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R A Eady

Showing results (121-130 of 206) with videos related to

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Journal of Cutaneous Pathology|April 1, 1992
Epidermolysis bullosa complicated by squamous cell carcinoma: report of 10 casesJ A McGrath, O M Schofield, B J Mayou, et al.
British Medical Journal|March 22, 1975
Plasma immunoreactive melanotrophic hormones in patients on maintenance haemodialysisJ J Gilkes, R A Eady, L H Rees, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 1, 2007
Prenatal diagnosis and management strategies in a family with a rare type of congenital ichthyosisS V Phadnis, D R Griffin, R A Eady, et al.
The British Journal of Dermatology|December 1, 1994
Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)A Ishida-Yamamoto, R A Eady, R A Underwood, et al.
The Journal of Investigative Dermatology|November 6, 1998
Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14)C S Shemanko, J E Mellerio, M J Tidman, et al.
The British Journal of Dermatology|September 5, 2001
New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of SiemensN V Whittock, G H Ashton, W A Griffiths, et al.
Clinical and Experimental Dermatology|September 1, 1977
A new method for recovery of exudates from normal and inflamed human skinA K Black, M W Greaves, C N Hensby, et al.
The Journal of Investigative Dermatology|April 1, 1995
Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosaJ A McGrath, L Pulkkinen, A M Christiano, et al.
Human Molecular Genetics|September 1, 1994
A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosaM G Dunnill, A J Richards, G Milana, et al.
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.
Pageof 21

Showing results (121-130 of 206) with videos related to

Sort By:
Pageof 21
Journal of Cutaneous Pathology|April 1, 1992
Epidermolysis bullosa complicated by squamous cell carcinoma: report of 10 casesJ A McGrath, O M Schofield, B J Mayou, et al.
British Medical Journal|March 22, 1975
Plasma immunoreactive melanotrophic hormones in patients on maintenance haemodialysisJ J Gilkes, R A Eady, L H Rees, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 1, 2007
Prenatal diagnosis and management strategies in a family with a rare type of congenital ichthyosisS V Phadnis, D R Griffin, R A Eady, et al.
The British Journal of Dermatology|December 1, 1994
Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)A Ishida-Yamamoto, R A Eady, R A Underwood, et al.
The Journal of Investigative Dermatology|November 6, 1998
Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14)C S Shemanko, J E Mellerio, M J Tidman, et al.
The British Journal of Dermatology|September 5, 2001
New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of SiemensN V Whittock, G H Ashton, W A Griffiths, et al.
Clinical and Experimental Dermatology|September 1, 1977
A new method for recovery of exudates from normal and inflamed human skinA K Black, M W Greaves, C N Hensby, et al.
The Journal of Investigative Dermatology|April 1, 1995
Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosaJ A McGrath, L Pulkkinen, A M Christiano, et al.
Human Molecular Genetics|September 1, 1994
A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosaM G Dunnill, A J Richards, G Milana, et al.
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.
Pageof 21