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Hidetoshi Hoshiya

Observed names: H Hoshiya, H. Hoshiya, Hoshiya, H, 星谷 英寿, 星谷, 英寿, 英寿 星谷
OpenAlex ID: A5086501720
Transplantation of Genetically Corrected Human iPSC-Derived Progenitors in Mice with Limb-Girdle Muscular Dystrophy
2012 · Francesco Saverio Tedesco, Mattia F. M. Gerli, et al. · Science Translational Medicine · 307
Complete Genetic Correction of iPS Cells From Duchenne Muscular Dystrophy
2009 · Yasuhiro Kazuki, Masaharu Hiratsuka, et al. · Molecular Therapy · 266
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Stem Cell–Mediated Transfer of a Human Artificial Chromosome Ameliorates Muscular Dystrophy
2011 · Francesco Saverio Tedesco, Hidetoshi Hoshiya, et al. · Science Translational Medicine · 155
A highly Stable and Nonintegrated Human Artificial Chromosome (HAC) Containing the 2.4 Mb Entire Human Dystrophin Gene
2008 · Hidetoshi Hoshiya, Yasuhiro Kazuki, et al. · Molecular Therapy · 114
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Refined human artificial chromosome vectors for gene therapy and animal transgenesis
2010 · Y Kazuki, H Hoshiya, et al. · Gene Therapy · 112
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Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma
2001 · Masakazu Kohda, Hidetoshi Hoshiya, et al. · Molecular Carcinogenesis · 96
Trans-chromosomic mice containing a human CYP3A cluster for prediction of xenobiotic metabolism in humans
2012 · Yasuhiro Kazuki, Kaoru Kobayashi, et al. · Human Molecular Genetics · 81
A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids
2003 · Chiga Okita, Makiko Meguro, et al. · Genomics · 80
Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression
2010 · Y. Iida, J.-H. Kim, et al. · DNA Research · 68
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Repair or replace? Exploiting novel gene and cell therapy strategies for muscular dystrophies
2013 · Sara Benedetti, Hidetoshi Hoshiya, et al. · FEBS Journal · 57
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A Novel Human Artificial Chromosome Vector Provides Effective Cell Lineage–Specific Transgene Expression in Human Mesenchymal Stem Cells
2005 · Xianying Ren, Motonobu Katoh, et al. · Stem Cells · 44
Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb
2003 · Akiko Kashiwagi, Makiko Meguro, et al. · Journal of Human Genetics · 44
Correction of a genetic defect in multipotent germline stem cells using a human artificial chromosome
2008 · Y Kazuki, H Hoshiya, et al. · Gene Therapy · 37
Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6
2003 · Hidetoshi Hoshiya, Makiko Meguro, et al. · Journal of Human Genetics · 35
Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next‐generation human artificial chromosomes for Duchenne muscular dystrophy
2017 · Sara Benedetti, Narumi Uno, et al. · EMBO Molecular Medicine · 32
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Mesoangioblasts at 20: From the embryonic aorta to the patient bed
2023 · Giulio Cossu, Rossana Tonlorenzi, et al. · Frontiers in Genetics · 17
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Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells
2005 · Masayuki Haruta, Makiko Meguro, et al. · Journal of Human Genetics · 1
Correction: Mesoangioblasts at 20: from the embryonic aorta to the patient bed
2026 · Giulio Cossu, Rossana Tonlorenzi, et al. · Frontiers in Genetics
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Combining iPS cell-derived myogenic progenitors and human artificial chromosomes as a potential genomic integration-free cell and gene therapy for Duchenne muscular dystrophy
2018 · G. Ferrari, H. Hoshiya, et al. · Neuromuscular Disorders
Human artificial chromosomes combined with iPS cells: a genomic integration-free therapy for Duchenne muscular dystrophy
2017 · G. Ferrari, H. Hoshiya, et al. · Neuromuscular Disorders
iPS cells and human artificial chromosomes: towards a genomic integration-free therapy for Duchenne muscular dystrophy
2016 · Giuliana Ferrari, Hidetoshi Hoshiya, et al. · UCL Discovery (University College London)
Reversible immortalisation, human artificial chromosomes, and induced pluripotency: new gene and cell therapy technologies for Duchenne muscular dystrophy
2016 · Sara Benedetti, Hidetoshi Hoshiya, et al. · The Lancet
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Human artificial chromosome-mediated genetic correction of human dystrophic skeletal muscle progenitors for the autologous cell therapy of Duchenne muscular dystrophy
2015 · Benedetti, S, Hoshiya, H, et al. · UCL Discovery (University College London)
Reversible immortalization allows human artificial chromosome-mediated gene correction of human dystrophic muscle progenitor cells
2015 · S. Benedetti, H. Hoshiya, et al. · Neuromuscular Disorders
Human artificial chromosome-mediated strategies for stem cell-based therapy of muscular dystrophy
2015 · Hidetoshi Hoshiya, Sara Benedetti, et al. · UCL Discovery (University College London)
Works count: 32
Citation count: 1,546
H-index: 16
I10-index: 16
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