Cargando…

Panel of human cell lines with human/mouse artificial chromosomes

Human artificial chromosomes (HACs) and mouse artificial chromosomes (MACs) are non-integrating chromosomal gene delivery vectors for molecular biology research. Recently, microcell-mediated chromosome transfer (MMCT) of HACs/MACs has been achieved in various human cells that include human immortali...

Descripción completa

Detalles Bibliográficos
Autores principales:	Uno, Narumi, Takata, Shuta, Komoto, Shinya, Miyamoto, Hitomaru, Nakayama, Yuji, Osaki, Mitsuhiko, Mayuzumi, Ryota, Miyazaki, Natsumi, Hando, Chiaki, Abe, Satoshi, Sakuma, Tetsushi, Yamamoto, Takashi, Suzuki, Teruhiko, Nakajima, Yoshihiro, Oshimura, Mitsuo, Tomizuka, Kazuma, Kazuki, Yasuhiro
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863800/ https://www.ncbi.nlm.nih.gov/pubmed/35194085 http://dx.doi.org/10.1038/s41598-022-06814-3

Ejemplares similares

Full-length human dystrophin on human artificial chromosome compensates for mouse dystrophin deficiency in a Duchenne muscular dystrophy mouse model
por: Hiramuki, Yosuke, et al.
Publicado: (2023)

Treatment of CHO cells with Taxol and reversine improves micronucleation and microcell-mediated chromosome transfer efficiency
por: Uno, Narumi, et al.
Publicado: (2023)

Development of a Safeguard System Using an Episomal Mammalian Artificial Chromosome for Gene and Cell Therapy
por: Uno, Narumi, et al.
Publicado: (2015)

Engineering of human induced pluripotent stem cells via human artificial chromosome vectors for cell therapy and disease modeling
por: Kazuki, Yasuhiro, et al.
Publicado: (2020)

CRISPR/Cas9-induced transgene insertion and telomere-associated truncation of a single human chromosome for chromosome engineering in CHO and A9 cells
por: Uno, Narumi, et al.
Publicado: (2017)

A luciferase complementation assay system using transferable mouse artificial chromosomes to monitor protein–protein interactions mediated by G protein-coupled receptors
por: Uno, Narumi, et al.
Publicado: (2018)

Retargeting of microcell fusion towards recipient cell-oriented transfer of human artificial chromosome
por: Hiratsuka, Masaharu, et al.
Publicado: (2015)

Integration-Free iPS Cells Engineered Using Human Artificial Chromosome Vectors
por: Hiratsuka, Masaharu, et al.
Publicado: (2011)

A pathway from chromosome transfer to engineering resulting in human and mouse artificial chromosomes for a variety of applications to bio-medical challenges
por: Oshimura, Mitsuo, et al.
Publicado: (2015)

miR-19b regulates hTERT mRNA expression through targeting PITX1 mRNA in melanoma cells
por: Ohira, Takahito, et al.
Publicado: (2015)

An efficient protein production system via gene amplification on a human artificial chromosome and the chromosome transfer to CHO cells
por: Ohira, Takahito, et al.
Publicado: (2019)

A Novel System for Simultaneous or Sequential Integration of Multiple Gene-Loading Vectors into a Defined Site of a Human Artificial Chromosome
por: Suzuki, Teruhiko, et al.
Publicado: (2014)

Simultaneous loading of PCR-based multiple fragments on mouse artificial chromosome vectors in DT40 cell for gene delivery
por: Yamazaki, Kyotaro, et al.
Publicado: (2022)

Publisher Correction: Simultaneous loading of PCR-based multiple fragments on mouse artificial chromosome vectors in DT40 cell for gene delivery
por: Yamazaki, Kyotaro, et al.
Publicado: (2023)

Real‐time fluorometric evaluation of hepatoblast proliferation in vivo and in vitro using the expression of CYP3A7 coding for human fetus‐specific P450
por: Okuyama, Shota, et al.
Publicado: (2020)

Efficient human-like antibody repertoire and hybridoma production in trans-chromosomic mice carrying megabase-sized human immunoglobulin loci
por: Satofuka, Hiroyuki, et al.
Publicado: (2022)

Establishment and Characterization of a Transgenic Mouse Model for In Vivo Imaging of Bmp4 Expression in the Pancreas
por: Yasunaga, Mayu, et al.
Publicado: (2011)

