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Tytuł:
MiR-155 promotes compensatory lung growth by inhibiting JARID2 activation of CD34+ endothelial progenitor cells.
Autorzy:
Zhao L; Department of Anesthesiology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, 650118, Yunnan, China.
Peng J; Department of Anesthesiology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, 650118, Yunnan, China.
Zhuang L; Department of Palliative Medicine, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, 650118, Yunnan, China.
Yan Z; Department of Gynaecologic Oncology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, 650118, Yunnan, China.
Liao F; Department of Anesthesiology, The 6th Affiliated Hospital of Kunming Medical University (The People's Hospital of Yuxi City), Yuxi, 653100, Yunnan, China.
Wang Y; Department of Anesthesiology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, 650118, Yunnan, China.
Shao S; Department of Anesthesiology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, 650118, Yunnan, China.
Wang W; Department of Thoracic Surgery Ⅱ, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, 650118, Yunnan, China.
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Źródło:
PloS one [PLoS One] 2024 Feb 23; Vol. 19 (2), pp. e0296671. Date of Electronic Publication: 2024 Feb 23 (Print Publication: 2024).
Typ publikacji:
Journal Article
MeSH Terms:
Endothelial Progenitor Cells*/metabolism
Lung*/metabolism
MicroRNAs*/genetics
MicroRNAs*/metabolism
Antigens, CD34/metabolism ; Cell Movement ; Cell Proliferation ; Animals ; Mice ; Polycomb Repressive Complex 2/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Myeloblasts transition to megakaryoblastic immunophenotypes over time in some patients with myelodysplastic syndromes.
Autorzy:
Ogata K; Department of Hematology, Metropolitan Research and Treatment Centre for Blood Disorders (MRTC Japan), Tokyo, Japan.
Mochimaru Y; Department of Hematology, Metropolitan Research and Treatment Centre for Blood Disorders (MRTC Japan), Tokyo, Japan.
Sei K; Department of Hematology, Metropolitan Research and Treatment Centre for Blood Disorders (MRTC Japan), Tokyo, Japan.
Kawahara N; Department of Hematology, Metropolitan Research and Treatment Centre for Blood Disorders (MRTC Japan), Tokyo, Japan.
Ogata M; Department of Hematology, Metropolitan Research and Treatment Centre for Blood Disorders (MRTC Japan), Tokyo, Japan.
Yamamoto Y; Department of Hematology, Metropolitan Research and Treatment Centre for Blood Disorders (MRTC Japan), Tokyo, Japan.
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Źródło:
PloS one [PLoS One] 2023 Sep 20; Vol. 18 (9), pp. e0291662. Date of Electronic Publication: 2023 Sep 20 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Granulocyte Precursor Cells*
Myelodysplastic Syndromes*
Humans ; Immunophenotyping ; Megakaryocyte Progenitor Cells ; Retrospective Studies ; Antigens, CD34
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Immunoregulatory properties of erythroid nucleated cells induced from CD34+ progenitors from bone marrow.
Autorzy:
Shevchenko JA; Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution 'Research Institute of Fundamental and Clinical Immunology', Novosibirsk, Russia.
Perik-Zavodskii RY; Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution 'Research Institute of Fundamental and Clinical Immunology', Novosibirsk, Russia.
Nazarov KV; Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution 'Research Institute of Fundamental and Clinical Immunology', Novosibirsk, Russia.
Denisova VV; Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution 'Research Institute of Fundamental and Clinical Immunology', Novosibirsk, Russia.
Perik-Zavodskaya OY; Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution 'Research Institute of Fundamental and Clinical Immunology', Novosibirsk, Russia.
Philippova YG; Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution 'Research Institute of Fundamental and Clinical Immunology', Novosibirsk, Russia.
Alsalloum A; Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution 'Research Institute of Fundamental and Clinical Immunology', Novosibirsk, Russia.
Sennikov SV; Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution 'Research Institute of Fundamental and Clinical Immunology', Novosibirsk, Russia.
