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Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 12, 2004
Functional assessment of ABCG2 (BCRP) gene polymorphisms to protein expression in human placentaDaisuke Kobayashi, Ichiro Ieiri, Takeshi Hirota, et al.
Neuroscience Research|July 7, 2005
No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese populationTetsuya Marui, Shinko Koishi, Ikuko Funatogawa, et al.
The Journal of Clinical Endocrinology and Metabolism|June 2, 2005
Mutation at cleavage site of insulin-like growth factor receptor in a short-stature child born with intrauterine growth retardationYuki Kawashima, Susumu Kanzaki, Fan Yang, et al.
BMC Neurology|August 19, 2018
Phenotypic variability of Niemann-Pick disease type C including a case with clinically pure schizophrenia: a case reportTomoya Kawazoe, Toshiyuki Yamamoto, Aya Narita, et al.
Journal of the Endocrine Society|December 22, 2017
Increased IRS2 mRNA Expression in SGA Neonates: PCR Analysis of Insulin/IGF Signaling in Cord BloodMasanobu Fujimoto, Yuki Kawashima Sonoyama, Kenji Fukushima, et al.
Psychiatric Genetics|May 23, 2008
Association study of the commonly recognized breakpoints in chromosome 15q11-q13 in Japanese autistic patientsChieko Kato, Mamoru Tochigi, Shinko Koishi, et al.
Journal of Human Genetics|October 25, 2007
No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese populationMamoru Tochigi, Chieko Kato, Shinko Koishi, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|May 16, 2022
sp2-Iminosugars targeting human lysosomal β-hexosaminidase as pharmacological chaperone candidates for late-onset Tay-Sachs diseaseManuel González-Cuesta, Irene Herrera-González, M Isabel García-Moreno, et al.
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