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Lung|July 20, 2007
Involvement of mutation-based inhibition of beta-catenin phosphorylation at Ser33 in the malignant progression of lung (pre)neoplastic lesions induced by N-nitrosobis(2-hydroxypropyl)amine in male Fischer 344 ratsMaki Igarashi, Midori Yoshida, Manabu Watanabe, et al.
Journal of Nutritional Science and Vitaminology|August 31, 2025
Validity of Digital Photographic Images for Dietary Assessment of Participants with Low Frequency of Home-Made Meal IntakeTomomi Nagahata, Maki Igarashi, Yuko Mekata, et al.
Scientific Reports|October 16, 2020
Nonsense-associated altered splicing of MAP3K1 in two siblings with 46,XY disorders of sex developmentMaki Igarashi, Yohei Masunaga, Yuichi Hasegawa, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 3, 2015
Novel Splice Site Mutation in MAMLD1 in a Patient with HypospadiasMaki Igarashi, Yuka Wada, Yoshiyuki Kojima, et al.
Human Genome Variation|September 7, 2025
DHX37 variants in patients with 46,XY disorders or differences of sex developmentYuko Katoh-Fukui, Daisuke Saito, Hiroko Narumi, et al.
Plos One|July 18, 2013
Cryptic genomic rearrangements in three patients with 46,XY disorders of sex developmentMaki Igarashi, Vu Chi Dung, Erina Suzuki, et al.
Biology of Sex Differences|November 12, 2016
The p.R92W variant of NR5A1/Nr5a1 induces testicular development of 46,XX gonads in humans, but not in mice: phenotypic comparison of human patients and mutation-induced miceMami Miyado, Masafumi Inui, Maki Igarashi, et al.
Plos One|November 8, 2018
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiencyHirohito Shima, Mie Hayashi, Takashi Tachibana, et al.
Journal of Cellular and Molecular Medicine|March 25, 2017
Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early pubertyMaki Fukami, Erina Suzuki, Yoko Izumi, et al.
Fertility and Sterility|July 28, 2014
Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadismYoko Izumi, Erina Suzuki, Susumu Kanzaki, et al.
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