Published in Dev Dyn on February 01, 1994
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The role of heparan sulphate in development: the ectodermal story. Int J Exp Pathol (2016) 0.75
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Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry. J Am Acad Dermatol (1991) 2.79
Altered triple helical structure of type I procollagen in lethal perinatal osteogenesis imperfecta. J Biol Chem (1985) 2.45
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Assembly of stratum corneum basic protein and keratin filaments in macrofibrils. Nature (1978) 1.96
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Abnormal alpha 2-chain in type I collagen from a patient with a form of osteogenesis imperfecta. J Clin Invest (1983) 1.71
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X-linked cutis laxa: defective cross-link formation in collagen due to decreased lysyl oxidase activity. N Engl J Med (1980) 1.62
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Comparison of endovascular and conventional vascular prostheses in an experimental infection model. J Vasc Surg (1996) 1.45
Abnormal collagen fibril structure in the gravis form (type I) of Ehlers-Danlos syndrome. Lab Invest (1979) 1.36
Heterozygosity for a large deletion in the alpha 2(I) collagen gene has a dramatic effect on type I collagen secretion and produces perinatal lethal osteogenesis imperfecta. J Biol Chem (1988) 1.34
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Regional differences in the thickness (cell layers) of the human stratum corneum: an ultrastructural analysis. J Invest Dermatol (1974) 1.31
Heterogeneity in harlequin ichthyosis, an inborn error of epidermal keratinization: variable morphology and structural protein expression and a defect in lamellar granules. J Invest Dermatol (1990) 1.23
Immunolocalization of epidermal growth factor receptors in normal developing human skin. J Invest Dermatol (1990) 1.23
The fine structure of developing human epidermis: light, scanning, and transmission electron microscopy of the periderm. J Invest Dermatol (1975) 1.23
Topical ocular antibiotics induce bacterial resistance at extraocular sites. Br J Ophthalmol (2005) 1.22
Genetic disorders of collagen metabolism. Adv Hum Genet (1982) 1.22
Structural abnormalities in the dermal collagen and elastic matrix from the skin of patients with inherited connective tissue disorders. J Invest Dermatol (1982) 1.22
Palmar-plantar keratoderma. A clinical, ultrastructural, and biochemical study. J Am Acad Dermatol (1988) 1.20
Pregnancy complications in type IV Ehlers-Danlos Syndrome. Lancet (1983) 1.16
Ichthyosis vulgaris: identification of a defect in synthesis of filaggrin correlated with an absence of keratohyaline granules. J Invest Dermatol (1985) 1.14
Properties of carcinogen altered mouse epidermal cells resistant to calcium-induced terminal differentiation. Carcinogenesis (1983) 1.13
Collagen types I, III, and V in human embryonic and fetal skin. Am J Anat (1986) 1.11
Abnormal lamellar granules in harlequin ichthyosis. J Invest Dermatol (1992) 1.10
A collagen and elastic network in the wing of the bat. J Anat (1978) 1.09
Periderm cells form cornified cell envelope in their regression process during human epidermal development. J Invest Dermatol (1999) 1.06
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Profilaggrin, a high-molecular-weight precursor of filaggrin in human epidermis and cultured keratinocytes. J Invest Dermatol (1985) 1.03
Infantile systemic hyalinosis in a black infant. Pediatr Dermatol (1994) 1.03
Prenatal diagnosis of lethal perinatal osteogenesis imperfecta (OI type II). J Pediatr (1982) 1.01
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Community treatment with azithromycin for trachoma is not associated with antibiotic resistance in Streptococcus pneumoniae at 1 year. Br J Ophthalmol (2003) 1.00
