about
The expression of epidermal lipoxygenases and transglutaminase-1 is perturbed by NIPAL4 mutations: indications of a common metabolic pathway essential for skin barrier homeostasisA single-nucleotide deletion in the POMP 5' UTR causes a transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosisOn the mechanism of biosynthesis of 19-hydroxyprostaglandins of human seminal fluid and expression of cyclooxygenase-2, PGH 19-hydroxylase (CYP4F8) and microsomal PGE synthase-1 in seminal vesicles and vas deferensBiosynthesis and function of all-trans- and 9-cis-retinoic acid in parathyroid cellsVitamin A esterification in human epidermis: a relation to keratinocyte differentiationRevertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26.Retinoid receptor expression and its correlation to retinoid sensitivity in non-M3 acute myeloid leukemia blast cells.Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris.siRNA silencing of proteasome maturation protein (POMP) activates the unfolded protein response and constitutes a model for KLICK genodermatosis.13-cis-retinoic acid competitively inhibits 3 alpha-hydroxysteroid oxidation by retinol dehydrogenase RoDH-4: a mechanism for its anti-androgenic effects in sebaceous glands?The effect of two endogenous retinoids on the mRNA expression profile in human primary keratinocytes, focusing on genes causing autosomal recessive congenital ichthyosisCloning and functional studies of a splice variant of CYP26B1 expressed in vascular cellsUV irradiation and topical vitamin A modulate retinol esterification in hairless mouse epidermis.Keratinocyte-based cell assays: their potential pitfalls.Protein kinase C-dependent upregulation of miR-203 induces the differentiation of human keratinocytes.Regulation of keratin expression by retinoids.A CYP26B1 polymorphism enhances retinoic acid catabolism and may aggravate atherosclerosis.Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome.Expression of cytosolic retinoid-binding protein genes in human skin biopsies and cultured keratinocytes and fibroblasts.Cellular retinoic acid-binding protein type II is expressed in adult human osteoblasts and in adult liver.Chemical chaperones protect epidermolysis bullosa simplex keratinocytes from heat stress-induced keratin aggregation: involvement of heat shock proteins and MAP kinases.Immortalized keratinocytes derived from patients with epidermolytic ichthyosis reproduce the disease phenotype: a useful in vitro model for testing new treatments.Characterization of immortalized human epidermolysis bullosa simplex (KRT5) cell lines: trimethylamine N-oxide protects the keratin cytoskeleton against disruptive stress condition.Differential effects of UV irradiation on nuclear retinoid receptor levels in cultured keratinocytes and melanocytes.Increased retinoid signaling in vascular smooth muscle cells by proinflammatory cytokines.Induction of CD36 by all-trans retinoic acid: retinoic acid receptor signaling in the pathogenesis of atherosclerosis.The vitamin A metabolism and expression of retinoid-binding proteins differ in HaCaT cells and normal human keratinocytes.Characterization of AT-1 cardiomyocytes as a model for studies of T3 effects on cardiac cells.Vitamin A metabolism and mRNA expression of retinoid-binding protein and receptor genes in human epidermal melanocytes and melanoma cells.Either chick embryo dermis or retinoid-treated mouse dermis can initiate glandular morphogenesis from mammalian epidermal tissue.Reverse transcription-polymerase chain reaction assay demonstrates that the 9-cis retinoic acid receptor alpha is expressed in human osteoblasts.Epidermolysis bullosa simplex due to KRT5 mutations: mutation-related differences in cellular fragility and the protective effects of trimethylamine N-oxide in cultured primary keratinocytes.Immunofluorescence localization of nuclear retinoid receptors in psoriasis versus normal human skin.Increased concentrations of 3,4-didehydroretinol and retinoic acid-binding protein (CRABPII) in human squamous cell carcinoma and keratoacanthoma but not in basal cell carcinoma of the skin.The expression of cellular retinoid binding proteins in non-APL leukemic cells and its association with retinoid sensitivity.CYP26B1 plays a major role in the regulation of all-trans-retinoic acid metabolism and signaling in human aortic smooth muscle cells.Keratins 2 and 4/13 in reconstituted human skin are reciprocally regulated by retinoids binding to nuclear receptor RARalpha.Keratinocyte differentiation induced by calcium, phorbol ester or interferon-gamma elicits distinct changes in the retinoid signalling pathways.Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis.High-performance liquid chromatography of natural and synthetic retinoids in human skin samples.