Thalidomide-induced limb abnormalities in a humanized CYP3A mouse model
por: Kazuki, Yasuhiro, et al.
Publicado: (2016)

Development of a multiple-gene-loading method by combining multi-integration system-equipped mouse artificial chromosome vector and CRISPR-Cas9
por: Honma, Kazuhisa, et al.
Publicado: (2018)

Down syndrome-associated haematopoiesis abnormalities created by chromosome transfer and genome editing technologies
por: Kazuki, Yasuhiro, et al.
Publicado: (2014)

PITX1 is a reliable biomarker for predicting prognosis in patients with oral epithelial dysplasia
por: NAKABAYASHI, MOTOKI, et al.
Publicado: (2014)

MTA1, a metastasis-associated protein, in endothelial cells is an essential molecule for angiogenesis
por: Ishikawa, Mizuho, et al.
Publicado: (2022)

Complete restoration of multiple dystrophin isoforms in genetically corrected Duchenne muscular dystrophy patient–derived cardiomyocytes
por: Zatti, Susi, et al.
Publicado: (2014)

Highly Efficient Transfer of Chromosomes to a Broad Range of Target Cells Using Chinese Hamster Ovary Cells Expressing Murine Leukemia Virus-Derived Envelope Proteins
por: Suzuki, Teruhiko, et al.
Publicado: (2016)

A Method for Producing Transgenic Cells Using a Multi-Integrase System on a Human Artificial Chromosome Vector
por: Yamaguchi, Shigeyuki, et al.
Publicado: (2011)

PITX1 protein interacts with ZCCHC10 to regulate hTERT mRNA transcription
por: Ohira, Takahito, et al.
Publicado: (2019)

Modification of single-nucleotide polymorphism in a fully humanized CYP3A mouse by genome editing technology
por: Abe, Satoshi, et al.
Publicado: (2017)

Exploitation of the interaction of measles virus fusogenic envelope proteins with the surface receptor CD46 on human cells for microcell-mediated chromosome transfer
por: Katoh, Motonobu, et al.
Publicado: (2010)

ATYPICAL CILIA IN HUMAN ENDOMETRIUM
por: Hando, T., et al.
Publicado: (1968)

MicroRNA-Based Diagnosis and Treatment of Metastatic Human Osteosarcoma
por: Sasaki, Ryo, et al.
Publicado: (2019)

A Human Artificial Chromosome Recapitulates the Metabolism of Native Telomeres in Mammalian Cells
por: Wakai, Michihito, et al.
Publicado: (2014)

Construction of Mouse A9 Clones Containing a Single Human Chromosome (X/Autosome Translocation) via Micro‐cell Fusion
por: Koi, Minoru, et al.
Publicado: (1989)

Normal Human Chromosome 1 Carries Suppressor Activity for Various Phenotypes of a Kirsten Murine Sarcoma Virus‐transformed NIH/3T3 Cell Line
por: Yamada, Hideto, et al.
Publicado: (1990)

Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next‐generation human artificial chromosomes for Duchenne muscular dystrophy
por: Benedetti, Sara, et al.
Publicado: (2017)

Transfer of a Mouse Artificial Chromosome into Spermatogonial Stem Cells Generates Transchromosomic Mice
por: Shinohara, Takashi, et al.
Publicado: (2017)

Subchromosomal Mapping of a Putative Transformation Suppressor Gene on Human Chromosome 1
por: Horikawa, Izumi, et al.
Publicado: (1995)

Construction of Mouse A9 Clones Containing a Single Human Chromosome Tagged with Neomycin‐resistance Gene via Microcell Fusion
por: Koi, Minoru, et al.
Publicado: (1989)

Is meeting the needs of tourists through ethnic tourism sustainable? Focus on Bali, Indonesia
por: Mayuzumi, Yoko
Publicado: (2021)

Survey of rural and urban happiness in Indonesia during the corona crisis
por: Mayuzumi, Yoko
Publicado: (2022)

Establishment of an antibody specific for AMIGO2 improves immunohistochemical evaluation of liver metastases and clinical outcomes in patients with colorectal cancer
por: Goto, Keisuke, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_5b5d6c5l2mh9f158p1ue7ln1lj