Showing results (161-170 of 193) with videos related to
Sort By:
Pageof 20
Scientific Reports|October 17, 2015
Artificial oxygen carriers rescue placental hypoxia and improve fetal development in the rat pre-eclampsia modelHeng Li, Hidenobu Ohta, Yu Tahara, et al.Scientific Reports|June 26, 2013
In vitro circadian period is associated with circadian/sleep preferenceAkiko Hida, Shingo Kitamura, Yosuke Ohsawa, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 10, 2020
Higd1a improves respiratory function in the models of mitochondrial disorderTakemasa Nagao, Yasunori Shintani, Takaharu Hayashi, et al.Annals of Neurology|June 4, 2019
COX6A2 variants cause a muscle-specific cytochrome c oxidase deficiencyMichio Inoue, Shumpei Uchino, Aritoshi Iida, et al.British Journal of Haematology|March 10, 2005
Methylation status of the p15 and p16 genes in paediatric myelodysplastic syndrome and juvenile myelomonocytic leukaemiaDaisuke Hasegawa, Atsushi Manabe, Takeo Kubota, et al.Drug Metabolism and Pharmacokinetics|December 25, 2004
Five novel single nucleotide polymorphisms in the EPHX1 gene encoding microsomal epoxide hydrolaseKisho Shiseki, Masaya Itoda, Yoshiro Saito, et al.Journal of Neuropathology and Experimental Neurology|July 9, 2014
Expression of astrocyte-related receptors in cortical dysplasia with intractable epilepsySayuri Sukigara, Hongmei Dai, Shin Nabatame, et al.Journal of Human Genetics|October 11, 2020
DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6AAkane Terasaki, Masayuki Nakamura, Yuka Urata, et al.Human Mutation|January 3, 2013
Mitochondrial complex III deficiency caused by a homozygous UQCRC2 mutation presenting with neonatal-onset recurrent metabolic decompensationNoriko Miyake, Shoji Yano, Chika Sakai, et al.Brain : a Journal of Neurology|February 5, 2019
Biallelic KARS pathogenic variants cause an early-onset progressive leukodystrophyMasayuki Itoh, Hongmei Dai, Shin-Ichi Horike, et al.Pageof 20