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Źródło:
PloS one [PLoS One] 2023 Jun 30; Vol. 18 (6), pp. e0287793. Date of Electronic Publication: 2023 Jun 30 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Bone Marrow*
Erythroid Cells*
Antigens, CD34 ; Bone Marrow Cells ; Cell Adhesion Molecules
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Gene knock-outs in human CD34+ hematopoietic stem and progenitor cells and in the human immune system of mice.
Autorzy:
Kuppers DA; Human Biology Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Linton J; Translational Science and Therapeutics Division, Program in Immunology, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Ortiz Espinosa S; Translational Science and Therapeutics Division, Program in Immunology, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
McKenna KM; Translational Science and Therapeutics Division, Program in Immunology, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Rongvaux A; Translational Science and Therapeutics Division, Program in Immunology, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.; Department of Immunology, University of Washington, Seattle, Washington, United States of America.
Paddison PJ; Human Biology Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
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Źródło:
PloS one [PLoS One] 2023 Jun 28; Vol. 18 (6), pp. e0287052. Date of Electronic Publication: 2023 Jun 28 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms:
Hematopoietic Stem Cells*
Hematopoietic Stem Cell Transplantation*/methods
Humans ; Mice ; Animals ; Antigens, CD34 ; Gene Knockout Techniques ; Immune System ; Mice, SCID
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Prediction of mobilized hematopoietic stem cell yield in patients with multiple myeloma: Usefulness of whole-body MRI-derived indices.
Autorzy:
Takasu M; Department of Diagnostic Radiology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.
Higashino R; Department of Diagnostic Radiology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.
Sueoka T; Department of Diagnostic Radiology, Hiroshima Prefectural Hospital, Hiroshima, Japan.
Kawai S; Department of Diagnostic Radiology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.
Tanitame N; Department of Diagnostic Radiology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.
Tamura A; Department of Diagnostic Radiology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.
Iida M; Department of Diagnostic Radiology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.
Kawase T; Department of Immune Regenerative Medicine, International Center for Cell and Gene Therapy, Research Promotion and Support Headquarters, Fujita Health University, Aichi, Japan.
Ichinohe T; Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine (RIRBM), Hiroshima University, Hiroshima, Japan.
Awai K; Department of Diagnostic Radiology, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
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Źródło:
PloS one [PLoS One] 2023 Mar 31; Vol. 18 (3), pp. e0283241. Date of Electronic Publication: 2023 Mar 31 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Multiple Myeloma*/diagnostic imaging
Multiple Myeloma*/therapy
Hematopoietic Stem Cell Transplantation*
Humans ; Retrospective Studies ; Hematopoietic Stem Cells/chemistry ; Antigens, CD34/analysis ; Magnetic Resonance Imaging ; Hematopoietic Stem Cell Mobilization/methods ; Granulocyte Colony-Stimulating Factor ; Transplantation, Autologous
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Human intracardiac SSEA4+CD34 cells show features of cycling, immature cardiomyocytes and are distinct from Side Population and C-kit+CD45- cells.
Autorzy:
Sandstedt M; Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Clinical Chemistry, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
Vukusic K; Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Clinical Chemistry, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
Ulfenborg B; Department of Biology and Bioinformatics, School of Bioscience, University of Skövde, Skövde, Sweden.
Jonsson M; Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Clinical Chemistry, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
Mattsson Hultén L; Department of Clinical Chemistry, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.; Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Dellgren G; Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Cardiothoracic Surgery, Region Västra Götaland, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.
Jeppsson A; Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Cardiothoracic Surgery, Region Västra Götaland, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.
Synnergren J; Department of Biology and Bioinformatics, School of Bioscience, University of Skövde, Skövde, Sweden.
Sandstedt J; Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Clinical Chemistry, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
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Źródło:
PloS one [PLoS One] 2022 Jun 16; Vol. 17 (6), pp. e0269985. Date of Electronic Publication: 2022 Jun 16 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Heart Failure*/metabolism
Myocytes, Cardiac*/metabolism
Antigens, CD34/metabolism ; Cell Differentiation/physiology ; Cells, Cultured ; Flow Cytometry ; Humans ; Proto-Oncogene Proteins c-kit/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Features of fibrosis regression abound in "non-cirrhotic" patients with resected hepatocellular carcinoma.
