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Yusuke Murakami

Showing results (201-210 of 212) with videos related to

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Frontiers in Immunology|January 23, 2023
Corrigendum: Intraocular human cytomegaloviruses of ocular diseases are distinct from those of viremia and are capable of escaping from innate and adaptive immunity by exploiting HLA-E-mediated peripheral and central toleranceMariko Shirane, Nobuyo Yawata, Daisuke Motooka, et al.
Journal of Medical Genetics|June 20, 2019
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patientsYoshito Koyanagi, Masato Akiyama, Koji M Nishiguchi, et al.
Frontiers in Immunology|November 7, 2022
Intraocular human cytomegaloviruses of ocular diseases are distinct from those of viremia and are capable of escaping from innate and adaptive immunity by exploiting HLA-E-mediated peripheral and central toleranceMariko Shirane, Nobuyo Yawata, Daisuke Motooka, et al.
NPJ Genomic Medicine|December 6, 2025
Clinical characteristics of EYS-associated retinal dystrophy in 291 Japanese patientsYoshito Koyanagi, Yusuke Murakami, Taro Kominami, et al.
Ophthalmology. Retina|February 26, 2021
Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese PatientsYusuke Murakami, Yoshito Koyanagi, Masatoshi Fukushima, et al.
American Journal of Ophthalmology|May 8, 2026
Genotype-phenotype correlations in RPGRIP1-associated retinal dystrophy in a nationwide Japanese cohortKei Mizobuchi, Taiga Inooka, Takuya Aoki, et al.
American Journal of Human Genetics|March 26, 2024
Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing readsMathieu Quinodoz, Karolina Kaminska, Francesca Cancellieri, et al.
Journal of Medical Genetics|March 18, 2024
Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseasesKensuke Goto, Yoshito Koyanagi, Masato Akiyama, et al.
Ophthalmology|July 18, 2024
Genetic Risk Stratification of Primary Open-Angle Glaucoma in Japanese IndividualsMasato Akiyama, Gen Tamiya, Kohta Fujiwara, et al.
Therapeutic Advances in Medical Oncology|June 19, 2025
Ramucirumab and erlotinib combination as first-line treatment for advanced or recurrent non-small cell lung cancer harboring <i>EGFR</i> Exon21 L858R mutation: a multicenter retrospective observational cohort study in Japan (REAL-SPEED)Masashi Ishihara, Takahisa Kawamura, Yukiko Namba, et al.
Pageof 22

Showing results (201-210 of 212) with videos related to

Sort By:
Pageof 22
Frontiers in Immunology|January 23, 2023
Corrigendum: Intraocular human cytomegaloviruses of ocular diseases are distinct from those of viremia and are capable of escaping from innate and adaptive immunity by exploiting HLA-E-mediated peripheral and central toleranceMariko Shirane, Nobuyo Yawata, Daisuke Motooka, et al.
Journal of Medical Genetics|June 20, 2019
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patientsYoshito Koyanagi, Masato Akiyama, Koji M Nishiguchi, et al.
Frontiers in Immunology|November 7, 2022
Intraocular human cytomegaloviruses of ocular diseases are distinct from those of viremia and are capable of escaping from innate and adaptive immunity by exploiting HLA-E-mediated peripheral and central toleranceMariko Shirane, Nobuyo Yawata, Daisuke Motooka, et al.
NPJ Genomic Medicine|December 6, 2025
Clinical characteristics of EYS-associated retinal dystrophy in 291 Japanese patientsYoshito Koyanagi, Yusuke Murakami, Taro Kominami, et al.
Ophthalmology. Retina|February 26, 2021
Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese PatientsYusuke Murakami, Yoshito Koyanagi, Masatoshi Fukushima, et al.
American Journal of Ophthalmology|May 8, 2026
Genotype-phenotype correlations in RPGRIP1-associated retinal dystrophy in a nationwide Japanese cohortKei Mizobuchi, Taiga Inooka, Takuya Aoki, et al.
American Journal of Human Genetics|March 26, 2024
Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing readsMathieu Quinodoz, Karolina Kaminska, Francesca Cancellieri, et al.
Journal of Medical Genetics|March 18, 2024
Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseasesKensuke Goto, Yoshito Koyanagi, Masato Akiyama, et al.
Ophthalmology|July 18, 2024
Genetic Risk Stratification of Primary Open-Angle Glaucoma in Japanese IndividualsMasato Akiyama, Gen Tamiya, Kohta Fujiwara, et al.
Therapeutic Advances in Medical Oncology|June 19, 2025
Ramucirumab and erlotinib combination as first-line treatment for advanced or recurrent non-small cell lung cancer harboring <i>EGFR</i> Exon21 L858R mutation: a multicenter retrospective observational cohort study in Japan (REAL-SPEED)Masashi Ishihara, Takahisa Kawamura, Yukiko Namba, et al.
Pageof 22