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Mamiko Yamada

Showing results (81-90 of 86) with videos related to

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CEN Case Reports|September 30, 2024
Effective calcineurin inhibitor treatment in adult-onset steroid-resistant nephrotic syndrome with a novel splice donor site variant of TRPC6: a case reportTomoki Nagasaka, Kiyotaka Uchiyama, Eriko Yoshida Hama, et al.
BMC Pulmonary Medicine|October 1, 2024
The first Japanese case of autosomal dominant cutis laxa with a frameshift mutation in exon 30 of the elastin gene complicated by small airway disease with 8 years of follow-upMasanori Kaji, Ho Namkoong, Shotaro Chubachi, et al.
Immunotherapy Advances|March 29, 2024
Janus kinase inhibitors ameliorate clinical symptoms in patients with STAT3 gain-of-functionShuya Kaneko, Fumiaki Sakura, Kay Tanita, et al.
The Keio Journal of Medicine|June 22, 2025
The Keio HBOC Center: A Model of Hereditary Breast and Ovarian Cancer ManagementYusuke Kobayashi, Kenta Masuda, Tomoko Seki, et al.
Frontiers in Endocrinology|December 25, 2024
Case report: Duplication of the <i>GCK</i> gene is a novel cause of nesidioblastosis: evidence from a case with Silver-Russell syndrome-like phenotype related to chromosome 7Takashi Shoji, Ichiro Yamauchi, Hidenori Kawasaki, et al.
The Journal of Pediatrics|February 8, 2022
Genome Analysis in Sick Neonates and Infants: High-yield Phenotypes and Contribution of Small Copy Number VariationsHisato Suzuki, Masatoshi Nozaki, Hiroshi Yoshihashi, et al.
Pageof 9

Showing results (81-90 of 86) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 86 results.
CEN Case Reports|September 30, 2024
Effective calcineurin inhibitor treatment in adult-onset steroid-resistant nephrotic syndrome with a novel splice donor site variant of TRPC6: a case reportTomoki Nagasaka, Kiyotaka Uchiyama, Eriko Yoshida Hama, et al.
BMC Pulmonary Medicine|October 1, 2024
The first Japanese case of autosomal dominant cutis laxa with a frameshift mutation in exon 30 of the elastin gene complicated by small airway disease with 8 years of follow-upMasanori Kaji, Ho Namkoong, Shotaro Chubachi, et al.
Immunotherapy Advances|March 29, 2024
Janus kinase inhibitors ameliorate clinical symptoms in patients with STAT3 gain-of-functionShuya Kaneko, Fumiaki Sakura, Kay Tanita, et al.
The Keio Journal of Medicine|June 22, 2025
The Keio HBOC Center: A Model of Hereditary Breast and Ovarian Cancer ManagementYusuke Kobayashi, Kenta Masuda, Tomoko Seki, et al.
Frontiers in Endocrinology|December 25, 2024
Case report: Duplication of the <i>GCK</i> gene is a novel cause of nesidioblastosis: evidence from a case with Silver-Russell syndrome-like phenotype related to chromosome 7Takashi Shoji, Ichiro Yamauchi, Hidenori Kawasaki, et al.
The Journal of Pediatrics|February 8, 2022
Genome Analysis in Sick Neonates and Infants: High-yield Phenotypes and Contribution of Small Copy Number VariationsHisato Suzuki, Masatoshi Nozaki, Hiroshi Yoshihashi, et al.
Pageof 9