Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Figura, Kurt von"'
Autor:
Koike, Masato, Shibata, Masahiro, Ohsawa, Yoshiyuki, Nakanishi, Hiroshi, Koga, Tomoyuki, Kametaka, Satoshi, Waguri, Satoshi, Momoi, Takashi, Kominami, Eiki, Peters, Christoph, Figura, Kurt von, Saftig, Paul, Uchiyama, Yasuo
Publikováno v:
In Molecular and Cellular Neuroscience 2003 22(2):146-161
Autor:
Waheed, Abdul1, Figura, Kurt von1
Publikováno v:
European Journal of Biochemistry. 10/5/90, Vol. 193 Issue 1, p47-54. 8p.
Publikováno v:
European Journal of Biochemistry. 8/17/90, Vol. 191 Issue 3, p627-631. 5p.
Autor:
Figura, Kurt von1
Publikováno v:
European Journal of Biochemistry. 11/1/77, Vol. 80 Issue 2, p525-533. 9p.
Autor:
Figura, Kurt von1
Publikováno v:
European Journal of Biochemistry. 11/1/77, Vol. 80 Issue 2, p535-542. 8p.
Autor:
Hanßke, Bengt, Thiel, Christian, Lübke, Torben, Hasilik, Martin, Höning, Stefan, Peters, Verena, Heidemann, Peter H., Hoffmann, Georg F., Berger, Eric G., Figura, Kurt von, Körner, Christian
Publikováno v:
Journal of Clinical Investigation. 109:725-733
Deficiency of the Golgi enzyme UDP-Gal:N-acetylglucosamine β-1,4-galactosyltransferase I (β4GalT I) (E.C.2.4.1.38) causes a new congenital disorder of glycosylation (CDG), designated type IId (CDG-IId), a severe neurologic disease characterized by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6106d4fa489ca1b9a3082a6aa924ef47
https://doi.org/10.1172/jci0214010
https://doi.org/10.1172/jci0214010
Autor:
Körner, Christian, Knauer, Roland, Stephani, Ulrich, Marquardt, Thorsten, Lehle, Ludwig, Figura, Kurt von
Type IV of the carbohydrate deficient glycoprotein syndromes (CDGp. is characterized by microcephaly, severe epilepsy, minimal psychomotor development and partial deficiency of sialic acids in serum glycoproteins. Here we show that the molecular defe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1688::27bba5fc294d3c9cd79a23d533e63d85
http://resolver.sub.uni-goettingen.de/purl?goescholar/3446
http://resolver.sub.uni-goettingen.de/purl?goescholar/3446
Autor:
Körner, Christian, Knauer, Roland, Holzbach, Ulrike, Hanefeld, Folker, Lehle, Ludwig, Figura, Kurt von
Deficiency of dolichyl-P-Glc:Man9GlcNAc2- PP-dolichyl glucosyltransferase is the cause of an additional type of carbohydrate-deficient glycoprotein syndrome (CDGS type V). Clinically this type resembles the classical type Ia of CDGS caused by the def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1688::bc236ad8c5d22ed1035baaffd3e868aa
http://resolver.sub.uni-goettingen.de/purl?goescholar/3444
http://resolver.sub.uni-goettingen.de/purl?goescholar/3444
Among the various coats involved in vesicular transport, the clathrin associated coats that contain the adaptor complexes AP-1 and AP-2 are the most extensively characterized. The function of the recently described adaptor complex AP-3, which is simi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1688::c1a3ea4d502e55aa1bf072b0b51f3121
http://resolver.sub.uni-goettingen.de/purl?goescholar/3443
http://resolver.sub.uni-goettingen.de/purl?goescholar/3443
In two children with an accumulation of guanidinoacetate in brain and a deficiency of creatine in blood, a severe deficiency of guanidinoacetate methyltransferase (GAMT) activity was detected in the liver. Two mutant GAMT alleles were identified that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1688::4d90146109f8b18b4a852e93294af976
http://resolver.sub.uni-goettingen.de/purl?goescholar/3442
http://resolver.sub.uni-goettingen.de/purl?goescholar/3442