Structure of the dermal matrix during development and in the adult. J Invest Dermatol (1982) 1.00
A new variety of spondyloepiphyseal dysplasia characterized by punctate corneal dystrophy and abnormal dermal collagen fibrils. Hum Genet (1978) 0.99
Phenotypic expression of epidermal cells in vitro: a review. J Invest Dermatol (1983) 0.98
Postinflammatory elastolysis and cutis laxa. A case report. J Am Acad Dermatol (1990) 0.98
Arrested epidermal morphogenesis in three newborn infants with a fatal genetic disorder (restrictive dermopathy). J Invest Dermatol (1987) 0.97
Dermatosparaxis in a Himalayan cat: I. Biochemical studies of dermal collagen. J Invest Dermatol (1980) 0.97
Dermatosparaxis in a Himalayan cat: II. Ultrastructural studies of dermal collagen. J Invest Dermatol (1980) 0.97
Mouse differentiation-specific keratins 1 and 10 require a preexisting keratin scaffold to form a filament network. J Cell Biol (1993) 0.96
Characteristic morphologic abnormality of harlequin ichthyosis detected in amniotic fluid cells. J Invest Dermatol (1994) 0.96
Fatal cardiovascular disease and cutis laxa following acute febrile neutrophilic dermatosis. J Pediatr (1983) 0.96
Label-retaining cells in human embryonic and fetal epidermis. J Invest Dermatol (1987) 0.96
Ontogeny of structural components at the dermal-epidermal junction in human embryonic and fetal skin: the appearance of anchoring fibrils and type VII collagen. J Invest Dermatol (1988) 0.95
Structure of the human fetal hair canal and initial hair eruption. J Invest Dermatol (1978) 0.95
Epidermolytic hyperkeratosis: ultrastructure and biochemistry of skin and amniotic fluid cells from two affected fetuses and a newborn infant. J Invest Dermatol (1983) 0.94
Human epidermal embryogenesis. Int J Dermatol (1979) 0.94
Factors influencing calcium-induced terminal differentiation in cultured mouse epidermal cells. J Cell Physiol (1983) 0.92
Characterization of hair follicle bulge in human fetal skin: the human fetal bulge is a pool of undifferentiated keratinocytes. J Invest Dermatol (1995) 0.92
Abnormal epidermal keratinization in the repeated epilation mutant mouse. J Cell Biol (1982) 0.91
Immunolocalization of FXIIIa+ dendritic cells in human burn wounds. J Surg Res (1995) 0.91
Molecular pathology in inherited disorders of collagen metabolism. Hum Pathol (1982) 0.89
Regional difference in expression of characteristic abnormality of harlequin ichthyosis in affected fetuses. Prenat Diagn (1998) 0.89
Ultrastructural characteristics of the skin in a form of the Ehlers-Danlos syndrome type IV. Storage in the rough endoplasmic reticulum. Lab Invest (1981) 0.88
The fine structure of the bursa of Fabricius: "B" cell surface configuration and lymphoepithelial organization as revealed by scanning and transmission electron microscopy. J Reticuloendothel Soc (1974) 0.88
Prenatal diagnosis and screening. Dermatol Clin (1987) 0.87
The appearance of four basement membrane zone antigens in developing human fetal skin. J Invest Dermatol (1984) 0.87
Growth factor and growth factor receptor localization in the hair follicle bulge and associated tissue in human fetus. J Invest Dermatol (1996) 0.86
Werner's syndrome. Evidence for preferential regional expression of a generalized mesenchymal cell defect. Arch Dermatol (1988) 0.86
Stratum corneum basic protein: an interfilamentous matrix protein of epidermal keratin. Curr Probl Dermatol (1980) 0.86
The appearance, density, and distribution of Merkel cells in human embryonic and fetal skin: their relation to sweat gland and hair follicle development. J Invest Dermatol (1995) 0.86
Keratinocytes cultured from subjects with ichthyosis vulgaris are phenotypically abnormal. J Invest Dermatol (1987) 0.86
An electron and light microscope study on the caecal tonsil: the basic unit of the caecal tonsil. Dev Comp Immunol (1981) 0.85
