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The British Journal of Dermatology|October 10, 1998
Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2S P Covello, F J Smith, J H Sillevis Smitt, et al.
The British Journal of Dermatology|December 22, 1999
Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1F J Smith, M Del Monaco, P M Steijlen, et al.
Experimental Dermatology|June 6, 2000
Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratodermaF J Smith, M P Fisher, E Healy, et al.
The American Journal of Physiology|October 1, 1996
Central infusions of leptin and GLP-1-(7-36) amide differentially stimulate c-FLI in the rat brainG Van Dijk, T E Thiele, J C Donahey, et al.
Protein Expression and Purification|March 31, 1998
Efficient secretion of biologically active recombinant OB protein (leptin) in Escherichia coli, purification from the periplasm and characterizationY Guisez, I Faché, L A Campfield, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|December 1, 1996
Intraventricular leptin reduces food intake and body weight of lean rats but not obese Zucker ratsR J Seeley, G van Dijk, L A Campfield, et al.
The Journal of Investigative Dermatology|March 12, 2002
Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenitaA Terrinoni, F J Smith, B Didona, et al.
Nature Genetics|June 1, 1997
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophyA D Irvine, L D Corden, O Swensson, et al.
The Journal of Investigative Dermatology|November 1, 1996
Effects of keratin 14 ablation on the clinical and cellular phenotype in a kindred with recessive epidermolysis bullosa simplexM F Jonkman, K Heeres, H H Pas, 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.
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