Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Heidemann, Peter H."'
Autor:
Vogt, Peter H., Besikoglu, Banu, Bettendorf, Markus, Frank-Herrmann, Petra, Zimmer, Jutta, Bender, Urike, Knauer-Fischer, Sabine, Choukair, Daniela, Sinn, Peter, Doerr, Helmuth-Guenther, Woelfle, Joachim, Heidemann, Peter H., Lau, Yun-Fai Chris, Strowitzki, Thomas
Publikováno v:
Syst Biol Reprod Med
“Differences of Sexual Development (DSD),” individuals with rearranged Y chromosome breaks in their 46,XY cells are reported with male and female gender phenotypes and differences in germ cell tumour (GCT) risk. This raised the question of whethe
Autor:
Gambineri, Eleonora, Perroni, Lucia, Passerini, Laura, Bianchi, Lucia, Doglioni, Claudio, Meschi, Franco, Bonfanti, Riccardo, Sznajer, Yves, Tommasini, Alberto, Lawitschka, Anita, Junker, Anne, Dunstheimer, Desiree, Heidemann, Peter H., Cazzola, Giantonio, Cipolli, Marco, Friedrich, Wilhelm, Janic, Dragana, Azzi, Nadira, Richmond, Erick, Vignola, Silvia, Barabino, Arrigo, Chiumello, Giuseppe, Azzari, Chiara, Roncarolo, Maria-Grazia, Bacchetta, Rosa
Publikováno v:
In The Journal of Allergy and Clinical Immunology 2008 122(6):1105-1112
Autor:
Vogt, Peter H., Besikoglu, Banu, Bettendorf, Markus, Frank-Herrmann, Petra, Zimmer, Jutta, Bender, Urike, Knauer-Fischer, Sabine, Choukair, Daniela, Sinn, Peter, Doerr, Helmuth-Guenther, Woelfle, Joachim, Heidemann, Peter H., Lau, Yun-Fai Chris, Strowitzki, Thomas
Publikováno v:
Systems Biology in Reproductive Medicine; Aug2022, Vol. 68 Issue 4, p247-257, 11p
Autor:
Hanßke, Bengt, Thiel, Christian, Lübke, Torben, Hasilik, Martin, Höning, Stefan, Peters, Verena, Heidemann, Peter H., Hoffmann, Georg F., Berger, Eric G., Figura, Kurt von, Körner, Christian
Publikováno v:
Journal of Clinical Investigation. 109:725-733
Deficiency of the Golgi enzyme UDP-Gal:N-acetylglucosamine β-1,4-galactosyltransferase I (β4GalT I) (E.C.2.4.1.38) causes a new congenital disorder of glycosylation (CDG), designated type IId (CDG-IId), a severe neurologic disease characterized by
Autor:
Hansske, Bengt, Thiel, Christian, Lübke, Torben, Hasilik, Martin, Höning, Stefan, Peters, Verena, Heidemann, Peter H., Hoffmann, Georg F., Berger, Eric G., von Figura, Kurt, Körner, Christian
Deficiency of the Golgi enzyme UDP-Gal:N-acetylglucosamine beta-1,4-galactosyltransferase I (beta4GalT I) (E.C.2.4.1.38) causes a new congenital disorder of glycosylation (CDG), designated type IId (CDG-IId), a severe neurologic disease characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::93db01c0d69ad23f7641c702e24001dc
https://pub.uni-bielefeld.de/record/1940103
https://pub.uni-bielefeld.de/record/1940103
Akademický článek
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Autor:
Müller, Eva, Dunstheimer, Desiree, Klammt, Jürgen, Friebe, Daniela, Kiess, Wieland, Kratzsch, Jürgen, Kruis, Tassilo, Laue, Sandy, Pfäffle, Roland, Wallborn, Tillmann, Heidemann, Peter H.
Publikováno v:
PLoS ONE; May2012, Vol. 7 Issue 5, p1-10, 10p
Publikováno v:
In Cancer Letters 2003 196(1):23-27
Publikováno v:
Hormone Research; 2004, Vol. 62 Issue 2, p84-87, 4p
Autor:
Frenzel, Sabine, Apel, Thomas W., Heidemann, Peter H., Zerres, Klaus, Neumann, Hartmut P. H., Dörr, Helmuth G., Frenzel, S, Apel, T W, Heidemann, P H, Zerres, K, Neumann, H P, Dörr, H G
Publikováno v:
European Journal of Pediatrics; 2001, Vol. 160 Issue 7, p421-424, 4p