G A Bennett|F J Smith - JoVE Visualize

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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.

Cell|January 10, 1997

Targeted disruption of the melanocortin-4 receptor results in obesity in miceD Huszar, C A Lynch, V Fairchild-Huntress, et al.

The British Journal of Dermatology|February 21, 1998

Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated casesJ E Mellerio, F J Smith, J R McMillan, et al.

Pageof 15

Showing results (131-140 of 143) with videos related to

Sort By:

Pageof 15

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.

Cell|January 10, 1997

Targeted disruption of the melanocortin-4 receptor results in obesity in miceD Huszar, C A Lynch, V Fairchild-Huntress, et al.

The British Journal of Dermatology|February 21, 1998

Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated casesJ E Mellerio, F J Smith, J R McMillan, et al.

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