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The Journal of Clinical Endocrinology and Metabolism
|
October 3, 2025
Comprehensive Molecular Studies in 88 Japanese Patients With Congenital Hypogonadotropic Hypogonadism
Wataru 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 FOXA2
Kaori 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 development
Maki 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 intestine
Hiromasa 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 cases
Takuya 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 3
Tatsuaki 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 Hypospadias
Yohei 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 sequencing
Takuya 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 Mutations
Yohei Masunaga, Takanobu Inoue, Kaori Yamoto, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
The Journal of Clinical Endocrinology and Metabolism
|
October 3, 2025
Comprehensive Molecular Studies in 88 Japanese Patients With Congenital Hypogonadotropic Hypogonadism
Wataru 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 FOXA2
Kaori 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 development
Maki 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 intestine
Hiromasa 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 cases
Takuya 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 3
Tatsuaki 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 Hypospadias
Yohei 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 sequencing
Takuya 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 Mutations
Yohei Masunaga, Takanobu Inoue, Kaori Yamoto, et al.
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of 4