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M J Arin

Showing results (1-10 of 14) with videos related to

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Trends in Molecular Medicine|September 1, 2001
Disease model: heritable skin blisteringM J Arin, D R Roop
The British Journal of Dermatology|August 27, 2005
Anti-CD20 monoclonal antibody (rituximab) in the treatment of pemphigusM J Arin, A Engert, T Krieg, et al.
Journal of Thrombosis and Haemostasis : JTH|February 3, 2007
More on: the 'ART' behind the clot: solving the mysteryR M Bauersachs, K Manolopoulos, I Hoppe, et al.
The Journal of Cell Biology|February 7, 2001
Focal activation of a mutant allele defines the role of stem cells in mosaic skin disordersM J Arin, M A Longley, X J Wang, et al.
Clinical and Experimental Dermatology|November 29, 2005
Chronic graft-versus-host disease with skin signs suggestive of dermatomyositisM J Arin, C Scheid, K Hübel, et al.
Experimental Dermatology|February 25, 2000
Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosisM J Arin, M A Longley, E H Epstein, et al.
The British Journal of Dermatology|January 29, 2011
Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosisM J Arin, V Oji, S Emmert, et al.
Research in Veterinary Science|July 1, 1988
Plasma protein binding of an N-pyrrolyl derivative penicillin in several mammalian speciesM T Teran, M Sierra, J J Garcia, et al.
Experimental Dermatology|May 8, 1999
An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosisM J Arin, M A Longley, W Küster, et al.
The Journal of Investigative Dermatology|March 20, 1999
A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of SiemensM J Arin, M A Longley, E H Epstein, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Trends in Molecular Medicine|September 1, 2001
Disease model: heritable skin blisteringM J Arin, D R Roop
The British Journal of Dermatology|August 27, 2005
Anti-CD20 monoclonal antibody (rituximab) in the treatment of pemphigusM J Arin, A Engert, T Krieg, et al.
Journal of Thrombosis and Haemostasis : JTH|February 3, 2007
More on: the 'ART' behind the clot: solving the mysteryR M Bauersachs, K Manolopoulos, I Hoppe, et al.
The Journal of Cell Biology|February 7, 2001
Focal activation of a mutant allele defines the role of stem cells in mosaic skin disordersM J Arin, M A Longley, X J Wang, et al.
Clinical and Experimental Dermatology|November 29, 2005
Chronic graft-versus-host disease with skin signs suggestive of dermatomyositisM J Arin, C Scheid, K Hübel, et al.
Experimental Dermatology|February 25, 2000
Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosisM J Arin, M A Longley, E H Epstein, et al.
The British Journal of Dermatology|January 29, 2011
Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosisM J Arin, V Oji, S Emmert, et al.
Research in Veterinary Science|July 1, 1988
Plasma protein binding of an N-pyrrolyl derivative penicillin in several mammalian speciesM T Teran, M Sierra, J J Garcia, et al.
Experimental Dermatology|May 8, 1999
An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosisM J Arin, M A Longley, W Küster, et al.
The Journal of Investigative Dermatology|March 20, 1999
A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of SiemensM J Arin, M A Longley, E H Epstein, et al.
Pageof 2