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Tytuł:
An image-guided microfluidic system for single-cell lineage tracking.
Autorzy:
Aslan Kamil M; Institute for Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, ETH Zürich, Zürich, Switzerland.
Fourneaux C; Laboratory of Biology and Modelling of the Cell, Université de Lyon, Ecole Normale Supérieure de Lyon, CNRS, UMR5239, Université Claude Bernard, Lyon, France.
Yilmaz A; Faculty of Medicine, Koç University, Istanbul, Turkey.
Stavros S; Institute for Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, ETH Zürich, Zürich, Switzerland.
Parmentier R; Ecole Pratique des Hautes Etudes, St-Antoine Research Center, Inserm U938, PSL Research University, Paris, France.
Paldi A; Ecole Pratique des Hautes Etudes, St-Antoine Research Center, Inserm U938, PSL Research University, Paris, France.
Gonin-Giraud S; Laboratory of Biology and Modelling of the Cell, Université de Lyon, Ecole Normale Supérieure de Lyon, CNRS, UMR5239, Université Claude Bernard, Lyon, France.
deMello AJ; Institute for Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, ETH Zürich, Zürich, Switzerland.
Gandrillon O; Laboratory of Biology and Modelling of the Cell, Université de Lyon, Ecole Normale Supérieure de Lyon, CNRS, UMR5239, Université Claude Bernard, Lyon, France.; Inria, France.
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Źródło:
PloS one [PLoS One] 2023 Aug 01; Vol. 18 (8), pp. e0288655. Date of Electronic Publication: 2023 Aug 01 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Microfluidics*/methods
Microfluidic Analytical Techniques*
Cell Lineage ; Cell Division ; Image Processing, Computer-Assisted ; Cell Survival ; Single-Cell Analysis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Consecutive deletions in a unique Uruguayan SARS-CoV-2 lineage evidence the genetic variability potential of accessory genes.
Autorzy:
Panzera Y; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Calleros L; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Goñi N; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Marandino A; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Techera C; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Grecco S; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Ramos N; Facultad de Ciencias, Sección Virología, Instituto de Biología e Instituto de Química Biológica, Universidad de la República, Montevideo, Uruguay.
Frabasile S; Facultad de Ciencias, Sección Virología, Instituto de Biología e Instituto de Química Biológica, Universidad de la República, Montevideo, Uruguay.
Tomás G; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Condon E; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Cortinas MN; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Ramas V; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Coppola L; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Sorhouet C; Laboratorio de Biología Molecular, Mutualista Médica Uruguaya, Montevideo, Uruguay.
Mogdasy C; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Chiparelli H; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Arbiza J; Facultad de Ciencias, Sección Virología, Instituto de Biología e Instituto de Química Biológica, Universidad de la República, Montevideo, Uruguay.
Delfraro A; Facultad de Ciencias, Sección Virología, Instituto de Biología e Instituto de Química Biológica, Universidad de la República, Montevideo, Uruguay.
Pérez R; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
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Źródło:
PloS one [PLoS One] 2022 Feb 17; Vol. 17 (2), pp. e0263563. Date of Electronic Publication: 2022 Feb 17 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cell Lineage*
Gene Deletion*
Genome, Viral*
COVID-19/*virology
Open Reading Frames/*genetics
SARS-CoV-2/*genetics
Viral Proteins/*genetics
Adult ; Aged ; COVID-19/epidemiology ; COVID-19/genetics ; Child ; Female ; High-Throughput Nucleotide Sequencing ; Humans ; Male ; Middle Aged ; Phylogeny ; SARS-CoV-2/classification ; SARS-CoV-2/isolation & purification ; Uruguay/epidemiology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Influence of FGF4 and BMP4 on FGFR2 dynamics during the segregation of epiblast and primitive endoderm cells in the pre-implantation mouse embryo.
