Publications by authors named "Sebastian Diecke"

42Publications

Generation of two human induced pluripotent stem cell lines derived from myoblasts (MDCi014-A) and from peripheral blood mononuclear cells (MDCi014-B) from the same donor.

Stem Cell Res 2020 10 17;48:101998. Epub 2020 Sep 17.

Muscle Research Unit, Experimental and Clinical Research Center, A Joint Cooperation of Charité, Universitätsmedizin Berlin and the Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany; Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.

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http://dx.doi.org/10.1016/j.scr.2020.101998DOI Listing
October 2020

Generation of three age and gender matched pairs of human induced pluripotent stem cells derived from myoblasts (MDCi011-A, MDCi012-A, MDCi013-A) and from peripheral blood mononuclear cells (MDCi011-B, MDCi012-B, MDCi013-B) from the same donor.

Stem Cell Res 2020 10 8;48:101987. Epub 2020 Sep 8.

Muscle Research Unit, Experimental and Clinical Research Center, a joint cooperation of Charité, Universitätsmedizin Berlin and the Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany; Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.

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http://dx.doi.org/10.1016/j.scr.2020.101987DOI Listing
October 2020

Methods for Automated Single Cell Isolation and Sub-Cloning of Human Pluripotent Stem Cells.

Curr Protoc Stem Cell Biol 2020 Dec;55(1):e123

Charité-Universitätsmedizin Berlin, Berlin, Germany.

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http://dx.doi.org/10.1002/cpsc.123DOI Listing
December 2020

Simple Workflow and Comparison of Media for hPSC-Cardiomyocyte Cryopreservation and Recovery.

Curr Protoc Stem Cell Biol 2020 Dec;55(1):e125

Core Facility Stem Cells, Max-Delbrück-Centrum, Berlin, Germany.

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http://dx.doi.org/10.1002/cpsc.125DOI Listing
December 2020

Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome.

Kidney Int 2020 07 24;98(1):159-167. Epub 2020 Mar 24.

Max-Delbrueck-Center for Molecular Medicine, Berlin, Germany; Department of Biomedicine, Faculty of Health Science, Aarhus University, Aarhus C, Denmark. Electronic address:

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http://dx.doi.org/10.1016/j.kint.2020.02.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322522PMC
July 2020

The Translational Landscape of the Human Heart.

Cell 2019 06 30;178(1):242-260.e29. Epub 2019 May 30.

Cardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), 13125 Berlin, Germany; DZHK (German Centre for Cardiovascular Research), Partner Site Berlin, 13347 Berlin, Germany; Berlin Institute of Health (BIH), 10178 Berlin, Germany; Charité-Universitätsmedizin, 10117 Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.cell.2019.05.010DOI Listing
June 2019

Human and equine endothelial cells in a live cell imaging scratch assay in vitro.

Clin Hemorheol Microcirc 2018 ;70(4):495-509

Freie Universität Berlin, Department of Veterinary Medicine, Institute for Veterinary Anatomy, Germany.

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http://www.medra.org/servlet/aliasResolver?alias=iospress&am
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http://dx.doi.org/10.3233/CH-189316DOI Listing
April 2019

Mutations in Disordered Regions Can Cause Disease by Creating Dileucine Motifs.

Cell 2018 09 6;175(1):239-253.e17. Epub 2018 Sep 6.

Proteome Dynamics, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Robert-Rössle-Str. 10, 13125 Berlin, Germany; Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.cell.2018.08.019DOI Listing
September 2018

FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells.

Dev Cell 2018 09 2;46(5):611-626.e12. Epub 2018 Aug 2.

Berlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, 13125 Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.devcel.2018.07.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137076PMC
September 2018

Autologous iPSC-Based Vaccines Elicit Anti-tumor Responses In Vivo.

Cell Stem Cell 2018 04 15;22(4):501-513.e7. Epub 2018 Feb 15.

Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cardiovascular Institute of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Radiology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address:

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http://dx.doi.org/10.1016/j.stem.2018.01.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134179PMC
April 2018

Alloimmune Responses of Humanized Mice to Human Pluripotent Stem Cell Therapeutics.

Cell Rep 2017 Aug;20(8):1978-1990

Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, USA; Department of Medicine, Stanford University School of Medicine, Stanford, California, USA; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, USA. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2017.08.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573767PMC
August 2017

A Comprehensive TALEN-Based Knockout Library for Generating Human-Induced Pluripotent Stem Cell-Based Models for Cardiovascular Diseases.

Circ Res 2017 May 28;120(10):1561-1571. Epub 2017 Feb 28.

