Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Uta, Gölnitz"'
Autor:
Gerhard Wunderlich, Fabiana P. Alves, Uta Gölnitz, Mauro S. Tada, Erney F.P. de Camargo, Luiz H. Pereira-da-Silva
Publikováno v:
Revista do Instituto de Medicina Tropical de São Paulo, Vol 47, Iss 4, Pp 195-201 (2005)
The var genes of Plasmodium falciparum code for the antigenically variant erythrocyte membrane proteins 1 (PfEMP1), a major factor for cytoadherence and immune escape of the parasite. Herein, we analyzed the var gene transcript turnover in two ongoin
Externí odkaz:
https://doaj.org/article/7fc2e6d5dcdf45d0a3ba5734186056e4
Autor:
Arndt Rolfs, Anne-Katrin Giese, Ulrike Grittner, Daniel Mascher, Deborah Elstein, Ari Zimran, Tobias Böttcher, Jan Lukas, Rayk Hübner, Uta Gölnitz, Anja Röhle, Ales Dudesek, Wolfgang Meyer, Matthias Wittstock, Hermann Mascher
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79732 (2013)
Gaucher disease (GD) is the most common lysosomal storage disorder (LSD). Based on a deficient β-glucocerebrosidase it leads to an accumulation of glucosylceramide. Standard diagnostic procedures include measurement of enzyme activity, genetic testi
Externí odkaz:
https://doaj.org/article/0c96da501419462db80565411c821dd8
Autor:
Luiz Hildebrando Pereira-da-Silva, Erney P. Camargo, Gerhard Wunderlich, Uta Gölnitz, Mauro Shugiro Tada, Fabiana Alves
Publikováno v:
Revista do Instituto de Medicina Tropical de São Paulo; Vol. 47 No. 4 (2005); 195-201
Revista do Instituto de Medicina Tropical de São Paulo; Vol. 47 Núm. 4 (2005); 195-201
Revista do Instituto de Medicina Tropical de São Paulo; v. 47 n. 4 (2005); 195-201
Revista do Instituto de Medicina Tropical de São Paulo
Instituto de Medicina Tropical (IMT)
instacron:IMT
Revista do Instituto de Medicina Tropical de São Paulo, Volume: 47, Issue: 4, Pages: 195-201, Published: AUG 2005
Revista do Instituto de Medicina Tropical de São Paulo; Vol. 47 Núm. 4 (2005); 195-201
Revista do Instituto de Medicina Tropical de São Paulo; v. 47 n. 4 (2005); 195-201
Revista do Instituto de Medicina Tropical de São Paulo
Instituto de Medicina Tropical (IMT)
instacron:IMT
Revista do Instituto de Medicina Tropical de São Paulo, Volume: 47, Issue: 4, Pages: 195-201, Published: AUG 2005
Os genes var de Plasmodium falciparum codificam as proteínas variantes da superfície do eritrócito infectado (PfEMP1). Neste estudo examinamos a mudança de transcritos destes genes var em duas infecções assintomáticas durante um curto prazo e
Autor:
Andreas Bräuer, Andreas Hermann, Arndt Rolfs, Georg Ziethe, Claudia Ricci, Ulrike Reuner, Uta Gölnitz
Publikováno v:
Amyotrophic Lateral Sclerosis. 12:382-384
Familial cases of amyotrophic lateral sclerosis are most frequently caused by mutation in the superoxide dismutase-1 (SOD1) gene. We report a heterozygous I113F mutation in a patient with familial ALS characterized by early and predominant bilateral
Autor:
Arndt Rolfs, Himesha Vandebona, Karl Ng, Christine Klein, David M. Sharpe, Viatcheslav Saviouk, Carolyn M. Sue, Nicholas F. Blair, Christina Liang, Anne Grünewald, Uta Gölnitz, Kishore R. Kumar
Publikováno v:
Journal of neurology. 260(10)
Molecular characterization is important for an accurate diagnosis in hereditary spastic paraplegia (HSP). Mutations in the gene SPAST (SPG4) are the most common cause of autosomal dominant forms. We performed targeted next generation sequencing (NGS)
Autor:
Ana, Westenberger, Raymond L, Rosales, Sascha, Heinitz, Karen, Freimann, Lilian V, Lee, Roland D, Jamora, Arlene R, Ng, Aloysius, Domingo, Katja, Lohmann, Uwe, Walter, Uta, Gölnitz, Arndt, Rolfs, Inga, Nagel, Gabriele, Gillessen-Kaesbach, Reiner, Siebert, Dirk, Dressler, Christine, Klein
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 28(5)
Recessive X-linked dystonia-parkinsonism almost exclusively affects men. We investigated the genetic mechanisms causing this disorder in a female patient.We confirmed the presence of an X-linked dystonia-parkinsonism-specific change in our patient by
Autor:
Anne-Katrin Giese, Michael Klingenhäger, Elisa Legnini, Sándor Túri, Olaf Bodamer, Uta Gölnitz, Adolf Mühl, Jan Lukas, Arndt Rolfs, Judit Wittmann, Gyula Wittmann, Eszter Karg
Publikováno v:
JIMD Reports ISBN: 9783642281280
Even though lysosomal storage disorders (LSDs) are considered to be orphan diseases, they pose a highly relevant cause for morbidity and mortality as their cumulative prevalence is estimated to be 1:4,000. This is especially important as treatment in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2f95b52708f25ab534140f03cd2a298
https://europepmc.org/articles/PMC3565645/
https://europepmc.org/articles/PMC3565645/
Publikováno v:
Malaria Journal
Malaria Journal, Vol 7, Iss 1, p 14 (2008)
Malaria Journal, Vol 7, Iss 1, p 14 (2008)
BackgroundCytoadherence ofPlasmodium falciparum-infected red blood cells is mediated byvargene-encodedP. falciparumerythrocyte membrane protein-1 and host receptor preference depends in most cases on which of the 50–60vargenes per genome is express
Publikováno v:
Journal of virology. 78(24)
Lassa virus is endemic to West Africa and causes hemorrhagic fever in humans. To facilitate the functional analysis of this virus, a replicon system was developed based on Lassa virus strain AV. Genomic and antigenomic minigenomes (MG) were construct
Autor:
Günter Pfaff, Herbert Schmitz, Marcel Asper, T Breuer, Uta Gölnitz, Klaus Fleischer, Petra Emmerich, Päivi Köhler, Stephan Günther, Walter Haas, Christian Drosten
Publikováno v:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 36(10)
This study sought to assess the risk of secondary transmission after import of Lassa fever into Europe. A total of 232 persons exposed to a case of Lassa fever imported into Germany were identified. The level of exposure was determined for 157 person