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Lily Ng

Showing results (51-60 of 57) with videos related to

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Endocrinology|November 20, 2012
Cerebellar abnormalities in mice lacking type 3 deiodinase and partial reversal of phenotype by deletion of thyroid hormone receptor α1Robin P Peeters, Arturo Hernandez, Lily Ng, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 6, 2010
Type 3 deiodinase, a thyroid-hormone-inactivating enzyme, controls survival and maturation of cone photoreceptorsLily Ng, Arkady Lyubarsky, Sergei S Nikonov, et al.
Human Molecular Genetics|October 24, 2002
Targeted disruption of Slc19a2, the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in miceKimihiko Oishi, Susanna Hofmann, George A Diaz, et al.
Human Molecular Genetics|April 13, 2022
An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutationYalan Hu, Peter Lauffer, Michelle Stewart, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2004
Hearing loss and retarded cochlear development in mice lacking type 2 iodothyronine deiodinaseLily Ng, Richard J Goodyear, Chad A Woods, et al.
Communications Biology|December 11, 2023
Thyroid hormone-regulated chromatin landscape and transcriptional sensitivity of the pituitary glandYoung-Wook Cho, Yulong Fu, Chen-Che Jeff Huang, et al.
Cancer Research|October 4, 2017
SKP2 Activation by Thyroid Hormone Receptor β2 Bypasses Rb-Dependent Proliferation in Rb-Deficient CellsXiaoliang L Xu, Zhengke Li, Aihong Liu, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Endocrinology|November 20, 2012
Cerebellar abnormalities in mice lacking type 3 deiodinase and partial reversal of phenotype by deletion of thyroid hormone receptor α1Robin P Peeters, Arturo Hernandez, Lily Ng, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 6, 2010
Type 3 deiodinase, a thyroid-hormone-inactivating enzyme, controls survival and maturation of cone photoreceptorsLily Ng, Arkady Lyubarsky, Sergei S Nikonov, et al.
Human Molecular Genetics|October 24, 2002
Targeted disruption of Slc19a2, the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in miceKimihiko Oishi, Susanna Hofmann, George A Diaz, et al.
Human Molecular Genetics|April 13, 2022
An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutationYalan Hu, Peter Lauffer, Michelle Stewart, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2004
Hearing loss and retarded cochlear development in mice lacking type 2 iodothyronine deiodinaseLily Ng, Richard J Goodyear, Chad A Woods, et al.
Communications Biology|December 11, 2023
Thyroid hormone-regulated chromatin landscape and transcriptional sensitivity of the pituitary glandYoung-Wook Cho, Yulong Fu, Chen-Che Jeff Huang, et al.
Cancer Research|October 4, 2017
SKP2 Activation by Thyroid Hormone Receptor β2 Bypasses Rb-Dependent Proliferation in Rb-Deficient CellsXiaoliang L Xu, Zhengke Li, Aihong Liu, et al.
Pageof 6