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O Swensson

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

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The Journal of Cell Biology|March 1, 1996
Gene targeting at the mouse cytokeratin 10 locus: severe skin fragility and changes of cytokeratin expression in the epidermisR M Porter, S Leitgeb, D W Melton, et al.
Experimental Eye Research|January 25, 2000
Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 geneL D Corden, O Swensson, B Swensson, et al.
The British Journal of Ophthalmology|April 27, 2000
A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophyL D Corden, O Swensson, B Swensson, et al.
Journal of Medical Genetics|October 1, 1993
Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinismA Meindl, D Hosenfeld, W Brückl, et al.
The Journal of Investigative Dermatology|September 1, 1999
Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutationsJ A McGrath, G H Ashton, J E Mellerio, et al.
The British Journal of Dermatology|January 20, 1999
Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stressO Swensson, L Langbein, J R McMillan, et al.
The Journal of Investigative Dermatology|March 1, 1995
Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratodermaH A Navsaria, O Swensson, R C Ratnavel, et al.
The British Journal of Ophthalmology|June 27, 2002
A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophyA D Irvine, C M Coleman, J E Moore, et al.
Nature Genetics|March 1, 1995
Keratin 16 and keratin 17 mutations cause pachyonychia congenitaW H McLean, E L Rugg, D P Lunny, et al.
Nature Genetics|June 1, 1997
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophyA D Irvine, L D Corden, O Swensson, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
The Journal of Cell Biology|March 1, 1996
Gene targeting at the mouse cytokeratin 10 locus: severe skin fragility and changes of cytokeratin expression in the epidermisR M Porter, S Leitgeb, D W Melton, et al.
Experimental Eye Research|January 25, 2000
Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 geneL D Corden, O Swensson, B Swensson, et al.
The British Journal of Ophthalmology|April 27, 2000
A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophyL D Corden, O Swensson, B Swensson, et al.
Journal of Medical Genetics|October 1, 1993
Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinismA Meindl, D Hosenfeld, W Brückl, et al.
The Journal of Investigative Dermatology|September 1, 1999
Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutationsJ A McGrath, G H Ashton, J E Mellerio, et al.
The British Journal of Dermatology|January 20, 1999
Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stressO Swensson, L Langbein, J R McMillan, et al.
The Journal of Investigative Dermatology|March 1, 1995
Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratodermaH A Navsaria, O Swensson, R C Ratnavel, et al.
The British Journal of Ophthalmology|June 27, 2002
A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophyA D Irvine, C M Coleman, J E Moore, et al.
Nature Genetics|March 1, 1995
Keratin 16 and keratin 17 mutations cause pachyonychia congenitaW H McLean, E L Rugg, D P Lunny, et al.
Nature Genetics|June 1, 1997
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophyA D Irvine, L D Corden, O Swensson, et al.
Pageof 2