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C G JUNG

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000

Genetic linkage analysis of X-ray hypersensitivity in the LEC mutant ratT Agui, T Miyamoto, C G Jung, et al.

Experimental Animals|August 23, 2001

Linkage mapping of the rat 8-oxoguanine DNA glycosylase gene to chromosome 4K Masuda, T Miyamoto, C G Jung, et al.

Molecular Endocrinology (Baltimore, Md.)|December 16, 2000

A missense mutation G2320R in the thyroglobulin gene causes non-goitrous congenital primary hypothyroidism in the WIC-rdw ratP S Kim, M Ding, S Menon, et al.

Glia|September 19, 2007

Functional consequences of S1P receptor modulation in rat oligodendroglial lineage cellsC G Jung, H J Kim, V E Miron, et al.

Pageof 2

Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000

Genetic linkage analysis of X-ray hypersensitivity in the LEC mutant ratT Agui, T Miyamoto, C G Jung, et al.

Experimental Animals|August 23, 2001

Linkage mapping of the rat 8-oxoguanine DNA glycosylase gene to chromosome 4K Masuda, T Miyamoto, C G Jung, et al.

Molecular Endocrinology (Baltimore, Md.)|December 16, 2000

A missense mutation G2320R in the thyroglobulin gene causes non-goitrous congenital primary hypothyroidism in the WIC-rdw ratP S Kim, M Ding, S Menon, et al.

Glia|September 19, 2007

Functional consequences of S1P receptor modulation in rat oligodendroglial lineage cellsC G Jung, H J Kim, V E Miron, et al.

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