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L Yamamoto

Showing results (111-120 of 161) with videos related to

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Toxicology Letters|July 26, 2005
Gene expression changes in human small airway epithelial cells exposed to Delta9-tetrahydrocannabinolTheodore Sarafian, Nancy Habib, Jenny T Mao, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Milder course in Duchenne patients with nonsense mutations and no muscle dystrophinM Zatz, R C M Pavanello, M Lazar, et al.
Cell Death & Disease|January 18, 2014
Ankrd2 is a modulator of NF-κB-mediated inflammatory responses during muscle differentiationC Bean, N K Verma, D L Yamamoto, et al.
American Journal of Physiology. Endocrinology and Metabolism|September 1, 2011
β₁-Adrenergic receptors increase UCP1 in human MADS brown adipocytes and rescue cold-acclimated β₃-adrenergic receptor-knockout mice via nonshivering thermogenesisCharlotte L Mattsson, Robert I Csikasz, Ekaterina Chernogubova, et al.
Journal of the Endocrine Society|March 14, 2022
Thyroid and Breast Cancer in 2 Sisters With Monoallelic Mutations in the Ataxia Telangiectasia Mutated (<i>ATM</i>) GeneFabíola Y Miasaki, Kelly C Saito, Guilherme L Yamamoto, et al.
Behavior Genetics|September 13, 2011
Mecp2 truncation in male mice promotes affiliative social behaviorB L Pearson, E B Defensor, R L H Pobbe, et al.
Archives of Medical Research|January 15, 1999
Prevalence of high blood pressure and associated coronary risk factors in an adult population of Mexico CityL Yamamoto-Kimura, J Zamora-Gonzalez, G Garcia de la Torre, et al.
Clinical and Experimental Obstetrics & Gynecology|October 20, 2004
Tamoxifen down-regulates CaMKII messenger RNA levels in normal human breast tissueI D C Guerreiro Da Silva, E Dias-Netto, F E Villanova, et al.
American Journal of Medical Genetics. Part A|January 12, 2022
The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestryTaccyanna M Ali, Bianca D W Linnenkamp, Guilherme L Yamamoto, et al.
Human Mutation|July 4, 2018
Rare RELN variants affect Reelin-DAB1 signal transduction in autism spectrum disorderSandra M Sánchez-Sánchez, Juliana Magdalon, Karina Griesi-Oliveira, et al.
Pageof 17

Showing results (111-120 of 161) with videos related to

Sort By:
Pageof 17
Toxicology Letters|July 26, 2005
Gene expression changes in human small airway epithelial cells exposed to Delta9-tetrahydrocannabinolTheodore Sarafian, Nancy Habib, Jenny T Mao, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Milder course in Duchenne patients with nonsense mutations and no muscle dystrophinM Zatz, R C M Pavanello, M Lazar, et al.
Cell Death & Disease|January 18, 2014
Ankrd2 is a modulator of NF-κB-mediated inflammatory responses during muscle differentiationC Bean, N K Verma, D L Yamamoto, et al.
American Journal of Physiology. Endocrinology and Metabolism|September 1, 2011
β₁-Adrenergic receptors increase UCP1 in human MADS brown adipocytes and rescue cold-acclimated β₃-adrenergic receptor-knockout mice via nonshivering thermogenesisCharlotte L Mattsson, Robert I Csikasz, Ekaterina Chernogubova, et al.
Journal of the Endocrine Society|March 14, 2022
Thyroid and Breast Cancer in 2 Sisters With Monoallelic Mutations in the Ataxia Telangiectasia Mutated (<i>ATM</i>) GeneFabíola Y Miasaki, Kelly C Saito, Guilherme L Yamamoto, et al.
Behavior Genetics|September 13, 2011
Mecp2 truncation in male mice promotes affiliative social behaviorB L Pearson, E B Defensor, R L H Pobbe, et al.
Archives of Medical Research|January 15, 1999
Prevalence of high blood pressure and associated coronary risk factors in an adult population of Mexico CityL Yamamoto-Kimura, J Zamora-Gonzalez, G Garcia de la Torre, et al.
Clinical and Experimental Obstetrics & Gynecology|October 20, 2004
Tamoxifen down-regulates CaMKII messenger RNA levels in normal human breast tissueI D C Guerreiro Da Silva, E Dias-Netto, F E Villanova, et al.
American Journal of Medical Genetics. Part A|January 12, 2022
The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestryTaccyanna M Ali, Bianca D W Linnenkamp, Guilherme L Yamamoto, et al.
Human Mutation|July 4, 2018
Rare RELN variants affect Reelin-DAB1 signal transduction in autism spectrum disorderSandra M Sánchez-Sánchez, Juliana Magdalon, Karina Griesi-Oliveira, et al.
Pageof 17