Autorzy:
Orr CE; Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada.
Wang PL; Department of Medicine, Division of Gastroenterology, Queen's University, Kingston, Ontario, Canada.
Chen L; Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
Wang T; Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada.
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Źródło:
PloS one [PLoS One] 2022 May 12; Vol. 17 (5), pp. e0267474. Date of Electronic Publication: 2022 May 12 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Carcinoma, Hepatocellular*/pathology
Liver Neoplasms*/pathology
Antigens, CD34/metabolism ; Cell Adhesion Molecules ; Fibrosis ; Humans ; Liver Cirrhosis/pathology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Sudden infant death syndrome: Melatonin, serotonin, and CD34 factor as possible diagnostic markers and prophylactic targets.
Autorzy:
Ivanov D; Saint-Petersburg State Pediatric Medical University, St. Petersburg, Russian Federation.
Mironova E; Saint Petersburg Institute of Bioregulation and Gerontology, St. Petersburg, Russian Federation.; Saint-Petersburg Research Institute of Phthisiopulmonology, St. Petersburg, Russian Federation.
Polyakova V; Saint-Petersburg State Pediatric Medical University, St. Petersburg, Russian Federation.
Evsyukova I; Ott Research Institute of Obstetrics, Gynecology and Reproductology, St. Petersburg, Russian Federation.
Osetrov M; Saint-Petersburg State Pediatric Medical University, St. Petersburg, Russian Federation.
Kvetnoy I; Saint-Petersburg Research Institute of Phthisiopulmonology, St. Petersburg, Russian Federation.; Saint-Petersburg State University, University Embankment, St. Petersburg, Russian Federation.
Nasyrov R; Saint-Petersburg State Pediatric Medical University, St. Petersburg, Russian Federation.
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Źródło:
PloS one [PLoS One] 2021 Sep 10; Vol. 16 (9), pp. e0256197. Date of Electronic Publication: 2021 Sep 10 (Print Publication: 2021).
Typ publikacji:
Journal Article; Retracted Publication
MeSH Terms:
Antigens, CD34/*metabolism
Biomarkers/*metabolism
Melatonin/*metabolism
Serotonin/*metabolism
Sudden Infant Death/*diagnosis
Case-Control Studies ; Female ; Humans ; Infant ; Male ; Risk Factors ; Russia/epidemiology ; Sudden Infant Death/epidemiology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
CD34 Promotes Pathological Epi-Retinal Neovascularization in a Mouse Model of Oxygen-Induced Retinopathy.
Autorzy:
Siemerink MJ; Ocular Angiogenesis Group, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Ophthalmology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Cell Biology and Histology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Hughes MR; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.; The Biomedical Research Centre, University of British Columbia, Vancouver, BC, Canada.
Dallinga MG; Ocular Angiogenesis Group, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Ophthalmology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Cell Biology and Histology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Gora T; Ocular Angiogenesis Group, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Ophthalmology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Cell Biology and Histology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Cait J; The Biomedical Research Centre, University of British Columbia, Vancouver, BC, Canada.; Department of Experimental Medicine, University of British Columbia, Vancouver, BC, Canada.
Vogels IM; Ocular Angiogenesis Group, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Ophthalmology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Cell Biology and Histology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Yetin-Arik B; Ocular Angiogenesis Group, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Ophthalmology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Cell Biology and Histology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Van Noorden CJ; Ocular Angiogenesis Group, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Ophthalmology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Cell Biology and Histology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Klaassen I; Ocular Angiogenesis Group, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Ophthalmology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Cell Biology and Histology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
McNagny KM; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.; The Biomedical Research Centre, University of British Columbia, Vancouver, BC, Canada.; Department of Experimental Medicine, University of British Columbia, Vancouver, BC, Canada.
Schlingemann RO; Ocular Angiogenesis Group, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Ophthalmology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.; Department of Cell Biology and Histology, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
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Źródło:
PloS one [PLoS One] 2016 Jun 28; Vol. 11 (6), pp. e0157902. Date of Electronic Publication: 2016 Jun 28 (Print Publication: 2016).
