C E Ogburn - JoVE Visualize

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Alzheimer Disease and Associated Disorders|January 1, 1993

Lack of detectable radiation hypersensitivity in lymphoblastoid cells from multiple pedigrees of familial Alzheimer diseaseE M Bryant, T D Bird, C E Ogburn, et al.

Human Genetics|September 10, 1999

Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell linesP R Prince, C E Ogburn, M J Moser, et al.

The American Journal of Pathology|December 10, 1998

Transgenic mice over-expressing the C-99 fragment of betaPP with an alpha-secretase site mutation develop a myopathy similar to human inclusion body myositisL W Jin, M G Hearn, C E Ogburn, et al.

Somatic Cell and Molecular Genetics|March 1, 1986

Resistance to paraquat in a mammalian cell lineJ Starr, S Sela, C M Disteche, et al.

Human Genetics|June 1, 1996

Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cellsV P Schulz, V A Zakian, C E Ogburn, et al.

The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|March 5, 2008

Cultured renal epithelial cells from birds and mice: enhanced resistance of avian cells to oxidative stress and DNA damageC E Ogburn, S N Austad, D J Holmes, et al.

Somatic Cell and Molecular Genetics|September 1, 1994

Oxygen-resistant multipotent embryonic carcinoma cell lines exhibit antimutator phenotypesC E Ogburn, M S Turker, T J Kavanagh, et al.

Experimental Neurology|June 1, 1994

Overexpression of a C-terminal portion of the beta-amyloid precursor protein in mouse brains by transplantation of transformed neuronal cellsK I Fukuchi, D D Kunkel, P A Schwartzkroin, et al.

Experimental Gerontology|November 1, 1994

Trypsin inhibitor activities of fibroblasts increase with age of donor and are unaltered in familial Alzheimer's diseaseM G Hearn, S D Edland, C E Ogburn, et al.

Human Genetics|December 24, 1997

An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutantsC E Ogburn, J Oshima, M Poot, et al.

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Showing results (11-20 of 28) with videos related to

Sort By:

Pageof 3

Alzheimer Disease and Associated Disorders|January 1, 1993

Lack of detectable radiation hypersensitivity in lymphoblastoid cells from multiple pedigrees of familial Alzheimer diseaseE M Bryant, T D Bird, C E Ogburn, et al.

Human Genetics|September 10, 1999

Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell linesP R Prince, C E Ogburn, M J Moser, et al.

The American Journal of Pathology|December 10, 1998

Transgenic mice over-expressing the C-99 fragment of betaPP with an alpha-secretase site mutation develop a myopathy similar to human inclusion body myositisL W Jin, M G Hearn, C E Ogburn, et al.

Somatic Cell and Molecular Genetics|March 1, 1986

Resistance to paraquat in a mammalian cell lineJ Starr, S Sela, C M Disteche, et al.

Human Genetics|June 1, 1996

Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cellsV P Schulz, V A Zakian, C E Ogburn, et al.

The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|March 5, 2008

Cultured renal epithelial cells from birds and mice: enhanced resistance of avian cells to oxidative stress and DNA damageC E Ogburn, S N Austad, D J Holmes, et al.

Somatic Cell and Molecular Genetics|September 1, 1994

Oxygen-resistant multipotent embryonic carcinoma cell lines exhibit antimutator phenotypesC E Ogburn, M S Turker, T J Kavanagh, et al.

Experimental Neurology|June 1, 1994

Overexpression of a C-terminal portion of the beta-amyloid precursor protein in mouse brains by transplantation of transformed neuronal cellsK I Fukuchi, D D Kunkel, P A Schwartzkroin, et al.

Experimental Gerontology|November 1, 1994

Trypsin inhibitor activities of fibroblasts increase with age of donor and are unaltered in familial Alzheimer's diseaseM G Hearn, S D Edland, C E Ogburn, et al.

Human Genetics|December 24, 1997

An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutantsC E Ogburn, J Oshima, M Poot, et al.

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