands.
Blokzijl H; Department of Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands.
de Meijer VE; Department of Surgery, Division of Hepato-Pancreato-Biliary Surgery and Liver Transplantation, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Faber KN; Department of Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands. .
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Źródło:
Stem cell research & therapy [Stem Cell Res Ther] 2023 Oct 05; Vol. 14 (1), pp. 288. Date of Electronic Publication: 2023 Oct 05.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Autocrine Communication*
Liver Diseases*/pathology
Humans ; Hepatic Stellate Cells/metabolism ; Liver/metabolism ; Liver Cirrhosis/pathology ; Stem Cells/metabolism ; Transforming Growth Factor beta1/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Droplet-based forward genetic screening of astrocyte-microglia cross-talk.
Autorzy:
Wheeler MA; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Clark IC; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Department of Bioengineering, College of Engineering, California Institute for Quantitative Biosciences, University of California Berkeley, Berkeley, CA 94720, USA.
Lee HG; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Li Z; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Linnerbauer M; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Rone JM; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Blain M; Neuroimmunology Unit, Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University, Montreal, QC H3A 2B4, Canada.
Akl CF; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Piester G; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA.
Giovannoni F; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Charabati M; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Lee JH; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Kye YC; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Evergrande Center for Immunologic Diseases, Harvard Medical School and Brigham and Women's Hospital, Boston, MA 02115, USA.
Choi J; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Evergrande Center for Immunologic Diseases, Harvard Medical School and Brigham and Women's Hospital, Boston, MA 02115, USA.
Sanmarco LM; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Srun L; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Chung EN; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Flausino LE; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Andersen BM; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Department of Neurology, Jamaica Plain Veterans Affairs Hospital, Harvard Medical School, Boston, MA 02130, USA.
Rothhammer V; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Department of Neurology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuernberg, Erlangen, Germany.
Yano H; Jill Roberts Institute for Research in Inflammatory Bowel Disease, Joan and Sanford I. Weill Department of Medicine, Department of Microbiology and Immunology, Weill Cornell Medicine, Cornell University, New York, NY 10021, USA.
Illouz T; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Zandee SEJ; Neuroimmunology Research Lab, Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Montreal, QC H2X 0A9, Canada.
Daniel C; Type 1 Diabetes Immunology, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany.; Deutsches Zentrum für Diabetesforschung, 85764 Munich-Neuherberg, Germany.; Division of Clinical Pharmacology, Department of Medicine IV, Ludwig-Maximilians-Universität München, 80337 Munich, Germany.
Artis D; Jill Roberts Institute for Research in Inflammatory Bowel Disease, Joan and Sanford I. Weill Department of Medicine, Department of Microbiology and Immunology, Weill Cornell Medicine, Cornell University, New York, NY 10021, USA.; Friedman Center for Nutrition and Inflammation, Joan and Sanford I. Weill Department of Medicine, Department of Microbiology and Immunology, Weill Cornell Medicine, Cornell University, New York, NY 10021, USA.
Prinz M; Institute of Neuropathology, University of Freiburg, D-79106 Freiburg, Germany.; Signaling Research Centres BIOSS and CIBSS, University of Freiburg, D-79106 Freiburg, Germany.; Center for Basics in NeuroModulation, Faculty of Medicine, University of Freiburg, D-79106 Freiburg, Germany.
Abate AR; Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, California Institute for Quantitative Biosciences, San Francisco, CA 94158, USA.; Chan Zuckerberg Biohub, San Francisco, CA, USA.
Kuchroo VK; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Evergrande Center for Immunologic Diseases, Harvard Medical School and Brigham and Women's Hospital, Boston, MA 02115, USA.
Antel JP; Neuroimmunology Unit, Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University, Montreal, QC H3A 2B4, Canada.
Prat A; Neuroimmunology Research Lab, Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Montreal, QC H2X 0A9, Canada.
Quintana FJ; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
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Źródło:
Science (New York, N.Y.) [Science] 2023 Mar 10; Vol. 379 (6636), pp. 1023-1030. Date of Electronic Publication: 2023 Mar 09.