Typ publikacji:
Journal Article
MeSH Terms:
Antigens, CD34/*metabolism
Neovascularization, Pathologic/*metabolism
Retinopathy of Prematurity/*metabolism
Animals ; Antigens, CD34/genetics ; Cell Line ; Cells, Cultured ; Endothelial Cells/metabolism ; Endothelium, Vascular/metabolism ; Humans ; Mice ; Mice, Inbred C57BL ; Oxygen/toxicity ; Retinal Vessels/metabolism ; Retinopathy of Prematurity/etiology ; Retinopathy of Prematurity/pathology ; Sialoglycoproteins/genetics ; Sialoglycoproteins/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Human hematopoietic microenvironments.
Autorzy:
Kristensen HB; Department of Clinical Cell Biology, Institute of Regional Health Science, University of Southern Denmark, Lillebaelt Hospital, Vejle, Denmark.; Department of Pathology, Clinical Cell Biology, Odense University Hospital, Odense, Denmark.; Department of Clinical Research and Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Andersen TL; Department of Clinical Cell Biology, Institute of Regional Health Science, University of Southern Denmark, Lillebaelt Hospital, Vejle, Denmark.; Department of Pathology, Clinical Cell Biology, Odense University Hospital, Odense, Denmark.; Department of Clinical Research and Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark.; Department of Forensic Medicine, Aarhus University, Aarhus, Denmark.
Patriarca A; Division of Hematology, Department of Oncology, Hospital 'Maggiore della Carità', Novara, Italy.
Kallenbach K; Department of Pathology, Zealand University Hospital, Roskilde, Denmark.
MacDonald B; Department of Clinical Cell Biology, Institute of Regional Health Science, University of Southern Denmark, Lillebaelt Hospital, Vejle, Denmark.
Sikjaer T; Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.
Ejersted C; Department of Endocrinology, Odense University Hospital, Odense, Denmark.
Delaisse JM; Department of Clinical Cell Biology, Institute of Regional Health Science, University of Southern Denmark, Lillebaelt Hospital, Vejle, Denmark.; Department of Pathology, Clinical Cell Biology, Odense University Hospital, Odense, Denmark.; Department of Clinical Research and Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
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Źródło:
PloS one [PLoS One] 2021 Apr 20; Vol. 16 (4), pp. e0250081. Date of Electronic Publication: 2021 Apr 20 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Bone Marrow Cells/*cytology
Hematopoietic Stem Cells/*cytology
Stem Cell Niche/*physiology
Adipocytes ; Adult ; Aged ; Antigens, CD34 ; Bone Marrow/metabolism ; Bone Marrow Cells/metabolism ; Bone Marrow Cells/physiology ; Cell Differentiation ; Cell Separation ; Cells, Cultured ; Female ; Flow Cytometry ; Hematopoiesis ; Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells/metabolism ; Hematopoietic Stem Cells/physiology ; Humans ; Immunophenotyping ; Megakaryocytes ; Membrane Glycoproteins ; Middle Aged
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Age-related changes in NG2-expressing telocytes of rat stomach.
Autorzy:
Tamura Y; Laboratory for Cellular Function Imaging, RIKEN Center for Biosystems Dynamics Research, Chuo-ku, Kobe, Japan.; Multi-Modal Microstructure Analysis Unit, RIKEN-JEOL Collaboration Center, Chuo-ku, Kobe, Japan.
Takata K; Laboratory for Cellular Function Imaging, RIKEN Center for Biosystems Dynamics Research, Chuo-ku, Kobe, Japan.; Multi-Modal Microstructure Analysis Unit, RIKEN-JEOL Collaboration Center, Chuo-ku, Kobe, Japan.
Eguchi A; Laboratory for Cellular Function Imaging, RIKEN Center for Biosystems Dynamics Research, Chuo-ku, Kobe, Japan.; Multi-Modal Microstructure Analysis Unit, RIKEN-JEOL Collaboration Center, Chuo-ku, Kobe, Japan.
