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Eric G. Berger

universite de franche-comte

45H指数
198论文数
8.1K被引数
收录论文 27
发表时间
Pathways commonly dysregulated in mouse and human obese adipose tissue: FAT/CD36 modulates differentiation and lipogenesis
err2015-01-26
err40
errOAAI
errBerger, E.; Heraud, S.; Mojallal, A.; Lequeux, C.; Weiss-Gayet, M.; Damour, O.; Geloen, A.
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Amyloid-Related Imaging Abnormalities in AβPP Duplication Carriers
err2013-10-10
err9
PREAI
errChamard, Ludivine; Wallon, David; Pijoff, Alexa; Berger, Eric; Viennet, Gabriel; Hannequin, Didier; Magnin, Eloi
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Golgi enzymes are enriched in perforated zones of Golgi cisternae but are depleted in COPI vesicles
err2004-10-01
err79
errOAAI
errKweon, HS; Beznoussenko, GV; Micaroni, M; Polishchuk, RS; Trucco, A; Martella, O; Di Giandomenico, D; Marra, P; Fusella, A; Di Pentima, A; Berger, EG; Geerts, WJC; Koster, AJ; Burger, KNJ; Luini, A; Mironov, AA
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Galactosyltransferase-still up and running
err2003-03-01
err23
PREAI
errBerger, EG; Rohrer, J
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Deficiency of UDP-galactose:N-acetylglucosamine β-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId
err2002-03-15
err125
errOAAI
errHansske, B; Thiel, C; Lübke, T; Hasilik, M; Höning, S; Peters, V; Heidemann, PH; Hoffmann, GF; Berger, EG; von Figura, K; Körner, C
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Small cargo proteins and large aggregates can traverse the Golgi by a common mechanism without leaving the lumen of cisternae
err2001-12-24
err185
errOAAI
errMironov, AA; Beznoussenko, GV; Nicoziani, P; Martella, O; Trucco, A; Kweon, HS; Di Giandomenico, D; Polishchuk, RS; Fusella, A; Lupetti, P; Berger, EG; Geerts, WJC; Koster, AJ; Burger, KNJ; Luini, A
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MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If
err2001-12-01
err121
errOAAI
errSchenk, B; Imbach, T; Frank, CG; Grubenmann, CE; Raymond, GV; Hurvitz, H; Raas-Rotschild, A; Luder, AS; Jaeken, J; Berger, EG; Matthijs, G; Hennet, T; Aebi, M
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Immobilisation on polystyrene of diazirine derivatives of mono- and disaccharides:: Biological activities of modified surfaces
err2001-11-01
err49
PREAI
errChevolot, Y; Martins, J; Milosevic, N; Léonard, D; Zeng, S; Malissard, M; Berger, EG; Maier, P; Mathieu, HJ; Crout, DHG; Sigrist, H
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Exploring the acceptor substrate recognition of the human β-galactoside α2,6-sialyltransferase
err2001-06-01
err65
errOAAI
errLegaigneur, P; Breton, C; El Battari, A; Guillemot, JC; Augé, C; Malissard, M; Berger, EG; Ronin, C
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Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic
err2000-05-30
err62
PREAI
errImbach, T; Grünewald, S; Schenk, B; Burda, P; Schollen, E; Wevers, RA; Jaeken, J; de Klerk, JBC; Berger, EG; Matthijs, G; Aebi, M; Hennet, T
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Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie
err2000-01-15
err144
errOAAI
errImbach, T; Schenk, B; Schollen, E; Burda, P; Stutz, A; Grünewald, S; Bailie, NM; King, MD; Jaeken, J; Matthijs, G; Berger, EG; Aebi, M; Hennet, T
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