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Issei Imoto

Showing results (151-160 of 241) with videos related to

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Human Genome Variation|April 16, 2016
DGCR6 at the proximal part of the DiGeorge critical region is involved in conotruncal heart defectsWenming Gao, Takashi Higaki, Minenori Eguchi-Ishimae, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|April 9, 2011
Genome-wide DNA methylation profiles in renal tumors of various histological subtypes and non-tumorous renal tissuesEri Arai, Saori Wakai-Ushijima, Hiroyuki Fujimoto, et al.
Cancer Science|May 3, 2008
Frequent silencing of a putative tumor suppressor gene melatonin receptor 1 A (MTNR1A) in oral squamous-cell carcinomaErina Nakamura, Ken-ichi Kozaki, Hitoshi Tsuda, et al.
Cancer Research|June 3, 2004
Frequent silencing of low density lipoprotein receptor-related protein 1B (LRP1B) expression by genetic and epigenetic mechanisms in esophageal squamous cell carcinomaItaru Sonoda, Issei Imoto, Jun Inoue, et al.
Cancer Science|February 26, 2022
Association between germline pathogenic variants and breast cancer risk in Japanese women: The HERPACC studyYumiko Kasugai, Tomohiro Kohmoto, Yukari Taniyama, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 10, 2015
A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disabilityToshitaka Kawarai, Atsushi Tajima, Yukiko Kuroda, et al.
The Journal of Cell Biology|March 15, 2006
The selective continued linkage of centromeres from mitosis to interphase in the absence of mammalian separaseKazuki Kumada, Ryoji Yao, Tokuichi Kawaguchi, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 11, 2015
Ectopic Aire Expression in the Thymic Cortex Reveals Inherent Properties of Aire as a Tolerogenic Factor within the MedullaHitoshi Nishijima, Satsuki Kitano, Hitoshi Miyachi, et al.
EMBO Molecular Medicine|May 5, 2011
SASPase regulates stratum corneum hydration through profilaggrin-to-filaggrin processingTakeshi Matsui, Kenichi Miyamoto, Akiharu Kubo, et al.
Human Genome Variation|August 10, 2017
The first Japanese patient with mandibular hypoplasia, deafness, progeroid features and lipodystrophy diagnosed via <i>POLD1</i> mutation detectionAsami Okada, Tomohiro Kohmoto, Takuya Naruto, et al.
Pageof 25

Showing results (151-160 of 241) with videos related to

Sort By:
Pageof 25
Human Genome Variation|April 16, 2016
DGCR6 at the proximal part of the DiGeorge critical region is involved in conotruncal heart defectsWenming Gao, Takashi Higaki, Minenori Eguchi-Ishimae, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|April 9, 2011
Genome-wide DNA methylation profiles in renal tumors of various histological subtypes and non-tumorous renal tissuesEri Arai, Saori Wakai-Ushijima, Hiroyuki Fujimoto, et al.
Cancer Science|May 3, 2008
Frequent silencing of a putative tumor suppressor gene melatonin receptor 1 A (MTNR1A) in oral squamous-cell carcinomaErina Nakamura, Ken-ichi Kozaki, Hitoshi Tsuda, et al.
Cancer Research|June 3, 2004
Frequent silencing of low density lipoprotein receptor-related protein 1B (LRP1B) expression by genetic and epigenetic mechanisms in esophageal squamous cell carcinomaItaru Sonoda, Issei Imoto, Jun Inoue, et al.
Cancer Science|February 26, 2022
Association between germline pathogenic variants and breast cancer risk in Japanese women: The HERPACC studyYumiko Kasugai, Tomohiro Kohmoto, Yukari Taniyama, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 10, 2015
A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disabilityToshitaka Kawarai, Atsushi Tajima, Yukiko Kuroda, et al.
The Journal of Cell Biology|March 15, 2006
The selective continued linkage of centromeres from mitosis to interphase in the absence of mammalian separaseKazuki Kumada, Ryoji Yao, Tokuichi Kawaguchi, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 11, 2015
Ectopic Aire Expression in the Thymic Cortex Reveals Inherent Properties of Aire as a Tolerogenic Factor within the MedullaHitoshi Nishijima, Satsuki Kitano, Hitoshi Miyachi, et al.
EMBO Molecular Medicine|May 5, 2011
SASPase regulates stratum corneum hydration through profilaggrin-to-filaggrin processingTakeshi Matsui, Kenichi Miyamoto, Akiharu Kubo, et al.
Human Genome Variation|August 10, 2017
The first Japanese patient with mandibular hypoplasia, deafness, progeroid features and lipodystrophy diagnosed via <i>POLD1</i> mutation detectionAsami Okada, Tomohiro Kohmoto, Takuya Naruto, et al.
Pageof 25