Maeda M; Laboratory for Cellular Function Imaging, RIKEN Center for Biosystems Dynamics Research, Chuo-ku, Kobe, Japan.; Multi-Modal Microstructure Analysis Unit, RIKEN-JEOL Collaboration Center, Chuo-ku, Kobe, Japan.
Kataoka Y; Laboratory for Cellular Function Imaging, RIKEN Center for Biosystems Dynamics Research, Chuo-ku, Kobe, Japan.; Multi-Modal Microstructure Analysis Unit, RIKEN-JEOL Collaboration Center, Chuo-ku, Kobe, Japan.
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Źródło:
PloS one [PLoS One] 2021 Apr 06; Vol. 16 (4), pp. e0249729. Date of Electronic Publication: 2021 Apr 06 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Antigens/*metabolism
Gastric Mucosa/*metabolism
Proteoglycans/*metabolism
Stomach/*physiology
Telocytes/*metabolism
Age Factors ; Animals ; Antigens, CD34/metabolism ; Mucous Membrane/cytology ; Mucous Membrane/metabolism ; Rats ; Rats, Transgenic ; Rats, Wistar ; Receptor, Platelet-Derived Growth Factor alpha/metabolism ; Stomach/cytology ; Telocytes/cytology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Compositional change of gut microbiome and osteocalcin expressing endothelial progenitor cells in patients with coronary artery disease.
Autorzy:
Toya T; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, United States of America.; Division of Cardiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Ozcan I; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, United States of America.
Corban MT; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, United States of America.
Sara JD; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, United States of America.
Marietta EV; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States of America.
Ahmad A; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, United States of America.
Horwath IE; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States of America.
Loeffler DL; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, United States of America.
Murray JA; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States of America.
Lerman LO; Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States of America.
Lerman A; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, United States of America.
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Źródło:
PloS one [PLoS One] 2021 Mar 25; Vol. 16 (3), pp. e0249187. Date of Electronic Publication: 2021 Mar 25 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gastrointestinal Microbiome*
Coronary Artery Disease/*pathology
Osteocalcin/*metabolism
AC133 Antigen/metabolism ; Adult ; Aged ; Antigens, CD34/metabolism ; Case-Control Studies ; Cells, Cultured ; Clostridiales/isolation & purification ; Clostridiales/physiology ; Coronary Artery Disease/metabolism ; Dysbiosis ; Endothelial Progenitor Cells/cytology ; Endothelial Progenitor Cells/metabolism ; Female ; Humans ; Male ; Methylamines/analysis ; Middle Aged ; Vascular Endothelial Growth Factor Receptor-2/metabolism
SCR Organism:
Ruminococcus gnavus
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Biological characteristics and metabolic profile of canine mesenchymal stem cells isolated from adipose tissue and umbilical cord matrix.
Autorzy:
Marcoccia R; Department of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia, Bologna, Italy.; Health Science and Technologies Interdepartmental Center for Industrial Research (HST-ICIR), University of Bologna, Bologna, Italy.
Nesci S; Department of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia, Bologna, Italy.
Merlo B; Department of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia, Bologna, Italy.; Health Science and Technologies Interdepartmental Center for Industrial Research (HST-ICIR), University of Bologna, Bologna, Italy.
Ballotta G; Department of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia, Bologna, Italy.
Algieri C; Department of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia, Bologna, Italy.
Pagliarani A; Department of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia, Bologna, Italy.
Iacono E; Department of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia, Bologna, Italy.; Health Science and Technologies Interdepartmental Center for Industrial Research (HST-ICIR), University of Bologna, Bologna, Italy.
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Źródło:
PloS one [PLoS One] 2021 Mar 04; Vol. 16 (3), pp. e0247567. Date of Electronic Publication: 2021 Mar 04 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Adipose Tissue/*cytology
Cell Separation/*methods
Mesenchymal Stem Cells/*metabolism
Metabolomics/*methods
Umbilical Cord/*cytology
Adenosine Triphosphate/metabolism ; Animals ; Antigens, CD34/genetics ; Cell Differentiation/genetics ; Cell Differentiation/physiology ; Cell Movement/genetics ; Cell Movement/physiology ; Cell Proliferation/genetics ; Cell Proliferation/physiology ; Cells, Cultured ; Dogs ; Gene Expression ; Hyaluronan Receptors/genetics ; Major Histocompatibility Complex/genetics ; Mesenchymal Stem Cells/cytology ; Reverse Transcriptase Polymerase Chain Reaction ; Thy-1 Antigens/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Network mapping of primary CD34+ cells by Ampliseq based whole transcriptome targeted resequencing identifies unexplored differentiation regulatory relationships.
