Search research articles
Contact Us
Filters
Showing results (31-40 of 73) with videos related to
Page
of 8
Sort By:
Rapid Communications in Mass Spectrometry : RCM
|
October 30, 2019
Characterization of 6-bromoferulic acid as a novel common-use matrix for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
Yosuke Kato, Narumi Hirosawa, Takeshi Sakamoto, et al.
American Journal of Medical Genetics. Part A
|
October 19, 2024
A Prevalent TMEM260 Deletion Causes Conotruncal Heart Defects, Including Truncus Arteriosus
Naoya Saijo, Hisao Yaoita, Jun Takayama, et al.
Genes & Genetic Systems
|
October 27, 2024
Next-generation sequencing analysis with a population-specific human reference genome
Tomohisa Suzuki, Kota Ninomiya, Takamitsu Funayama, et al.
Case Reports in Neurology
|
July 9, 2026
Relative Efficacy of Self-Managed Caffeine Supplementation in Maintaining Daily Activity in a Patient with ADCY5-Related Dyskinesia: A Case Report
Kaori Kodama, Haruhiko Nakamura, Aritomo Kawashima, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 17, 2019
Potent HIV-1 protease inhibitors incorporating squaramide-derived P2 ligands: Design, synthesis, and biological evaluation
Arun K Ghosh, Jacqueline N Williams, Satish Kovela, et al.
Journal of Human Genetics
|
November 4, 2025
PHOX2B deletion in congenital central hypoventilation syndrome: is this sufficient for pathogenesis?
Kiyoshi Hayasaka, Ayako Sasaki, Yumiko Kishikawa, et al.
Molecular Therapy. Nucleic Acids
|
April 24, 2026
From N-of-1 to versatility in propionic acidemia: Antisense oligonucleotide-mediated skipping of a constitutive <i>PCCA</i> pseudoexon
Eriko Totsune, Yoichi Wada, Yasuko Mikami-Saito, et al.
Journal of Human Genetics
|
February 13, 2024
Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population
Hisao Yaoita, Eiichiro Kawai, Jun Takayama, et al.
Brain & Development
|
August 30, 2021
A patient with early-onset SMAX3 and a novel variant of ATP7A
Moriei Shibuya, Hisao Yaoita, Kaori Kodama, et al.
Clinical Genetics
|
May 8, 2024
A fine-scale genetic map of the Japanese population
Jun Takayama, Satoshi Makino, Takamitsu Funayama, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 73) with videos related to
Sort By:
Page
of 8
Rapid Communications in Mass Spectrometry : RCM
|
October 30, 2019
Characterization of 6-bromoferulic acid as a novel common-use matrix for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
Yosuke Kato, Narumi Hirosawa, Takeshi Sakamoto, et al.
American Journal of Medical Genetics. Part A
|
October 19, 2024
A Prevalent TMEM260 Deletion Causes Conotruncal Heart Defects, Including Truncus Arteriosus
Naoya Saijo, Hisao Yaoita, Jun Takayama, et al.
Genes & Genetic Systems
|
October 27, 2024
Next-generation sequencing analysis with a population-specific human reference genome
Tomohisa Suzuki, Kota Ninomiya, Takamitsu Funayama, et al.
Case Reports in Neurology
|
July 9, 2026
Relative Efficacy of Self-Managed Caffeine Supplementation in Maintaining Daily Activity in a Patient with ADCY5-Related Dyskinesia: A Case Report
Kaori Kodama, Haruhiko Nakamura, Aritomo Kawashima, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 17, 2019
Potent HIV-1 protease inhibitors incorporating squaramide-derived P2 ligands: Design, synthesis, and biological evaluation
Arun K Ghosh, Jacqueline N Williams, Satish Kovela, et al.
Journal of Human Genetics
|
November 4, 2025
PHOX2B deletion in congenital central hypoventilation syndrome: is this sufficient for pathogenesis?
Kiyoshi Hayasaka, Ayako Sasaki, Yumiko Kishikawa, et al.
Molecular Therapy. Nucleic Acids
|
April 24, 2026
From N-of-1 to versatility in propionic acidemia: Antisense oligonucleotide-mediated skipping of a constitutive <i>PCCA</i> pseudoexon
Eriko Totsune, Yoichi Wada, Yasuko Mikami-Saito, et al.
Journal of Human Genetics
|
February 13, 2024
Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population
Hisao Yaoita, Eiichiro Kawai, Jun Takayama, et al.
Brain & Development
|
August 30, 2021
A patient with early-onset SMAX3 and a novel variant of ATP7A
Moriei Shibuya, Hisao Yaoita, Kaori Kodama, et al.
Clinical Genetics
|
May 8, 2024
A fine-scale genetic map of the Japanese population
Jun Takayama, Satoshi Makino, Takamitsu Funayama, et al.
Page
of 8