Zobrazeno 1 - 10
of 926
pro vyhledávání: '"Rascher Wolfgang"'
Autor:
Fahlbusch Fabian B, Ruebner Matthias, Volkert Gudrun, Offergeld Ramona, Hartner Andrea, Menendez-Castro Carlos, Strick Reiner, Rauh Manfred, Rascher Wolfgang, Dötsch Jörg
Publikováno v:
Reproductive Biology and Endocrinology, Vol 10, Iss 1, p 80 (2012)
Abstract Background The placental syncytiotrophoblast is the major source of maternal plasma corticotropin-releasing hormone (CRH) in the second half of pregnancy. Placental CRH exerts multiple functions in the maternal organism: It induces the adren
Externí odkaz:
https://doaj.org/article/80b916ff6c214983810df90c40eb508d
Autor:
Hinkes Bernward, Hilgers Karl F, Bolz Hanno J, Goppelt-Struebe Margarete, Amann Kerstin, Nagl Sandra, Bergmann Carsten, Rascher Wolfgang, Eckardt Kai-Uwe, Jacobi Johannes
Publikováno v:
BMC Nephrology, Vol 13, Iss 1, p 27 (2012)
Abstract Background Microdeletions on chromosome 17q12 cause of diverse spectrum of disorders and have only recently been identified as a rare cause of Mayer-Rokitansky-Kuester-Hauser-Syndrome (MRKH), which is characterized by uterus aplasia ± parti
Externí odkaz:
https://doaj.org/article/241326cf2f8448d8be1d2929af0393d1
Publikováno v:
Thrombosis Journal, Vol 10, Iss 1, p 6 (2012)
Abstract The clinical use of Sodium nitroprusside (SNP) may be associated with an alteration of platelet function. The main focus of this study was the effect of SNP on platelet aggregation in the absence or presence of endothelial cells. Methods: Pl
Externí odkaz:
https://doaj.org/article/ceb0c40792f943ceae8c03d22e269218
Autor:
Hilgers Karl F, Goppelt-Struebe Margarete, Özcan Zehra, Zürn Christina, Fahlbusch Fabian, Jahn Angelika, Volkert Gudrun, Marek Ines, Rascher Wolfgang, Hartner Andrea
Publikováno v:
BMC Cell Biology, Vol 11, Iss 1, p 102 (2010)
Abstract Background Extracellular matrix receptors of the integrin family are known to regulate cell adhesion, shape and functions. The α8 integrin chain is expressed in glomerular mesangial cells and in vascular smooth muscle cells. Mice deficient
Externí odkaz:
https://doaj.org/article/4f388a89d10644df9a419f763377952f
Autor:
Weigel Corina, Topf Hans G, Schellmoser Stefan, Zschocke Johannes, Knerr Ina, Dötsch Jörg, Rascher Wolfgang
Publikováno v:
BMC Pediatrics, Vol 5, Iss 1, p 5 (2005)
Abstract Background Phenylketonuria is an inborn error of amino acid metabolism which can cause severe damage to the patient or, in the case of maternal phenylketonuria, to the foetus. The maternal phenylketonuria syndrome is caused by high blood phe
Externí odkaz:
https://doaj.org/article/5ad7d6bf60414f80ae7a281212ff75b6
Publikováno v:
In Journal of Pediatric Urology February 2020 16(1):71-79
Autor:
Knieling, Ferdinand, Gonzales Menezes, Jean, Claussen, Jing, Schwarz, Mathias, Neufert, Clemens, Fahlbusch, Fabian B., Rath, Timo, Thoma, Oana-Maria, Kramer, Viktoria, Menchicchi, Bianca, Kersten, Christina, Scheibe, Kristina, Schürmann, Sebastian, Carlé, Birgitta, Rascher, Wolfgang, Neurath, Markus F., Ntziachristos, Vasilis, Waldner, Maximilian J.
Publikováno v:
In Gastroenterology March 2018 154(4):807-809
Akademický článek
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Akademický článek
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Publikováno v:
In Ultrasound in Medicine & Biology March 2017 43(3):662-669