Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Anne Kosfeld"'
Autor:
Anne Kosfeld, Knut Jahreis
Publikováno v:
Metabolites, Vol 2, Iss 4, Pp 756-774 (2012)
Escherichia coli is a widely used microorganism in biotechnological processes. An obvious goal for current scientific and technical research in this field is the search for new tools to optimize productivity. Usually glucose is the preferred carbon s
Externí odkaz:
https://doaj.org/article/d8e0aff69e3a4dfa9ecb63144d63ab60
Publikováno v:
Medizinische Genetik. 30:448-460
Zusammenfassung Der Begriff CAKUT (Congenital Anomalies of the Kidney and Urinary Tract) bezeichnet diverse angeborene Fehlbildungen der Nieren und ableitenden Harnwege. Da alle CAKUT-Phänotypen zusammengenommen etwa 15–30 % aller pränatal diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::158b3b77729d6de06c0ca13829777267
https://doi.org/10.1007/s11825-018-0226-y
https://doi.org/10.1007/s11825-018-0226-y
Autor:
Lars Pape, Frank Brand, Stephanie Schubert, Dieter Haffner, Ruthild G. Weber, Kerstin Amann, Lars Krogvold, Imke Hennies, Jan Hinrich Bräsen, Michaela Goerk, Christoph Daniel, Anna Bjerre, Andreas Kispert, Anne-Kathrin Schäfer, Anne Kosfeld, Vera Riehmer, Helge Martens, Anna-Carina Weiss, Martin Kreuzer
Publikováno v:
Human Molecular Genetics. 26:1716-1731
Congenital anomalies of the kidneys and urinary tract (CAKUT) are the most common cause of chronic kidney disease in children. As CAKUT is a genetically heterogeneous disorder and most cases are genetically unexplained, we aimed to identify new CAKUT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4340673b40d9fe752632b42bc6e97e96
https://doi.org/10.1093/hmg/ddx086
https://doi.org/10.1093/hmg/ddx086
Autor:
Frank Brand, Alisa Förster, Marc S. Raab, Michael Weller, Peter Claus, Carina M. Thome, Ruthild G. Weber, Andreas von Deimling, Martin Bucher, Manfred Westphal, Bettina Hentschel, Torsten Pietsch, Anne Kosfeld, Guido Reifenberger
Publikováno v:
Neuro Oncol
In search of novel genes associated with glioma pathogenesis, we have previously shown that KIAA1797/FOCAD is frequently deleted in malignant gliomas and that the encoded focadhesin functions as a tumor suppressor impacting proliferation and migratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e4c184ebc96293a0205069a1165f7a4
https://europepmc.org/articles/PMC6847672/
https://europepmc.org/articles/PMC6847672/
Autor:
Frank Brand, Alexandra Chadt, Dieter Haffner, Michael Klintschar, Anne-Kathrin Schäfer, Hadi Al-Hasani, Anna-Carina Weiss, Martin Kreuzer, Cécile Jeanpierre, Jan Hinrich Bräsen, Christoph Daniel, Ruthild G. Weber, Andreas Kispert, Anne Kosfeld, Lars Pape, Kerstin Amann, Vera Riehmer
Publikováno v:
Human Genetics. 135:69-87
Congenital anomalies of the kidneys and urinary tract (CAKUT) are genetically highly heterogeneous leaving most cases unclear after mutational analysis of the around 30 causative genes known so far. Assuming that phenotypes frequently showing dominan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2598528bb87e98d0b1ad8c7b36b7b46
https://doi.org/10.1007/s00439-015-1610-1
https://doi.org/10.1007/s00439-015-1610-1
Autor:
Peter Raab, Isolde Rangnau, Susanne Abdulla, Susanne Petri, Ruthild G. Weber, Alma Osmanovic, Bernd Auber, Matthias Preller, Claas Janssen, Anne Kosfeld
Publikováno v:
European journal of human genetics : EJHG. 25(3)
We aimed to identify the genetic cause of the devastating neurodegenerative disease amyotrophic lateral sclerosis (ALS) in a German family with two affected individuals, and to assess the prevalence of variants in the identified risk gene, FIG4, in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f6fd12cbb6ba15b7dc7a7affa82167b
https://pubmed.ncbi.nlm.nih.gov/28051077
https://pubmed.ncbi.nlm.nih.gov/28051077
Autor:
Ian A. Wilson, Knut Jahreis, Hsiu-Ju Chiu, Mark W. Knuth, Heath E. Klock, M.A. Elsliger, Qingping Xu, Adam Godzik, Anna-Katharina Göhler, Dennis Carlton, Anne Kosfeld, Ashley M. Deacon, Mitchell D. Miller, Scott A. Lesley
Publikováno v:
Journal of Bacteriology. 194:2987-2999
MtfA of Escherichia coli (formerly YeeI) was previously identified as a regulator of the phosphoenolpyruvate (PEP)-dependent:glucose phosphotransferase system. MtfA homolog proteins are highly conserved, especially among beta- and gammaproteobacteria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72ac7e434010689505cd9e673d4f8b0c
https://doi.org/10.1128/jb.00038-12
https://doi.org/10.1128/jb.00038-12
Autor:
Anna-Katharina Göhler, Ariane Staab, Elisabeth Gabor, Anne Kosfeld, Janna-Eleni Muus, Karina Homann, Jana Selina Wulftange, Elisabeth Klang, Knut Jahreis
Publikováno v:
Journal of Bacteriology. 194:1024-1035
The glucose-phosphotransferase system (PTS) in Escherichia coli K-12 is a complex sensory and regulatory system. In addition to its central role in glucose uptake, it informs other global regulatory networks about carbohydrate availability and the ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d29e827f94f396db31afb6984914598f
https://doi.org/10.1128/jb.06387-11
https://doi.org/10.1128/jb.06387-11
Autor:
Ariane Staab, Elisabeth Gabor, Anne Kosfeld, Andreas Kremling, Anna-Katharina Göhler, Knut Jahreis
Publikováno v:
European Journal of Cell Biology. 90:711-720
The phosphoenolpyruvate-(PEP)-dependent-carbohydrate:phosphotransferase systems (PTSs) of enteric bacteria constitute a complex transport and sensory system. Such a PTS usually consists of two cytoplasmic energy-coupling proteins, Enzyme I (EI) and H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3f0f76edb16497d687d65a6e62a42ae
https://doi.org/10.1016/j.ejcb.2011.04.002
https://doi.org/10.1016/j.ejcb.2011.04.002
Autor:
Vera Riehmer, Sascha Tierling, Sarah Kabisch, Dieter Haffner, Stefanie Heilmann, Christina Landwehr, Hartmut Engels, Frank Schacherer, Carl Friedrich Classen, Ruthild G. Weber, Anne Kosfeld, C Scholz, Miroslav Zivicnjak
Publikováno v:
Human genetics. 132(7)
When a known microimbalance affecting multiple genes is detected in a patient with syndromic intellectual disability, it is usually presumed causative for all observed features. Whole exome sequencing (WES) allows questioning this assumption. In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25fc40a73d506eefac413a7e8ef859c4
https://pubmed.ncbi.nlm.nih.gov/23552953
https://pubmed.ncbi.nlm.nih.gov/23552953