Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
International Journal of Molecular Sciences|February 13, 2026
Quercetin Dilates Retinal Arterioles via Nitric Oxide-Dependent Mechanisms in RatsAsami Mori, Akihiro Sakurai, Sarina Takimoto, et al.
Endocrine|March 23, 2004
Clinical and genetic features of patients with multiple endocrine tumors who have neither family history nor MEN1 germline mutationsAkihiro Sakurai, Miyuki Katai, Wataru Yumita, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 11, 2021
Extra-endocrine phenotypes at infancy in multiple endocrine neoplasia type 2B: A case series of six Japanese patientsRie Matsushita, Akihiro Sakurai, Kanshi Minamitani, et al.
International Journal of Cancer|January 8, 2003
Suppression of insulin-induced AP-1 transactivation by menin accompanies inhibition of c-Fos inductionWataru Yumita, Yasuto Ikeo, Keishi Yamauchi, et al.
Endocrine Journal|July 1, 2009
Unusual clinical and pathological presentation of a neuroendocrine tumor in a patient with multiple endocrine neoplasia type 1Akihiro Sakurai, Akiko Murakami, Kenji Sano, et al.
Endocrine Journal|August 11, 2012
Application of an intracellular stability test of a novel missense menin mutant to the diagnosis of multiple endocrine neoplasia type 1Yuko Nagamura, Masanori Yamazaki, Satoko Shimazu, et al.
Journal of Pharmacological Sciences|September 11, 2004
Carbachol-induced secretion and homologous desensitization in rat basophilic leukemia (RBL-2H3) cells transfected with human m2 muscarinic acetylcholine receptorsKazuhiko Oishi, Akihiro Sakurai, Noriyasu Seki, et al.
Ophthalmic Genetics|September 17, 2020
A variant in the RP1L1 gene in a family with occult macular dystrophy in a predicted intrinsically disordered regionMiki Hiraoka, Aki Ishikawa, Fumiko Matsuzawa, et al.
Endocrine Journal|May 3, 2005
Octreotide as a rapid and effective painkiller for metastatic carcinoid tumorMiyuki Katai, Akihiro Sakurai, Hidefumi Inaba, et al.
Endocrine Journal|March 27, 2012
A novel splice site mutation of the MEN1 gene identified in a patient with primary hyperparathyroidismYuko Nagamura, Masanori Yamazaki, Satoko Shimazu, et al.
Pageof 8