An adaptive variant of TRIB2, rs1057001, is associated with higher expression levels of thermogenic genes in human subcutaneous and visceral adipose tissues

por Nakayama, Kazuhiro, Iwamoto, Sadahiko
Publicado 2017

Seasonal effects of the UCP3 and the RPTOR gene polymorphisms on obesity traits in Japanese adults

por Nakayama, Kazuhiro, Miyashita, Hiroshi, Iwamoto, Sadahiko
Publicado 2014

Kbtbd11 gene expression in adipose tissue increases in response to feeding and affects adipocyte differentiation

por Watanabe, Kazuhisa, Yoshida, Ken, Iwamoto, Sadahiko
Publicado 2019

Genome-wide DNA methylation status of Mongolians exhibits signs of cellular stress response related to their nomadic lifestyle

por Inaba, Yuta, Iwamoto, Sadahiko, Nakayama, Kazuhiro
Publicado 2022

Seasonal Effects of UCP1 Gene Polymorphism on Visceral Fat Accumulation in Japanese Adults

por Nakayama, Kazuhiro, Miyashita, Hiroshi, Yanagisawa, Yoshiko, Iwamoto, Sadahiko
Publicado 2013

N4BP2L1 interacts with dynactin and contributes to GLUT4 trafficking and glucose uptake in adipocytes

por Watanabe, Kazuhisa, Matsumoto, Ayumi, Tsuda, Hidetoshi, Iwamoto, Sadahiko
Publicado 2021

KBTBD11, encoding a novel PPARγ target gene, is involved in NFATc1 proteolysis by interacting with HSC70 and HSP60

por Watanabe, Kazuhisa, Matsumoto, Ayumi, Tsuda, Hidetoshi, Iwamoto, Sadahiko
Publicado 2022

Association of CTXN3-SLC12A2 polymorphisms and schizophrenia in a Thai population

por Panichareon, Benjaporn, Nakayama, Kazuhiro, Iwamoto, Sadahiko, Thurakitwannakarn, Wanpen, Sukhumsirichart, Wasana
Publicado 2012

A novel upstream transcription factor 1 target gene N4bp2l1 that regulates adipogenesis

por Watanabe, Kazuhisa, Yokota, Kazuha, Yoshida, Ken, Matsumoto, Ayumi, Iwamoto, Sadahiko
Publicado 2019

Kbtbd11 contributes to adipocyte homeostasis through the activation of upstream stimulatory factor 1

por Watanabe, Kazuhisa, Yokota, Kazuha, Yoshida, Ken, Matsumoto, Ayumi, Iwamoto, Sadahiko
Publicado 2019

Novel BEST1 mutation in autosomal recessive bestrophinopathy in Japanese siblings

por Yamada, Rika, Takagi, Rina, Iwamoto, Sadahiko, Shimada, Shoichi, Kakehashi, Akihiro
Publicado 2021

Identification of deleterious rare variants in MTTP, PNPLA3, and TM6SF2 in Japanese males and association studies with NAFLD

por Boonvisut, Supichaya, Yoshida, Ken, Nakayama, Kazuhiro, Watanabe, Kazuhisa, Miyashita, Hiroshi, Iwamoto, Sadahiko
Publicado 2017

ILDR2 stabilization is regulated by its interaction with GRP78

por Watanabe, Kazuhisa, Nakayama, Kazuhiro, Ohta, Satoshi, Matsumoto, Ayumi, Tsuda, Hidetoshi, Iwamoto, Sadahiko
Publicado 2021

Lack of GPR180 ameliorates hepatic lipid depot via downregulation of mTORC1 signaling

por Yoshida, Ken, Yokota, Kazuha, Watanabe, Kazuhisa, Tsuda, Hidetoshi, Matsumoto, Ayumi, Mizukami, Hiroaki, Iwamoto, Sadahiko
Publicado 2023

Replication analysis of genetic association of the NCAN-CILP2 region with plasma lipid levels and non-alcoholic fatty liver disease in Asian and Pacific ethnic groups

por Boonvisut, Supichaya, Nakayama, Kazuhiro, Makishima, Saho, Watanabe, Kazuhisa, Miyashita, Hiroshi, Lkhagvasuren, Munkhtulga, Kagawa, Yasuo, Iwamoto, Sadahiko
Publicado 2016

Probiotics suppress nonalcoholic steatohepatitis and carcinogenesis progression in hepatocyte-specific PTEN knockout mice

por Arai, Naoshi, Miura, Kouichi, Aizawa, Kenichi, Sekiya, Mariko, Nagayama, Manabu, Sakamoto, Hirotsugu, Maeda, Hiroshi, Morimoto, Naoki, Iwamoto, Sadahiko, Yamamoto, Hironori
Publicado 2022

The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis

por Fujita-Jimbo, Eriko, Tanabe, Yuko, Yu, Zhiling, Kojima, Karin, Mori, Masato, Li, Hong, Iwamoto, Sadahiko, Yamagata, Takanori, Momoi, Mariko Y, Momoi, Takashi
Publicado 2015

Genome‐Wide Association Study of Lean Nonalcoholic Fatty Liver Disease Suggests Human Leukocyte Antigen as a Novel Candidate Locus

por Yoshida, Ken, Yokota, Kazuha, Kutsuwada, Yukinobu, Nakayama, Kazuhiro, Watanabe, Kazuhisa, Matsumoto, Ayumi, Miyashita, Hiroshi, Khor, Seik‐soon, Tokunaga, Katsushi, Kawai, Yosuke, Nagasaki, Masao, Iwamoto, Sadahiko
Publicado 2020

A case of congenital fiber‐type disproportion syndrome presenting dilated cardiomyopathy with ACTA1 mutation

por Matsumoto, Ayumi, Tsuda, Hidetoshi, Furui, Sadahiro, Kawada‐Nagashima, Masako, Anzai, Tatsuya, Seki, Mitsuru, Watanabe, Kazuhisa, Muramatsu, Kazuhiro, Osaka, Hitoshi, Iwamoto, Sadahiko, Nishino, Ichizo, Yamagata, Takanori
Publicado 2022

Investigation of Maternal Diet and FADS1 Polymorphism Associated with Long-Chain Polyunsaturated Fatty Acid Compositions in Human Milk

por Niwa, Sakurako, Kawabata, Terue, Shoji, Kumiko, Ogata, Hiromitsu, Kagawa, Yasuo, Nakayama, Kazuhiro, Yanagisawa, Yoshiko, Iwamoto, Sadahiko, Tatsuta, Nozomi, Asato, Kaname, Arima, Takahiro, Yaegashi, Nobuo, Nakai, Kunihiko
Publicado 2022