Regional development of the human epidermis in the first trimester embryo and the second trimester fetus (ages related to the timing of amniocentesis and fetal biopsy). J Invest Dermatol (1980) 0.84
Ultrastructural aspects of human skin during the embryonic, fetal, premature, neonatal, and adult periods of life. Birth Defects Orig Artic Ser (1981) 0.84
Cutis laxa. Johns Hopkins Med J (1982) 0.82
Age-related changes in collagenase expression in cultured embryonic and fetal human skin fibroblasts. Exp Cell Res (1985) 0.82
Potassium mediation of calcium-induced terminal differentiation of epidermal cells in culture. J Invest Dermatol (1983) 0.82
Embryogenesis of the dermis in human skin. Pediatr Dermatol (1986) 0.82
Restrictive dermopathy. Report of two affected siblings and a review of the literature. Arch Dermatol (1992) 0.82
Antisense profilaggrin RNA delays and decreases profilaggrin expression and alters in vitro differentiation of rat epidermal keratinocytes. J Invest Dermatol (1993) 0.82
Ontogeny of Langerhans cells in human embryonic and fetal skin: cell densities and phenotypic expression relative to epidermal growth. Am J Anat (1989) 0.81
Ontogeny and characterization of factor XIIIa+ cells in developing human skin. Anat Embryol (Berl) (1996) 0.80
Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis). Br J Dermatol (1994) 0.80
Congenital migratory ichthyosiform dermatosis with neurologic and ophthalmologic abnormalities. Arch Dermatol (1985) 0.80
Contact sites between lymphoid cells of the bursa of Fabricius, in vivo and in vitro. Anat Rec (1977) 0.80
Prenatal diagnosis of Herlitz junctional epidermolysis bullosa by amniocentesis. Prenat Diagn (1995) 0.80
Molecular mechanisms of connective tissue abnormalities in the Ehlers-Danlos syndrome. Coll Relat Res (1981) 0.80
Molecular basis of clinical heterogeneity in the Ehlers-Danlos syndrome. Ann N Y Acad Sci (1985) 0.80
Heterogeneity of elastin expression in cutis laxa fibroblast strains. J Invest Dermatol (1989) 0.79
Platelet adherence in endothelial cell cultures. Blood Vessels (1979) 0.79
Antenatal diagnosis of recessive dystrophic epidermolysis bullosa: collagenase expression in cultured fibroblasts as a biochemical marker. J Invest Dermatol (1986) 0.79
Electron microscopy as an aid to diagnosis of disorders of the extracellular matrix: a new type of spondyloepiphyseal dysplasia. Birth Defects Orig Artic Ser (1978) 0.79
Development of human embryonic and fetal dermal vasculature. J Invest Dermatol (1989) 0.79
Skin lipid content during early fetal development. J Invest Dermatol (1988) 0.79
The structure and function of dermal connective tissue in normal individuals and patients with inherited connective tissue disorders. Scan Electron Microsc (1982) 0.78
Embedding prolene for the development of fiducial markers. Anat Rec (1989) 0.78
The nerve-dependency of Merkel cell proliferation in cultured human fetal glabrous skin. Yonsei Med J (2001) 0.78
Repeated epilation (ER): a semidominant autosomal gene reducing synthesis of skin filaggrin in mice. Prog Clin Biol Res (1982) 0.78
Developmental expression of human epidermal keratins and filaggrin. Curr Top Dev Biol (1987) 0.78
Morphometric and statistical analyses describing the in utero growth of human epidermis. Anat Rec (1988) 0.78
Familial pityriasis rubra pilaris. Arch Dermatol (1995) 0.78
Prenatal diagnosis of congenital non-bullous ichthyosiform erythroderma (lamellar ichthyosis). Prenat Diagn (1987) 0.77
Cell surface and cytoskeletal changes associated with epidermal stratification and differentiation in organ cultures of embryonic human skin. Dev Biol (1987) 0.77
Proliferation of human embryonic and fetal epidermal cells in organ culture. Am J Anat (1986) 0.77
Biochemical examination of fetal skin biopsy specimens obtained by fetoscopy: use of the method for analysis of keratins and filaggrin. Prenat Diagn (1986) 0.77