Autorzy:
Goissis MD; Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Bradshaw B; Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Posfai E; Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Rossant J; Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
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Źródło:
PloS one [PLoS One] 2023 Jul 20; Vol. 18 (7), pp. e0279515. Date of Electronic Publication: 2023 Jul 20 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Endoderm*/metabolism
Germ Layers*/metabolism
Animals ; Mice ; Blastocyst/metabolism ; Cell Differentiation ; Cell Lineage ; Embryo, Mammalian/metabolism ; Fibroblast Growth Factors/metabolism ; Gene Expression Regulation, Developmental
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Evolution of cancer stem cell lineage involving feedback regulation.
Autorzy:
Batool I; Faculty of Mechanical and Process Engineering, Technische Universität Kaiserslautern, Kaiserslautern, Rheinland Pfalz, Germany.
Bajcinca N; Faculty of Mechanical and Process Engineering, Technische Universität Kaiserslautern, Kaiserslautern, Rheinland Pfalz, Germany.
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Źródło:
PloS one [PLoS One] 2021 May 20; Vol. 16 (5), pp. e0251481. Date of Electronic Publication: 2021 May 20 (Print Publication: 2021).
Typ publikacji:
Journal Article
MeSH Terms:
Cell Lineage*
Neoplasms/*pathology
Neoplastic Stem Cells/*pathology
Cell Differentiation ; Computer Simulation ; Feedback, Physiological ; Humans ; Models, Biological ; Mutation ; Neoplasms/genetics ; Neoplastic Stem Cells/cytology ; Neoplastic Stem Cells/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
A network approach to analyze neuronal lineage and layer innervation in the Drosophila optic lobes.
Autorzy:
Del Valle Rodríguez A; Center for Genomics and Systems Biology, New York University Abu Dhabi (NYUAD), Abu Dhabi, UAE.
Cera M; Departamento de Matemática Aplicada I, Universidad de Sevilla, Sevilla, Spain.; Instituto Universitario de Investigación de Matemáticas de la Universidad de Sevilla (IMUS), Sevilla, Spain.
Portillo JR; Departamento de Matemática Aplicada I, Universidad de Sevilla, Sevilla, Spain.; Instituto Universitario de Investigación de Matemáticas de la Universidad de Sevilla (IMUS), Sevilla, Spain.
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Źródło:
PloS one [PLoS One] 2020 Feb 05; Vol. 15 (2), pp. e0227897. Date of Electronic Publication: 2020 Feb 05 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cell Lineage*
Drosophila melanogaster/*cytology
Neurons/*cytology
Optic Lobe, Nonmammalian/*cytology
Animals ; Clone Cells ; Reproducibility of Results
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Cytochrome b marker reveals an independent lineage of Stenella coeruleoalba in the Gulf of Taranto.
Autorzy:
Ciccarese S; Dipartimento di Biologia, Sezioni di Genetica e Biologia Animale ed Ambientale, Università di Bari 'Aldo Moro', Bari, Italy.
Carlucci R; Dipartimento di Biologia, Sezioni di Genetica e Biologia Animale ed Ambientale, Università di Bari 'Aldo Moro', Bari, Italy.
Ciani E; Dipartimento di Bioscienze, Biotecnologie e Biofarmaceutica, Università di Bari 'Aldo Moro', Bari, Italy.
Corcella E; Dipartimento di Biologia, Sezioni di Genetica e Biologia Animale ed Ambientale, Università di Bari 'Aldo Moro', Bari, Italy.
Cosentino A; Dipartimento di Biologia, Sezioni di Genetica e Biologia Animale ed Ambientale, Università di Bari 'Aldo Moro', Bari, Italy.
Fanizza C; Ionian Dolphin Conservation, Taranto, Italy.
Linguiti G; Dipartimento di Biologia, Sezioni di Genetica e Biologia Animale ed Ambientale, Università di Bari 'Aldo Moro', Bari, Italy.
Antonacci R; Dipartimento di Biologia, Sezioni di Genetica e Biologia Animale ed Ambientale, Università di Bari 'Aldo Moro', Bari, Italy.
