J T Hernandez|F J Smith - JoVE Visualize

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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.

Journal of Bacteriology|May 1, 1980

Location of the multivalent control site for the ilvEDA operon of Escherichia coliD J Gayda, T D Leathers, J D Noti, et al.

Nature Genetics|November 1, 1993

Missing links: Weber-Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton functionE L Rugg, S M Morley, F J Smith, et al.

The American Journal of Physiology|February 1, 1997

Central infusion of GLP-1, but not leptin, produces conditioned taste aversions in ratsT E Thiele, G Van Dijk, L A Campfield, et al.

The Journal of Investigative Dermatology|November 6, 1998

Genomic organization and fine mapping of the keratin 2e gene (KRT2E): K2e V1 domain polymorphism and novel mutations in ichthyosis bullosa of SiemensF J Smith, C Maingi, S P Covello, et al.

The Journal of Investigative Dermatology|December 18, 1998

Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern IrelandS P Covello, A D Irvine, K E McKenna, et al.

Pageof 10

Showing results (71-80 of 95) with videos related to

Sort By:

Pageof 10

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.

Journal of Bacteriology|May 1, 1980

Location of the multivalent control site for the ilvEDA operon of Escherichia coliD J Gayda, T D Leathers, J D Noti, et al.

Nature Genetics|November 1, 1993

Missing links: Weber-Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton functionE L Rugg, S M Morley, F J Smith, et al.

The American Journal of Physiology|February 1, 1997

Central infusion of GLP-1, but not leptin, produces conditioned taste aversions in ratsT E Thiele, G Van Dijk, L A Campfield, et al.

The Journal of Investigative Dermatology|November 6, 1998

Genomic organization and fine mapping of the keratin 2e gene (KRT2E): K2e V1 domain polymorphism and novel mutations in ichthyosis bullosa of SiemensF J Smith, C Maingi, S P Covello, et al.

The Journal of Investigative Dermatology|December 18, 1998

Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern IrelandS P Covello, A D Irvine, K E McKenna, et al.

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