about
The L-type Ca2+ channels blocker nifedipine represses mesodermal fate determination in murine embryonic stem cells.Bioluminescent imaging of genetically selected induced pluripotent stem cell-derived cardiomyocytes after transplantation into infarcted heart of syngeneic recipientsThe novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac deathThe ER aminopeptidase ERAP1 enhances or limits antigen presentation by trimming epitopes to 8-9 residuesThe cytosolic endopeptidase, thimet oligopeptidase, destroys antigenic peptides and limits the extent of MHC class I antigen presentationPathway for degradation of peptides generated by proteasomes: a key role for thimet oligopeptidase and other metallopeptidasesInduced pluripotent mesenchymal stromal cell clones retain donor-derived differences in DNA methylation profiles.Effective Hypothermic Storage of Human Pluripotent Stem Cell-Derived Cardiomyocytes Compatible With Global Distribution of Cells for Clinical Applications and Toxicology TestingThe disease-specific phenotype in cardiomyocytes derived from induced pluripotent stem cells of two long QT syndrome type 3 patients.Protein degradation and the generation of MHC class I-presented peptides.The importance of the proteasome and subsequent proteolytic steps in the generation of antigenic peptides.The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus.Indoleamine 2,3-dioxygenase-expressing dendritic cells form suppurative granulomas following Listeria monocytogenes infectionDynamic Support Culture of Murine Skeletal Muscle-Derived Stem Cells Improves Their Cardiogenic Potential In VitroRegionally diverse mitochondrial calcium signaling regulates spontaneous pacing in developing cardiomyocytes.Conversion of Human Fibroblasts to Stably Self-Renewing Neural Stem Cells with a Single Zinc-Finger Transcription Factor.Concise review: role and function of the ubiquitin-proteasome system in mammalian stem and progenitor cells.Immunological barriers to embryonic stem cell-derived therapies.Conserved TCP domain of Sas-4/CPAP is essential for pericentriolar material tethering during centrosome biogenesis.Mesenchymal stem cells and their conditioned medium improve integration of purified induced pluripotent stem cell-derived cardiomyocyte clusters into myocardial tissueInduced pluripotent stem cells as cardiac arrhythmic in vitro models and the impact for drug discovery.Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2.Ascorbic Acid-Induced Cardiac Differentiation of Murine Pluripotent Stem Cells: Transcriptional Profiling and Effect of a Small Molecule Synergist of Wnt/β-Catenin Signaling Pathway.Optimized Generation of Functional Neutrophils and Macrophages from Patient-Specific Induced Pluripotent Stem Cells: Ex Vivo Models of X(0)-Linked, AR22(0)- and AR47(0)- Chronic Granulomatous DiseasesHuman cardiac extracellular matrix supports myocardial lineage commitment of pluripotent stem cells.Electrophysiological integration and action potential properties of transplanted cardiomyocytes derived from induced pluripotent stem cells.Ca2+ signaling in human induced pluripotent stem cell-derived cardiomyocytes (iPS-CM) from normal and catecholaminergic polymorphic ventricular tachycardia (CPVT)-afflicted subjects.In vitro model for assessing arrhythmogenic properties of drugs based on high-resolution impedance measurements.A Cre-based double fluorescence indicator system for monitoring cell fusion events and selection of fused cells.Functional characterization of cardiomyocytes derived from murine induced pluripotent stem cells in vitro.Infection of myeloid dendritic cells with Listeria monocytogenes leads to the suppression of T cell function by multiple inhibitory mechanisms.Serpin-6 expression protects embryonic stem cells from lysis by antigen-specific CTL.Susceptibility of murine induced pluripotent stem cell-derived cardiomyocytes to hypoxia and nutrient deprivation.Detection of the substance immunologically cross-reactive with insulin in insulin RIA is an artifact caused by insulin tracer degradation: involvement of the insulin-degrading enzyme.Epigenetic rejuvenation of mesenchymal stromal cells derived from induced pluripotent stem cellsComparison of contractile behavior of native murine ventricular tissue and cardiomyocytes derived from embryonic or induced pluripotent stem cells.Regulation of the multidrug resistance transporter P-glycoprotein in multicellular prostate tumor spheroids by hyperthermia and reactive oxygen species.CD25 and indoleamine 2,3-dioxygenase are up-regulated by prostaglandin E2 and expressed by tumor-associated dendritic cells in vivo: additional mechanisms of T-cell inhibition.Scalable selection of hepatocyte- and hepatocyte precursor-like cells from culture of differentiating transgenically modified murine embryonic stem cells.Murine embryonic stem cell differentiation into cardiomyocytes requires L-type Ca2+ channel activity.