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Źródło:
PloS one [PLoS One] 2019 Mar 20; Vol. 14 (3), pp. e0213826. Date of Electronic Publication: 2019 Mar 20 (Print Publication: 2019).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cell Lineage*
Genetic Heterogeneity*
Population Dynamics*
Biomarkers/*analysis
Cytochromes b/*genetics
Stenella/*genetics
Animals ; Ecology ; Mediterranean Sea ; Phylogeny ; Stenella/classification
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Media composition modulates human embryonic stem cell morphology and may influence preferential lineage differentiation potential.
Autorzy:
Harkness L; Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, Australia.
Chen X; Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, Australia.
Gillard M; Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, Australia.
Gray PP; Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, Australia.
Davies AM; Translational Cell Imaging Queensland, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Australia.
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Źródło:
PloS one [PLoS One] 2019 Mar 19; Vol. 14 (3), pp. e0213678. Date of Electronic Publication: 2019 Mar 19 (Print Publication: 2019).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cell Differentiation*
Cell Lineage*
Culture Media/*chemistry
Human Embryonic Stem Cells/*cytology
Pluripotent Stem Cells/*cytology
Cell Culture Techniques ; Cell Line ; Cluster Analysis ; Cytoskeleton/metabolism ; Ectoderm/cytology ; Embryoid Bodies ; Endoderm/cytology ; Gene Expression Profiling ; Humans ; Mesoderm/cytology ; Microscopy, Fluorescence ; Transcription, Genetic
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Vertebral body versus iliac crest bone marrow as a source of multipotential stromal cells: Comparison of processing techniques, tri-lineage differentiation and application on a scaffold for spine fusion.
Autorzy:
Fragkakis EM; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom.; The Leeds Department of Neurosciences, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
El-Jawhari JJ; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom.; Clinical pathology department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Dunsmuir RA; The Leeds Department of Neurosciences, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Millner PA; The Leeds Department of Neurosciences, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Rao AS; The Leeds Department of Neurosciences, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Henshaw KT; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom.
Pountos I; Academic Unit of Trauma and Orthopaedic Surgery, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Jones E; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom.
Giannoudis PV; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom.; Academic Unit of Trauma and Orthopaedic Surgery, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
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Źródło:
PloS one [PLoS One] 2018 May 24; Vol. 13 (5), pp. e0197969. Date of Electronic Publication: 2018 May 24 (Print Publication: 2018).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cell Differentiation*
Cell Lineage*
Bone Marrow Cells/*cytology
Ilium/*cytology
Spinal Diseases/*therapy
Spinal Fusion/*methods
Spine/*cytology
Stromal Cells/*cytology
Adolescent ; Adult ; Aged ; Bone Marrow Cells/physiology ; Cell Proliferation ; Cells, Cultured ; Chondrogenesis ; Female ; Humans ; Ilium/physiology ; Male ; Middle Aged ; Osteogenesis ; Spinal Diseases/pathology ; Spine/physiology ; Stem Cell Transplantation ; Stromal Cells/physiology ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
GM-CSF perturbs cell identity in mouse pre-implantation embryos.
Autorzy:
Pock T; Centre of Reproductive Medicine and Andrology (CeRA), University of Münster, Münster, Germany.
Schulte K; Central Animal Facility of the Faculty of Medicine, University of Münster, Münster, Germany.
Schlatt S; Centre of Reproductive Medicine and Andrology (CeRA), University of Münster, Münster, Germany.
Boiani M; Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Nordhoff V; Centre of Reproductive Medicine and Andrology (CeRA), University of Münster, Münster, Germany.
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Źródło:
PloS one [PLoS One] 2022 Feb 10; Vol. 17 (2), pp. e0263793. Date of Electronic Publication: 2022 Feb 10 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Blastocyst/*cytology
Embryo Culture Techniques/*methods
Granulocyte-Macrophage Colony-Stimulating Factor/*pharmacology
Nanog Homeobox Protein/*metabolism
Animals ; Blastocyst/drug effects ; Blastocyst/metabolism ; Cell Count ; Cell Lineage/drug effects ; Culture Media/chemistry ; Embryo Implantation/drug effects ; Female ; Humans ; Mice ; Pregnancy
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Actin and myosin II modulate differentiation of pluripotent stem cells.
