Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Shuntaro, Morikawa"'
Autor:
Hisato Segoe, Akie Nakamura, Kimiaki Uetake, Nozomi Hishimura, Naoya Kaneko, Shuntaro Morikawa, Akari Nakamura-Utsunomiya, Takeshi Yamaguchi
Publikováno v:
Clinical Pediatric Endocrinology; 2024, Vol. 33 Issue 3, p163-168, 6p
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, optic nerve atrophy, hearing loss, diabetes insipidus, and progressive neurodegeneration. Pathogenic variants in the WFS1 gene are the main causes of Wolfr
Externí odkaz:
https://doaj.org/article/82ca11f920cc43ecacd9214f61ba4b0d
Autor:
Noriko Namatame-Ohta, Shuntaro Morikawa, Akie Nakamura, Kumihiro Matsuo, Masahide Nakajima, Kazuhiro Tomizawa, Yusuke Tanahashi, Toshihiro Tajima
Publikováno v:
Case Reports in Pediatrics, Vol 2018 (2018)
Almost 90% of nephrogenic diabetes insipidus (NDI) is caused by mutations in the arginine vasopressin receptor 2 gene (AVPR2) on the X chromosome. Herein, we reported clinical and biochemical parameters in four cases of three unrelated Japanese famil
Externí odkaz:
https://doaj.org/article/76be6b75f4f345c797756203763e47b1
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 19, Iss 3, Pp 117-121 (2014)
Congenital central hypothyroidism (C-CH) is a rare disease in which thyroid hormone deficiency is caused by insufficient thyrotropin (TSH) stimulation of a normally-located thyroid gland. Most patients with C-CH have low free thyroxine levels and ina
Externí odkaz:
https://doaj.org/article/1f028bd1519c4cb59d2b0745d9556024
Autor:
Takuya Yagi, Cris M. Brown, Simin Lu, Fumihiko Urano, Jana Mahadevan, Damien Abreu, Kohsuke Kanekura, Shuntaro Morikawa
Publikováno v:
Laboratory Investigation; a Journal of Technical Methods and Pathology
Endoplasmic reticulum (ER) stress-mediated cell death is an emerging target for human chronic disorders, including neurodegeneration and diabetes. However, there is currently no treatment for preventing ER stress-mediated cell death. Here, we show th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3a4178c88c3cabafbe73677193704a3
https://doi.org/10.1038/s41374-020-0436-1
https://doi.org/10.1038/s41374-020-0436-1
Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, optic nerve atrophy, hearing loss, diabetes insipidus, and progressive neurodegeneration. Pathogenic variants in the WFS1 gene are the main causes of Wolfr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a46635ac4afe954814d9984b757bb7dc
https://doi.org/10.1101/2022.02.09.479773
https://doi.org/10.1101/2022.02.09.479773
Autor:
Guifang Dong, Sangeeta Adak, George Spyropoulos, Qiang Zhang, Chu Feng, Li Yin, Sarah L. Speck, Zeenat Shyr, Shuntaro Morikawa, Rie Asada Kitamura, Rahul S. Kathayat, Bryan C. Dickinson, Xue Wen Ng, David W. Piston, Fumihiko Urano, Maria S. Remedi, Xiaochao Wei, Clay F. Semenkovich
Publikováno v:
Cell Metabolism. 35:332-344.e7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13921b899fa0512e7cf14ba5544f1bf0
https://doi.org/10.1016/j.cmet.2022.12.012
https://doi.org/10.1016/j.cmet.2022.12.012
Autor:
Fumihiko Urano, Shuntaro Morikawa
Publikováno v:
International Journal of Molecular Sciences. 24:230
The endoplasmic reticulum (ER) is a cytosolic organelle that plays an essential role in the folding and processing of new secretory proteins, including insulin. The pathogenesis of diabetes, a group of metabolic disorders caused by dysfunctional insu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe38a2a2d0abbbd700e66b9d3f976497
https://doi.org/10.3390/ijms24010230
https://doi.org/10.3390/ijms24010230
Publikováno v:
Journal of the Endocrine Society. 6:A338-A338
Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, optic nerve atrophy, hearing loss, diabetes insipidus, and progressive neurodegeneration. Pathogenic variants in the WFS1 gene are the main causes of Wolfr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8fabbbb6920236255adf765fa12ac13
https://doi.org/10.1210/jendso/bvac150.702
https://doi.org/10.1210/jendso/bvac150.702
Autor:
Shuntaro Morikawa, Yukihiro Hasegawa, Rumi Hachiya, Kentaro Sawano, Akie Nakamura, Takeshi Yamaguchi, Sayaka Watanabe-Yamamoto
Publikováno v:
Diabetes Research and Clinical Practice. 147:87-92
There are as yet no cohort studies of hypoglycemia in type 1 diabetes before starting insulin therapy. Our aim was to determine the frequency and clinical features of hypoglycemia in patients with type 1A diabetes prior to commencing insulin therapy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11eb06f8e559a14afbfa5afd469b2866
https://doi.org/10.1016/j.diabres.2018.11.011
https://doi.org/10.1016/j.diabres.2018.11.011