Showing results (111-120 of 143) with videos related to
Sort By:
Pageof 15
Biochemistry|October 5, 2001
Benign synthesis of 2-ethylhexanoic acid by cytochrome P450cam: enzymatic, crystallographic, and theoretical studiesK J French, M D Strickler, D A Rock, et al.The Journal of Investigative Dermatology|May 12, 2001
Novel keratin 17 mutations in pachyonychia congenita type 2F J Smith, C M Coleman, N M Bayoumy, et al.The British Journal of Dermatology|May 8, 1999
Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literatureT Basarab, F J Smith, V M Jolliffe, et al.The Journal of Clinical Investigation|November 15, 1996
A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophyS Chavanas, L Pulkkinen, Y Gache, et al.The Journal of Investigative Dermatology|June 9, 2000
A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevusA Terrinoni, P Puddu, B Didona, et al.The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Weekly subcutaneous pegylated recombinant native human leptin (PEG-OB) administration in obese menC J Hukshorn, W H Saris, M S Westerterp-Plantenga, et al.Experimental Dermatology|May 8, 1999
A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1F J Smith, K E McKenna, A D Irvine, et al.Human Molecular Genetics|June 9, 1998
A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2F J Smith, M F Jonkman, H van Goor, et al.Human Molecular Genetics|October 1, 1996
Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophyL Pulkkinen, F J Smith, H Shimizu, et al.Obesity Research|November 1, 1995
Insulin normalization as an approach to the pharmacological treatment of obesityL A Campfield, F J Smith, G Mackie, et al.Pageof 15