Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Sebastian Weidinger"'
Autor:
Sebastian Weidinger, Benjamin Kaltenbach, Lukas Lenga, Rouben Czwikla, Moritz H. Albrecht, Simon S. Martin, Julian L. Wichmann, Thomas J. Vogl
Publikováno v:
Investigative radiology. 53(3)
Objectives The aim of this study was to investigate the value of third-generation dual-source dual-energy computed tomography (DECT) iodine and fat quantification in differentiating adrenal gland adenomas from metastases. Materials and methods Sixty-
Publikováno v:
Pediatric Pulmonology. 18:3-7
In cystic fibrosis (CF) neutrophil released serine proteinase activity may facilitate Pseudomonas aeruginosa lung colonization, leading to chronic infection. Since such activity is mostly controlled by alpha 1-antitrypsin (alpha 1-AT), we postulated
Autor:
S. Scholz, Sebastian Weidinger, K. Tief, Klaus Olek, M. Fischer, M. Kirchgesser, H.-H. Heidtmann, W. Poller, J.-P. Faber
Publikováno v:
Genomics. 17:740-743
Using denaturing gradient gel electrophoresis and direct sequencing of amplified genomic DNA, the authors have identified two defective mutants of the human [alpha][sub 1]-antichymotrypsin (ACT) gene associated with chronic obstructive pulmonary dise
Autor:
Sebastian Weidinger
Publikováno v:
Electrophoresis. 13:234-239
Genetically determined phenotypes of the highly polymorphic human alpha 1-antitrypsin were examined by hybrid isoelectric focusing in a narrow immobilized pH gradient. The chosen pH range from 4.45 to 4.75 was useful for identification and classifica
Autor:
Sebastian Weidinger, Frank Merklein, Anja Haack, Henry Fechner, Sonja Schneider-Rasp, Ioannis Anagnostopoulos, Wolfgang Poller, Haili Wang
Publikováno v:
European journal of human genetics : EJHG. 7(3)
Deficiency of the serine proteinase inhibitor (serpin) alpha 1-antitrypsin (alpha 1AT) is the most common autosomal recessive genetic disorder in Northern Europe. alpha 1AT is the physiological regulator of the proteolytic enzyme neutrophil elastase
Publikováno v:
Scopus-Elsevier
The genetic structure of the human population in a random sample of 238 unrelated individuals from Garfagnana (Tuscany, Italy) was studied for five highly polymorphic serum proteins (GC, TF, PI, AHSG, ORM1) and three red cell isozymes (ACP, PGM1, ESD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a42625f06e8b8de8caad159eb56b4d41
http://hdl.handle.net/11568/26626
http://hdl.handle.net/11568/26626
Autor:
B.C. Eap, Isao Yuasa, J.-C. Duche, K. Suenaga, Pierre Baumann, G. Ishimoto, Sebastian Weidinger, Kazuo Umetsu
Publikováno v:
Vox sanguinis. 64(1)
There are two forms of orosomucoid (ORM) in the sera of most individuals. They are encoded by two separate but closely linked loci, ORM1 and ORM2. A number of variants have been identified in various populations. Duplication and nonexpression are als
Publikováno v:
Lancet (London, England). 339(8808)
Publikováno v:
Human genetics. 88(6)
A new 6-phosphogluconate dehydrogenase variant tentatively named PGD Port Elizabeth is presented.
Publikováno v:
Advances in Forensic Haemogenetics ISBN: 9783540551942
Alpha-1-antitrypsin (α1AT) is the major protease inhibitor (PI) in human plasma. It is a 52-kD glycoprotein which consists of a single polypeptide chain of 394 amino acids with three complex asparaginyl-linked carbohydrate chains (Carrell et al. 198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74e3db396dda92d4c3c20dba4f102b43
https://doi.org/10.1007/978-3-642-77324-2_90
https://doi.org/10.1007/978-3-642-77324-2_90