L E King
Affiliation: Vanderbilt University
- Chlamydia pneumoniae and chronic skin wounds: a focused reviewL E King
Department of Medicine Dermatology, Nashville Veterans Administration Medical Centers, Tennessee, USA
J Investig Dermatol Symp Proc 6:233-7. 2001..Evidence that C. pneumoniae is an opportunistic pathogen in chronic skin ulcers and other inflammatory skin conditions analogous to its role in atherosclerosis is reviewed...
- Increased epidermal growth factor receptor in fsn/fsn miceL B Nanney
Department of Plastic Surgery, Vanderbilt School of Medicine, Nashville, Tennessee, USA
J Invest Dermatol 106:1169-74. 1996..Modulations of the flaky phenotype in response to injury and three different treatments suggest that fsn/fsn is a useful in vivo model for examining new treatment modalities for psoriasiform skin diseases...
- Tamoxifen-induced remission of psoriasisA S Boyd
Department of Medicine Dermatology, Vanderbilt University, Nashville, Tennessee, USA
J Am Acad Dermatol 41:887-9. 1999..Several lines of evidence suggest that female sex hormones such as estrogen and progesterone affect this condition. We describe a patient whose psoriasis responded favorably to administration of the antiestrogen compound tamoxifen...
- Differentiating keratinocytes express a novel cytochrome P450 enzyme, CYP2B19, having arachidonate monooxygenase activityD S Keeney
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232 0146, USA
J Biol Chem 273:32071-9. 1998....
- Cutaneous ultrastructural features of the flaky skin (fsn) mouse mutationK Morita
Department of Medicine, Vanderbilt School of Medicine, Nashville, TN, USA
J Dermatol 22:385-95. 1995..This constellation of ultrastructural aberrations is typically found in psoriasis vulgaris and supports the theory that the flaky skin mouse mutation is a naturally occurring analog to one variety of human psoriasis vulgaris...
- Radiographic joint damage in rheumatoid arthritis is associated with differences in cartilage turnover and can be predicted by serum biomarkers: an evaluation from 1 to 4 years after diagnosisS M M Verstappen
Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, The Netherlands
Arthritis Res Ther 8:R31. 2006....
- What is the 'true' function of skin?C M Chuong
Department of Pathology, University of Southern California, Los Angeles, 90033, USA
Exp Dermatol 11:159-87. 2002....
- Histologic features of actinic keratoses in solid organ transplant recipients and healthy controlsA S Boyd
Department of Medicine, Division of Dermatology, and the Department of Pathology, Vanderbilt University, Nashville, TN, USA
J Am Acad Dermatol 45:217-21. 2001..CONCLUSION: Certain histopathologic features are more common in AKs of immunosuppressed transplant recipients and may be used to distinguish between those removed from otherwise healthy persons...
- Massive xanthomatosis and altered composition of atherosclerotic lesions in hyperlipidemic mice lacking acyl CoA:cholesterol acyltransferase 1M Accad
Gladstone Institute of Cardiovascular Disease, San Francisco, California 94141, USA
J Clin Invest 105:711-9. 2000....
- Epidermal growth factor receptors in genetically induced hyperproliferative skin disordersL B Nanney
Department of Plastic Surgery and Cell Biology, Vanderbilt University, Nashville, Tennessee
Pediatr Dermatol 7:256-65. 1990..The finding that EGF-R levels are not always increased in congenital epidermal disorders indicated that the presence of this receptor pathway is not simply a marker for aberrant epidermis...
- The genetic basis of "Scarsdale Gourmet Diet" variegate porphyria: a missense mutation in the protoporphyrinogen oxidase geneJ Frank
Department of Dermatology, Columbia University, College of Physicians and Surgeons, New York, NY 10032, USA
Arch Dermatol Res 290:441-5. 1998..Our study established that a missense mutation in the PPO gene was the underlying mutation in this patient with VP and explained the occurrence of the phenotype in this family...
- Lanceolate hair (lah): a recessive mouse mutation with alopecia and abnormal hairX Montagutelli
Unite de Genetique des Mammiferes, Institut Pasteur, Paris, France
J Invest Dermatol 107:20-5. 1996..These features are found in the Netherton's syndrome of the human, for which this mouse mutation may represent a model. The lah mutation has been localized to the centromeric end of mouse Chromosome 18...
- Transgenic mice as a model to study the role of TGF-beta-related molecules in hair folliclesM Blessing
Department of Cell Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232
Genes Dev 7:204-15. 1993....
- Defects of pelage hairs in 20 mouse mutationsM E Hogan
Jackson Laboratory, Bar Harbor, ME 04609 1500, USA
J Invest Dermatol 104:31S-32S. 1995
- Reactive site-dependent phenotypic alterations in plasminogen activator inhibitor-1 transgenic miceM Eren
Division of Cardiovascular Medicine, Department of Medicine and Pharmacology, Vanderbilt University Medical Center, Nashville, TN 37232, USA
J Thromb Haemost 5:1500-8. 2007....