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British Journal of Clinical Pharmacology
|
February 1, 1980
Elevated blood histamine levels and mast cell degranulation in solar urticaria
J L Hawk, R A Eady, A V Challoner, et al.
The Journal of Investigative Dermatology
|
May 1, 1990
Production of rabbit antibodies against carboxy-terminal epitopes encoded by bullous pemphigoid cDNA
T Tanaka, N J Korman, H Shimizu, et al.
The Journal of Investigative Dermatology
|
May 1, 1988
Type VII collagen is a normal component of epidermal basement membrane, which shows altered expression in recessive dystrophic epidermolysis bullosa
I M Leigh, R A Eady, A H Heagerty, et al.
The British Journal of Dermatology
|
December 1, 1985
Abnormal binding of an anti-amnion antibody to epidermal basement membrane provides a novel diagnostic probe for junctional epidermolysis bullosa
A R Kennedy, A H Heagerty, J P Ortonne, et al.
The British Journal of Dermatology
|
May 8, 1999
Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literature
T Basarab, F J Smith, V M Jolliffe, et al.
The Journal of Investigative Dermatology
|
April 5, 2001
Novel splice site mutation in keratin 1 underlies mild epidermolytic palmoplantar keratoderma in three kindreds
S J Hatsell, R A Eady, L Wennerstrand, et al.
The British Journal of Dermatology
|
April 16, 1998
Acquired junctional epidermolysis bullosa associated with IgG autoantibodies to the beta subunit of laminin-5
G Kirtschig, F Caux, J R McMillan, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
January 1, 1991
Monoclonal antibody GB3 defines a widespread defect of several basement membranes and a keratinocyte dysfunction in patients with lethal junctional epidermolysis bullosa
P Verrando, C Blanchet-Bardon, A Pisani, et al.
The British Journal of Dermatology
|
July 17, 1998
Frameshift mutations in the type VII collagen gene (COL7A1) in five Mexican cousins with recessive dystrophic epidermolysis bullosa
J C Salas-Alanis, J E Mellerio, M Amaya-Guerra, et al.
The Journal of Investigative Dermatology
|
August 1, 1996
Clinicopathological correlations of compound heterozygous COL7A1 mutations in recessive dystrophic epidermolysis bullosa
M G Dunnill, J A McGrath, A J Richards, et al.
Page
of 21
Search research articles
Search
Showing results (141-150 of 206) with videos related to
Sort By:
Page
of 21
British Journal of Clinical Pharmacology
|
February 1, 1980
Elevated blood histamine levels and mast cell degranulation in solar urticaria
J L Hawk, R A Eady, A V Challoner, et al.
The Journal of Investigative Dermatology
|
May 1, 1990
Production of rabbit antibodies against carboxy-terminal epitopes encoded by bullous pemphigoid cDNA
T Tanaka, N J Korman, H Shimizu, et al.
The Journal of Investigative Dermatology
|
May 1, 1988
Type VII collagen is a normal component of epidermal basement membrane, which shows altered expression in recessive dystrophic epidermolysis bullosa
I M Leigh, R A Eady, A H Heagerty, et al.
The British Journal of Dermatology
|
December 1, 1985
Abnormal binding of an anti-amnion antibody to epidermal basement membrane provides a novel diagnostic probe for junctional epidermolysis bullosa
A R Kennedy, A H Heagerty, J P Ortonne, et al.
The British Journal of Dermatology
|
May 8, 1999
Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literature
T Basarab, F J Smith, V M Jolliffe, et al.
The Journal of Investigative Dermatology
|
April 5, 2001
Novel splice site mutation in keratin 1 underlies mild epidermolytic palmoplantar keratoderma in three kindreds
S J Hatsell, R A Eady, L Wennerstrand, et al.
The British Journal of Dermatology
|
April 16, 1998
Acquired junctional epidermolysis bullosa associated with IgG autoantibodies to the beta subunit of laminin-5
G Kirtschig, F Caux, J R McMillan, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
January 1, 1991
Monoclonal antibody GB3 defines a widespread defect of several basement membranes and a keratinocyte dysfunction in patients with lethal junctional epidermolysis bullosa
P Verrando, C Blanchet-Bardon, A Pisani, et al.
The British Journal of Dermatology
|
July 17, 1998
Frameshift mutations in the type VII collagen gene (COL7A1) in five Mexican cousins with recessive dystrophic epidermolysis bullosa
J C Salas-Alanis, J E Mellerio, M Amaya-Guerra, et al.
The Journal of Investigative Dermatology
|
August 1, 1996
Clinicopathological correlations of compound heterozygous COL7A1 mutations in recessive dystrophic epidermolysis bullosa
M G Dunnill, J A McGrath, A J Richards, et al.
Page
of 21