L. Smith

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Mutations in the COL3A1 gene result in the Ehlers-Danlos syndrome type IV and alterations in the size and distribution of the major collagen fibrils of the dermis.

P. Byers, U. Schwarze, J. Goldstein, 1997, The Journal of investigative dermatology.

Structure of the dermal matrix during development and in the adult.

P. Byers, K. Holbrook, L. Smith, 1982, The Journal of investigative dermatology.

Expression of amphiregulin is regulated in cultured human keratinocytes and in developing fetal skin.

R. Underwood, M. Piepkorn, L. Smith, 1995, The Journal of investigative dermatology.

Prevalence of hypopigmented macules in a healthy population.

R. Pagon, V. Sybert, S. Vanderhooft, 1996, The Journal of pediatrics.

Marfan syndrome: abnormal alpha 2 chain in type I collagen.

P. Byers, D. Rowe, K. Holbrook, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.

K. Stephens, M. Weaver, V. Sybert, 1999, American journal of human genetics.

Ultrastructural findings in epidermolysis bullosa.

L. Smith, Lynne T. Smith, 1993, Archives of dermatology.

Prenatal diagnosis of genetic skin disease using fetal skin biopsy samples.

K. Holbrook, S. Elias, L. Smith, 1993, Archives of dermatology.

Expression of a truncated keratin 5 may contribute to severe palmar--plantar hyperkeratosis in epidermolysis bullosa simplex patients.

R. Livingston, K. Stephens, V. Sybert, 2001, The Journal of investigative dermatology.

Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in the COL1A1 and COL1A2 genes of type I collagen.

S. Krane, P. Byers, R. Matalon, 1997, American journal of medical genetics.

Outcome after surgical repair of junctional epidermolysis bullosa-pyloric atresia syndrome: a report of 3 cases and review of the literature.

V. Sybert, J. Waldhausen, L. Smith, 1999, Archives of dermatology.

Expression of transglutaminase activity in developing human epidermis

M. Akiyama, H. Shimizu, L. Smith, 2000, The British journal of dermatology.

E. Bauer, K. Holbrook, G. Stricklin, 1985, Experimental cell research.

Altered secretion of type III procollagen in a form of type IV Ehlers-Danlos syndrome. Biochemical studies in cultured fibroblasts.

G. Barsh, P. Byers, K. Holbrook, 1981, Laboratory investigation; a journal of technical methods and pathology.

Mitochondrial ultrastructure in embryos after implantation.

T. Shepard, L. Muffley, L. Smith, 2000, Human reproduction.

Regional difference in expression of characteristic abnormality of harlequin ichthyosis in affected fetuses

M. Akiyama, H. Shimizu, K. Holbrook, 1998, Prenatal diagnosis.

Buschke-Ollendorff syndrome associated with elevated elastin production by affected skin fibroblasts in culture.

F. Arnett, J. Davidson, M. Duvic, 1992, The Journal of investigative dermatology.

Intra-epidermal retention of type VII collagen in a patient with recessive dystrophic epidermolysis bullosa.

V. Sybert, L. Smith, 1990, The Journal of investigative dermatology.

Ontogeny of structural components at the dermal-epidermal junction in human embryonic and fetal skin: the appearance of anchoring fibrils and type VII collagen.

R. Burgeson, K. Holbrook, L. Sakai, 1988, The Journal of investigative dermatology.

The appearance of four basement membrane zone antigens in developing human fetal skin.

K. Holbrook, S. Katz, J. Fine, 1984, The Journal of investigative dermatology.

Growth factor and growth factor receptor localization in the hair follicle bulge and associated tissue in human fetus.

M. Akiyama, K. Holbrook, L. Smith, 1996, The Journal of investigative dermatology.

Collagen types I, III, and V in human embryonic and fetal skin.

K. Holbrook, J. Madri, L. Smith, 1986, The American journal of anatomy.

Dermatosparaxis in children. A case report and review of the newly recognized phenotype.

