Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Mami Matsuo"'
Autor:
Rui Li, Hazuki Tsuboi, Hidenori Ito, Daigo Takagi, Yun-Hsuan Chang, Tomoya Shimizu, Yutaka Arai, Mami Matsuo-Takasaki, Michiya Noguchi, Yukio Nakamura, Kiyoshi Ohnuma, Satoru Takahashi, Yohei Hayashi
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103584- (2024)
Glucose transporter 1 deficiency syndrome (GLUT1DS), caused by impaired glucose transport at the blood–brain barriers, leads to various central nervous system dysfunctions. A comprehensive understanding of the underlying disease pathogenesis is sti
Externí odkaz:
https://doaj.org/article/8b7969b8fad1436f8846449618613ed6
Autor:
Mami Matsuo-Takasaki, Sho Kambayashi, Yasuko Hemmi, Tamami Wakabayashi, Tomoya Shimizu, Yuri An, Hidenori Ito, Kazuhiro Takeuchi, Masato Ibuki, Terasu Kawashima, Rio Masayasu, Manami Suzuki, Yoshikazu Kawai, Masafumi Umekage, Tomoaki M Kato, Michiya Noguchi, Koji Nakade, Yukio Nakamura, Tomoyuki Nakaishi, Naoki Nishishita, Masayoshi Tsukahara, Yohei Hayashi
Publikováno v:
eLife, Vol 12 (2024)
Human induced pluripotent stem cells (hiPSCs) are promising resources for producing various types of tissues in regenerative medicine; however, the improvement in a scalable culture system that can precisely control the cellular status of hiPSCs is n
Externí odkaz:
https://doaj.org/article/9741ffd7753d4338bddd028973796412
Autor:
Daigo Takagi, Satomi Tsukamoto, Koji Nakade, Tomoya Shimizu, Yutaka Arai, Mami Matsuo-Takasaki, Michiya Noguchi, Yukio Nakamura, Norihiro Yumoto, Jiro Kawada, Tadayoshi Hayata, Yohei Hayashi
Publikováno v:
Stem Cell Research, Vol 79, Iss , Pp 103493- (2024)
Myelin basic protein (MBP) is a major component of the myelin sheaths of oligodendrocytes in the central nervous system and Schwann cells of the peripheral nervous system. Here we generated heterozygous fluorescent reporter of MBP gene in human induc
Externí odkaz:
https://doaj.org/article/9cbe5412d3a94a889af7b882c8c6ff7c
Autor:
Yutaka Arai, Hidenori Ito, Tomoya Shimizu, Yuzuno Shimoda, Dan Song, Mami Matsuo-Takasaki, Tadayoshi Hayata, Yohei Hayashi
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
Juvenile nephronophthisis is an inherited renal ciliopathy with cystic kidney disease, renal fibrosis, and end-stage renal failure in children and young adults. Mutations in the NPHP1 gene encoding nephrocystin-1 protein have been identified as the m
Externí odkaz:
https://doaj.org/article/47959d363cb542d9ac07e26428f2cb66
Autor:
Miyu Mori, Shoko Yoshii, Michiya Noguchi, Daigo Takagi, Tomoya Shimizu, Hidenori Ito, Mami Matsuo-Takasaki, Yukio Nakamura, Satoru Takahashi, Hiromichi Hamada, Kiyoshi Ohnuma, Tadashi Shiohama, Yohei Hayashi
Publikováno v:
Stem Cell Research, Vol 77, Iss , Pp 103432- (2024)
Rett syndrome is characterized by severe global developmental impairments with autistic features and loss of purposeful hand skills. Here we show that human induced pluripotent stem cell (hiPSC) lines derived from four Japanese female patients with R
Externí odkaz:
https://doaj.org/article/6962a75bf8ac4d788cddea596e42be9a
Autor:
Tomoya Shimizu, Mami Matsuo-Takasaki, Dorian Luijkx, Miho Takami, Yutaka Arai, Michiya Noguchi, Yukio Nakamura, Tadayoshi Hayata, Megumu K. Saito, Yohei Hayashi
Publikováno v:
Stem Cell Research, Vol 61, Iss , Pp 102744- (2022)
DiGeorge syndrome (22q11.2 deletion syndrome, or CATCH22 syndrome), caused by hemizygous deletion of chromosome 22q11.2, results in the poor development of multiple organs. Here we have generated DiGeorge syndrome-specific human induced pluripotsnt s
Externí odkaz:
https://doaj.org/article/1d22e84c5d9641c7b2f967bda61b628c
Autor:
Evgeniia Borisova, Ken Nishimura, Yuri An, Miho Takami, Jingyue Li, Dan Song, Mami Matsuo-Takasaki, Dorian Luijkx, Shiho Aizawa, Akihiro Kuno, Eiji Sugihara, Taka-aki Sato, Fumiaki Yumoto, Tohru Terada, Koji Hisatake, Yohei Hayashi
Publikováno v:
iScience, Vol 25, Iss 1, Pp 103525- (2022)
Summary: Non-genetically modified somatic cells can only be inefficiently and stochastically reprogrammed to pluripotency by exogenous expression of reprogramming factors. Low competence of natural reprogramming factors may prevent the majority of ce
Externí odkaz:
https://doaj.org/article/39f12cba9f554b229646605931796070
Autor:
Yuji Kuramochi, Tomonari Awaya, Mami Matsuo-Takasaki, Miho Takami, Yuri An, Jingyue Li, Yasuko Hemmi, Tamami Wakabayashi, Yutaka Arai, Jun Inoue, Michiya Noguchi, Yukio Nakamura, Isao Asaka, Kazunori Akimoto, Megumu K. Saito, Yohei Hayashi
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102337- (2021)
Adrenoleukodystrophy (ALD) is an X-linked genetic disorder, characterized by demyelination in the central nervous system and adrenal insufficiency. Human induced pluripotent stem cell (hiPSC) lines derived from two Japanese male patients with ALD wer
Externí odkaz:
https://doaj.org/article/193cf00ce38e4473be44dc32ab02b779
Autor:
Satomi Tsukamoto, Koji Nakade, Tamami Wakabayashi, Kenichi Nakashima, Miho Takami, Yasuko Hemmi, Yuji Kuramochi, Tomoya Shimizu, Yutaka Arai, Mami Matsuo-Takasaki, Michiya Noguchi, Yukio Nakamura, Yoshihiro Miwa, Yohei Hayashi
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102363- (2021)
ISL1 encodes a member of the LIM/homeodomain family of transcription factors. This encoded protein plays central roles in the development of motor neuron, pancreas, and secondary heart field. Here we generated heterozygous fluorescent reporters of th
Externí odkaz:
https://doaj.org/article/f0a084e1f66742a1b47f6d8af2db44f6
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Chromosomal abnormality causes congenital and acquired intractable diseases. In general, there are no fundamental treatments for these diseases. To establish platforms to develop therapeutics for these diseases, patient-derived induced pluripotent st
Externí odkaz:
https://doaj.org/article/12e389c157fc44b38b73af795e9b349b