Autorzy:
Boraas LC; Department of Biomedical Engineering, Tulane University, New Orleans, Louisiana, United States of America.
Pineda ET; Department of Biomedical Engineering, Tulane University, New Orleans, Louisiana, United States of America.
Ahsan T; Department of Biomedical Engineering, Tulane University, New Orleans, Louisiana, United States of America.; RoosterBio Inc., Frederick, Maryland, United States of America.
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Źródło:
PloS one [PLoS One] 2018 Apr 17; Vol. 13 (4), pp. e0195588. Date of Electronic Publication: 2018 Apr 17 (Print Publication: 2018).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Cell Differentiation*
Cell Lineage*
Actins/*metabolism
Embryoid Bodies/*cytology
Embryonic Stem Cells/*cytology
Myosin Type II/*metabolism
Pluripotent Stem Cells/*cytology
Animals ; Cells, Cultured ; Ectoderm/cytology ; Ectoderm/metabolism ; Embryoid Bodies/metabolism ; Embryonic Stem Cells/metabolism ; Gene Expression Regulation, Developmental ; Mesoderm/cytology ; Mesoderm/metabolism ; Mice ; Pluripotent Stem Cells/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Automated C. elegans embryo alignments reveal brain neuropil position invariance despite lax cell body placement.
Autorzy:
Insley P; Laboratory of Developmental Genetics, The Rockefeller University, New York, NY, United States of America.
Shaham S; Laboratory of Developmental Genetics, The Rockefeller University, New York, NY, United States of America.
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Źródło:
PloS one [PLoS One] 2018 Mar 28; Vol. 13 (3), pp. e0194861. Date of Electronic Publication: 2018 Mar 28 (Print Publication: 2018).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Cell Lineage*
Brain/*cytology
Caenorhabditis elegans/*growth & development
Caenorhabditis elegans Proteins/*metabolism
Cell Body/*physiology
Embryo, Nonmammalian/*cytology
Neuropil/*cytology
Algorithms ; Animals ; Automation ; Brain/metabolism ; Caenorhabditis elegans/genetics ; Caenorhabditis elegans/metabolism ; Caenorhabditis elegans Proteins/genetics ; Embryo, Nonmammalian/metabolism ; Neurogenesis/physiology ; Neuropil/metabolism ; Spatio-Temporal Analysis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Charting the transcriptional landscape of cells of renin lineage following podocyte depletion.
Autorzy:
McClelland AD; Division of Nephrology, University of Washington, Seattle, Washington, United States of America.
Lichtnekert J; Division of Nephrology, University of Washington, Seattle, Washington, United States of America.
Eng DG; Division of Nephrology, University of Washington, Seattle, Washington, United States of America.
Pippin JW; Division of Nephrology, University of Washington, Seattle, Washington, United States of America.
Gross KW; Department of Molecular and Cellular Biology, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Gharib SA; Computational Medicine Core, Center for Lung Biology, Division of Pulmonary, Critical Care and Sleep Medicine, University of Washington, Seattle, Washington, United States of America.
Shankland SJ; Division of Nephrology, University of Washington, Seattle, Washington, United States of America.
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Źródło:
PloS one [PLoS One] 2017 Dec 12; Vol. 12 (12), pp. e0189084. Date of Electronic Publication: 2017 Dec 12 (Print Publication: 2017).
Typ publikacji:
Journal Article; Validation Study
MeSH Terms:
Cell Lineage*
Transcription, Genetic*
Podocytes/*metabolism
Renin/*biosynthesis
Animals ; Cell Separation ; Flow Cytometry ; Gene Expression Regulation ; Kidney Cortex/cytology ; Kidney Cortex/metabolism ; Mice ; Mice, Transgenic ; Podocytes/cytology ; RNA/isolation & purification ; Real-Time Polymerase Chain Reaction ; Transcription Factors/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Dynamic regulation of EZH2 from HPSc to hepatocyte-like cell fate.