Autorzy:
Schwaber JL; Avectas, Toronto, Ontario, Canada.
Korbie D; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia, Queensland, Australia.
Andersen S; Australian Institute for Molecular Bioscience, The University of Queensland, St Lucia, Queensland, Australia.
Lin E; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia, Queensland, Australia.
Chrysanthopoulos PK; BlueRock Therapeutics, Toronto, Ontario, Canada.
Trau M; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia, Queensland, Australia.
Nielsen LK; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia, Queensland, Australia.
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Źródło:
PloS one [PLoS One] 2021 Feb 05; Vol. 16 (2), pp. e0246107. Date of Electronic Publication: 2021 Feb 05 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Regulatory Networks*
Antigens, CD34/*metabolism
Fetal Blood/*cytology
Gene Expression Profiling/*methods
Neutrophils/*cytology
RNA, Untranslated/*genetics
Aryl Hydrocarbon Receptor Nuclear Translocator/genetics ; Basic Helix-Loop-Helix Transcription Factors/genetics ; Cell Differentiation ; Cell Lineage ; Cell Proliferation ; DNA-Binding Proteins/genetics ; Female ; Fetal Blood/immunology ; Gene Expression Regulation ; Humans ; Mass Spectrometry ; Neutrophils/immunology ; Pregnancy ; Primary Cell Culture ; Proteomics ; Proto-Oncogene Proteins/genetics ; Sequence Analysis, RNA ; Trans-Activators/genetics ; Exome Sequencing
Czasopismo naukowe
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Tytuł:
Small RNA Sequencing Uncovers New miRNAs and moRNAs Differentially Expressed in Normal and Primary Myelofibrosis CD34+ Cells.
Autorzy:
Guglielmelli P; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Bisognin A; Department of Molecular Medicine, University of Padova, Padova, Italy.
Saccoman C; Department of Biology, University of Padova, Padova, Italy.
Mannarelli C; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Coppe A; Department of Molecular Medicine, University of Padova, Padova, Italy.
Vannucchi AM; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Bortoluzzi S; Department of Molecular Medicine, University of Padova, Padova, Italy.
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Źródło:
PloS one [PLoS One] 2015 Oct 15; Vol. 10 (10), pp. e0140445. Date of Electronic Publication: 2015 Oct 15 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Antigens, CD34/*metabolism
Lymphocytes/*metabolism
MicroRNAs/*genetics
Primary Myelofibrosis/*metabolism
Adaptor Proteins, Signal Transducing/genetics ; Adaptor Proteins, Signal Transducing/metabolism ; Antigens, CD34/genetics ; Base Sequence ; Case-Control Studies ; Gene Expression Regulation, Neoplastic ; Granulocytes/metabolism ; Humans ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Molecular Sequence Data ; Primary Myelofibrosis/genetics ; Receptors, Fibroblast Growth Factor/genetics ; Receptors, Fibroblast Growth Factor/metabolism
Czasopismo naukowe
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Tytuł:
Primary myelofibrosis marrow-derived CD14+/CD34- monocytes induce myelofibrosis-like phenotype in immunodeficient mice and give rise to megakaryocytes.
