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Toxicology Letters
|
July 26, 2005
Gene expression changes in human small airway epithelial cells exposed to Delta9-tetrahydrocannabinol
Theodore 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 dystrophin
M 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 differentiation
C 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 thermogenesis
Charlotte 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>) Gene
Fabíola Y Miasaki, Kelly C Saito, Guilherme L Yamamoto, et al.
Behavior Genetics
|
September 13, 2011
Mecp2 truncation in male mice promotes affiliative social behavior
B 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 City
L 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 tissue
I 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 ancestry
Taccyanna 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 disorder
Sandra M Sánchez-Sánchez, Juliana Magdalon, Karina Griesi-Oliveira, et al.
Page
of 17
Search research articles
Search
Showing results (111-120 of 161) with videos related to
Sort By:
Page
of 17
Toxicology Letters
|
July 26, 2005
Gene expression changes in human small airway epithelial cells exposed to Delta9-tetrahydrocannabinol
Theodore 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 dystrophin
M 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 differentiation
C 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 thermogenesis
Charlotte 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>) Gene
Fabíola Y Miasaki, Kelly C Saito, Guilherme L Yamamoto, et al.
Behavior Genetics
|
September 13, 2011
Mecp2 truncation in male mice promotes affiliative social behavior
B 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 City
L 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 tissue
I 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 ancestry
Taccyanna 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 disorder
Sandra M Sánchez-Sánchez, Juliana Magdalon, Karina Griesi-Oliveira, et al.
Page
of 17