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Circulation Journal : Official Journal of the Japanese Circulation Society
|
June 5, 2024
Sex Differences in Cardiovascular Disease-Related Hospitalization and Mortality in Japan - Analysis of Health Records From a Nationwide Claim-Based Database, the Japanese Registry of All Cardiac and Vascular Disease (JROAD)
Satsuki Noma, Katsuhito Kato, Toshiaki Otsuka, et al.
Japanese Journal of Ophthalmology
|
February 25, 2021
Regional differences in genes and variants causing retinitis pigmentosa in Japan
Yoshito Koyanagi, Masato Akiyama, Koji M Nishiguchi, et al.
Communications Biology
|
January 30, 2021
A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa
Koji M Nishiguchi, Fuyuki Miya, Yuka Mori, et al.
American Journal of Medical Genetics. Part A
|
October 3, 2022
Comprehensive genetic screening for vascular Ehlers-Danlos syndrome through an amplification-based next-generation sequencing system
Tomomi Yamaguchi, Shujiro Hayashi, Daisuke Hayashi, et al.
Investigative Ophthalmology & Visual Science
|
March 27, 2019
Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease Spectrum
Sanne K Verbakel, Ramon A C van Huet, Anneke I den Hollander, et al.
Cardiovascular Research
|
November 18, 2025
Immune regulation following allogeneic iPSC-derived cardiomyocyte transplantation in non-human primates
Shuji Chino, Hajime Ichimura, Shugo Tohyama, et al.
Journal of Medical Genetics
|
June 20, 2019
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients
Yoshito Koyanagi, Masato Akiyama, Koji M Nishiguchi, et al.
Nature Communications
|
June 30, 2019
A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy
Konstantinos Nikopoulos, Katarina Cisarova, Mathieu Quinodoz, 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 reads
Mathieu Quinodoz, Karolina Kaminska, Francesca Cancellieri, et al.
Circulation. Genomic and Precision Medicine
|
July 26, 2021
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> Variants
Krystian Kozek, Yuko Wada, Luca Sala, et al.
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of 25
Search research articles
Search
Showing results (231-240 of 250) with videos related to
Sort By:
Page
of 25
Circulation Journal : Official Journal of the Japanese Circulation Society
|
June 5, 2024
Sex Differences in Cardiovascular Disease-Related Hospitalization and Mortality in Japan - Analysis of Health Records From a Nationwide Claim-Based Database, the Japanese Registry of All Cardiac and Vascular Disease (JROAD)
Satsuki Noma, Katsuhito Kato, Toshiaki Otsuka, et al.
Japanese Journal of Ophthalmology
|
February 25, 2021
Regional differences in genes and variants causing retinitis pigmentosa in Japan
Yoshito Koyanagi, Masato Akiyama, Koji M Nishiguchi, et al.
Communications Biology
|
January 30, 2021
A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa
Koji M Nishiguchi, Fuyuki Miya, Yuka Mori, et al.
American Journal of Medical Genetics. Part A
|
October 3, 2022
Comprehensive genetic screening for vascular Ehlers-Danlos syndrome through an amplification-based next-generation sequencing system
Tomomi Yamaguchi, Shujiro Hayashi, Daisuke Hayashi, et al.
Investigative Ophthalmology & Visual Science
|
March 27, 2019
Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease Spectrum
Sanne K Verbakel, Ramon A C van Huet, Anneke I den Hollander, et al.
Cardiovascular Research
|
November 18, 2025
Immune regulation following allogeneic iPSC-derived cardiomyocyte transplantation in non-human primates
Shuji Chino, Hajime Ichimura, Shugo Tohyama, et al.
Journal of Medical Genetics
|
June 20, 2019
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients
Yoshito Koyanagi, Masato Akiyama, Koji M Nishiguchi, et al.
Nature Communications
|
June 30, 2019
A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy
Konstantinos Nikopoulos, Katarina Cisarova, Mathieu Quinodoz, 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 reads
Mathieu Quinodoz, Karolina Kaminska, Francesca Cancellieri, et al.
Circulation. Genomic and Precision Medicine
|
July 26, 2021
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> Variants
Krystian Kozek, Yuko Wada, Luca Sala, et al.
Page
of 25