Search Results - "Eckl, K."

Update: advanced methods in three-dimensional organotypic tissue engineering for congenital ichthyosis and other rare keratinization disorders by Eckl, K.M.

“…ORIGINAL ARTICLE, p 1347…”
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Quality of life and clinical characteristics of self‐improving congenital ichthyosis within the disease spectrum of autosomal‐recessive congenital ichthyosis by Hake, L., Süßmuth, K., Komlosi, K., Kopp, J., Drerup, C., Metze, D., Traupe, H., Hausser, I., Eckl, K.M., Hennies, H.C., Fischer, J., Oji, V.

“…Background Autosomal‐recessive congenital ichthyosis (ARCI) is a heterogeneous group of ichthyoses presenting at birth. Self‐improving congenital ichthyosis…”
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Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations by Gruber, R., Rainer, G., Weiss, A., Udvardi, A., Thiele, H., Eckl, K.M., Schupart, R., Nürnberg, P., Zschocke, J., Schmuth, M., Volc‐Platzer, B., Hennies, H.C.

“…Summary Autosomal recessive congenital ichthyosis (ARCI) caused by mutations in CYP4F22 is very rare. CyP4F22, a protein of the cytochrome‐P450 family 4,…”
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CEDNIK syndrome results from loss-of-function mutations in SNAP29 by Fuchs-Telem, D., Stewart, H., Rapaport, D., Nousbeck, J., Gat, A., Gini, M., Lugassy, Y., Emmert, S., Eckl, K., Hennies, H.C., Sarig, O., Goldsher, D., Meilik, B., Ishida-Yamamoto, A., Horowitz, M., Sprecher, E.

“…Summary Background  CEDNIK (cerebral dysgenesis, neuropathy, ichthyosis and keratoderma) syndrome is a rare genodermatosis which was shown 5 years ago in one…”
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Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss‐of‐function mutation in CSTA by Moosbrugger‐Martinz, V., Jalili, A., Schossig, A.S., Jahn‐Bassler, K., Zschocke, J., Schmuth, M., Stingl, G., Eckl, K.M., Hennies, H.C., Gruber, R.

“…Summary Autosomal recessive exfoliative ichthyosis (AREI) results from mutations in CSTA, encoding cysteine protease inhibitor A (cystatin A). We present a…”
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Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates by ECKL, Katja Martina, STEVENS, Howard P, REIS, André, HENNIES, Hans Christian, LESTRINGANT, Gilles G, WESTENBERGER-TREUMANN, Margaretha, TRAUPE, Heiko, HINZ, Britta, FROSSARD, Philippe M, STADLER, Rudolf, LEIGH, Irene M, NÜRNBERG, Peter

“…Mal de Meleda (MDM) or keratosis palmoplantaris transgrediens of Siemens is an autosomal recessive skin disorder characterized by diffuse palmoplantar…”
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Krankheitsspezifische Hautmodelle: In-vitro-Modelle für die Entwicklung von Therapien bei angeborenen Verhornungsstörungen am Beispiel der kongenitalen Ichthyosen by Eckl, K.-M., Hennies, H.C.

“…Zusammenfassung In den letzten Jahren wurden Hautmodelle besonders für die Behandlung von Verbrennungsopfern, aber auch zur molekularen und zellbiologischen…”
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Computing support-minimal subfunctions during functional decomposition by Legl, C., Wurth, B., Eckl, K.

“…The growing popularity of look-up table (LUT)-based field programmable gate arrays (FPGA's) has renewed the interest in functional or Roth-Karp decomposition…”
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Pharmacokinetics of temocapril and temocaprilat after 14 once daily oral doses of temocapril in hypertensive patients with varying degrees of renal impairment by Püchler, K., Eckl, K. M., Fritsche, L., Renneisen, K., Neumayer, H.‐H., Sierakowski, B., Lavrijssen, A. T. J., Thomsen, T., Roots, I.

“…Aims The aim of this study was to determine the potential influence of renal impairment on the pharmacokinetics of temocapril and its pharmacologically active…”
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Voglibose has no effect on the pharmacokinetics of hydrochlorothiazide by KLEIST, P, SUZUKI, Y, THOMSEN, T, MÖLLER, M, RÖMER, A, HUCKE, H. P, KUROWSKI, M, ECKL, K. M

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Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling by Kim, Mi-Ran, Oji, Vinzenz, Valentin, Frederic, Traupe, Heiko, Nofer, Jerzy-Roch, Hausser, Ingrid, Hennies, Hans Christian, Eckl, Katja, Wudy, Stefan A, Sánchez-Guijo, Alberto, Kerschke, Laura, Fischer, Judith, Süßmuth, Kira

“…Data on vitamin D status of patients with inherited ichthyosis in Europe is scarce and unspecific concerning the genetic subtype. This study determined serum…”
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Genetic and Clinical Heterogeneity in Transgressive Palmoplantar Keratoderma by Lestringant, Gilles G., Frossard, Philippe M., Eckl, Katja-Martina, Reis, André, Hennies, Hans Christian

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Retiming sequential circuits with multiple register classes by Eckl, K., Legl, C.

“…Retiming is an efficient technique for redistributing registers in synchronous circuits in order to improve the circuit performance. However, the traditional…”
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A Boolean approach to performance-directed technology mapping for LUT-based FPGA designs by Legl, C., Wurth, B., Eckl, K.

“…This paper presents a novel Boolean approach to LUT-based FPGA technology mapping targeting high performance. At the core of the approach, we have developed a…”
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The pharmacokinetics of paroxetine in patients with liver cirrhosis by Krastev, Z, Terziivanov, D, Vlahov, V, Maleev, A, Greb, W H, Eckl, K M, Dierdorf, H D, Wolf, D

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Phase transitions in plant cuticles by Eckl, K, Gruler, H

“…The effect of temperature on wet plant cuticles has been investigated with the following techniques: Calorimetry, densitometry, spin-label…”
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Krankheitsspezifische Hautmodelle by Eckl, K.-M., Hennies, H.C.

“…In den letzten Jahren wurden Hautmodelle besonders für die Behandlung von Verbrennungsopfern, aber auch zur molekularen und zellbiologischen Aufklärung von…”
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Krankheitsspezifische Hautmodelle: In-vitro-Modelle für die Entwicklung von Therapien bei angeborenen Verhornungsstörungen am Beispiel der kongenitalen Ichthyosen by Eckl, K.-M., Hennies, H.C.

“…Zusammenfassung In den letzten Jahren wurden Hautmodelle besonders für die Behandlung von Verbrennungsopfern, aber auch zur molekularen und zellbiologischen…”
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Water permeability of plant cuticles: The effect of temperature on diffusion of water by Schönherr, J, Eckl, K, Gruler, H

“…The effect of temperature on water permeability of plant cuticles (astomatous Citrus leaf cuticles) has been investigated. The Arrhenius plot (logarithm of the…”
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CEDNIK syndrome results from loss-of-function mutations in SNAP29: CEDNIK syndrome by Fuchs-Telem, D., Stewart, H., Rapaport, D., Nousbeck, J., Gat, A., Gini, M., Lugassy, Y., Emmert, S., Eckl, K., Hennies, H.C., Sarig, O., Goldsher, D., Meilik, B., Ishida-Yamamoto, A., Horowitz, M., Sprecher, E.

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