From the Stanford Cardiovascular Institute (I.K., V.T., J.L., S.D., I.I., M.A., R.S., H.W., N.M., N.-Y.S., T.S., N.W., K.D.W., E.M., J.C.W.), Department of Cardiothoracic Surgery (I.K.), Division of Cardiovascular Medicine, Department of Medicine (V.T., J.C.W.), CA; Institute of Stem Cell Biology and Regenerative Medicine (D.A.C., V.S., J.C.W.), Departments of Pediatrics (A.H., M.H.P.), Pathology (K.D.W.), and Obstetrics and Gynecology (V.S.), Stanford University School of Medicine, CA; Berlin Institute of Health, Germany (S.D.); and Max Delbrueck Center, Berlin, Germany (S.D.).

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http://dx.doi.org/10.1161/CIRCRESAHA.116.309948DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429194PMC
May 2017

Generation of Functional Cardiomyocytes from the Synoviocytes of Patients with Rheumatoid Arthritis via Induced Pluripotent Stem Cells.

Sci Rep 2016 09 9;6:32669. Epub 2016 Sep 9.

Division of Rheumatology, Department of Internal Medicine, College of Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul, South Korea.

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http://dx.doi.org/10.1038/srep32669DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016736PMC
September 2016

Reprogramming and transdifferentiation for cardiovascular development and regenerative medicine: where do we stand?

EMBO Mol Med 2015 Sep;7(9):1090-103

Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA Department of Medicine, Division of Cardiology, Stanford University School of Medicine, Stanford, CA, USA Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, USA

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http://dx.doi.org/10.15252/emmm.201504395DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4568945PMC
September 2015

Modeling Cardiovascular Diseases with Patient-Specific Human Pluripotent Stem Cell-Derived Cardiomyocytes.

Methods Mol Biol 2016 ;1353:119-30

Department of Medicine (Division of Cardiology), Stanford Cardiovascular Institute, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, 265 Campus Drive, Room G1120B, Stanford, CA, 94305-5454, USA.

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http://dx.doi.org/10.1007/7651_2015_196DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962608PMC
August 2016

Novel codon-optimized mini-intronic plasmid for efficient, inexpensive, and xeno-free induction of pluripotency.

Sci Rep 2015 Jan 28;5:8081. Epub 2015 Jan 28.

1] Institute for Stem Cell Biology and Regenerative Medicine; Stanford University School of Medicine, Stanford, California 94305, USA [2] Stanford Cardiovascular Institute; Stanford University School of Medicine, Stanford, California 94305, USA [3] Department of Medicine, Division of Cardiology; Stanford University School of Medicine, Stanford, California 94305, USA.

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http://www.nature.com/articles/srep08081
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http://dx.doi.org/10.1038/srep08081DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4308704PMC
January 2015

Improved approach for chondrogenic differentiation of human induced pluripotent stem cells.

Stem Cell Rev Rep 2015 Apr;11(2):242-53

Department of Radiology, and Molecular Imaging Program at Stanford (MIPS), Stanford School of Medicine, Stanford, CA, 94304, USA.

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http://dx.doi.org/10.1007/s12015-014-9581-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412587PMC
April 2015

Pravastatin reverses obesity-induced dysfunction of induced pluripotent stem cell-derived endothelial cells via a nitric oxide-dependent mechanism.

Eur Heart J 2015 Apr 2;36(13):806-16. Epub 2014 Nov 2.

Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, USA Division of Cardiology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA

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http://dx.doi.org/10.1093/eurheartj/ehu411DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381134PMC
April 2015

Characterization of the molecular mechanisms underlying increased ischemic damage in the aldehyde dehydrogenase 2 genetic polymorphism using a human induced pluripotent stem cell model system.

Sci Transl Med 2014 Sep;6(255):255ra130

Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA 94305, USA. Division of Cardiology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA. Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.

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http://dx.doi.org/10.1126/scitranslmed.3009027DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215699PMC
September 2014

Recent technological updates and clinical applications of induced pluripotent stem cells.

Korean J Intern Med 2014 Sep 28;29(5):547-57. Epub 2014 Aug 28.

Division of Rheumatology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.

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http://dx.doi.org/10.3904/kjim.2014.29.5.547DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164716PMC
September 2014

Second generation codon optimized minicircle (CoMiC) for nonviral reprogramming of human adult fibroblasts.

Methods Mol Biol 2014 ;1181:1-13

Lorry I. Lokey Stem Cell Research Building, Stanford University School of Medicine, 265 Campus Drive, Room G1105, Stanford, CA, 94305-5454, USA.

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http://link.springer.com/10.1007/978-1-4939-1047-2_1
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http://dx.doi.org/10.1007/978-1-4939-1047-2_1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385867PMC
March 2015

Human induced pluripotent stem cell-derived cardiomyocytes as an in vitro model for coxsackievirus B3-induced myocarditis and antiviral drug screening platform.

