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Noriyuki Namba

Showing results (81-90 of 103) with videos related to

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European Journal of Pediatrics|June 24, 2009
Increased type 3 iodothyronine deiodinase activity in a regrown hepatic hemangioma with consumptive hypothyroidismKazuhiko Bessho, Yuri Etani, Hiroaki Ichimori, et al.
Endocrine Journal|October 30, 2018
Functional analysis of monocarboxylate transporter 8 mutations in Japanese Allan-Herndon-Dudley syndrome patientsMohammad Saiful Islam, Noriyuki Namba, Yasuhisa Ohata, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 29, 2014
Elevated fibroblast growth factor 23 exerts its effects on placenta and regulates vitamin D metabolism in pregnancy of Hyp miceYasuhisa Ohata, Miwa Yamazaki, Masanobu Kawai, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 8, 2020
Monthly intravenous alendronate treatment can maintain bone strength in osteogenesis imperfecta patients following cyclical pamidronate treatmentDaisuke Harada, Hiroko Kashiwagi, Kaoru Ueyama, et al.
Plos One|August 8, 2012
An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 geneKohji Miura, Noriyuki Namba, Makoto Fujiwara, et al.
American Journal of Medical Genetics. Part A|November 15, 2015
Acromesomelic dysplasia, type maroteaux caused by novel loss-of-function mutations of the NPR2 gene: Three case reportsWei Wang, Mi Hyun Song, Kohji Miura, et al.
Yonago Acta Medica|May 26, 2026
Transient Oxygen Desaturation Associated with Persistent Right Venous Valve-Mediated Right-to-Left Atrial Shunt in Term NeonatesYoichi Mino, Hitoshi Uemasu, Juntaro Yamasaki, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|January 8, 2025
Urodele amphibian newt bridges the missing link in evo-devo of the pancreasRyosuke Morozumi, Kazuko Okamoto, Eriko Enomoto, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 8, 2018
A case of perinatal hypophosphatasia with a novel mutation in the <i>ALPL</i> gene: clinical course and review of the literatureMaki Oyachi, Daisuke Harada, Natsuko Sakamoto, et al.
Nature Medicine|August 6, 2002
SHIP-deficient mice are severely osteoporotic due to increased numbers of hyper-resorptive osteoclastsSunao Takeshita, Noriyuki Namba, Jenny J Zhao, et al.
Pageof 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
European Journal of Pediatrics|June 24, 2009
Increased type 3 iodothyronine deiodinase activity in a regrown hepatic hemangioma with consumptive hypothyroidismKazuhiko Bessho, Yuri Etani, Hiroaki Ichimori, et al.
Endocrine Journal|October 30, 2018
Functional analysis of monocarboxylate transporter 8 mutations in Japanese Allan-Herndon-Dudley syndrome patientsMohammad Saiful Islam, Noriyuki Namba, Yasuhisa Ohata, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 29, 2014
Elevated fibroblast growth factor 23 exerts its effects on placenta and regulates vitamin D metabolism in pregnancy of Hyp miceYasuhisa Ohata, Miwa Yamazaki, Masanobu Kawai, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 8, 2020
Monthly intravenous alendronate treatment can maintain bone strength in osteogenesis imperfecta patients following cyclical pamidronate treatmentDaisuke Harada, Hiroko Kashiwagi, Kaoru Ueyama, et al.
Plos One|August 8, 2012
An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 geneKohji Miura, Noriyuki Namba, Makoto Fujiwara, et al.
American Journal of Medical Genetics. Part A|November 15, 2015
Acromesomelic dysplasia, type maroteaux caused by novel loss-of-function mutations of the NPR2 gene: Three case reportsWei Wang, Mi Hyun Song, Kohji Miura, et al.
Yonago Acta Medica|May 26, 2026
Transient Oxygen Desaturation Associated with Persistent Right Venous Valve-Mediated Right-to-Left Atrial Shunt in Term NeonatesYoichi Mino, Hitoshi Uemasu, Juntaro Yamasaki, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|January 8, 2025
Urodele amphibian newt bridges the missing link in evo-devo of the pancreasRyosuke Morozumi, Kazuko Okamoto, Eriko Enomoto, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 8, 2018
A case of perinatal hypophosphatasia with a novel mutation in the <i>ALPL</i> gene: clinical course and review of the literatureMaki Oyachi, Daisuke Harada, Natsuko Sakamoto, et al.
Nature Medicine|August 6, 2002
SHIP-deficient mice are severely osteoporotic due to increased numbers of hyper-resorptive osteoclastsSunao Takeshita, Noriyuki Namba, Jenny J Zhao, et al.
Pageof 11