His primary scientific interests are in Molecular biology, Haematopoiesis, Immunology, Cellular differentiation and Progenitor cell. His Molecular biology research includes elements of Myeloid, Methylation, CRISPR and Autologous transplantation. As part of his Stem cell and Cell biology and Haematopoiesis studies, Marcus O. Muench is studying Haematopoiesis.
He has researched Stem cell in several fields, including Fms-Like Tyrosine Kinase 3, ROR1, Tropomyosin receptor kinase C, Platelet-derived growth factor receptor and Receptor tyrosine kinase. The Cellular differentiation study combines topics in areas such as Natural killer cell, T lymphocyte, Clonogenic assay and Sialyltransferase. His Progenitor cell study combines topics from a wide range of disciplines, such as Immune system and Glycan.
His main research concerns Immunology, Haematopoiesis, Stem cell, Molecular biology and Progenitor cell. His Immunology research incorporates elements of Fetus, Ex vivo and Transplantation. His study in the field of Stem cell factor is also linked to topics like Population.
His studies deal with areas such as Blood cell and Cancer research as well as Stem cell. His research in Molecular biology focuses on subjects like Methylation, which are connected to Epigenetics. Marcus O. Muench interconnects Endocrinology and Internal medicine in the investigation of issues within Progenitor cell.
Marcus O. Muench mainly investigates Virology, Antibody, In vivo, Flow cytometry and Platelet. His study in the field of Tissue tropism also crosses realms of Attenuated vaccine. His studies in In vivo integrate themes in fields like Apoptosis, In vitro and Immune system, Immune tolerance.
His Flow cytometry study improves the overall literature in Molecular biology. His Platelet study is concerned with the field of Immunology as a whole. His Immunology study frequently draws connections between related disciplines such as Ex vivo.
Marcus O. Muench spends much of his time researching Salivary gland, Cell biology, Stem cell, Progenitor cell and Myoepithelial cell. The concepts of his Salivary gland study are interwoven with issues in Ductal cells, Intercalated duct, Progenitor and Cellular differentiation. His Cell biology study focuses mostly on Haematopoiesis and Cell therapy.
His research on Stem cell often connects related topics like Myeloid. His research in Myoepithelial cell intersects with topics in CD34, CD90, Mesenchymal stem cell and Salivary Gland Disorder. CD90 connects with themes related to Stromal cell in his study.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Maternal Alloantigens Promote the Development of Tolerogenic Fetal Regulatory T Cells in Utero
Jeff E. Mold;Jakob Michaëlsson;Trevor D. Burt;Marcus O. Muench.
Ligand for FLT3/FLK2 receptor tyrosine kinase regulates growth of haematopoietic stem cells and is encoded by variant RNAs
C. Hannum;J. Culpepper;D. Campbell;T. McClanahan.
Seamless gene correction of β-thalassemia mutations in patient-specific iPSCs using CRISPR/Cas9 and piggyBac
Fei Xie;Lin Ye;Judy C. Chang;Ashley I. Beyer.
Genome Research (2014)
Differential Downregulation of ACE2 by the Spike Proteins of Severe Acute Respiratory Syndrome Coronavirus and Human Coronavirus NL63
Ilona Glowacka;Stephanie Bertram;Petra Herzog;Susanne Pfefferle.
Journal of Virology (2010)
Seamless modification of wild-type induced pluripotent stem cells to the natural CCR5Δ32 mutation confers resistance to HIV infection
Lin Ye;Jiaming Wang;Ashley I. Beyer;Fernando Teque.
Proceedings of the National Academy of Sciences of the United States of America (2014)
Identification of a common T/natural killer cell progenitor in human fetal thymus.
María José Sánchez;Marcus O. Muench;Maria Grazia Roncarolo;Lewis L. Lanier.
Journal of Experimental Medicine (1994)
Whole-genome fingerprint of the DNA methylome during human B cell differentiation
Marta Kulis;Angelika Merkel;Simon Heath;Ana C Queirós.
Nature Genetics (2015)
Bone marrow transplantation with interleukin-1 plus kit-ligand ex vivo expanded bone marrow accelerates hematopoietic reconstitution in mice without the loss of stem cell lineage and proliferative potential
Marcus O. Muench;Meri T. Firpo;Malcolm A.S. Moore.
Exosomes from red blood cell units bind to monocytes and induce proinflammatory cytokines, boosting T-cell responses in vitro
Ali Danesh;Heather C. Inglis;Rachael P. Jackman;Shiquan Wu.
Genome editing using CRISPR-Cas9 to create the HPFH genotype in HSPCs: An approach for treating sickle cell disease and β-thalassemia
Lin Ye;Jiaming Wang;Yuting Tan;Ashley I. Beyer.
Proceedings of the National Academy of Sciences of the United States of America (2016)
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