Autorzy:
Pistoni M; KU Leuven-Department Development and Regeneration, Stem Cell Institute (SCIL), Leuven, Belgium.
Helsen N; KU Leuven-Department Development and Regeneration, Stem Cell Institute (SCIL), Leuven, Belgium.
Vanhove J; KU Leuven-Department Development and Regeneration, Stem Cell Institute (SCIL), Leuven, Belgium.
Boon R; KU Leuven-Department Development and Regeneration, Stem Cell Institute (SCIL), Leuven, Belgium.
Xu Z; KU Leuven-Department Development and Regeneration, Stem Cell Institute (SCIL), Leuven, Belgium.
Ordovas L; KU Leuven-Department Development and Regeneration, Stem Cell Institute (SCIL), Leuven, Belgium.
Verfaillie CM; KU Leuven-Department Development and Regeneration, Stem Cell Institute (SCIL), Leuven, Belgium.
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Źródło:
PloS one [PLoS One] 2017 Nov 01; Vol. 12 (11), pp. e0186884. Date of Electronic Publication: 2017 Nov 01 (Print Publication: 2017).
Typ publikacji:
Journal Article
MeSH Terms:
Cell Lineage*
Enhancer of Zeste Homolog 2 Protein/*metabolism
Hepatocytes/*metabolism
Pluripotent Stem Cells/*cytology
Cell Differentiation ; Enhancer of Zeste Homolog 2 Protein/genetics ; HEK293 Cells ; Hepatocytes/cytology ; Humans ; MicroRNAs/metabolism ; RNA, Messenger/metabolism ; Reverse Transcriptase Polymerase Chain Reaction
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
MicroRNA-16 feedback loop with p53 and Wip1 can regulate cell fate determination between apoptosis and senescence in DNA damage response.
Autorzy:
Issler MVC; Department of Physics, Universidade Federal de Santa Maria, Santa Maria, Rio Grande do Sul, Brazil.
Mombach JCM; Department of Physics, Universidade Federal de Santa Maria, Santa Maria, Rio Grande do Sul, Brazil.
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Źródło:
PloS one [PLoS One] 2017 Oct 02; Vol. 12 (10), pp. e0185794. Date of Electronic Publication: 2017 Oct 02 (Print Publication: 2017).
Typ publikacji:
Journal Article
MeSH Terms:
Apoptosis*
Cell Lineage*
Cellular Senescence*
DNA Damage*
MicroRNAs/*metabolism
Protein Phosphatase 2C/*metabolism
Tumor Suppressor Protein p53/*metabolism
Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Heading towards a dead end: The role of DND1 in germ line differentiation of human iPSCs.
Autorzy:
Mall EM; Max Planck Institute for Molecular Biomedicine, Münster, Germany.; Centre of Reproductive Medicine and Andrology, Münster, Germany.
Lecanda A; Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Drexler HCA; Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Raz E; Institute of Cell Biology, ZMBE, Münster, Germany.
Schöler HR; Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Schlatt S; Centre of Reproductive Medicine and Andrology, Münster, Germany.
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Źródło:
PloS one [PLoS One] 2021 Oct 15; Vol. 16 (10), pp. e0258427. Date of Electronic Publication: 2021 Oct 15 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Germ Cells/*metabolism
Neoplasm Proteins/*metabolism
CRISPR-Cas Systems/genetics ; Cell Differentiation ; Cell Lineage ; Cell Proliferation ; Gene Editing ; Gene Expression ; Germ Cells/cytology ; Humans ; Induced Pluripotent Stem Cells/cytology ; Induced Pluripotent Stem Cells/metabolism ; Neoplasm Proteins/genetics ; Positive Regulatory Domain I-Binding Factor 1/genetics ; Positive Regulatory Domain I-Binding Factor 1/metabolism ; Principal Component Analysis ; RNA/chemistry ; RNA/genetics ; RNA/metabolism ; RNA, Guide, CRISPR-Cas Systems/metabolism ; RNA-Binding Proteins/genetics ; RNA-Binding Proteins/metabolism ; Single-Cell Analysis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Differential expression profile of gluten-specific T cells identified by single-cell RNA-seq.
