Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nina Rind"'
Autor:
Berthil H.C.M.T. Prinsen, Jürgen Lübbehusen, Daniel Ungar, Nina Rind, Christian Thiel, Tom J. de Koning, Peter M. van Hasselt, Christian Körner
Publikováno v:
Human Molecular Genetics, 19(18), 3623-3633. Oxford University Press
Deficiency of subunit 6 of the conserved oligomeric Golgi (COG6) complex causes a new combined N- and O-glycosylation deficiency of the congenital disorders of glycosylation, designated as CDG-IIL (COG6-CDG). The index patient presented with a severe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2020dc89cf5c31b7f6fe8a326953ac85
https://hdl.handle.net/11370/bc70e4fe-7d09-45cf-b961-f20a71fbd932
https://hdl.handle.net/11370/bc70e4fe-7d09-45cf-b961-f20a71fbd932
Autor:
Gert Matthijs, Kristen Hanson, Craig R. Adamski, Christian Körner, Georg F. Hoffmann, Nina Rind, Rhonda Scanlon, Neophytos Apeshiotis, Diana Popovici, Charlotte Thiels, Marie Lambert, Robert L. Conway, Christian Thiel, Elizabeth Butler
Publikováno v:
Human Mutation. 33:485-487
Congenital disorders of glycosylation (CDG) comprise a clinically and biochemically heterogeneous group of monogenetic-inherited, multisystemic diseases that affect the biosynthesis of N- and/or O-glycans linked to glycoconjugates. Recently, we ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fc8fe71f474b22b00262d88548c7e4c
https://doi.org/10.1002/humu.22019
https://doi.org/10.1002/humu.22019
Autor:
Nina Rind
Publikováno v:
Beziehungsanalysen. Bildende Künste in Westdeutschland nach 1945 ISBN: 9783658029166
Im Jahr 1958 eroffnet die Galerie Seide als eine von zwei Nachkriegsgalerien fur zeitgenossische Kunst in Hannover. Anders als beim Mitstreiter Brusberg ist die Galerie Seide jedoch nicht vorrangig kommerziell ausgerichtet. Sie ist vielmehr Treffpunk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f4fa0bb7d3d6a1a28a6bf31a662d2ec
https://doi.org/10.1007/978-3-658-02917-3_6
https://doi.org/10.1007/978-3-658-02917-3_6
Autor:
Christian Thiel, Julia Hocks, Jürgen Lübbehusen, Ekkehard Wilichowski, Ludwig Lehle, Birgit Absmanner, Christian Körner, Verena Schmeiser, Nina Rind, Neophytos Apeshiotis
Publikováno v:
Human molecular genetics. 19(8)
A new type of congenital disorders of glycosylation, designated CDG-Ip, is caused by the deficiency of GDP-Man:Man3GlcNAc2-PP-dolichol-alpha1,2-mannosyltransferase, encoded by the human ortholog of ALG11 from yeast. The patient presented with a multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60f3964490ebbc359cbd10358e9aab7d
https://pubmed.ncbi.nlm.nih.gov/20080937
https://pubmed.ncbi.nlm.nih.gov/20080937
Autor:
Peter W. Mathieson, Johannes Zschocke, Hans-Peter Hammes, Jochen Meyer, Daniela Hohenadel, Ivan Rychlik, Benito A. Yard, Verena Peters, Christine Fischer, Stephan J. L. Bakker, Moin A. Saleem, Nina Rind, Paul T. Brinkkoetter, Emile de Heer, Fokko J. van der Woude, Claus R. Bartram, Sibylle Sauerhoefer, Marianna Romzova, Bart Janssen, Hannes Koppel, Peter P. Nawroth, Hans J. Baelde, Mahmoud Zirie, Eric Rondeau, Marie Cerna
Publikováno v:
University of Bristol-PURE
The risk of diabetic nephropathy is partially genetically determined. Diabetic nephropathy is linked to a gene locus on chromosome 18q22.3-q23. We aimed to identify the causative gene on chromosome 18 and to study the mechanism by which the product o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31f6830d9f48d506738b4618d5638cfb
https://research-information.bris.ac.uk/en/publications/ee8a0905-0557-4ed9-91f2-f44d8297740d
https://research-information.bris.ac.uk/en/publications/ee8a0905-0557-4ed9-91f2-f44d8297740d