Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R A Eady

Showing results (181-190 of 206) with videos related to

Pageof 21
Sort By:
Arthritis and Rheumatism|June 1, 1982
Adult-onset Still's disease. Twenty-year followup and further studies of patients with active diseaseK B Elkon, G R Hughes, E G Bywaters, 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 Journal of Investigative Dermatology|November 1, 1988
Prenatal diagnosis of dominant and recessive dystrophic epidermolysis bullosa: application and limitations in the use of KF-1 and LH 7:2 monoclonal antibodies and immunofluorescence mapping techniqueJ D Fine, R A Eady, M L Levy, et al.
The Journal of Investigative Dermatology|June 1, 1997
Bullous pemphigoid and cicatricial pemphigoid autoantibodies react with ultrastructurally separable epitopes on the BP180 ectodomain: evidence that BP180 spans the lamina lucidaC Bédane, J R McMillan, S D Balding, et al.
Biochemical and Biophysical Research Communications|October 12, 2000
Genomic organization and amplification of the human desmosomal cadherin genes DSC1 and DSC3, encoding desmocollin types 1 and 3N V Whittock, D M Hunt, L Rickman, et al.
Human Molecular Genetics|May 1, 1995
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosaS Kivirikko, J A McGrath, C Baudoin, et al.
Journal of Medical Genetics|October 1, 1994
Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalitiesM G Dunnill, A J Richards, G Milana, et al.
Lancet (London, England)|December 19, 1992
Oral and gastrointestinal manifestations of epidermolysis bullosaS P Travis, J A McGrath, A J Turnbull, et al.
The British Journal of Dermatology|September 6, 2000
A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe diseaseK Batta, E L Rugg, N J Wilson, et al.
The British Journal of Dermatology|April 1, 1996
First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus samplingJ A McGrath, M G Dunnill, A M Christiano, et al.
Pageof 21

Showing results (181-190 of 206) with videos related to

Sort By:
Pageof 21
Arthritis and Rheumatism|June 1, 1982
Adult-onset Still's disease. Twenty-year followup and further studies of patients with active diseaseK B Elkon, G R Hughes, E G Bywaters, 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 Journal of Investigative Dermatology|November 1, 1988
Prenatal diagnosis of dominant and recessive dystrophic epidermolysis bullosa: application and limitations in the use of KF-1 and LH 7:2 monoclonal antibodies and immunofluorescence mapping techniqueJ D Fine, R A Eady, M L Levy, et al.
The Journal of Investigative Dermatology|June 1, 1997
Bullous pemphigoid and cicatricial pemphigoid autoantibodies react with ultrastructurally separable epitopes on the BP180 ectodomain: evidence that BP180 spans the lamina lucidaC Bédane, J R McMillan, S D Balding, et al.
Biochemical and Biophysical Research Communications|October 12, 2000
Genomic organization and amplification of the human desmosomal cadherin genes DSC1 and DSC3, encoding desmocollin types 1 and 3N V Whittock, D M Hunt, L Rickman, et al.
Human Molecular Genetics|May 1, 1995
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosaS Kivirikko, J A McGrath, C Baudoin, et al.
Journal of Medical Genetics|October 1, 1994
Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalitiesM G Dunnill, A J Richards, G Milana, et al.
Lancet (London, England)|December 19, 1992
Oral and gastrointestinal manifestations of epidermolysis bullosaS P Travis, J A McGrath, A J Turnbull, et al.
The British Journal of Dermatology|September 6, 2000
A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe diseaseK Batta, E L Rugg, N J Wilson, et al.
The British Journal of Dermatology|April 1, 1996
First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus samplingJ A McGrath, M G Dunnill, A M Christiano, et al.
Pageof 21