Items where Author is "Kielar, Danuta"
 | Up a level |
Article
Kielar, Danuta and Kaminski, Wolfgang E. and Liebisch, Gerhard and Piehler, Armin and Wenzel, Juergen J. and Moehle, Christoph and Heimerl, Susanne and Langmann, Thomas and Friedrich, Sven O. and Boettcher, Alfred and Barlage, Stefan and Drobnik, Wolfgang and Schmitz, Gerd (2003) Adenosine triphosphate binding cassette (ABC) transporters are expressed and regulated during terminal keratinocyte differentiation: A potential role for ABCA7 in epidermal lipid reorganization. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 121 (3). pp. 465-474. ISSN 0022-202X
Langmann, Thomas and Porsch-Özcürümez, Mustafa and Heimerl, Susanne and Probst, Mario and Moehle, Christoph and Taher, Mohammed and Borsukova, Hana and Kielar, Danuta and Kaminski, Wolfgang E. and Dittrich-Wengenroth, Elke and Schmitz, Gerd (2002) Identification of sterol-independent regulatory elements in the human ATP-binding cassette transporter A1 promoter - Role of Sp1/3, E-box binding factors, and an oncostatin M-responsive element. JOURNAL OF BIOLOGICAL CHEMISTRY, 277 (17). pp. 14443-14450. ISSN 0021-9258
Brousseau, Margaret E. and Bodzioch, Marek and Schaefer, Ernst J. and Goldkamp, Allison L. and Kielar, Danuta and Probst, Mario and Ordovas, Jose M. and Aslanidis, Charalampos and Lackner, Karl J. and Bloomfield Rubins, Hanna and Collins, Dorothea and Robins, Sander J. and Wilson, Peter W. F. and Schmitz, Gerd (2001) Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low HDL cholesterol levels and coronary heart disease. ATHEROSCLEROSIS, 154 (3). pp. 607-611. ISSN 0021-9150
Lapicka-Bodzioch, Katarzyna and Bodzioch, Marek and Kruell, Matthias and Kielar, Danuta and Probst, Mario and Kiec, Beata and Andrikovics, Hajnalka and Boettcher, Alfred and Hubacek, Jaroslav and Aslanidis, Charalampos and Suttorp, Norbert and Schmitz, Gerd (2001) Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1537 (1). pp. 42-48. ISSN 0925-4439