P50
Q24336160-974F33EA-46F4-4792-9D0D-517E343F60FCQ24602843-DA024F59-9863-4538-9D92-68D049DC3191Q28241664-7C038A65-9F46-4AAA-BAA8-61A9DA88DC64Q28301958-958805E4-79EB-4876-98EA-9ACB27C38D33Q28332923-A2F3F43C-E45F-4AC9-9D54-E5E2EC444FC5Q30847249-F77189C5-CE95-43D8-A869-B90550FA7B4FQ32107309-A9C90D6B-B09B-429E-800B-33D496783ABDQ34099095-57718A60-B94D-4EFA-BE64-CF15AB2333C7Q34123701-C0D3508A-967A-4737-B9D9-80A883CAA1C1Q34184730-311A2ACE-5CD3-41A3-BB77-B0A3F5F9D014Q34207520-2BAC207A-1519-4008-BFB5-119540652088Q34292431-B255330D-100D-43E2-B2E2-709CB0B572CBQ34408460-A6321232-3B84-451C-9FA2-939901D6752CQ34415612-D3D91078-4814-41DE-A57C-3EAD3F4D17F2Q35003441-26340DF2-9E7D-4F41-B100-C00B069EF2EDQ35558870-B67F0368-5E7F-4139-9D6D-374F4E19E332Q36071717-8216B9DF-B120-4545-A559-14E93B575B6BQ37301205-5EE3E59A-EF61-41F2-9291-2952DAFDEED7Q38305902-6144EFF2-4B3F-4300-A32D-015AFD577234Q38323364-7E05BF3A-030A-43DD-B1AA-541EED49627AQ39559114-2CF5D6D8-5C38-42D9-984B-D9810837F84FQ39639706-51AA4E4E-D197-417A-AD68-1FB7B62ED662Q39892835-0E0D3CCA-DB2A-4F3D-A33B-312B5DAE03ABQ40539946-A6C65A9F-4D03-4EDD-85C6-B0292E13120AQ40786945-3257BCAA-5A19-49F5-85D6-05C12E86011CQ40807194-4859CEBD-78AC-4E99-9DFE-883250149B33Q40939641-419D7520-E883-4D4C-BE5B-8FAAE63399E5Q41093599-E376F2B9-6A8F-499B-8E3A-9FB8B37E60D7Q41096102-942E2B9E-F4B4-4215-BB63-ABD9F38CF05FQ41212572-6A8699B2-1829-4950-A4F6-FEE836A6DDE3Q41553893-55750B65-7F77-442D-883F-E51229982AE5Q42466779-41835363-3362-44B0-9359-5149AC68B511Q42467599-7D23EEC6-6074-49F7-B72F-B30106612F82Q42516918-09EC6D06-ACE3-4DAF-9B99-94CA81B6DA36Q42524425-D022B464-501C-4C87-AC0F-21A10924BD2FQ42981256-3B4FAC94-CB50-4EAA-9FA5-BD7DC62DEB3CQ43067702-D13C73DD-416C-47FE-A75B-2DFC9722AD1DQ43178159-BFD47FF7-2BC0-4ECA-AD40-C39D6709EA71Q43814372-EE2D4689-400E-4934-80C7-8DD4D4805B35Q43821350-AACC0B32-0904-4E21-9C63-C1459E68AF8F
P50
description
Zweeds onderzoeker
@nl
hulumtues
@sq
researcher
@en
հետազոտող
@hy
name
Hans Törmä
@ast
Hans Törmä
@en
Hans Törmä
@es
Hans Törmä
@nl
Hans Törmä
@sl
type
label
Hans Törmä
@ast
Hans Törmä
@en
Hans Törmä
@es
Hans Törmä
@nl
Hans Törmä
@sl
prefLabel
Hans Törmä
@ast
Hans Törmä
@en
Hans Törmä
@es
Hans Törmä
@nl
Hans Törmä
@sl
P1053
F-8152-2011
P106
P21
P27
P31
P3829
P496
0000-0002-3617-8551