M. Seashore, E. Petty, I. Braverman, 1993, Archives of dermatology.

Initial observations of human dermatosparaxis: Ehlers-Danlos syndrome type VIIC.

P. Byers, W. Wertelecki, L. Smith, 1992, The Journal of pediatrics.

Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen.

M. Seashore, E. Petty, I. Braverman, 1992, American journal of human genetics.

Prenatal detection of epidermolysis bullosa letalis with pyloric atresia in a fetus by abnormal ultrasound and elevated alpha-fetoprotein.

V. Sybert, L. Smith, C. Dolan, 1993, American journal of medical genetics.

Dystrophic epidermolysis bullosa inversa: report of two cases with further correlation between electron microscopic and immunofluorescence studies.

J. Fine, A. Lin, L. Smith, 1995, Journal of the American Academy of Dermatology.

Partial COL1A2 gene duplication produces features of osteogenesis imperfecta and Ehlers-Danlos syndrome type VII

P. Byers, W. Craigen, D. Keene, 1999, Human Genetics.

Periderm cells form cornified cell envelope in their regression process during human epidermal development.

M. Akiyama, H. Shimizu, K. Holbrook, 1999, The Journal of investigative dermatology.

Patterns of type VI collagen compared to types I, III and V collagen in human embryonic and fetal skin and in fetal skin-derived cell cultures.

L. Smith, 1994, Matrix biology : journal of the International Society for Matrix Biology.

Changing patterns of localization of putative stem cells in developing human hair follicles.

M. Akiyama, H. Shimizu, L. Smith, 2000, The Journal of investigative dermatology.

Trichodysplasia spinulosa--a newly described folliculocentric viral infection in an immunocompromised host.

J. Sundberg, S. E. Miller, D. Howell, 1999, The journal of investigative dermatology. Symposium proceedings.

Development of dermal connective tissue in human embryonic and fetal skin.

K. Holbrook, L. Smith, 1982, Scanning electron microscopy.

Embryogenesis of the Dermis in Human Skin

K. Holbrook, L. Smith, 1986, Pediatric dermatology.

A common uptake system for serotonin and dopamine in human platelets.

G S Omenn, G. Omenn, L T Smith, 1978, The Journal of clinical investigation.

Histopathologic characteristics and ultrastructure of aging skin.

L. Smith, 1989, Cutis.

Transglutaminase and major cornified cell envelope precursor proteins, loricrin, small proline-rich proteins 1 and 2, and involucrin are coordinately expressed in the sites defined to form hair canal in developing human hair follicle.

M. Akiyama, H. Shimizu, K. Holbrook, 1999, Experimental dermatology.

Basic fibroblast growth factor enhances the coupling of intimal hyperplasia and proliferation of vasa vasorum in injured rat arteries.

E. Edelman, M. Nugent, M. Karnovsky, 1992, The Journal of clinical investigation.

Expression of morphogens during human follicle development in vivo and a model for studying follicle morphogenesis in vitro.

K. Holbrook, R. Underwood, S. Minami, 1993, The Journal of investigative dermatology.

Severe perinatal Marfan syndrome.

N. Glass, M. Duvic, H. Rosenberg, 1989, Pediatrics.

Localization of type I human skin collagenase in developing embryonic and fetal skin.

E. Bauer, K. McGowan, L. Smith, 1994, The Journal of investigative dermatology.

Two-dimensional fourier analysis of electron micrographs of human skin for quantification of the collagen fiber organization in the dermis.

S. Vaezy, L. Smith, J. Clark, 1995, Journal of Electron Microscopy.

Markers of adult skin expressed in the skin of the first trimester fetus.

E. Bauer, K. Holbrook, C. A. Foster, 1987, Current problems in dermatology.

Ultrastructural aspects of human skin during the embryonic, fetal, premature, neonatal, and adult periods of life.

K. Holbrook, L. Smith, 1981, Birth defects original article series.

The natural history of human dermatosparaxis (Ehlers‐Danlos syndrome type VIIC)

B. Lake, L. Smith, M. Rossiter, 1995, Clinical dysmorphology.