Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Andreas Walter Kuss"'
Autor:
Simone Venz, Viola von Bohlen und Halbach, Christian Hentschker, Heike Junker, Andreas Walter Kuss, Thomas Sura, Elke Krüger, Uwe Völker, Oliver von Bohlen und Halbach, Lars Riff Jensen, Elke Hammer
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 14, p 11308 (2023)
Tissue sections, which are widely used in research and diagnostic laboratories and have already been examined by immunohistochemistry (IHC), may subsequently provide a resource for proteomic studies, even though only small amount of protein is availa
Externí odkaz:
https://doaj.org/article/3234f7ace0294bc5bd6b43daea2c5562
Autor:
Hammer, Simone Venz, Viola von Bohlen und Halbach, Christian Hentschker, Heike Junker, Andreas Walter Kuss, Thomas Sura, Elke Krüger, Uwe Völker, Oliver von Bohlen und Halbach, Lars Riff Jensen, Elke
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 14; Pages: 11308
Tissue sections, which are widely used in research and diagnostic laboratories and have already been examined by immunohistochemistry (IHC), may subsequently provide a resource for proteomic studies, even though only small amount of protein is availa
Autor:
Wenke, Seifert, Muriel, Holder-Espinasse, Jirko, Kühnisch, Kimia, Kahrizi, Andreas, Tzschach, Masoud, Garshasbi, Hossein, Najmabadi, Andreas, Walter Kuss, Wolfram, Kress, Geneviève, Laureys, Bart, Loeys, Eva, Brilstra, Grazia M S, Mancini, Hélène, Dollfus, Karin, Dahan, Kira, Apse, Hans Christian, Hennies, Denise, Horn
Publikováno v:
Human mutation. 30(2)
Cohen syndrome is characterised by mental retardation, postnatal microcephaly, facial dysmorphism, pigmentary retinopathy, myopia, and intermittent neutropenia. Mutations in COH1 (VPS13B) have been found in patients with Cohen syndrome from diverse e