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Showing results (151-160 of 206) with videos related to

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The British Journal of Dermatology|August 1, 1991
Detection of a novel basement membrane antigen by GDA-J/F3 anti-human sperm fibrous sheath monoclonal antibodyA Jassim, O Schofield, P Whitehead, et al.
Nature|March 19, 1992
A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blisteringE B Lane, E L Rugg, H Navsaria, et al.
Nature Genetics|September 1, 1995
Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosaJ A McGrath, B Gatalica, A M Christiano, et al.
Lancet (London, England)|April 12, 1986
GB3 monoclonal antibody for diagnosis of junctional epidermolysis bullosaA H Heagerty, A R Kennedy, R A Eady, et al.
Human Molecular Genetics|January 15, 1999
Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratodermaD K Armstrong, K E McKenna, P E Purkis, et al.
Archives of Dermatological Research|January 1, 1990
Common antigen expression between human periderm and other tissues identified by GB1-monoclonal antibodyO M Schofield, J N McDonald, D Fredj-Reygrobellet, et al.
The Journal of Investigative Dermatology|September 21, 2000
The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21N V Whittock, C M Coleman, W H McLean, et al.
The American Journal of Pathology|June 1, 1996
Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentitionJ A McGrath, B Gatalica, K Li, 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|September 1, 1987
Rapid prenatal diagnosis of epidermolysis bullosa letalis using GB3 monoclonal antibodyA H Heagerty, R A Eady, A R Kennedy, et al.
Pageof 21

Showing results (151-160 of 206) with videos related to

Sort By:
Pageof 21
The British Journal of Dermatology|August 1, 1991
Detection of a novel basement membrane antigen by GDA-J/F3 anti-human sperm fibrous sheath monoclonal antibodyA Jassim, O Schofield, P Whitehead, et al.
Nature|March 19, 1992
A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blisteringE B Lane, E L Rugg, H Navsaria, et al.
Nature Genetics|September 1, 1995
Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosaJ A McGrath, B Gatalica, A M Christiano, et al.
Lancet (London, England)|April 12, 1986
GB3 monoclonal antibody for diagnosis of junctional epidermolysis bullosaA H Heagerty, A R Kennedy, R A Eady, et al.
Human Molecular Genetics|January 15, 1999
Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratodermaD K Armstrong, K E McKenna, P E Purkis, et al.
Archives of Dermatological Research|January 1, 1990
Common antigen expression between human periderm and other tissues identified by GB1-monoclonal antibodyO M Schofield, J N McDonald, D Fredj-Reygrobellet, et al.
The Journal of Investigative Dermatology|September 21, 2000
The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21N V Whittock, C M Coleman, W H McLean, et al.
The American Journal of Pathology|June 1, 1996
Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentitionJ A McGrath, B Gatalica, K Li, 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|September 1, 1987
Rapid prenatal diagnosis of epidermolysis bullosa letalis using GB3 monoclonal antibodyA H Heagerty, R A Eady, A R Kennedy, et al.
Pageof 21