Typ publikacji:
Journal Article
MeSH Terms:
Astrocytes*/physiology
Genetic Testing*/methods
Microfluidic Analytical Techniques*/methods
Microglia*/physiology
Amphiregulin*/genetics
Autocrine Communication*/genetics
High-Throughput Screening Assays ; Gene Expression ; Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Autocrine signaling can explain the emergence of Allee effects in cancer cell populations.
Autorzy:
Gerlee P; Mathematical Sciences, Chalmers University of Technology, Gothenburg, Sweden.; Mathematical Sciences, University of Gothenburg, Gothenburg, Sweden.
Altrock PM; Department of Integrated Mathematical Oncology, Moffitt Cancer Center, Tampa, Florida, United States of America.; Department of Evolutionary Theory, Max Planck Institute for Evolutionary Biology, Plön, Germany.
Malik A; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Krona C; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Nelander S; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
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Źródło:
PLoS computational biology [PLoS Comput Biol] 2022 Mar 03; Vol. 18 (3), pp. e1009844. Date of Electronic Publication: 2022 Mar 03 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Autocrine Communication*
Neoplasms*
Ecology ; Feedback ; Humans ; Models, Biological ; Population Density ; Population Dynamics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Doxorubicin-Resistant TNBC Cells Exhibit Rapid Growth with Cancer Stem Cell-like Properties and EMT Phenotype, Which Can Be Transferred to Parental Cells through Autocrine Signaling.
Autorzy:
Paramanantham A; Departments of Internal Medicine, Institute of Health Sciences, Gyeongsang National University Hospital, Gyeongsang National University College of Medicine, 90 Chilam-dong, Jinju 660-702, Korea.; School of Veterinary and Institute of Life Science, Gyeongsang National University, 900 Gajwadong, Jinju 660-701, Korea.
Jung EJ; Departments of Internal Medicine, Institute of Health Sciences, Gyeongsang National University Hospital, Gyeongsang National University College of Medicine, 90 Chilam-dong, Jinju 660-702, Korea.
Kim HJ; Departments of Pharmacology, Institute of Health Sciences, Gyeongsang National University Hospital, Gyeongsang National University School of Medicine, Jinju 660-702, Korea.
Jeong BK; Departments of Radiation Oncology, Institute of Health Sciences, Gyeongsang National University Hospital, Gyeongsang National University College of Medicine, 90 Chilam-dong, Jinju 660-702, Korea.
Jung JM; Departments of Neurosurgery, Institute of Health Sciences, Gyeongsang National University Hospital, Gyeongsang National University College of Medicine, 90 Chilam-dong, Jinju 660-702, Korea.
Kim GS; School of Veterinary and Institute of Life Science, Gyeongsang National University, 900 Gajwadong, Jinju 660-701, Korea.
Chan HS; Department of Surgery, Institute of Health Sciences, Gyeongsang National University Hospital, Gyeongsang National University School of Medicine, Jinju 660-702, Korea.
Lee WS; Departments of Internal Medicine, Institute of Health Sciences, Gyeongsang National University Hospital, Gyeongsang National University College of Medicine, 90 Chilam-dong, Jinju 660-702, Korea.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Nov 18; Vol. 22 (22). Date of Electronic Publication: 2021 Nov 18.
