Zobrazeno 1 - 10
of 141
pro vyhledávání: '"H U, Schweikert"'
Autor:
H. U. Schweikert, Olaf Hiort, Ole Ammerpohl, Susanne Bens, Hendrik G. Stunnenberg, Alexandra Kulle, Paul-Martin Holterhus, Nina C. Hubner, Ralf Werner, Anne Katrin Eckstein, Annemarie Verrijn-Stuart, Martine Cools, Helmuth G. Dörr, Susanne Gonzalves, Reiner Siebert, Nadine Hornig, Maik Welzel, Pascal Rodens
Publikováno v:
The Journal of clinical endocrinology and metabolism, 103(12), 4617. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 103, 12, pp. 4617-4627
Journal of Clinical Endocrinology and Metabolism, 103, 4617-4627
Journal of Clinical Endocrinology and Metabolism, 103, 12, pp. 4617-4627
Journal of Clinical Endocrinology and Metabolism, 103, 4617-4627
Contains fulltext : 197541.pdf (Publisher’s version ) (Closed access) Context: Inactivating mutations within the AR-gene are present in only around 40% of individuals with clinically and hormonally diagnosed androgen insensitivity syndrome (AIS). P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62e58acb268e331df0c790daa943f487
https://dspace.library.uu.nl/handle/1874/373771
https://dspace.library.uu.nl/handle/1874/373771
Autor:
R. Ziegler, W. Sippell, O. Butenandt, Nikolaus Stahnke, Jürgen Brämswig, F. Kollmann, H. U. Schweikert, M. B. Ranke, P. Stubbe, K.-D. Schönberg, H. Stolecke, U. Heinrich, P. Beyer, P. Bittner, B. Stöver, J. R. Bierich, H. Borkenstein
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 111:483-489
During the period from 1982 to 1985, biosynthetic growth hormone (methionyl-hGH) was administered to 55 children with pituitary growth deficiency, 49 with idiopathic, six with other forms of the disorder. Preparations with a relatively high content o
Autor:
C de Beaufort, Martin Ukat, H. U. Schweikert, Alexandra Kulle, Ole Ammerpohl, Sls Drop, M Welzel, Reiner Siebert, Gaby Wehner, Olaf Hiort, C. Seif, Martine Cools, Ieuan A. Hughes, Paul Martin Holterhus, Nadine Hornig, Rebecca E. Werner, Anne Katrin Eckstein, C. Van Der Horst
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 122
Androgen insensitivity syndrome (AIS) is characterized by a partial to complete lack of genital virilization in genetically male individuals. It is classically caused by inactivating mutations in the coding region of the X-chromosomal androgen recept
Autor:
Ute M. Liegibel, Ulrike Hilscher, Christian Kasperk, H. U. Schweikert, Peter P. Nawroth, Angelika Bierhaus, Irma Boercsoek, U. Sommer
Publikováno v:
Steroids. 68:1179-1187
Two isoforms of the androgen receptor (AR-A and AR-B), differing by a lack of the first 187 amino acids in the NH2-terminal transactivation domain of AR-A, are expressed in connective tissue and bone. Transient transfections of normal human osteoblas
Autor:
Sedika Issa, Doris Schnabel, Maritta Feix, David W. Russell, Lutz Wolf, Hans E. Schaefer, H. U. Schweikert
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 87:5401-5407
In previous studies we established that human bone and human osteoblast-like cells (hOB cells) cultured from bone express 5alpha-reductase (5alpha-R) activity, as demonstrated by the conversion of testosterone and androstenedione to their correspondi
Publikováno v:
International Journal of Human Genetics. 2:213-221
Gonosomal mosaicism with a Y-chromo- some present in at least one cell system was investi- gated in 29 patients. In 15 cases the Y-chromosome was structurally normal, in 14 cases different structural aberrations were analysed. 17 patients were phenot
Publikováno v:
Der Internist. 42:1413-1417
Ein primarer Hypoparathyreoidismus ist eine seltene Manifestation der hereditaren Hamochromatose. Dabei kann es infolge einer inadaquat niedrigen Parathormonsekretion zu einer Hypokalzamie mit dem Leitsymptom der Tetanien kommen. Bei der Hamochromato
Publikováno v:
Der Urologe B. 37:14-23
Fehlentwicklungen der embryonalen Sexualdifferenzierung lassen sich in solche des chromosomalen, gonadalen und phanotypischen Geschlechts unterteilen. Bei der Gonadendysgenesie und der Gemischten Gonadendysgenesie handelt es sich um Fehlentwicklungen
Publikováno v:
Phytomedicine. 1:127-133
Summary The inhibition of testosterone 5oc-reductase (EC 1.3.99.5) (5αR) in vitro by lipophilic extracts from Sabal serrulata fruits effective on Benign Prostatic hyperplasia (BPH) treatment is due entirely to free fatty acid content. In order to fi
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