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The Journal of Investigative Dermatology
|
December 18, 1998
Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern Ireland
S P Covello, A D Irvine, K E McKenna, et al.
The British Journal of Dermatology
|
October 10, 1998
Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
S 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 1
F 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 keratoderma
F 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 brain
G 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 characterization
Y 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 rats
R 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 congenita
A 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 dystrophy
A 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 simplex
M F Jonkman, K Heeres, H H Pas, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 117) with videos related to
Sort By:
Page
of 12
The Journal of Investigative Dermatology
|
December 18, 1998
Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern Ireland
S P Covello, A D Irvine, K E McKenna, et al.
The British Journal of Dermatology
|
October 10, 1998
Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
S 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 1
F 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 keratoderma
F 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 brain
G 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 characterization
Y 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 rats
R 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 congenita
A 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 dystrophy
A 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 simplex
M F Jonkman, K Heeres, H H Pas, et al.
Page
of 12