Typ publikacji:
Journal Article
MeSH Terms:
Antibiotics, Antineoplastic/*pharmacology
Autocrine Communication/*drug effects
Doxorubicin/*pharmacology
Drug Resistance, Neoplasm/*genetics
Epithelial-Mesenchymal Transition/*drug effects
Neoplastic Stem Cells/*drug effects
Antigens, CD/genetics ; Antigens, CD/metabolism ; Autocrine Communication/genetics ; Cadherins/genetics ; Cadherins/metabolism ; Cell Line, Tumor ; Cell Movement/drug effects ; Cell Proliferation/drug effects ; Cyclin D1/genetics ; Cyclin D1/metabolism ; Epithelial Cells/drug effects ; Epithelial Cells/metabolism ; Epithelial Cells/pathology ; Epithelial-Mesenchymal Transition/genetics ; ErbB Receptors/genetics ; ErbB Receptors/metabolism ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; Intercellular Adhesion Molecule-1/genetics ; Intercellular Adhesion Molecule-1/metabolism ; Matrix Metalloproteinase 2/genetics ; Matrix Metalloproteinase 2/metabolism ; Matrix Metalloproteinase 9/genetics ; Matrix Metalloproteinase 9/metabolism ; Mitogen-Activated Protein Kinase 1/genetics ; Mitogen-Activated Protein Kinase 1/metabolism ; Mitogen-Activated Protein Kinase 3/genetics ; Mitogen-Activated Protein Kinase 3/metabolism ; Neoplastic Stem Cells/metabolism ; Neoplastic Stem Cells/pathology ; Proto-Oncogene Proteins c-akt/genetics ; Proto-Oncogene Proteins c-akt/metabolism ; Signal Transduction ; Triple Negative Breast Neoplasms/genetics ; Triple Negative Breast Neoplasms/metabolism ; Triple Negative Breast Neoplasms/pathology ; beta Catenin/genetics ; beta Catenin/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The Role of the α Cell in the Pathogenesis of Diabetes: A World beyond the Mirror.
Autorzy:
Martínez MS; MedStar Health Internal Medicine, Georgetown University Affiliated, Baltimore, MD 21218-2829, USA.
Manzano A; Endocrine and Metabolic Diseases Research Center, School of Medicine, Universidad del Zulia, Maracaibo 4002, Venezuela.
Olivar LC; Endocrine and Metabolic Diseases Research Center, School of Medicine, Universidad del Zulia, Maracaibo 4002, Venezuela.
Nava M; Endocrine and Metabolic Diseases Research Center, School of Medicine, Universidad del Zulia, Maracaibo 4002, Venezuela.
Salazar J; Endocrine and Metabolic Diseases Research Center, School of Medicine, Universidad del Zulia, Maracaibo 4002, Venezuela.
D'Marco L; Department of Nephrology, Hospital Clinico Universitario de Valencia, INCLIVA, University of Valencia, 46010 Valencia, Spain.
Ortiz R; Facultad de Medicina, Universidad Católica de Cuenca, Ciudad de Cuenca, Azuay 010105, Ecuador.
Chacín M; Facultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080022, Colombia.
Guerrero-Wyss M; Escuela de Nutrición y Dietética, Facultad de Ciencias Para el Cuidado de la Salud, Universidad San Sebastián, Valdivia 5090000, Chile.
Cabrera de Bravo M; City of Houston Health Department, Houston, TX 77054, USA.
Cano C; Endocrine and Metabolic Diseases Research Center, School of Medicine, Universidad del Zulia, Maracaibo 4002, Venezuela.
Bermúdez V; Facultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080022, Colombia.
Angarita L; Escuela de Nutrición y Dietética, Facultad de Medicina, Universidad Andres Bello, Sede Concepción 4260000, Chile.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Sep 01; Vol. 22 (17). Date of Electronic Publication: 2021 Sep 01.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Autocrine Communication*
Paracrine Communication*
Diabetes Mellitus, Type 1/*metabolism
Diabetes Mellitus, Type 2/*metabolism
Glucagon-Secreting Cells/*metabolism
Insulin-Secreting Cells/*metabolism
Animals ; Diabetes Mellitus, Type 1/drug therapy ; Diabetes Mellitus, Type 1/pathology ; Diabetes Mellitus, Type 2/drug therapy ; Diabetes Mellitus, Type 2/pathology ; Dipeptidyl-Peptidase IV Inhibitors/therapeutic use ; Glucagon/metabolism ; Glucagon-Like Peptide 1/antagonists & inhibitors ; Glucagon-Like Peptide 1/metabolism ; Glucagon-Secreting Cells/pathology ; Humans ; Hypoglycemic Agents/therapeutic use ; Insulin-Secreting Cells/pathology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Oxytocin and Bone: Review and Perspectives.
