The Role of ER Stress in Diabetes: Exploring Pathological Mechanisms Using Wolfram Syndrome

por Morikawa, Shuntaro, Urano, Fumihiko
Publicado 2022

Clinical features and molecular basis of pseudohypoaldosteronism type 1

por Tajima, Toshihiro, Morikawa, Shuntaro, Nakamura, Akie
Publicado 2017

ODP254 WFS1 Loss of Function Causes ER Stress-Mediated Inflammation in Pancreatic β-Cells

por Morikawa, Shuntaro, Blaher, Lindsey, Urano, Fumihiko
Publicado 2022

Neonatal screening and a new cause of congenital central hypothyroidism

por Tajima, Toshihiro, Nakamura, Akie, Morikawa, Shuntaro, Ishizu, Katsura
Publicado 2014

Loss of Function of WFS1 Causes ER Stress-Mediated Inflammation in Pancreatic Beta-Cells

por Morikawa, Shuntaro, Blacher, Lindsey, Onwumere, Chinyere, Urano, Fumihiko
Publicado 2022

Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of NR3C2

por Morikawa, Shuntaro, Komatsu, Nagisa, Sakata, Sonoko, Nakamura-Utsunomiya, Akari, Okada, Satoshi, Tajima, Toshihiro
Publicado 2015

Results from 28 Years of Newborn Screening for Congenital Adrenal Hyperplasia in Sapporo

por Morikawa, Shuntaro, Nakamura, Akie, Fujikura, Kaori, Fukushi, Masaru, Hotsubo, Tomoyuki, Miyata, Jun, Ishizu, Katsura, Tajima, Toshihiro
Publicado 2014

Two siblings with congenital central hypothyroidism caused by a novel mutation in the IGSF1 gene

por Oguma, Makiko, Kobayashi, Mizuki, Yamazaki, Masayo, Yokoyama, Koji, Morikawa, Shuntaro, Yamaguchi, Takeshi, Yamagata, Takanori, Tajima, Toshihiro
Publicado 2018

Four Japanese Patients with Congenital Nephrogenic Diabetes Insipidus due to the AVPR2 Mutations

por Namatame-Ohta, Noriko, Morikawa, Shuntaro, Nakamura, Akie, Matsuo, Kumihiro, Nakajima, Masahide, Tomizawa, Kazuhiro, Tanahashi, Yusuke, Tajima, Toshihiro
Publicado 2018

A soluble endoplasmic reticulum factor as regenerative therapy for Wolfram syndrome

por Mahadevan, Jana, Morikawa, Shuntaro, Yagi, Takuya, Abreu, Damien, Lu, Simin, Kanekura, Kohsuke, Brown, Cris M., Urano, Fumihiko
Publicado 2020

(Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty

por Suzuki, Erina, Shima, Hirohito, Kagami, Masayo, Soneda, Shun, Tanaka, Toshiaki, Yatsuga, Shuichi, Nishioka, Junko, Oto, Yuji, Kamiya, Toshiya, Naiki, Yasuhiro, Ogata, Tsutomu, Fujisawa, Yasuko, Nakamura, Akie, Kawashima, Sayaka, Morikawa, Shuntaro, Horikawa, Reiko, Sano, Shinichiro, Fukami, Maki
Publicado 2019