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Hidehito Inagaki

Showing results (71-80 of 98) with videos related to

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Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 3, 2023
SEGA-like circumscribed astrocytoma in a non-NF1 patient, harboring molecular profile of GBM. A case reportSeiji Yamada, Motoki Tanikawa, Yuko Matsushita, et al.
JIMD Reports|January 13, 2023
Transport and Golgi organization 2 deficiency with a prominent elevation of C14:1 during a metabolic crisis: A case reportKatsuyuki Yokoi, Yoko Nakajima, Yoshihisa Takahashi, et al.
Case Reports in Obstetrics and Gynecology|October 31, 2019
Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion SyndromeMasatake Toshimitsu, Shinichi Nagaoka, Shuusaku Kobori, et al.
Journal of Clinical Medicine|August 12, 2022
Characterization of the <i>MG828507</i> lncRNA Located Upstream of the <i>FLT1</i> Gene as an Etiology for Pre-EclampsiaHikari Yoshizawa, Haruki Nishizawa, Hidehito Inagaki, et al.
BMC Cancer|November 28, 2020
An aggressive systemic mastocytosis preceded by ovarian dysgerminomaMakiko Tsutsumi, Hiroki Miura, Hidehito Inagaki, et al.
Nature Communications|July 18, 2020
The Bartonella autotransporter BafA activates the host VEGF pathway to drive angiogenesisKentaro Tsukamoto, Naoaki Shinzawa, Akito Kawai, et al.
Human Genome Variation|April 16, 2016
Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndromeIkuya Tsuge, Masashi Morishita, Takema Kato, et al.
Reproductive Medicine and Biology|December 21, 2017
Preimplantation genetic diagnosis/screening by comprehensive molecular testingHiroki Kurahashi, Takema Kato, Jun Miyazaki, et al.
Scientific Reports|April 3, 2014
Dual roles for the telomeric repeats in chromosomally integrated human herpesvirus-6Tamae Ohye, Hidehito Inagaki, Masaru Ihira, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 22, 2018
Compound heterozygous RYR1 mutations by whole exome sequencing in a family with three repeated affected fetuses with fetal akinesiaNobuhiro Suzumori, Hidehito Inagaki, Ayano Ohtani, et al.
Pageof 10

Showing results (71-80 of 98) with videos related to

Sort By:
Pageof 10
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 3, 2023
SEGA-like circumscribed astrocytoma in a non-NF1 patient, harboring molecular profile of GBM. A case reportSeiji Yamada, Motoki Tanikawa, Yuko Matsushita, et al.
JIMD Reports|January 13, 2023
Transport and Golgi organization 2 deficiency with a prominent elevation of C14:1 during a metabolic crisis: A case reportKatsuyuki Yokoi, Yoko Nakajima, Yoshihisa Takahashi, et al.
Case Reports in Obstetrics and Gynecology|October 31, 2019
Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion SyndromeMasatake Toshimitsu, Shinichi Nagaoka, Shuusaku Kobori, et al.
Journal of Clinical Medicine|August 12, 2022
Characterization of the <i>MG828507</i> lncRNA Located Upstream of the <i>FLT1</i> Gene as an Etiology for Pre-EclampsiaHikari Yoshizawa, Haruki Nishizawa, Hidehito Inagaki, et al.
BMC Cancer|November 28, 2020
An aggressive systemic mastocytosis preceded by ovarian dysgerminomaMakiko Tsutsumi, Hiroki Miura, Hidehito Inagaki, et al.
Nature Communications|July 18, 2020
The Bartonella autotransporter BafA activates the host VEGF pathway to drive angiogenesisKentaro Tsukamoto, Naoaki Shinzawa, Akito Kawai, et al.
Human Genome Variation|April 16, 2016
Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndromeIkuya Tsuge, Masashi Morishita, Takema Kato, et al.
Reproductive Medicine and Biology|December 21, 2017
Preimplantation genetic diagnosis/screening by comprehensive molecular testingHiroki Kurahashi, Takema Kato, Jun Miyazaki, et al.
Scientific Reports|April 3, 2014
Dual roles for the telomeric repeats in chromosomally integrated human herpesvirus-6Tamae Ohye, Hidehito Inagaki, Masaru Ihira, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 22, 2018
Compound heterozygous RYR1 mutations by whole exome sequencing in a family with three repeated affected fetuses with fetal akinesiaNobuhiro Suzumori, Hidehito Inagaki, Ayano Ohtani, et al.
Pageof 10