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Journal of Hepatology|April 24, 2012
Increased activity of serum mitochondrial isoenzyme of creatine kinase in hepatocellular carcinoma patients predominantly with recurrenceYoko Soroida, Ryunosuke Ohkawa, Hayato Nakagawa, et al.BMC Genomics|May 5, 2006
Construction of a nurse shark (Ginglymostoma cirratum) bacterial artificial chromosome (BAC) library and a preliminary genome surveyMeizhong Luo, Hyeran Kim, Dave Kudrna, et al.Nucleic Acids Research|December 1, 2022
Structural basis of transcription regulation by CNC family transcription factor, Nrf2Toru Sengoku, Masaaki Shiina, Kae Suzuki, et al.Journal of Gastroenterology|March 23, 2012
Systemic combination therapy of intravenous continuous 5-fluorouracil and subcutaneous pegylated interferon alfa-2a for advanced hepatocellular carcinomaKoji Uchino, Shuntaro Obi, Ryosuke Tateishi, et al.Plant Molecular Biology|July 29, 2009
AtObgC, a plant ortholog of bacterial Obg, is a chloroplast-targeting GTPase essential for early embryogenesisWoo Young Bang, Akira Hata, In Sil Jeong, et al.Journal of Hepatology|March 1, 2015
Sarcopenia, intramuscular fat deposition, and visceral adiposity independently predict the outcomes of hepatocellular carcinomaNaoto Fujiwara, Hayato Nakagawa, Yotaro Kudo, et al.European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|September 2, 2024
Impact of causative organism identification on clinical outcomes after minimally invasive posterior fixation for thoracolumbar pyogenic spondylitis: multicenter retrospective cohort studyHisanori Gamada, Toru Funayama, Tomoyuki Asada, 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.Clinical Genetics|October 4, 2018
GRIN2D variants in three cases of developmental and epileptic encephalopathyNaomi Tsuchida, Keisuke Hamada, Masaaki Shiina, et al.American Journal of Human Genetics|August 13, 2011
Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardationHiroshi Doi, Kunihiro Yoshida, Takao Yasuda, et al.Pageof 188