Zobrazeno 1 - 6 of 6 pro vyhledávání: '"F K, Jugert"'
1
An improved and rapid method to construct skin equivalents from human hair follicles and fibroblasts
Autor: D, Hoeller, B, Huppertz, T C, Roos, P, Poblete Gutiérrez, H F, Merk, J, Frank, F K, Jugert
Publikováno v: Experimental dermatology. 10(4)
To produce sufficient amounts of high quality skin equivalents (SE), either allogenic for dermatopharmacological and dermatotoxicological studies or autologous for transplantation purposes, we established a rapid, easy and cost effective three-dimens
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0e7515abcf5ceee1480546a2bcada272
https://pubmed.ncbi.nlm.nih.gov/11493315
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2
Molekularbiologische Untersuchungen zur Erythropoetischen Protoporphyrie: die genetische Analyse ist sensitiver und spezifischer als biochemische und klinische Untersuchungstechniken zur Diagnosefindung
Autor: G. Goerz, F. K. Jugert, H. F. Merk, H. Lam, Angela M. Christiano, Wasim Ahmad, Katrin Kalka, Jorge Frank
Publikováno v: Dermatologie an der Schwelle zum neuen Jahrtausend ISBN: 9783642630422
Die Erythropoetische Protoporphyrie (EPP) resultiert aus einer angeborenen katalytischen Defizienz der Ferrochelatase (FC), des achten Enzym der Porphyrin-Ham-Biosynthese. Die erniedrigte FC-Aktivitat fuhrt zur ubermasigen Akkumulation und Deposition
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aa2549f1d19ad73d11befca4f4b0e59a
https://doi.org/10.1007/978-3-642-57191-6_26
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3
Erythropoietic protoporphyria: identification of novel mutations in the ferrochelatase gene and comparison of biochemical markers versus molecular analysis as diagnostic strategies
Autor: J, Frank, J, Nelson, X, Wang, L, Yang, W, Ahmad, H, Lam, F K, Jugert, K, Kalka, M B, Poh-Fitzpatrick, G, Goerz, H F, Merk, A M, Christiano
Publikováno v: Journal of investigative medicine : the official publication of the American Federation for Clinical Research. 47(6)
Erythropoietic protoporphyria (EPP) results from an inherited deficiency of the last enzyme of the heme biosynthetic pathway, ferrochelatase (FC). EPP is usually inherited in an autosomal dominant fashion, and the mutations in the FC gene on chromoso
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::14e8871628d1065d65e3c2623cf32a2b
https://pubmed.ncbi.nlm.nih.gov/10431482
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4
Vitamin D3 and its synthetic analogue secocholestra-trien-1,2, 24-triol influence the metabolism and the isomerization of retinoic acid in human keratinocytes
Autor: F K, Jugert, T C, Roos, I, Notzon, H F, Merk
Publikováno v: Skin pharmacology and applied skin physiology. 11(3)
Vitamin D and vitamin A acid share metabolic pathways thereby influencing their benefit as a given drug. Little is known concerning their metabolic interactions in epidermal cells. We compared the influence of 1,25-dihydroxycholecalciferol (vitamin D
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9dd65f6178a749a15cdf164ff31e0012
https://pubmed.ncbi.nlm.nih.gov/9745143
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5
Recurrent missense mutation in the protoporphyrinogen oxidase gene underlies variegate porphyria
Autor: J, Frank, F K, Jugert, C, Breitkopf, G, Goerz, H F, Merk, A M, Christiano
Publikováno v: American journal of medical genetics. 79(1)
The porphyrias represent a heterogeneous group of disorders of porphyrin or porphyrin-precursor metabolism, resulting from the inherited or acquired dysregulation of one of the eight enzymes in the porphyrin-heme biosynthetic pathway. Variegate porph
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::52bec07c045417dda3b2ba7e01413fa4
https://pubmed.ncbi.nlm.nih.gov/9738863
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