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S Munro

Showing results (301-310 of 335) with videos related to

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The Journal of Investigative Dermatology|October 3, 1999
Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotypeB P Korge, H Hamm, C S Jury, et al.
The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.
The Journal of Investigative Dermatology|February 18, 2011
Filaggrin null mutations are not a protective factor for acne vulgarisJohn E A Common, Sara J Brown, Rebecca L Haines, et al.
The British Journal of Dermatology|April 1, 1997
Treatment of psoriasis with intermittent short course cyclosporin (Neoral). A multicentre studyJ Berth-Jones, C A Henderson, C S Munro, et al.
Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, et al.
Experimental Dermatology|August 10, 1999
Point mutation in the helix termination peptide (HTP) of human type II hair keratin hHb6 causes monilethrix in five familiesB P Korge, E Healy, H Traupe, et al.
The Journal of General Virology|January 7, 2020
Characterization of ranaviruses isolated from lumpfish <i>Cyclopterus lumpus</i> L. in the North Atlantic area: proposal for a new ranavirus species (European North Atlantic Ranavirus)Hannah E B Stagg, Sigríður Guðmundsdóttir, Niccolò Vendramin, et al.
The Journal of Investigative Dermatology|February 10, 2012
Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skinAileen Sandilands, Sara J Brown, Christabelle S Goh, et al.
American Journal of Human Genetics|July 9, 2013
Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratodermaDiana C Blaydon, Lisbet K Lind, Vincent Plagnol, et al.
Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.
Pageof 34

Showing results (301-310 of 335) with videos related to

Sort By:
Pageof 34
The Journal of Investigative Dermatology|October 3, 1999
Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotypeB P Korge, H Hamm, C S Jury, et al.
The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.
The Journal of Investigative Dermatology|February 18, 2011
Filaggrin null mutations are not a protective factor for acne vulgarisJohn E A Common, Sara J Brown, Rebecca L Haines, et al.
The British Journal of Dermatology|April 1, 1997
Treatment of psoriasis with intermittent short course cyclosporin (Neoral). A multicentre studyJ Berth-Jones, C A Henderson, C S Munro, et al.
Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, et al.
Experimental Dermatology|August 10, 1999
Point mutation in the helix termination peptide (HTP) of human type II hair keratin hHb6 causes monilethrix in five familiesB P Korge, E Healy, H Traupe, et al.
The Journal of General Virology|January 7, 2020
Characterization of ranaviruses isolated from lumpfish <i>Cyclopterus lumpus</i> L. in the North Atlantic area: proposal for a new ranavirus species (European North Atlantic Ranavirus)Hannah E B Stagg, Sigríður Guðmundsdóttir, Niccolò Vendramin, et al.
The Journal of Investigative Dermatology|February 10, 2012
Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skinAileen Sandilands, Sara J Brown, Christabelle S Goh, et al.
American Journal of Human Genetics|July 9, 2013
Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratodermaDiana C Blaydon, Lisbet K Lind, Vincent Plagnol, et al.
Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.
Pageof 34