Zobrazeno 1 - 10
of 16
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::e6dd4bcd80bcf6024d716ba11bed2f14
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2231f99a771f407422c1949e65b4e6e5
https://pubmed.ncbi.nlm.nih.gov/19006247
https://pubmed.ncbi.nlm.nih.gov/19006247
Autor:
Venz, Simone1 (AUTHOR) simone.venz@med.uni-greifswald.de, von Bohlen und Halbach, Viola2 (AUTHOR) viola.bohlenundhalbach@uni-greifswald.de, Hentschker, Christian3 (AUTHOR) hentschkec@uni-greifswald.de, Junker, Heike1 (AUTHOR) elke.krueger@med.uni-greifswald.de, Kuss, Andreas Walter3 (AUTHOR) kussa@uni-greifswald.de, Sura, Thomas3 (AUTHOR) thomas.sura@uni-greifswald.de, Krüger, Elke1 (AUTHOR), Völker, Uwe3 (AUTHOR) voelker@uni-greifswald.de, von Bohlen und Halbach, Oliver2 (AUTHOR) oliver.vonbohlen@uni-greifswald.de, Jensen, Lars Riff3 (AUTHOR) jensenl@uni-greifswald.de, Hammer, Elke3 (AUTHOR) simone.venz@med.uni-greifswald.de
Publikováno v:
International Journal of Molecular Sciences. Jul2023, Vol. 24 Issue 14, p11308. 13p.
Autor:
Kuss, Andreas, Chen, Wei
Publikováno v:
Current Neurology & Neuroscience Reports; May2008, Vol. 8 Issue 3, p190-197, 8p
Autor:
Shafeghati, Yousef1, Kahrizi, Kimia1, Najmabadi, Hossein1, Kuss, Andreas Walter2, Ropers, Hans-Hilger2, Tzschach, Andreas2 tzschach@molgen.mpg.de
Publikováno v:
European Journal of Pediatrics. Dec2010, Vol. 169 Issue 12, p1535-1539. 5p. 1 Color Photograph, 1 Black and White Photograph, 1 Chart.
Autor:
Frints, Suzanna Gerarda Maria1,2 suzanne.frints@gen.unimaas.nl, Lenzner, Steffen3, Bauters, Mareike4, Jensen, Lars Riff3, Van Esch, Hilde5, des Portes, Vincent6, Moog, Ute1, Macville, Merryn Victor Erik1, van Roozendaal, Kees1, Schrander-Stumpel, Constance Theresia Rimbertha Maria1,2, Tzschach, Andreas3, Marynen, Peter4, Fryns, Jean-Pierre5, Hamel, Ben7, van Bokhoven, Hans7, Chelly, Jamel8, Beldjord, Chérif8, Turner, Gillian9, Gecz, Jozef10, Moraine, Claude11
Publikováno v:
European Journal of Human Genetics. Sep2008, Vol. 16 Issue 9, p1029-1037. 9p. 3 Black and White Photographs, 2 Diagrams, 1 Chart, 1 Graph.
Autor:
Moheb, Lia Abbasi1, Tzschach, Andreas2, Garshasbi, Masoud2, Kahrizi, Kimia3, Darvish, Hossein3, Heshmati, Yaser3, Kordi, Alireza3, Najmabadi, Hossein3, Ropers, Hans Hilger2, Kuss, Andreas Walter2 kuss_a@molgen.mpg.de
Publikováno v:
European Journal of Human Genetics. Feb2008, Vol. 16 Issue 2, p270-273. 4p. 2 Diagrams, 1 Chart.
Publikováno v:
American Journal of Medical Genetics. Part A; Aug2011, Vol. 155A Issue 8, pfm i-fm vi, 6p
Autor:
Garshasbi, Masoud, Kahrizi, Kimia, Hosseini, Masoumeh, Nouri Vahid, Leila, Falah, Masoumeh, Hemmati, Sahel, Hu, Hao, Tzschach, Andreas, Ropers, Hans Hilger, Najmabadi, Hossein, Kuss, Andreas Walter
Publikováno v:
American Journal of Medical Genetics. Part A; Aug2011, Vol. 155A Issue 8, p1976-1980, 5p