Autorzy:
Yao Y; Department of Immunology, University of Oslo, Oslo, Norway.; Centre for Immune Regulation, University of Oslo, Oslo, Norway.; K.G. Jebsen Coeliac Disease Research Centre, University of Oslo, Oslo, Norway.
Wyrozżemski Ł; Department of Immunology, University of Oslo, Oslo, Norway.; K.G. Jebsen Coeliac Disease Research Centre, University of Oslo, Oslo, Norway.
Lundin KEA; Department of Immunology, University of Oslo, Oslo, Norway.; Centre for Immune Regulation, University of Oslo, Oslo, Norway.; K.G. Jebsen Coeliac Disease Research Centre, University of Oslo, Oslo, Norway.
Sandve GK; K.G. Jebsen Coeliac Disease Research Centre, University of Oslo, Oslo, Norway.; Department of Informatics, University of Oslo, Oslo, Norway.
Qiao SW; Department of Immunology, University of Oslo, Oslo, Norway.; Centre for Immune Regulation, University of Oslo, Oslo, Norway.; K.G. Jebsen Coeliac Disease Research Centre, University of Oslo, Oslo, Norway.
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Źródło:
PloS one [PLoS One] 2021 Oct 07; Vol. 16 (10), pp. e0258029. Date of Electronic Publication: 2021 Oct 07 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Celiac Disease/*genetics
Cell Lineage/*genetics
Gene Expression Regulation/*genetics
Glutens/*genetics
T-Lymphocytes/*metabolism
Celiac Disease/pathology ; Gene Expression Profiling ; Glutens/biosynthesis ; Humans ; RNA-Seq ; Receptors, Antigen, T-Cell/genetics ; Single-Cell Analysis ; T-Lymphocytes/classification ; Th1 Cells/metabolism ; Th1 Cells/pathology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Sensitive timing of undifferentiation in oligodendrocyte progenitor cells and their enhanced maturation in primary visual cortex of binocularly enucleated mice.
Autorzy:
Shin H; Department of Bioinformatics, Graduate School of Engineering, Soka University, Hachioji, Tokyo, Japan.
Kawai HD; Department of Bioinformatics, Graduate School of Engineering, Soka University, Hachioji, Tokyo, Japan.; Department of Biosciences, Graduate School of Science and Engineering, Soka University, Hachioji, Tokyo, Japan.
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Źródło:
PloS one [PLoS One] 2021 Sep 17; Vol. 16 (9), pp. e0257395. Date of Electronic Publication: 2021 Sep 17 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Hedgehog Proteins/*genetics
Oligodendroglia/*cytology
Stem Cells/*cytology
Visual Cortex/*physiology
Animals ; Cell Differentiation ; Cell Division ; Cell Lineage ; Cell Proliferation ; Eye ; Mice ; Mice, Inbred C57BL ; Models, Statistical ; Neurogenesis ; Oligodendrocyte Precursor Cells/metabolism ; Signal Transduction ; Veratrum Alkaloids/pharmacology ; Visual Cortex/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Single-cell transcriptome analysis of the zebrafish embryonic trunk.
Autorzy:
Metikala S; Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.; Department of Pathology and Cell Biology, USF Health Heart Institute, University of South Florida, Tampa, FL, United States of America.
Casie Chetty S; Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.; Molecular and Developmental Biology Graduate Program, University of Cincinnati, Cincinnati, OH, United States of America.
Sumanas S; Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.; Department of Pathology and Cell Biology, USF Health Heart Institute, University of South Florida, Tampa, FL, United States of America.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States of America.