Autorzy:
Breuil V; Faculté de Médecine Nice, UMR E-4320 TIRO-MATOs CEA/DRF/Institut Joliot, Université Côte d'Azur, CEDEX 2, 06107 Nice, France.
Trojani MC; Faculté de Médecine Nice, UMR E-4320 TIRO-MATOs CEA/DRF/Institut Joliot, Université Côte d'Azur, CEDEX 2, 06107 Nice, France.
Ez-Zoubir A; French National Centre for Scientific Research (CNRS), Inserm, iBV, Université Côte d'Azur, CEDEX 2, 06107 Nice, France.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Aug 09; Vol. 22 (16). Date of Electronic Publication: 2021 Aug 09.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Autocrine Communication*
Bone Density*
Paracrine Communication*
Sex Characteristics*
Bone and Bones/*metabolism
Oxytocin/*metabolism
Amenorrhea/metabolism ; Animals ; Anorexia Nervosa/metabolism ; Bone and Bones/pathology ; Breast Neoplasms/metabolism ; Breast Neoplasms/pathology ; Cardiovascular Diseases/metabolism ; Cardiovascular Diseases/pathology ; Cognitive Dysfunction/metabolism ; Cognitive Dysfunction/pathology ; Diabetes Mellitus/metabolism ; Diabetes Mellitus/pathology ; Estrogens/deficiency ; Estrogens/metabolism ; Female ; Humans ; Male ; Osteoporosis, Postmenopausal/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Autocrine signaling by receptor tyrosine kinases in urothelial carcinoma of the bladder.
Autorzy:
Lee YH; Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Lee MM; Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
De Silva DM; Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Roy A; Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Wright CE; Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Wong TK; Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Costello R; Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Olaku O; Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Grubb RL 3rd; Department of Urology, Medical University of South Carolina, Charleston, South Carolina, United States of America.
Agarwal PK; Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Apolo AB; Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Bottaro DP; Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
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Źródło:
PloS one [PLoS One] 2021 Jul 22; Vol. 16 (7), pp. e0241766. Date of Electronic Publication: 2021 Jul 22 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, N.I.H., Intramural
MeSH Terms:
Autocrine Communication*
Receptor Protein-Tyrosine Kinases/*metabolism
Urinary Bladder Neoplasms/*pathology
Animals ; Cell Line, Tumor ; Databases, Factual ; Epithelial-Mesenchymal Transition/genetics ; Gene Expression Regulation, Neoplastic ; Humans ; Intercellular Signaling Peptides and Proteins/genetics ; Intercellular Signaling Peptides and Proteins/metabolism ; Kaplan-Meier Estimate ; Mice ; Neoplasm Invasiveness ; Protein-Tyrosine Kinases/genetics ; Protein-Tyrosine Kinases/metabolism ; Proto-Oncogene Proteins/antagonists & inhibitors ; Proto-Oncogene Proteins/genetics ; Proto-Oncogene Proteins/metabolism ; RNA Interference ; RNA, Small Interfering/metabolism ; Receptor Protein-Tyrosine Kinases/antagonists & inhibitors ; Receptor Protein-Tyrosine Kinases/genetics ; Receptors, Granulocyte-Macrophage Colony-Stimulating Factor/genetics ; Receptors, Granulocyte-Macrophage Colony-Stimulating Factor/metabolism ; Transplantation, Heterologous ; Urinary Bladder Neoplasms/metabolism ; Urinary Bladder Neoplasms/mortality ; Axl Receptor Tyrosine Kinase
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The Roles of Various Prostaglandins in Fibrosis: A Review.
Autorzy:
Li K; Department of Ophthalmology, The Second Hospital of Jilin University, Changchun 130000, China.
Zhao J; Department of Ophthalmology, The Second Hospital of Jilin University, Changchun 130000, China.
Wang M; Department of Ophthalmology, The Second Hospital of Jilin University, Changchun 130000, China.
Niu L; Department of Ophthalmology, The Second Hospital of Jilin University, Changchun 130000, China.
Wang Y; Department of Ophthalmology, The Second Hospital of Jilin University, Changchun 130000, China.
