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J W Kim

Showing results (431-440 of 691) with videos related to

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Physical Review Letters|May 26, 2018
Ferromagnetism and Charge Order from a Frozen Electron Configuration in Strained Epitaxial LaCoO_{3}G E Sterbinsky, R Nanguneri, J X Ma, et al.
The Journal of Biological Chemistry|June 26, 1999
3-deazaadenosine, a S-adenosylhomocysteine hydrolase inhibitor, has dual effects on NF-kappaB regulation. Inhibition of NF-kappaB transcriptional activity and promotion of IkappaBalpha degradationS Y Jeong, S G Ahn, J H Lee, et al.
The Laryngoscope|February 24, 2001
Regulation of mucociliary motility by nitric oxide and expression of nitric oxide synthase in the human sinus epithelial cellsJ W Kim, Y G Min, C S Rhee, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|April 12, 2013
Genotyping of Mycobacterium intracellulare isolates and clinical characteristics of lung diseaseS-Y Kim, S-T Lee, B-H Jeong, et al.
The Journal of International Medical Research|August 9, 2011
Silencing of the GnRH type 1 receptor blocks the antiproliferative effect of the GnRH agonist, leuprolide, on the androgen-independent prostate cancer cell line DU145Y H Ko, Y R Ha, J W Kim, et al.
The Review of Scientific Instruments|July 5, 2012
A novel approach for x-ray scattering experiments in magnetic fields utilizing trapped flux in type-II superconductorsR K Das, Z Islam, J P C Ruff, et al.
Biochemistry and Molecular Biology International|November 14, 1997
Cloning of the human cDNA sequence encoding the NADH:ubiquinone oxidoreductase MLRQ subunitJ W Kim, Y Lee, H B Kang, et al.
Psychological Medicine|May 29, 2015
Associations between serotonin transporter gene (SLC6A4) methylation and clinical characteristics and cortical thickness in children with ADHDS Park, J-M Lee, J-W Kim, et al.
Oral Diseases|January 15, 2016
Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfectaY-J Kim, F Seymen, M Koruyucu, et al.
Journal of Dental Research|October 9, 2020
<i>FAM83H</i> and Autosomal Dominant Hypocalcified Amelogenesis ImperfectaS K Wang, H Zhang, C Y Hu, et al.
Pageof 70

Showing results (431-440 of 691) with videos related to

Sort By:
Pageof 70
Physical Review Letters|May 26, 2018
Ferromagnetism and Charge Order from a Frozen Electron Configuration in Strained Epitaxial LaCoO_{3}G E Sterbinsky, R Nanguneri, J X Ma, et al.
The Journal of Biological Chemistry|June 26, 1999
3-deazaadenosine, a S-adenosylhomocysteine hydrolase inhibitor, has dual effects on NF-kappaB regulation. Inhibition of NF-kappaB transcriptional activity and promotion of IkappaBalpha degradationS Y Jeong, S G Ahn, J H Lee, et al.
The Laryngoscope|February 24, 2001
Regulation of mucociliary motility by nitric oxide and expression of nitric oxide synthase in the human sinus epithelial cellsJ W Kim, Y G Min, C S Rhee, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|April 12, 2013
Genotyping of Mycobacterium intracellulare isolates and clinical characteristics of lung diseaseS-Y Kim, S-T Lee, B-H Jeong, et al.
The Journal of International Medical Research|August 9, 2011
Silencing of the GnRH type 1 receptor blocks the antiproliferative effect of the GnRH agonist, leuprolide, on the androgen-independent prostate cancer cell line DU145Y H Ko, Y R Ha, J W Kim, et al.
The Review of Scientific Instruments|July 5, 2012
A novel approach for x-ray scattering experiments in magnetic fields utilizing trapped flux in type-II superconductorsR K Das, Z Islam, J P C Ruff, et al.
Biochemistry and Molecular Biology International|November 14, 1997
Cloning of the human cDNA sequence encoding the NADH:ubiquinone oxidoreductase MLRQ subunitJ W Kim, Y Lee, H B Kang, et al.
Psychological Medicine|May 29, 2015
Associations between serotonin transporter gene (SLC6A4) methylation and clinical characteristics and cortical thickness in children with ADHDS Park, J-M Lee, J-W Kim, et al.
Oral Diseases|January 15, 2016
Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfectaY-J Kim, F Seymen, M Koruyucu, et al.
Journal of Dental Research|October 9, 2020
<i>FAM83H</i> and Autosomal Dominant Hypocalcified Amelogenesis ImperfectaS K Wang, H Zhang, C Y Hu, et al.
Pageof 70