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染色体または遺伝子に変化を伴う症候群分化誘導法掲載論文一覧


Patient-derived iPSCs show premature neural differentiation and neuron type-specific phenotypes relevant to neurodevelopment. 2017, Mol Psychiatry, PubMed ID: 29158583
E. Yeh, D. Q. Dao, Z. Y. Wu, S. M. Kandalam, F. M. Camacho, C. Tom, W. Zhang, R. Krencik, K. A. Rauen, E. M. Ullian and L. A. Weiss

Autonomous and Non-autonomous Defects Underlie Hypertrophic Cardiomyopathy in BRAF-Mutant hiPSC-Derived Cardiomyocytes. 2016, Stem Cell Reports, 7, 355-369, PubMed ID: 27569062
R. Josowitz, S. Mulero-Navarro, N. A. Rodriguez, C. Falce, N. Cohen, E. M. Ullian, L. A. Weiss, K. A. Rauen, E. A. Sobie and B. D. Gelb

Human Engineered Cardiac Tissues Created Using Induced Pluripotent Stem Cells Reveal Functional Characteristics of BRAF-Mediated Hypertrophic Cardiomyopathy. 2016, PLoS One, 11, e0146697, PubMed ID: 26784941
T. J. Cashman, R. Josowitz, B. V. Johnson, B. D. Gelb and K. D. Costa

Enhanced SMAD1 Signaling Contributes to Impairments of Early Development in CFC-iPSCs. 2015, Stem Cells, 33, 1447-55, PubMed ID: 25639853
K. M. Han, S. K. Kim, D. Kim, J. Y. Choi, I. Im, K. S. Hwang, C. H. Kim, B. H. Lee, H. W. Yoo and Y. M. Han

The Potential of iPSCs for the Treatment of Premature Aging Disorders. 2017, Int J Mol Sci, 18, PubMed ID: 29112121
C. Compagnucci and E. Bertini

Cell-fate determination by ubiquitin-dependent regulation of translation. 2015, Nature, 525, 523-7, PubMed ID: 26399832
A. Werner, S. Iwasaki, C. A. McGourty, S. Medina-Ruiz, N. Teerikorpi, I. Fedrigo, N. T. Ingolia and M. Rape

Reprogramming suppresses premature senescence phenotypes of Werner syndrome cells and maintains chromosomal stability over long-term culture. 2014, PLoS One, 9, e112900, PubMed ID: 25390333
A. Shimamoto, H. Kagawa, K. Zensho, Y. Sera, Y. Kazuki, M. Osaki, M. Oshimura, Y. Ishigaki, K. Hamasaki, Y. Kodama, S. Yuasa, K. Fukuda, K. Hirashima, H. Seimiya, H. Koyama, T. Shimizu, M. Takemoto, K. Yokote, M. Goto and H. Tahara

Telomerase protects werner syndrome lineage-specific stem cells from premature aging. 2014, Stem Cell Reports, 2, 534-46, PubMed ID: 24749076
H. H. Cheung, X. Liu, L. Canterel-Thouennon, L. Li, C. Edmonson and O. M. Rennert

A role for the Werner syndrome protein in epigenetic inactivation of the pluripotency factor Oct4. 2010, Aging Cell, 9, 580-91, PubMed ID: 20477760
J. A. Smith, A. M. Ndoye, K. Geary, M. P. Lisanti, O. Igoucheva and R. Daniel

Cockayne syndrome-derived neurons display reduced synapse density and altered neural network synchrony. 2016, Hum Mol Genet, 25, 1271-80, PubMed ID: 26755826
A. T. Vessoni, R. H. Herai, J. V. Karpiak, A. M. Leal, C. A. Trujillo, A. Quinet, L. F. Agnez Lima, C. F. Menck and A. R. Muotri

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes. 2010, Proc Natl Acad Sci U S A, 107, 17668-73, PubMed ID: 20876107
S. J. Chamberlain, P. F. Chen, K. Y. Ng, F. Bourgois-Rocha, F. Lemtiri-Chlieh, E. S. Levine and M. Lalande

Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome. 2010, Nature, 465, 808-12, PubMed ID: 20535210
X. Carvajal-Vergara, A. Sevilla, S. L. D’Souza, Y. S. Ang, C. Schaniel, D. F. Lee, L. Yang, A. D. Kaplan, E. D. Adler, R. Rozov, Y. Ge, N. Cohen, L. J. Edelmann, B. Chang, A. Waghray, J. Su, S. Pardo, K. D. Lichtenbelt, M. Tartaglia, B. D. Gelb and I. R. Lemischka