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The Journal of Investigative Dermatology
|
July 18, 2009
Keratin K6c mutations cause focal palmoplantar keratoderma
Neil J Wilson, Andrew G Messenger, Sancy A Leachman, et al.
Archives of Dermatology
|
May 18, 2011
Paternal germ cell mosaicism in autosomal dominant pachyonychia congenita
Lana N Pho, Frances J D Smith, David Konecki, et al.
The Journal of Investigative Dermatology
|
March 10, 2012
Generic and personalized RNAi-based therapeutics for a dominant-negative epidermal fragility disorder
Deena M Leslie Pedrioli, Dun Jack Fu, Emilio Gonzalez-Gonzalez, et al.
The Journal of Investigative Dermatology
|
July 28, 2007
Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis
Haihui Liao, Alex J Waters, David R Goudie, et al.
The Journal of Investigative Dermatology
|
September 1, 2007
Development of therapeutic siRNAs for pachyonychia congenita
Frances J D Smith, Robyn P Hickerson, Jane M Sayers, et al.
The Journal of Allergy and Clinical Immunology
|
May 29, 2007
Filaggrin null mutations are associated with increased asthma severity in children and young adults
Colin N A Palmer, Tahmina Ismail, Simon P Lee, et al.
Journal of the American Academy of Dermatology
|
May 24, 2011
An appraisal of oral retinoids in the treatment of pachyonychia congenita
Robert Gruber, Michael Edlinger, Roger L Kaspar, et al.
The Journal of Investigative Dermatology
|
August 22, 2013
Keratin 9 is required for the structural integrity and terminal differentiation of the palmoplantar epidermis
Dun Jack Fu, Calum Thomson, Declan P Lunny, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
January 7, 2009
Keratin 7 promoter selectively targets transgene expression to normal and neoplastic pancreatic ductal cells in vitro and in vivo
Judit Pujal, Meritxell Huch, Anabel José, et al.
Investigative Ophthalmology & Visual Science
|
December 13, 2012
Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy
Edwin H A Allen, Sarah D Atkinson, Haihui Liao, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 52) with videos related to
Sort By:
Page
of 6
The Journal of Investigative Dermatology
|
July 18, 2009
Keratin K6c mutations cause focal palmoplantar keratoderma
Neil J Wilson, Andrew G Messenger, Sancy A Leachman, et al.
Archives of Dermatology
|
May 18, 2011
Paternal germ cell mosaicism in autosomal dominant pachyonychia congenita
Lana N Pho, Frances J D Smith, David Konecki, et al.
The Journal of Investigative Dermatology
|
March 10, 2012
Generic and personalized RNAi-based therapeutics for a dominant-negative epidermal fragility disorder
Deena M Leslie Pedrioli, Dun Jack Fu, Emilio Gonzalez-Gonzalez, et al.
The Journal of Investigative Dermatology
|
July 28, 2007
Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis
Haihui Liao, Alex J Waters, David R Goudie, et al.
The Journal of Investigative Dermatology
|
September 1, 2007
Development of therapeutic siRNAs for pachyonychia congenita
Frances J D Smith, Robyn P Hickerson, Jane M Sayers, et al.
The Journal of Allergy and Clinical Immunology
|
May 29, 2007
Filaggrin null mutations are associated with increased asthma severity in children and young adults
Colin N A Palmer, Tahmina Ismail, Simon P Lee, et al.
Journal of the American Academy of Dermatology
|
May 24, 2011
An appraisal of oral retinoids in the treatment of pachyonychia congenita
Robert Gruber, Michael Edlinger, Roger L Kaspar, et al.
The Journal of Investigative Dermatology
|
August 22, 2013
Keratin 9 is required for the structural integrity and terminal differentiation of the palmoplantar epidermis
Dun Jack Fu, Calum Thomson, Declan P Lunny, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
January 7, 2009
Keratin 7 promoter selectively targets transgene expression to normal and neoplastic pancreatic ductal cells in vitro and in vivo
Judit Pujal, Meritxell Huch, Anabel José, et al.
Investigative Ophthalmology & Visual Science
|
December 13, 2012
Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy
Edwin H A Allen, Sarah D Atkinson, Haihui Liao, et al.
Page
of 6