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Źródło:
PloS one [PLoS One] 2021 Jul 07; Vol. 16 (7), pp. e0254024. Date of Electronic Publication: 2021 Jul 07 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Profiling*
Single-Cell Analysis*
Embryo, Nonmammalian/*metabolism
Torso/*embryology
Zebrafish/*embryology
Zebrafish/*genetics
Animals ; Cell Lineage/genetics ; Ectoderm/cytology ; Ectoderm/embryology ; Endoderm/cytology ; Endoderm/embryology ; Endothelium, Vascular/cytology ; Endothelium, Vascular/embryology ; Erythrocytes/metabolism ; Fibroblasts/cytology ; Gene Expression Regulation, Developmental ; Mesoderm/cytology ; Mesoderm/embryology ; Muscle, Skeletal/embryology ; Muscle, Skeletal/metabolism ; Zebrafish Proteins/genetics ; Zebrafish Proteins/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The Chromatin Modifier MSK1/2 Suppresses Endocrine Cell Fates during Mouse Pancreatic Development.
Autorzy:
Bhat N; Institute for Regenerative Medicine, Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Civic Center Blvd., Philadelphia, PA, United States of America.
Park J; Howard Hughes Medical Institute, Department of Molecular and Human Genetics, Baylor College of Medicine, and Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, United States of America.
Zoghbi HY; Howard Hughes Medical Institute, Department of Molecular and Human Genetics, Baylor College of Medicine, and Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, United States of America.
Arthur JS; Medical Research Council Protein Phosphorylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Zaret KS; Institute for Regenerative Medicine, Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Civic Center Blvd., Philadelphia, PA, United States of America.
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Źródło:
PloS one [PLoS One] 2016 Dec 14; Vol. 11 (12), pp. e0166703. Date of Electronic Publication: 2016 Dec 14 (Print Publication: 2016).
Typ publikacji:
Journal Article
MeSH Terms:
Cell Lineage*
Pancreas/*embryology
Ribosomal Protein S6 Kinases, 90-kDa/*metabolism
Alleles ; Animals ; Apoptosis ; Bridged Bicyclo Compounds, Heterocyclic/chemistry ; Cell Differentiation ; Cell Proliferation ; Chromatin/chemistry ; Endocrine System ; Female ; Gene Expression Profiling ; Histones/chemistry ; Insulin-Secreting Cells/cytology ; Male ; Mice ; Mice, Inbred C3H ; Mice, Knockout ; Oxadiazoles/chemistry ; Phosphorylation ; Promoter Regions, Genetic ; Signal Transduction
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Phosphorylations of Serines 21/9 in Glycogen Synthase Kinase 3α/β Are Not Required for Cell Lineage Commitment or WNT Signaling in the Normal Mouse Intestine.
Autorzy:
Hey F; Department of Molecular Cell Biology, Henry Wellcome Building, University of Leicester, Leicester, United Kingdom.
Giblett S; Department of Molecular Cell Biology, Henry Wellcome Building, University of Leicester, Leicester, United Kingdom.
Forrest S; Department of Molecular Cell Biology, Henry Wellcome Building, University of Leicester, Leicester, United Kingdom.
Herbert C; Department of Molecular Cell Biology, Henry Wellcome Building, University of Leicester, Leicester, United Kingdom.
Pritchard C; Department of Molecular Cell Biology, Henry Wellcome Building, University of Leicester, Leicester, United Kingdom.; Department of Cancer Studies, Robert Kilpatrick Clinical Sciences Building, University of Leicester, Leicester, United Kingdom.
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Źródło:
PloS one [PLoS One] 2016 Jun 10; Vol. 11 (6), pp. e0156877. Date of Electronic Publication: 2016 Jun 10 (Print Publication: 2016).
Typ publikacji:
Journal Article
MeSH Terms:
Cell Lineage*/genetics
Wnt Signaling Pathway*/genetics
Glycogen Synthase Kinase 3/*metabolism
Glycogen Synthase Kinase 3 beta/*metabolism
Intestinal Mucosa/*metabolism
Serine/*metabolism
Animals ; Cell Differentiation/genetics ; Female ; Glycogen Synthase Kinase 3/genetics ; Glycogen Synthase Kinase 3 beta/genetics ; Intestinal Mucosa/physiology ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Phosphorylation/genetics ; Serine/genetics ; beta Catenin/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Wyświetlanie 1-20 z 700

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