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1-9 of 9
Keywords: Induced pluripotent stem cells
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Journal Articles
Julie Bejoy, Justin M. Farry, Eddie S. Qian, Curtis H. Dearing, Lorraine B. Ware, Julie A. Bastarache, Lauren E. Woodard
Journal:
Disease Models & Mechanisms
Dis Model Mech (2023) 16 (12): dmm050342.
Published: 1 December 2023
... into the circulation of patients with severe sepsis and the levels of CFH are independently associated with mortality. CFH treatment increased cytotoxicity in the human tubular epithelial cell line HK-2. To better model the intact kidney, we cultured human kidney organoids derived from induced pluripotent stem cells...
Includes: Supplementary data
Journal Articles
In collection:
Developmental Disorders
Kseniia Sarieva, Felix Hildebrand, Theresa Kagermeier, Zeynep Yentür, Katharina Becker, Simone Mayer
Journal:
Disease Models & Mechanisms
Dis Model Mech (2023) 16 (11): dmm050306.
Published: 3 November 2023
.... , Abyzov , A. and Vaccarino , F. M. ( 2017 ). Human induced pluripotent stem cells for modelling neurodevelopmental disorders . Nat. Rev. Neurol. 13 , 265 - 278 . 10.1038/nrneurol.2017.45 Atladóttir , H. Ó. , Thorsen , P. , Østergaard , L. , Schendel , D. E...
Includes: Supplementary data
Journal Articles
Martyna M. Grochowska, Federico Ferraro, Ana Carreras Mascaro, Domenico Natale, Amber Winkelaar, Valerie Boumeester, Guido J. Breedveld, Vincenzo Bonifati, Wim Mandemakers
Journal:
Disease Models & Mechanisms
Dis Model Mech (2023) 16 (6): dmm049980.
Published: 23 June 2023
... ventral midbrain patterned astrocytes. Human astrocytes Ventral midbrain Induced pluripotent stem cells Disease modeling Parkinson's disease Calcium imaging data analysis Human stem cell-based models Stichting ParkinsonFonds http://dx.doi.org/10.13039/501100008383 110875 110825...
Includes: Supplementary data
Journal Articles
In collection:
Rare Disease Translational Research
Sueanne Chear, Sharn Perry, Richard Wilson, Aidan Bindoff, Jana Talbot, Tyson L. Ware, Alexandra Grubman, James C. Vickers, Alice Pébay, Jonathan B. Ruddle, Anna E. King, Alex W. Hewitt, Anthony L. Cook
Journal:
Disease Models & Mechanisms
Dis Model Mech (2022) 15 (12): dmm049651.
Published: 13 December 2022
... that is caused by mutations in CLN3 , with most affected individuals carrying at least one allele with a 966 bp deletion. Using CRISPR/Cas9, we corrected the 966 bp deletion mutation in human induced pluripotent stem cells (iPSCs) of a compound heterozygous patient ( CLN3 Δ 966 bp and E295K). We differentiated...
Includes: Supplementary data
Journal Articles
CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neurons
Open AccessS. Schuster, E. Heuten, A. Velic, J. Admard, M. Synofzik, S. Ossowski, B. Macek, S. Hauser, L. Schöls
Journal:
Disease Models & Mechanisms
Dis Model Mech (2020) 13 (10): dmm045096.
Published: 12 October 2020
... recovery in patient- compared to control-fibroblasts. As SCAR16 primarily affects the central nervous system we next investigated the HSR in cortical neurons (CNs) derived from induced pluripotent stem cells of SCAR16 patients. We found CNs of patients and controls to be surprisingly resistant to heat...
Includes: Supplementary data
Journal Articles
Neuromuscular disease modeling on a chip
Open Access
Journal:
Disease Models & Mechanisms
Dis Model Mech (2020) 13 (7): dmm044867.
Published: 7 July 2020
... sclerosis Induced pluripotent stem cells Tissue engineering Microfluidic devices University of Southern California Viterbi School of Engineering Women in Science and Engineering, University of Southern California 10.13039/100009251 Rose Hills Foundation 10.13039...
Journal Articles
Decreased N-TAF1 expression in X-linked dystonia-parkinsonism patient-specific neural stem cells
Open AccessIn collection:
Neurodegenerative Disorders
Naoto Ito, William T. Hendriks, Jyotsna Dhakal, Christine A. Vaine, Christina Liu, David Shin, Kyle Shin, Noriko Wakabayashi-Ito, Marisela Dy, Trisha Multhaupt-Buell, Nutan Sharma, Xandra O. Breakefield, D. Cristopher Bragg
Journal:
Disease Models & Mechanisms
Dis Model Mech (2016) 9 (4): 451–462.
Published: 1 April 2016
..., N-TAF1, which showed decreased expression in post-mortem XDP brain compared with control tissue. Here, we generated XDP patient and control fibroblasts and induced pluripotent stem cells (iPSCs) in order to further probe cellular defects associated with this disease. As initial validation...
Includes: Supplementary data
Journal Articles
Journal:
Disease Models & Mechanisms
Dis Model Mech (2016) 9 (1): 39–49.
Published: 1 January 2016
... type 1 patient-specific induced pluripotent stem cells (iPSCs) and differentiating these cells into spinal motor neurons. The initial specification of spinal motor neurons was not affected, but these SMA spinal motor neurons specifically degenerated following long-term culture. Moreover, at an early...
Includes: Supplementary data
Journal Articles
Bo Lin, Yang Li, Lu Han, Aaron D. Kaplan, Ying Ao, Spandan Kalra, Glenna C. L. Bett, Randall L. Rasmusson, Chris Denning, Lei Yang
Journal:
Disease Models & Mechanisms
Dis Model Mech (2015) 8 (5): 457–466.
Published: 1 May 2015
... for individuals with late-stage DMD. Results Cardiomyocytes (CMs) were derived from DMD patient-specific induced pluripotent stem cells (iPSCs) and control iPSCs. DMD iPSC-CMs exhibited dystrophin deficiency, as well as increased levels of cytosolic Ca 2+ , mitochondria damage, caspase-3 (CASP3) activation...
Includes: Supplementary data