Li Y; Department of Ophthalmology, The Second Hospital of Jilin University, Changchun 130000, China.
Zheng Y; Department of Ophthalmology, The Second Hospital of Jilin University, Changchun 130000, China.
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Źródło:
Biomolecules [Biomolecules] 2021 May 24; Vol. 11 (6). Date of Electronic Publication: 2021 May 24.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Autocrine Communication*
Paracrine Communication*
Prostaglandin-Endoperoxide Synthases*
Prostaglandins/*metabolism
Animals ; Chronic Disease ; Fibrosis ; Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Autocrine TGF-β in Cancer: Review of the Literature and Caveats in Experimental Analysis.
Autorzy:
Ungefroren H; First Department of Medicine, University Hospital Schleswig-Holstein, Campus Lübeck, D-23538 Lübeck, Germany.; Clinic for General Surgery, Visceral, Thoracic, Transplantation and Pediatric Surgery, University Hospital Schleswig-Holstein, Campus Kiel, D-24105 Kiel, Germany.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Jan 19; Vol. 22 (2). Date of Electronic Publication: 2021 Jan 19.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Autocrine Communication*/drug effects
Autocrine Communication*/physiology
Neoplasms/*metabolism
Transforming Growth Factor beta/*physiology
Animals ; Biomedical Research/methods ; Biomedical Research/standards ; Feedback, Physiological/drug effects ; Feedback, Physiological/physiology ; Gene Expression Regulation, Neoplastic ; Humans ; Neoplasms/genetics ; Neoplasms/pathology ; Receptors, Transforming Growth Factor beta/genetics ; Receptors, Transforming Growth Factor beta/metabolism ; Research Design ; Transforming Growth Factor beta/pharmacology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Autocrine and Paracrine Effects of Vascular Endothelial Cells Promote Cutaneous Wound Healing.
Autorzy:
Lu Y; Department of Plastic Surgery, The First Affiliated Hospital of Jinan University, Key Laboratory of Regenerative Medicine, Ministry of Education, Guangzhou, Guangdong Province 510630, China.
Yang Y; Department of Orthopedics, The First Affiliated Hospital of Jinan University, No. 613, Whampoa Avenue West, Guangzhou, Guangdong Province, China.
Xiao L; Department of Plastic Surgery, The First Affiliated Hospital of Jinan University, Key Laboratory of Regenerative Medicine, Ministry of Education, Guangzhou, Guangdong Province 510630, China.
Li S; Department of Plastic Surgery, The First Affiliated Hospital of Jinan University, Key Laboratory of Regenerative Medicine, Ministry of Education, Guangzhou, Guangdong Province 510630, China.
Liao X; Department of Plastic Surgery, The First Affiliated Hospital of Jinan University, Key Laboratory of Regenerative Medicine, Ministry of Education, Guangzhou, Guangdong Province 510630, China.
Liu H; Department of Plastic Surgery, The First Affiliated Hospital of Jinan University, Key Laboratory of Regenerative Medicine, Ministry of Education, Guangzhou, Guangdong Province 510630, China.
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Źródło:
BioMed research international [Biomed Res Int] 2021 Apr 10; Vol. 2021, pp. 6695663. Date of Electronic Publication: 2021 Apr 10 (Print Publication: 2021).
Typ publikacji:
Journal Article
MeSH Terms:
Autocrine Communication*/drug effects
Paracrine Communication*/drug effects
Wound Healing*/drug effects
Human Umbilical Vein Endothelial Cells/*metabolism
Skin/*pathology
Antigens, CD/metabolism ; Biomarkers/metabolism ; Cell Movement/drug effects ; Cell Proliferation/drug effects ; Culture Media, Conditioned/pharmacology ; Cytokines/metabolism ; Fibroblasts/cytology ; Fibroblasts/drug effects ; Human Embryonic Stem Cells/cytology ; Human Embryonic Stem Cells/drug effects ; Human Umbilical Vein Endothelial Cells/drug effects ; Humans ; Mesenchymal Stem Cells/cytology ; Mesenchymal Stem Cells/drug effects
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-10 z 478

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