C L Freund - JoVE Visualize

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The Journal of Cell Biology|January 1, 1991

Sequence of the clathrin heavy chain from Saccharomyces cerevisiae and requirement of the COOH terminus for clathrin functionS K Lemmon, A Pellicena-Palle, K Conley, et al.

Human Molecular Genetics|April 1, 1996

A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disordersD A Swanson, C L Freund, L Ploder, et al.

Genome Research|May 1, 1997

A differential hybridization scheme to identify photoreceptor-specific genesD A Swanson, C L Freund, J M Steel, et al.

American Journal of Human Genetics|October 30, 1998

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor geneM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.

Investigative Ophthalmology & Visual Science|November 6, 1998

Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.

Cell|December 9, 1997

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.

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Showing results (1-10 of 6) with videos related to

Sort By:

Pageof 1

The Journal of Cell Biology|January 1, 1991

Sequence of the clathrin heavy chain from Saccharomyces cerevisiae and requirement of the COOH terminus for clathrin functionS K Lemmon, A Pellicena-Palle, K Conley, et al.

Human Molecular Genetics|April 1, 1996

A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disordersD A Swanson, C L Freund, L Ploder, et al.

Genome Research|May 1, 1997

A differential hybridization scheme to identify photoreceptor-specific genesD A Swanson, C L Freund, J M Steel, et al.

American Journal of Human Genetics|October 30, 1998

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor geneM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.

Investigative Ophthalmology & Visual Science|November 6, 1998

Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.

Cell|December 9, 1997

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.

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