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Satomi Inoue

Showing results (21-30 of 29) with videos related to

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Human Genome Variation|December 18, 2021
A Japanese boy with double diagnoses of 2p15p16.1 microdeletion syndrome and RP2-associated retinal disorderKazuki Yamazawa, Kenji Shimizu, Hirofumi Ohashi, et al.
Human Genome Variation|January 17, 2022
A novel pathogenic variant of the FH gene in a family with hereditary leiomyomatosis and renal cell carcinomaYasuto Yagi, Naoko Abeto, Junichi Shiraishi, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|October 14, 2025
Association of supportive care team intervention with nutritional status, adverse events, and treatment status in patients with head and neck cancer undergoing concurrent chemoradiotherapyAkiho Yamashita, Masayuki Kaku, Misato Otsuka, et al.
Mitochondrion|May 22, 2025
Auditory neuropathy spectrum disorder and related auditory features in patients with hearing loss associated with the MT-TS1 m.7471dup variantShujiro Minami, Amina Kida, Satomi Inoue, et al.
Biology|November 11, 2022
Identification of <i>NRAS</i> Downstream Genes with CRISPR Activation ScreeningAkiya Tatsumi, Haruka Hirakochi, Satomi Inoue, et al.
Cancer Science|April 17, 2023
The pathogenic role of the BRCA2 c.7847C>T (p.Ser2616Phe) variant in breast and ovarian cancer predispositionKazuki Yamazawa, Kokichi Sugano, Kohji Tanakaya, et al.
Human Genetics|January 4, 2025
Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity searchHideki Mutai, Fuyuki Miya, Kiyomitsu Nara, et al.
BMC Pregnancy and Childbirth|February 19, 2020
Qualitative investigation of the factors that generate ambivalent feelings in women who give birth after receiving negative results from non-invasive prenatal testingJunko Yotsumoto, Akihiko Sekizawa, Satomi Inoue, et al.
Journal of Medical Genetics|March 19, 2026
Comprehensive evidence for the pathogenicity of the <i>BRCA2</i> c.7847C>T (p.Ser2616Phe) variant specific to the Japanese populationKazuki Yamazawa, Arisa Ueki, Asami Kuga, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Human Genome Variation|December 18, 2021
A Japanese boy with double diagnoses of 2p15p16.1 microdeletion syndrome and RP2-associated retinal disorderKazuki Yamazawa, Kenji Shimizu, Hirofumi Ohashi, et al.
Human Genome Variation|January 17, 2022
A novel pathogenic variant of the FH gene in a family with hereditary leiomyomatosis and renal cell carcinomaYasuto Yagi, Naoko Abeto, Junichi Shiraishi, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|October 14, 2025
Association of supportive care team intervention with nutritional status, adverse events, and treatment status in patients with head and neck cancer undergoing concurrent chemoradiotherapyAkiho Yamashita, Masayuki Kaku, Misato Otsuka, et al.
Mitochondrion|May 22, 2025
Auditory neuropathy spectrum disorder and related auditory features in patients with hearing loss associated with the MT-TS1 m.7471dup variantShujiro Minami, Amina Kida, Satomi Inoue, et al.
Biology|November 11, 2022
Identification of <i>NRAS</i> Downstream Genes with CRISPR Activation ScreeningAkiya Tatsumi, Haruka Hirakochi, Satomi Inoue, et al.
Cancer Science|April 17, 2023
The pathogenic role of the BRCA2 c.7847C>T (p.Ser2616Phe) variant in breast and ovarian cancer predispositionKazuki Yamazawa, Kokichi Sugano, Kohji Tanakaya, et al.
Human Genetics|January 4, 2025
Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity searchHideki Mutai, Fuyuki Miya, Kiyomitsu Nara, et al.
BMC Pregnancy and Childbirth|February 19, 2020
Qualitative investigation of the factors that generate ambivalent feelings in women who give birth after receiving negative results from non-invasive prenatal testingJunko Yotsumoto, Akihiko Sekizawa, Satomi Inoue, et al.
Journal of Medical Genetics|March 19, 2026
Comprehensive evidence for the pathogenicity of the <i>BRCA2</i> c.7847C>T (p.Ser2616Phe) variant specific to the Japanese populationKazuki Yamazawa, Arisa Ueki, Asami Kuga, et al.
Pageof 3