A Novel Missense Mutation (P366T) of the LHX4 Gene Causes Severe Combined Pituitary Hormone Deficiency with Pituitary Hypoplasia, Ectopic Posterior Lobe and a Poorly Developed Sella Turcica
TAJIMA, Toshihiro, HATTORI, Tsukasa, NAKAJIMA, Takeo, OKUHARA, Koji, TSUBAKI, Junko, FUJIEDA, Kenji
Published in Endocrine Journal (2007)
Published in Endocrine Journal (2007)
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Four Japanese Patients with Adrenal Hypoplasia Congenita and Hypogonadotropic Hypogonadism Caused by DAX-1 Gene Mutations: Mutant DAX-1 Failed to Repress Steroidogenic Acute Regulatory Protein (StAR) and Luteinizing Hormone β-subunit Gene Promoter Activity
OKUHARA, Koji, ABE, Shuji, KONDO, Takuma, FUJITA, Keinosuke, KODA, Noya, MOCHIZUKI, Hiroshi, FUJIEDA, Kenji, TAJIMA, Toshihiro
Published in Endocrine Journal (2008)
Published in Endocrine Journal (2008)
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A Novel Deletion Mutation of SLC16A2 Encoding Monocarboxylate Transporter (MCT) 8 in a 26-year-old Japanese Patient with Allan-Herndon-Dudley Syndrome
Yamamoto, Sayaka, Okuhara, Koji, Tonoki, Hidefumi, Iizuka, Susumu, Nihei, Noriko, Tajima, Toshihiro
Published in Clinical Pediatric Endocrinology (01.10.2013)
Published in Clinical Pediatric Endocrinology (01.10.2013)
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Central Congenital Hypothyroidism Detected by Neonatal Screening in Sapporo, Japan (2000-2004): It's Prevalence and Clinical Characteristics
Fujiwara, Fumie, Fujikura, Kaori, Okuhara, Koji, Tsubaki, Jyunko, Fukushi, Masaru, Fujita, Kozo, Fujieda, Kenji, Tajima, Toshihiro
Published in Clinical Pediatric Endocrinology (01.01.2008)
Published in Clinical Pediatric Endocrinology (01.01.2008)
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A DNA unwinding factor involved in DNA replication in cell-free extracts of Xenopus eggs
Okuhara, Koji, Ohta, Kunihiro, Seo, Hidetaka, Shioda, Masaki, Yamada, Takatomi, Tanaka, Yasuhiro, Dohmae, Naoshi, Seyama, Yousuke, Shibata, Takehiko, Murofushi, Hiromu
Published in Current biology (08.04.1999)
Published in Current biology (08.04.1999)
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Crosstalk of Prolyl Isomerases, Pin1/Ess1, and Cyclophilin A
Fujimori, Fumihiro, Gunji, Wataru, Kikuchi, Junko, Mogi, Tomoko, Ohashi, Yoko, Makino, Tohru, Oyama, Akira, Okuhara, Koji, Uchida, Takafumi, Murakami, Yasufumi
Published in Biochemical and biophysical research communications (23.11.2001)
Published in Biochemical and biophysical research communications (23.11.2001)
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Journal Article
A Novel Deletion Mutation of SLC16A2 Encoding Monocarboxylate Transporter (MCT) 8 in a 26-year-old Japanese Patient with Allan-Herndon-Dudley Syndrome
Sayaka Yamamoto, Koji Okuhara, Hidefumi Tonoki, Susumu Iizuka, Noriko Nihei, Toshihiro Tajima
Published in Clinical Pediatric Endocrinology (01.10.2013)
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Published in Clinical Pediatric Endocrinology (01.10.2013)
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