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Showing results (111-120 of 121) with videos related to

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The Journal of Investigative Dermatology|February 11, 1998
Cycloheximide facilitates the identification of aberrant transcripts resulting from a novel splice-site mutation in COL17A1 in a patient with generalized atrophic benign epidermolysis bullosaT N Darling, C Yee, B Koh, et al.
The Journal of Investigative Dermatology|February 11, 1998
A deletion mutation in COL17A1 in five Austrian families with generalized atrophic benign epidermolysis bullosa represents propagation of an ancestral alleleT N Darling, B B Koh, S J Bale, et al.
Mechanisms of Ageing and Development|April 21, 2010
Aberrant heterodimerization of keratin 16 with keratin 6A in HaCaT keratinocytes results in diminished cellular migrationA Trost, P Desch, V Wally, et al.
The British Journal of Dermatology|December 3, 1999
Ocular involvement in IgA-epidermolysis bullosa acquisitaJ W Bauer, H Schaeppi, D Metze, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 29, 2010
Nosocomial Staphylococcal scalded skin syndrome caused by intra-articular injectionM Emberger, J Koller, M Laimer, et al.
Actas Dermo-Sifiliograficas|October 23, 2010
[Immunofluorescence mapping for diagnosis of congenital epidermolysis bullosa]R Cepeda-Valdés, G Pohla-Gubo, J R Borbolla-Escoboza, et al.
European Journal of Ophthalmology|December 28, 2006
Ocular involvement in anti-epiligrin cicatricial pemphigoidC Nischler, E Sadler, Z Lazarova, et al.
The Journal of Investigative Dermatology|October 26, 2001
Pathogenesis of the permeability barrier abnormality in epidermolytic hyperkeratosisM Schmuth, G Yosipovitch, M L Williams, et al.
The Journal of Investigative Dermatology|April 1, 1997
Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosaT N Darling, J A McGrath, C Yee, et al.
The American Journal of Pathology|February 13, 2001
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyJ W Bauer, F Rouan, B Kofler, et al.
Pageof 13

Showing results (111-120 of 121) with videos related to

Sort By:
Pageof 13
The Journal of Investigative Dermatology|February 11, 1998
Cycloheximide facilitates the identification of aberrant transcripts resulting from a novel splice-site mutation in COL17A1 in a patient with generalized atrophic benign epidermolysis bullosaT N Darling, C Yee, B Koh, et al.
The Journal of Investigative Dermatology|February 11, 1998
A deletion mutation in COL17A1 in five Austrian families with generalized atrophic benign epidermolysis bullosa represents propagation of an ancestral alleleT N Darling, B B Koh, S J Bale, et al.
Mechanisms of Ageing and Development|April 21, 2010
Aberrant heterodimerization of keratin 16 with keratin 6A in HaCaT keratinocytes results in diminished cellular migrationA Trost, P Desch, V Wally, et al.
The British Journal of Dermatology|December 3, 1999
Ocular involvement in IgA-epidermolysis bullosa acquisitaJ W Bauer, H Schaeppi, D Metze, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 29, 2010
Nosocomial Staphylococcal scalded skin syndrome caused by intra-articular injectionM Emberger, J Koller, M Laimer, et al.
Actas Dermo-Sifiliograficas|October 23, 2010
[Immunofluorescence mapping for diagnosis of congenital epidermolysis bullosa]R Cepeda-Valdés, G Pohla-Gubo, J R Borbolla-Escoboza, et al.
European Journal of Ophthalmology|December 28, 2006
Ocular involvement in anti-epiligrin cicatricial pemphigoidC Nischler, E Sadler, Z Lazarova, et al.
The Journal of Investigative Dermatology|October 26, 2001
Pathogenesis of the permeability barrier abnormality in epidermolytic hyperkeratosisM Schmuth, G Yosipovitch, M L Williams, et al.
The Journal of Investigative Dermatology|April 1, 1997
Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosaT N Darling, J A McGrath, C Yee, et al.
The American Journal of Pathology|February 13, 2001
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyJ W Bauer, F Rouan, B Kofler, et al.
Pageof 13