Literature DB >> 4607617

Ultrastructure of inborn errors of keratinization. VI. Inherited ichthyoses--a model system for heterogeneities in keratinization disturbances.

I Anton-Lamprecht, U W Schnyder.   

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Year:  1974        PMID: 4607617

Source DB:  PubMed          Journal:  Arch Dermatol Forsch        ISSN: 0003-9187


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  60 in total

Review 1.  INHIBITION OF KERATINIZING STRUCTURES BY SYSTEMIC DRUGS.

Authors:  P FLESCH
Journal:  Pharmacol Rev       Date:  1963-12       Impact factor: 25.468

2.  [Studies on the phytol metabolism in lipoidosis heredopathia atactica polyneuritiformis (Refsum's syndrome). The transformation of 3H-phytol into the 3,7,11,15-tetramethylhexadecanoic acid (phytanic acid) of the plasma lipoid fractions].

Authors:  W Kahlke; H Wagener; H Dieckmann
Journal:  Klin Wochenschr       Date:  1965-12-15

3.  Electron cytochemical demonstration of sulfhydryl groups in keratohyalin granules and in the peripheral envelope of cornified cells.

Authors:  H Jessen
Journal:  Histochemie       Date:  1973

4.  [Erythrodermia ichthyosiformis congenita bullosa brocq. on the so-called granular degeneration. I. Introduction and report of cases].

Authors:  Y Ishibashi; G Klingmüller
Journal:  Arch Klin Exp Dermatol       Date:  1968-05-09

5.  A case of biphasic ichthyosiform dermatosis: light and electron microscopic study.

Authors:  H Pinkus; S Nagao
Journal:  Arch Klin Exp Dermatol       Date:  1970

6.  [Nevus verrucosus (2nd presentation)].

Authors:  Y Edelson; C Grupper; E Beltzer-Garelly; M Pruniéras
Journal:  Bull Soc Fr Dermatol Syphiligr       Date:  1970

7.  Ichthyosis vulgaris. A clinical and histopathological study of patients and their close relatives in the autosomal dominant and sex-linked forms of the disease.

Authors:  K Kuokkanen
Journal:  Acta Derm Venereol Suppl (Stockh)       Date:  1969

8.  [On the clinical aspects, histology and genetics of congenital ichthyosiform bullus erythroderma (Brocq)].

Authors:  U Gasser
Journal:  Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg       Date:  1963

9.  X-linked ichthyosis and ichthyosis vulgaris. Clinical and genetic distinctions in a second series of families.

Authors:  R S Wells; M C Jennings
Journal:  JAMA       Date:  1967-11-06       Impact factor: 56.272

Review 10.  Sjögren-Larsson syndrome. Oligophrenia--ichthyosis--di-tetraplegia.

Authors:  U Theile
Journal:  Humangenetik       Date:  1974-05-17
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  18 in total

1.  Bicomponent keratohyalin in normal human ridged skin.

Authors:  I Kastl; I Anton-Lamprecht
Journal:  Arch Dermatol Res       Date:  1990       Impact factor: 3.017

2.  Keratohyalin granules are heterogeneous in ridged and non-ridged human skin: evidence from anti-filaggrin immunogold labelling of normal skin and skin of autosomal dominant ichthyosis vulgaris patients.

Authors:  S Günzel; B Weidenthaler; I Hausser; I Anton-Lamprecht
Journal:  Arch Dermatol Res       Date:  1991       Impact factor: 3.017

3.  Desmosomes, corneosomes and desquamation. An ultrastructural study of adult pig epidermis.

Authors:  S J Chapman; A Walsh
Journal:  Arch Dermatol Res       Date:  1990       Impact factor: 3.017

4.  The effect of glycerol and humidity on desmosome degradation in stratum corneum.

Authors:  A Rawlings; C Harding; A Watkinson; J Banks; C Ackerman; R Sabin
Journal:  Arch Dermatol Res       Date:  1995       Impact factor: 3.017

5.  Prenatal diagnosis of genetic disorders of the skin by means of electron microscopy.

Authors:  I Anton-Lamprecht
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity.

Authors:  J Fischer; A Faure; B Bouadjar; C Blanchet-Bardon; A Karaduman; I Thomas; S Emre; S Cure; M Ozgüc; J Weissenbach; J F Prud'homme
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

7.  Placental steroid deficiency: association with arylsulfatase A deficiency.

Authors:  J Vidgoff; M M Buxman; L J Shapiro; R L Dimond; T G Wilson; C A Hepburn; T Tabei; W R Heinrichs
Journal:  Am J Hum Genet       Date:  1982-05       Impact factor: 11.025

8.  An ultrastructural study of epidermolytic leukoplakia.

Authors:  G Kolde; F Vakilzadeh
Journal:  Arch Dermatol Res       Date:  1983       Impact factor: 3.017

9.  Transgenic mice expressing a mutant keratin 10 gene reveal the likely genetic basis for epidermolytic hyperkeratosis.

Authors:  E Fuchs; R A Esteves; P A Coulombe
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-01       Impact factor: 11.205

10.  Ultrastructural study of the skin in Sjögren-Larsson syndrome.

Authors:  M Ito; K Oguro; Y Sato
Journal:  Arch Dermatol Res       Date:  1991       Impact factor: 3.017

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