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J C Salas

Showing results (11-20 of 29) with videos related to

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The British Journal of Dermatology|March 20, 2014
High levels of type VII collagen expression in recessive dystrophic epidermolysis bullosa cutaneous squamous cell carcinoma keratinocytes increases PI3K and MAPK signalling, cell migration and invasionC Pourreyron, M Chen, J A McGrath, et al.
Clinical Genetics|May 20, 2003
Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked traitM Tadin-Strapps, J C Salas-Alanis, L Moreno, et al.
Clinical and Experimental Dermatology|May 15, 2009
Sabinas syndrome in monozygotic twinsD R López-García, J C Salas-Alanis, A M Christiano, et al.
Australian Dental Journal|February 28, 2015
Clinical features of gingival lesions in patients with dystrophic epidermolysis bullosa: a cross-sectional studyG Fortuna, M Aria, R Cepeda-Valdes, 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 bullosaJ C Salas-Alanis, J E Mellerio, M Amaya-Guerra, et al.
Clinical and Experimental Dermatology|May 16, 2020
Novel p.Ala675Thr missense mutation in TRPV3 in Olmsted syndromeF P-C Chiu, J C Salas-Alanis, M Amaya-Guerra, 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.
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.
Clinical and Experimental Dermatology|March 22, 2001
Three cases of de novo dominant dystrophic epidermolysis bullosa associated with the mutation G2043R in COL7A1V Wessagowit, G H Ashton, R Mohammedi, et al.
Experimental Dermatology|April 17, 1999
A recurrent frameshift mutation in exon 19 of the type VII collagen gene (COL7A1) in Mexican patients with recessive dystrophic epidermolysis bullosaJ E Mellerio, J C Salas-Alanis, M Amaya-Guerra, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
The British Journal of Dermatology|March 20, 2014
High levels of type VII collagen expression in recessive dystrophic epidermolysis bullosa cutaneous squamous cell carcinoma keratinocytes increases PI3K and MAPK signalling, cell migration and invasionC Pourreyron, M Chen, J A McGrath, et al.
Clinical Genetics|May 20, 2003
Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked traitM Tadin-Strapps, J C Salas-Alanis, L Moreno, et al.
Clinical and Experimental Dermatology|May 15, 2009
Sabinas syndrome in monozygotic twinsD R López-García, J C Salas-Alanis, A M Christiano, et al.
Australian Dental Journal|February 28, 2015
Clinical features of gingival lesions in patients with dystrophic epidermolysis bullosa: a cross-sectional studyG Fortuna, M Aria, R Cepeda-Valdes, 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 bullosaJ C Salas-Alanis, J E Mellerio, M Amaya-Guerra, et al.
Clinical and Experimental Dermatology|May 16, 2020
Novel p.Ala675Thr missense mutation in TRPV3 in Olmsted syndromeF P-C Chiu, J C Salas-Alanis, M Amaya-Guerra, 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.
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.
Clinical and Experimental Dermatology|March 22, 2001
Three cases of de novo dominant dystrophic epidermolysis bullosa associated with the mutation G2043R in COL7A1V Wessagowit, G H Ashton, R Mohammedi, et al.
Experimental Dermatology|April 17, 1999
A recurrent frameshift mutation in exon 19 of the type VII collagen gene (COL7A1) in Mexican patients with recessive dystrophic epidermolysis bullosaJ E Mellerio, J C Salas-Alanis, M Amaya-Guerra, et al.
Pageof 3