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Yoichi Shinkai

Showing results (141-150 of 149) with videos related to

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Scientific Reports|January 18, 2023
A novel NONO variant that causes developmental delay and cardiac phenotypesToshiyuki Itai, Atsushi Sugie, Yohei Nitta, et al.
Molecular Cell|August 15, 2017
Methylation of DNA Ligase 1 by G9a/GLP Recruits UHRF1 to Replicating DNA and Regulates DNA MethylationLaure Ferry, Alexandra Fournier, Takeshi Tsusaka, et al.
Human Molecular Genetics|November 24, 2012
Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndromeMonique C M Balemans, Nael Nadif Kasri, Maksym V Kopanitsa, et al.
Nature Communications|January 12, 2023
A specific G9a inhibitor unveils BGLT3 lncRNA as a universal mediator of chemically induced fetal globin gene expressionShohei Takase, Takashi Hiroyama, Fumiyuki Shirai, et al.
Molecular Psychiatry|July 15, 2021
A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brainShabeesh Balan, Yoshimi Iwayama, Tetsuo Ohnishi, et al.
Nature Communications|September 7, 2021
C9orf72-derived arginine-rich poly-dipeptides impede phase modifiersHitoki Nanaura, Honoka Kawamukai, Ayano Fujiwara, et al.
Cell Reports|July 28, 2025
Glucose-activated JMJD1A drives visceral adipogenesis via α-ketoglutarate-dependent chromatin remodelingChenxu Yang, Makoto Arai, Eko Fuji Ariyanto, et al.
Nature Communications|February 10, 2021
The methyltransferase METTL9 mediates pervasive 1-methylhistidine modification in mammalian proteomesErna Davydova, Tadahiro Shimazu, Maren Kirstin Schuhmacher, et al.
American Journal of Human Genetics|July 16, 2024
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndromeDmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
Pageof 15

Showing results (141-150 of 149) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 149 results.
Scientific Reports|January 18, 2023
A novel NONO variant that causes developmental delay and cardiac phenotypesToshiyuki Itai, Atsushi Sugie, Yohei Nitta, et al.
Molecular Cell|August 15, 2017
Methylation of DNA Ligase 1 by G9a/GLP Recruits UHRF1 to Replicating DNA and Regulates DNA MethylationLaure Ferry, Alexandra Fournier, Takeshi Tsusaka, et al.
Human Molecular Genetics|November 24, 2012
Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndromeMonique C M Balemans, Nael Nadif Kasri, Maksym V Kopanitsa, et al.
Nature Communications|January 12, 2023
A specific G9a inhibitor unveils BGLT3 lncRNA as a universal mediator of chemically induced fetal globin gene expressionShohei Takase, Takashi Hiroyama, Fumiyuki Shirai, et al.
Molecular Psychiatry|July 15, 2021
A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brainShabeesh Balan, Yoshimi Iwayama, Tetsuo Ohnishi, et al.
Nature Communications|September 7, 2021
C9orf72-derived arginine-rich poly-dipeptides impede phase modifiersHitoki Nanaura, Honoka Kawamukai, Ayano Fujiwara, et al.
Cell Reports|July 28, 2025
Glucose-activated JMJD1A drives visceral adipogenesis via α-ketoglutarate-dependent chromatin remodelingChenxu Yang, Makoto Arai, Eko Fuji Ariyanto, et al.
Nature Communications|February 10, 2021
The methyltransferase METTL9 mediates pervasive 1-methylhistidine modification in mammalian proteomesErna Davydova, Tadahiro Shimazu, Maren Kirstin Schuhmacher, et al.
American Journal of Human Genetics|July 16, 2024
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndromeDmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
Pageof 15