Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Nakayuki Naritaka"'
Autor:
Anh-Hoa Nguyen Pham, MD, PhD, Kim-Oanh Bui Thi, MD, Mai-Huong Nguyen Thi, MD, Diem-Ngoc Ngo, MD, Nakayuki Naritaka, MD, Hiroshi Nittono, MD, Hisamitsu Hayashi, MD, Trang Thi Dao, MD, Kim-Huong Thi Nguyen, MD, Hoai-Nghia Nguyen, PhD, Hoa Giang, PhD, Hung-Sang Tang, MD, Tat-Thanh Nguyen, MD, Dinh-Kiet Truong, PhD, Minh-Dien Tran, MD
Publikováno v:
Medicine, Vol 101, Iss 25, p e29476 (2022)
Abstract. Rationale:. Congenital bile acid synthesis defect (BASD) is a rare disease caused by mutations in the aldo-keto reductase 1D1 gene, which encodes the primary Δ4-3-oxosteroid 5β-reductase enzyme. Early disease diagnosis is critical for ear
Externí odkaz:
https://doaj.org/article/07ebe75c38304d43ba06851477b8609f
Autor:
Akihiko Kimura, Tatehiro Kagawa, Hajime Takei, Yoshihiro Maruo, Hiroshi Sakugawa, Takahiro Sasaki, Tsuyoshi Murai, Nakayuki Naritaka, Hajime Takikawa, Hiroshi Nittono
Publikováno v:
Hepatology Communications, Vol 5, Iss 4, Pp 629-633 (2021)
Organic anion transporting polypeptide (OATP) 1B1 (gene, solute carrier organic anion transporter family member 1B1 [SLCO1B1]) and OATP1B3 (SLCO1B3) serve as transporters for hepatic uptake of important endogenous substances and several commonly pres
Externí odkaz:
https://doaj.org/article/213cc16824da4eaaacfce35e91b4bb77
Autor:
Eitaro Aihara, Ayumu Mizutani, Nakayuki Naritaka, Hiroyuki Kusuhara, Yusuke Sabu, Aiko Fukami, Kenneth D. R. Setchell, Christopher N. Mayhew, Takanori Takebe, Akihiro Asai, Shuhei Osaka, Hisamitsu Hayashi, Masahide Sakabe, Kokoro Sakabe, Takahisa Nakamura, Eriko Kishimoto, Yueh Chiang Hu, Wujuan Zhang, Stacey S. Huppert
Publikováno v:
Stem Cell Reports
Summary The bile salt export pump (BSEP) is responsible for the export of bile acid from hepatocytes. Impaired transcellular transport of bile acids in hepatocytes with mutations in BSEP causes cholestasis. Compensatory mechanisms to regulate the int
Autor:
Yoshihiro Maruo, Tatehiro Kagawa, Hajime Takikawa, Hiroshi Nittono, Tsuyoshi Murai, Hiroshi Sakugawa, Akihiko Kimura, Hajime Takei, Takahiro Sasaki, Nakayuki Naritaka
Publikováno v:
Hepatology Communications
Hepatology Communications, Vol 5, Iss 4, Pp 629-633 (2021)
Hepatology Communications, Vol 5, Iss 4, Pp 629-633 (2021)
Organic anion transporting polypeptide (OATP) 1B1 (gene, solute carrier organic anion transporter family member 1B1 [SLCO1B1]) and OATP1B3 (SLCO1B3) serve as transporters for hepatic uptake of important endogenous substances and several commonly pres
Autor:
Koichiro Wada, Haruki Usuda, Michael Camilleri, Hajime Takei, Keiichi Ashikari, Atsushi Nakajima, Akiko Fuyuki, Takaomi Kessoku, Noboru Misawa, Tomohiro Takatsu, Hiroshi Nittono, Nakayuki Naritaka, Tetsuya Matsuura, Michihiro Iwaki, Takashi Kobayashi, Mitsuharu Matsumoto, Hidenori Ohkubo, Takuma Higurashi, Akira Honda, Tsutomu Yoshihara
Publikováno v:
Alimentary Pharmacology & Therapeutics. 52:821-828
BACKGROUND Elobixibat, a novel inhibitor of apical sodium-dependent bile acid transporter for treating chronic constipation, increases colonic bile acid concentrations, stimulating bowel function. However, it is not clear which bile acids are altered
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 64(1)
Autor:
Hiroshi Nittono, Takao Kurosawa, Keiko Sato, Genta Kakiyama, Mitsuyoshi Suzuki, Hiroaki Sato, Akihiko Kimura, Toshiaki Shimizu, Hajime Takei, William M. Pandak, Tsuyoshi Murai, Nakayuki Naritaka
Publikováno v:
Steroids. 164
Bile acid compositions are known to change dramatically after birth with aging. However, no reports have described the transition of conjugated urinary bile acids from the neonatal period to adulthood, and such findings would noninvasively offer insi
Autor:
Pinyada Kaewplang, Nakayuki Naritaka, Takao Kurosawa, Hiroshi Nittono, Mitsuyoshi Suzuki, Seek‐hi Oh, Huey-Ling Chen, Toshiaki Shimizu, Chunhua Zhang, Akihiko Kimura, Tsuyoshi Murai, Hajime Takei
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 61(5)
BACKGROUND In pediatric patients with cholestasis of unknown cause, inborn errors of bile acid (BA) synthesis (IEBAS) may be considered. For the initial screening for IEBAS, clarification of the urine BA profile is essential. The transportation of ur
Autor:
Tomoaki Yokokura, Nakayuki Naritaka, Satoshi Nakano, Seiji Kawasaki, Hiroyuki Sugo, Mitsuyoshi Suzuki, Toshiaki Shimizu, Naho Obayashi, Yoshikazu Ohtsuka
Publikováno v:
Pediatrics International. 57:1205-1207
Increasingly, food allergy associated with tacrolimus after pediatric living-donor liver transplantation (LT) has been reported. Tacrolimus prevents the activation of T cells by blocking calcineurin, thus producing an immunosuppressive effect, but ta
Autor:
Yumiko Sakurai, Jin K. Sai, Kei Minowa, Mitsuyoshi Suzuki, Toshiaki Shimizu, Nakayuki Naritaka, Satoshi Nakano, Nobutomo Saito
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 63(4)
Causes of acute recurrent pancreatitis (ARP) or chronic pancreatitis (CP) are sometimes difficult to determine in children. In such patients, genetic analysis may prove helpful. The present study analyzed mutations of cationic trypsinogen (PRSS1), se