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L Kuo

Showing results (521-530 of 570) with videos related to

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Nature Genetics|July 1, 1997
Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1L Li, I D Krantz, Y Deng, et al.
Allergy|September 26, 2017
A composite of exhaled LTB<sub>4</sub> , LXA<sub>4</sub> , FeNO, and FEV<sub>1</sub> as an "asthma classification ratio" characterizes childhood asthmaL-C Chen, H-M Tseng, M-L Kuo, et al.
Ophthalmic Surgery, Lasers & Imaging Retina|January 10, 2023
Functional Imaging of Mitochondria in Age-Related Macular Degeneration Using Flavoprotein FluorescenceJustin C Muste, Matthew W Russell, Andrew X Chen, et al.
Oncogene|September 8, 2009
LARG at chromosome 11q23 has functional characteristics of a tumor suppressor in human breast and colorectal cancerD C T Ong, Y M Ho, C Rudduck, et al.
American Journal of Human Genetics|October 30, 1998
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomalyA J Mears, T Jordan, F Mirzayans, et al.
The British Journal of Surgery|July 9, 2021
Prevalence of nodal involvement in rectal cancer after chemoradiotherapyH E Haak, G L Beets, K Peeters, et al.
Journal of Internal Medicine|February 29, 2020
A roadmap to build a phenotypic metric of ageing: insights from the Baltimore Longitudinal Study of AgingP-L Kuo, J A Schrack, M D Shardell, et al.
Human Molecular Genetics|February 28, 1998
Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomesB J Trask, C Friedman, A Martin-Gallardo, et al.
Neurology|October 15, 2013
Quinacrine treatment trial for sporadic Creutzfeldt-Jakob diseaseMichael D Geschwind, Amy L Kuo, Katherine S Wong, et al.
Oncogene|March 14, 2012
MiR-520h-mediated FOXC2 regulation is critical for inhibition of lung cancer progression by resveratrolY-H Yu, H-A Chen, P-S Chen, et al.
Pageof 57

Showing results (521-530 of 570) with videos related to

Sort By:
Pageof 57
Nature Genetics|July 1, 1997
Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1L Li, I D Krantz, Y Deng, et al.
Allergy|September 26, 2017
A composite of exhaled LTB<sub>4</sub> , LXA<sub>4</sub> , FeNO, and FEV<sub>1</sub> as an "asthma classification ratio" characterizes childhood asthmaL-C Chen, H-M Tseng, M-L Kuo, et al.
Ophthalmic Surgery, Lasers & Imaging Retina|January 10, 2023
Functional Imaging of Mitochondria in Age-Related Macular Degeneration Using Flavoprotein FluorescenceJustin C Muste, Matthew W Russell, Andrew X Chen, et al.
Oncogene|September 8, 2009
LARG at chromosome 11q23 has functional characteristics of a tumor suppressor in human breast and colorectal cancerD C T Ong, Y M Ho, C Rudduck, et al.
American Journal of Human Genetics|October 30, 1998
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomalyA J Mears, T Jordan, F Mirzayans, et al.
The British Journal of Surgery|July 9, 2021
Prevalence of nodal involvement in rectal cancer after chemoradiotherapyH E Haak, G L Beets, K Peeters, et al.
Journal of Internal Medicine|February 29, 2020
A roadmap to build a phenotypic metric of ageing: insights from the Baltimore Longitudinal Study of AgingP-L Kuo, J A Schrack, M D Shardell, et al.
Human Molecular Genetics|February 28, 1998
Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomesB J Trask, C Friedman, A Martin-Gallardo, et al.
Neurology|October 15, 2013
Quinacrine treatment trial for sporadic Creutzfeldt-Jakob diseaseMichael D Geschwind, Amy L Kuo, Katherine S Wong, et al.
Oncogene|March 14, 2012
MiR-520h-mediated FOXC2 regulation is critical for inhibition of lung cancer progression by resveratrolY-H Yu, H-A Chen, P-S Chen, et al.
Pageof 57