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High levels of oxysterol sulfates in serum of patients with steroid sulfatase deficiency.
Not available
S-EPMC4306693
|
biostudies-literature
Cite
Oral liarozole in the treatment of patients with moderate/severe lamellar ichthyosis: results of a randomized, double-blind, multinational, placebo-controlled phase II/III trial.
Not available
S-EPMC4232915
|
biostudies-literature
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Topical enzyme-replacement therapy restores transglutaminase 1 activity and corrects architecture of transglutaminase-1-deficient skin grafts.
Not available
S-EPMC3791258
|
biostudies-literature
Cite
Long-term faithful recapitulation of transglutaminase 1-deficient lamellar ichthyosis in a skin-humanized mouse model, and insights from proteomic studies.
Not available
S-EPMC3375344
|
biostudies-literature
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Mutations in ASPRV1 Cause Dominantly Inherited Ichthyosis.
Not available
S-EPMC7332602
|
biostudies-literature
Cite
Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13.
Not available
S-EPMC1287873
|
biostudies-literature
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Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients.
Not available
S-EPMC2593025
|
biostudies-literature
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Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion.
Not available
S-EPMC3188842
|
biostudies-literature
Cite
Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease.
Not available
S-EPMC2917721
|
biostudies-literature
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Psoriasis is associated with increased beta-defensin genomic copy number.
Not available
S-EPMC2447885
|
biostudies-literature
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