P50
Q27321569-5431E180-1751-4274-92CC-F415B056D88EQ27347592-82AF41B3-38C6-4BCF-A6BB-AC94531184ADQ28114840-013F7E98-3CD8-4C58-8EC5-8E9A5F2CD3CDQ28115737-75BA4F08-97C7-406D-B7B9-96F6C4EA34C1Q28185221-192BCF33-22B1-4395-B02F-E79FEA39433FQ28278713-243EE420-AA55-49FF-9FE7-D01EE80EE197Q30531604-A75781B9-C6C8-4917-AEB3-2B0CF16FB9A5Q30743853-E5A013A7-8331-48B2-9244-AA335C0FF658Q33163638-270283C5-1E72-47F4-9635-A364AD4A3EA6Q34700398-C7D58135-D29A-4488-8114-B9B000E0890DQ34801799-0478EB88-E801-44CE-BD49-67D738A75842Q35112121-B6B015E4-0E5E-4DAF-8495-328F876ACEF7Q35131219-B19D153F-55C6-4384-9112-A07BEE004529Q36016039-F9F5D1F8-1CF6-478D-A641-26872EFD334DQ36497604-41CD3AE8-B098-4EB1-AFF2-5E39CE32F3F6Q36805048-111328B4-52D5-4BFA-AAA2-9E192CF53615Q36886735-4B34DF7B-E5C9-46CA-AC63-D77B5894D937Q37095718-6C45EB68-5665-4890-BAE6-6642B3DEFF72Q37519676-063A8CB9-407F-4725-A34E-6B21993E8DB8Q37610637-E03EF16B-7ACA-4D5A-8C49-D310502B2ED3Q38167806-E693694C-B797-4465-8FBD-67093E59227CQ38761970-8B9A34D2-3A00-456F-B6BA-16C35A90BA1CQ38869985-AAF0D174-FBD1-4260-B55F-18973B3E6593Q38932710-EB429866-2975-428E-98FC-F4834890AAE5Q39000461-D3A36AE8-56BD-4D61-AA8B-54712F93DA64Q39094991-F86DAAF0-4F05-4CF8-BCBE-2FF5FC431054Q39150543-01BAF2DD-7BEA-428A-8754-3644682CE7F5Q39344963-66A36A27-9A84-4C83-AE58-2B58B69595B0Q39720061-BF6D0670-2920-4B84-BB4B-B4C2177A8A29Q39808804-F844F3D8-3143-48F4-A085-6B84A348A0A0Q39938261-5C49AC91-74BB-4524-8833-4CD3ECB072CCQ40163001-1F88D996-14F5-41B5-8319-70325536B268Q41137829-9B2CE36C-BA91-4C5C-A4FB-0F8426315FA0Q41418835-13C0BEC1-7B82-4D1A-A9E0-B30F003BC987Q42625062-3A4FB84E-FE83-47F4-8021-4DCF1D9D15F2Q43108108-75C93364-B2F9-4AF5-9639-81F9FE4C2747Q45076159-D304CDFB-D3B2-438D-9323-B1D8C64C5026Q46979779-D4200A3E-0816-42B8-804F-F22A3CDF7628Q47633864-8D6FF666-1137-4C82-BFD9-8EA6ED73849DQ48324526-B1305A7B-900D-4B56-B088-4B1353C20120
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Tomo Saric
@ast
Tomo Saric
@en
Tomo Saric
@es
Tomo Saric
@nl
Tomo Saric
@sl
type
label
Tomo Saric
@ast
Tomo Saric
@en
Tomo Saric
@es
Tomo Saric
@nl
Tomo Saric
@sl
prefLabel
Tomo Saric
@ast
Tomo Saric
@en
Tomo Saric
@es
Tomo Saric
@nl
Tomo Saric
@sl
P1053
B-3415-2015
P106
P1153
6603401782
P21
P31
P3829
P496
0000-0001-8344-1095
P569
2000-01-01T00:00:00Z