Autorzy:
Manshouri T; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Verstovsek S; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Harris DM; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Veletic I; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Zhang X; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Post SM; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Bueso-Ramos CE; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Estrov Z; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
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Źródło:
PloS one [PLoS One] 2019 Sep 30; Vol. 14 (9), pp. e0222912. Date of Electronic Publication: 2019 Sep 30 (Print Publication: 2019).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Immunocompromised Host*
Bone Marrow Cells/*immunology
Fibroblasts/*immunology
Hyperplasia/*immunology
Monocytes/*immunology
Primary Myelofibrosis/*immunology
Splenomegaly/*immunology
Adoptive Transfer ; Animals ; Antigens, CD34/genetics ; Antigens, CD34/immunology ; Bone Marrow Cells/pathology ; Female ; Fibroblasts/pathology ; Fibroblasts/transplantation ; Gene Expression ; HLA Antigens/genetics ; HLA Antigens/immunology ; Humans ; Hyperplasia/etiology ; Hyperplasia/genetics ; Hyperplasia/pathology ; Janus Kinase 2/genetics ; Janus Kinase 2/immunology ; Lipopolysaccharide Receptors/genetics ; Lipopolysaccharide Receptors/immunology ; Megakaryocytes/immunology ; Megakaryocytes/pathology ; Mice ; Mice, Inbred NOD ; Mice, SCID ; Monocytes/pathology ; Monocytes/transplantation ; Mutation ; Primary Myelofibrosis/etiology ; Primary Myelofibrosis/genetics ; Primary Myelofibrosis/pathology ; Splenomegaly/etiology ; Splenomegaly/genetics ; Splenomegaly/pathology
Czasopismo naukowe
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Tytuł:
Normal myeloid progenitor cell subset-associated gene signatures for acute myeloid leukaemia subtyping with prognostic impact.
Autorzy:
Schönherz AA; Department of Clinical Medicine, Faculty of Medicine, Aalborg University, Aalborg, Denmark.; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.; Department of Molecular Biology and Genetics, Center for Quantitative Genetics and Genomics, Aarhus University, Aarhus, Denmark.
Bødker JS; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Schmitz A; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Brøndum RF; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Jakobsen LH; Department of Clinical Medicine, Faculty of Medicine, Aalborg University, Aalborg, Denmark.; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Roug AS; Department of Clinical Medicine, Faculty of Medicine, Aalborg University, Aalborg, Denmark.; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Severinsen MT; Department of Clinical Medicine, Faculty of Medicine, Aalborg University, Aalborg, Denmark.; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
El-Galaly TC; Department of Clinical Medicine, Faculty of Medicine, Aalborg University, Aalborg, Denmark.; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Jensen P; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Johnsen HE; Department of Clinical Medicine, Faculty of Medicine, Aalborg University, Aalborg, Denmark.; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Bøgsted M; Department of Clinical Medicine, Faculty of Medicine, Aalborg University, Aalborg, Denmark.; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Dybkær K; Department of Clinical Medicine, Faculty of Medicine, Aalborg University, Aalborg, Denmark.; Department of Haematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
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Źródło:
PloS one [PLoS One] 2020 Apr 23; Vol. 15 (4), pp. e0229593. Date of Electronic Publication: 2020 Apr 23 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Hematopoietic Stem Cells/*metabolism
Leukemia, Myeloid, Acute/*genetics
Myeloid Cells/*metabolism
Stem Cells/*metabolism
ADP-ribosyl Cyclase 1/genetics ; Antigens, CD34/genetics ; Cell Differentiation/genetics ; Cell Lineage/genetics ; Core Binding Factor Alpha 2 Subunit/genetics ; Female ; Gene Expression Regulation, Neoplastic/genetics ; Hematopoietic Stem Cells/pathology ; Humans ; Isocitrate Dehydrogenase/genetics ; Leukemia, Myeloid, Acute/pathology ; Leukocyte Common Antigens/genetics ; Male ; Middle Aged ; Mutation/genetics ; Myeloid Cells/pathology ; Principal Component Analysis ; Regression Analysis ; Stem Cells/pathology ; WT1 Proteins/genetics
Czasopismo naukowe
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Tytuł:
Development of an ex vivo xenogeneic bone environment producing human platelet-like cells.
Autorzy:
Fujiyama S; Central Research Laboratories, Sysmex Corporation, Kobe-shi, Hyogo, Japan.
Hori N; Central Research Laboratories, Sysmex Corporation, Kobe-shi, Hyogo, Japan.