Circ Res 2014 Aug 11;115(6):556-66. Epub 2014 Jul 11.

From the Department of Medicine, Division of Cardiology (A.S., R.H., P.W.B., K.R., J.M.C., H.W., K.I.S., E.M., A.C.S., Y.C., A.E., S.D., P.L., S.M.W., J.C.W.), Institute for Stem Cell Biology and Regenerative Medicine (A.S., R.H., P.W.B., K.R., J.M.C., H.W., K.I.S., E.M., A.C.S., Y.C., A.E., S.D., P.L., S.M.W., J.C.W.), Stanford Cardiovascular Institute (A.S., R.H., P.W.B., K.R., J.M.C., H.W., K.I.S., E.M., A.C.S., Y.C., A.E., S.D., P.L., K.R.-H., S.M.W., J.C.W.), Department of Biology (A.S., R.H., K.R.-H.), Department of Microbiology and Immunology (C.M., J.E.C.), and Department of Radiology, Molecular Imaging Program (J.C.W.), Stanford University School of Medicine, CA.

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http://dx.doi.org/10.1161/CIRCRESAHA.115.303810DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149868PMC
August 2014

Chemically defined generation of human cardiomyocytes.

Nat Methods 2014 Aug 15;11(8):855-60. Epub 2014 Jun 15.

1] Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, USA. [2] Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, USA. [3] Department of Medicine, Division of Cardiology, Stanford University School of Medicine, Stanford, California, USA.

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http://dx.doi.org/10.1038/nmeth.2999DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4169698PMC
August 2014

Transplanted terminally differentiated induced pluripotent stem cells are accepted by immune mechanisms similar to self-tolerance.

Nat Commun 2014 May 30;5:3903. Epub 2014 May 30.

1] Departments of Medicine and Radiology, Stanford University School of Medicine, Stanford, California 94305-5323, USA [2] Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California 94305-5323, USA [3] Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305-5323, USA.

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http://dx.doi.org/10.1038/ncomms4903DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075468PMC
May 2014

Costimulation-adhesion blockade is superior to cyclosporine A and prednisone immunosuppressive therapy for preventing rejection of differentiated human embryonic stem cells following transplantation.

Stem Cells 2013 Nov;31(11):2354-63

Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, USA; Department of Medicine, Stanford University School of Medicine, Stanford, California, USA; Department of Radiology, Stanford University School of Medicine, Stanford, California, USA.

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http://dx.doi.org/10.1002/stem.1501DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938393PMC
November 2013

The role of SIRT6 protein in aging and reprogramming of human induced pluripotent stem cells.

J Biol Chem 2013 Jun 7;288(25):18439-47. Epub 2013 May 7.

Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.

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http://dx.doi.org/10.1074/jbc.M112.405928DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689986PMC
June 2013

Pushing the reset button: chemical-induced conversion of amniotic fluid stem cells into a pluripotent state.

Mol Ther 2012 Oct;20(10):1839-41

Division of Cardiology, Department of Medicine, Stanford University School of Medicine, Stanford, California94305, USA.

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http://dx.doi.org/10.1038/mt.2012.192DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464646PMC
October 2012

E-cadherin is crucial for embryonic stem cell pluripotency and can replace OCT4 during somatic cell reprogramming.

EMBO Rep 2011 Jul 1;12(7):720-6. Epub 2011 Jul 1.

Max Delbrueck Center, Robert-Roessle-Strasse 10, 13125 Berlin, Germany; Freie Universität Berlin, Department of Biology, Chemistry and Pharmacy, Takustrasse 3, 14195 Berlin, Germany.

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http://embor.embopress.org/cgi/doi/10.1038/embor.2011.88
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http://dx.doi.org/10.1038/embor.2011.88DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128971PMC
July 2011

FGF2 signaling in mouse embryonic fibroblasts is crucial for self-renewal of embryonic stem cells.

Cells Tissues Organs 2008 11;188(1-2):52-61. Epub 2008 Mar 11.

Max Delbrück Center, Berlin, Germany.

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http://dx.doi.org/10.1159/000121282DOI Listing
September 2008

Identification of prion protein binding proteins by combined use of far-Western immunoblotting, two dimensional gel electrophoresis and mass spectrometry.

Proteomics 2006 Jan;6(1):26-34

Molecular Medicine, Ottawa Health Research Institute, Lab N1, Box 221, 501 Smyth Road, Ottawa, Ontario K1H 8L6, Canada.

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http://dx.doi.org/10.1002/pmic.200500066DOI Listing
January 2006