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Yohei Masunaga

Showing results (21-30 of 31) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|October 3, 2025
Comprehensive Molecular Studies in 88 Japanese Patients With Congenital Hypogonadotropic HypogonadismWataru Tanikawa, Shingo Okamoto, Osamu Ohara, et al.
European Journal of Endocrinology|March 31, 2026
Novel HK1 intronic variant in congenital hyperinsulinism: impaired transactivation function for FOXA2Kaori Yamoto, Sachiko Miyamoto, Shinichiro Sano, 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.
Journal of Immunology (Baltimore, Md. : 1950)|December 26, 2001
Identification of multiple isolated lymphoid follicles on the antimesenteric wall of the mouse small intestineHiromasa Hamada, Takachika Hiroi, Yasuhiro Nishiyama, et al.
Brain & Development|July 8, 2026
Recurrent RNU4-2 n.64_65insT variant in ReNU syndrome identified in exome-negative casesTakuya Hiraide, Kenji Shimizu, Taiju Hayashi, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 13, 2005
A novel, selective, and orally available antagonist for CC chemokine receptor 3Tatsuaki Morokata, Keiko Suzuki, Yohei Masunaga, et al.
The Journal of Clinical Endocrinology and Metabolism|April 3, 2023
Microdeletion at ESR1 Intron 6 (DEL_6_75504) Is a Susceptibility Factor for Cryptorchidism and HypospadiasYohei Masunaga, Yasuko Fujisawa, Francesco Massart, et al.
Clinical Genetics|March 1, 2021
Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole-exome sequencingTakuya Hiraide, Kaori Yamoto, Yohei Masunaga, et al.
Scientific Reports|October 12, 2022
Clinical and molecular findings in three Japanese patients with N-acetylneuraminic acid synthetase-congenital disorder of glycosylation (NANS-CDG)Yohei Masunaga, Gen Nishimura, Koji Takahashi, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 2019
IGF2 MutationsYohei Masunaga, Takanobu Inoue, Kaori Yamoto, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
The Journal of Clinical Endocrinology and Metabolism|October 3, 2025
Comprehensive Molecular Studies in 88 Japanese Patients With Congenital Hypogonadotropic HypogonadismWataru Tanikawa, Shingo Okamoto, Osamu Ohara, et al.
European Journal of Endocrinology|March 31, 2026
Novel HK1 intronic variant in congenital hyperinsulinism: impaired transactivation function for FOXA2Kaori Yamoto, Sachiko Miyamoto, Shinichiro Sano, 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.
Journal of Immunology (Baltimore, Md. : 1950)|December 26, 2001
Identification of multiple isolated lymphoid follicles on the antimesenteric wall of the mouse small intestineHiromasa Hamada, Takachika Hiroi, Yasuhiro Nishiyama, et al.
Brain & Development|July 8, 2026
Recurrent RNU4-2 n.64_65insT variant in ReNU syndrome identified in exome-negative casesTakuya Hiraide, Kenji Shimizu, Taiju Hayashi, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 13, 2005
A novel, selective, and orally available antagonist for CC chemokine receptor 3Tatsuaki Morokata, Keiko Suzuki, Yohei Masunaga, et al.
The Journal of Clinical Endocrinology and Metabolism|April 3, 2023
Microdeletion at ESR1 Intron 6 (DEL_6_75504) Is a Susceptibility Factor for Cryptorchidism and HypospadiasYohei Masunaga, Yasuko Fujisawa, Francesco Massart, et al.
Clinical Genetics|March 1, 2021
Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole-exome sequencingTakuya Hiraide, Kaori Yamoto, Yohei Masunaga, et al.
Scientific Reports|October 12, 2022
Clinical and molecular findings in three Japanese patients with N-acetylneuraminic acid synthetase-congenital disorder of glycosylation (NANS-CDG)Yohei Masunaga, Gen Nishimura, Koji Takahashi, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 2019
IGF2 MutationsYohei Masunaga, Takanobu Inoue, Kaori Yamoto, et al.
Pageof 4