Sato T; Central Research Laboratories, Sysmex Corporation, Kobe-shi, Hyogo, Japan.
Enosawa S; Department of Organ Fabrication, Keio University School of Medicine, Tokyo, Japan.; Division of Advanced Medical Sciences, National Center for Child Health and Development, Tokyo, Japan.
Murata M; Department of Laboratory Medicine, Keio University School of Medicine, Tokyo, Japan.
Kobayashi E; Department of Organ Fabrication, Keio University School of Medicine, Tokyo, Japan.
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Źródło:
PloS one [PLoS One] 2020 Apr 07; Vol. 15 (4), pp. e0230507. Date of Electronic Publication: 2020 Apr 07 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Blood Platelets/*metabolism
Bone Marrow Cells/*cytology
Animals ; Antigens, CD34/metabolism ; Blood Platelets/cytology ; Cell Differentiation/drug effects ; Humans ; Integrin beta3/metabolism ; Megakaryocytes/cytology ; Megakaryocytes/metabolism ; Swine ; Thrombin/pharmacology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
A profile of circulating vascular progenitor cells in human neovascular age-related macular degeneration.
Autorzy:
Catchpole T; Retina Foundation of the Southwest, Dallas, Texas, United States of America.
Nguyen TD; Retina Foundation of the Southwest, Dallas, Texas, United States of America.
Gilfoyle A; Retina Foundation of the Southwest, Dallas, Texas, United States of America.
Csaky KG; Retina Foundation of the Southwest, Dallas, Texas, United States of America.; Department of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.
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Źródło:
PloS one [PLoS One] 2020 Feb 27; Vol. 15 (2), pp. e0229504. Date of Electronic Publication: 2020 Feb 27 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Choroidal Neovascularization/*blood
Choroidal Neovascularization/*pathology
Macular Degeneration/*blood
Macular Degeneration/*pathology
Stem Cells/*pathology
Aged ; Aged, 80 and over ; Angiogenesis Inhibitors/administration & dosage ; Antigens, CD34/blood ; Cell Differentiation ; Cell Proliferation ; Cell Separation ; Choroidal Neovascularization/drug therapy ; Drug Resistance ; Endothelial Cells/metabolism ; Endothelial Cells/pathology ; Female ; Humans ; Macular Degeneration/drug therapy ; Male ; Pericytes/metabolism ; Pericytes/pathology ; Stem Cells/metabolism ; Vascular Endothelial Growth Factor A/antagonists & inhibitors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Tissue-resident macrophages can be generated de novo in adult human skin from resident progenitor cells during substance P-mediated neurogenic inflammation ex vivo.
Autorzy:
Gherardini J; Monasterium Laboratory GmbH, Münster, Germany.
Uchida Y; Department of Dermatology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Hardman JA; Centre for Dermatology Research and NIHR Manchester Biomedical Research Centre University of Manchester, Manchester, United Kingdom.
Chéret J; Dr. Phillip Frost Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, Florida, United States of America.
Mace K; Division of Cell Matrix Biology and Regenerative Medicine, University of Manchester, Manchester, United Kingdom.
Bertolini M; Monasterium Laboratory GmbH, Münster, Germany.
Paus R; Monasterium Laboratory GmbH, Münster, Germany.; Centre for Dermatology Research and NIHR Manchester Biomedical Research Centre University of Manchester, Manchester, United Kingdom.; Dr. Phillip Frost Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, Florida, United States of America.
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Źródło:
PloS one [PLoS One] 2020 Jan 23; Vol. 15 (1), pp. e0227817. Date of Electronic Publication: 2020 Jan 23 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Macrophages/*immunology
Neurogenic Inflammation/*immunology
Skin/*immunology
Stem Cells/*immunology
Substance P/*immunology
Adult ; Antigens, CD/immunology ; Antigens, CD34/immunology ; Antigens, Differentiation, Myelomonocytic/immunology ; Apoptosis ; Cell Differentiation ; Female ; Humans ; Macrophages/cytology ; Organ Culture Techniques ; Skin/cytology ; Stem Cells/cytology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 263

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