Authors:
Zhuo, D
Zhao, WD
Wright, FA
Yang, HY
Wang, JP
Sears, R
Baer, T
Kwon, DH
Gordon, D
Gibbs, S
Dai, D
Yang, Q
Spitzner, J
Krahe, R
Stredney, D
Stutz, A
Yuan, B
Citation: D. Zhuo et al., Assembly, annotation, and integration of UNIGENE clusters into the human genome draft, GENOME RES, 11(5), 2001, pp. 904-918
Citation: A. Gould et al., A method to measure the ratio of total to selective extinction toward Baade's window, ASTROPHYS J, 547(2), 2001, pp. 590-593
Authors:
Aebi, M
Helenius, A
Schenk, B
Barone, R
Fiumara, A
Berger, EG
Hennet, T
Imbach, T
Stutz, A
Bjursell, C
Uller, A
Wahlstrom, JG
Briones, P
Cardo, E
Clayton, P
Winchester, B
Cormier-Daire, V
de Lonlay, P
Cuer, M
Dupre, T
Seta, N
de Koning, T
Dorland, L
de Loos, F
Kupers, L
Fabritz, L
Hasilik, M
Marquardt, T
Niehues, R
Freeze, H
Grunewald, S
Heykants, L
Jaeken, J
Matthijs, G
Schollen, E
Keir, G
Kjaergaard, S
Schwartz, M
Skovby, F
Klein, A
Roussel, P
Korner, C
Lubke, T
Thiel, C
von Figura, K
Koscielak, J
Krasnewich, D
Lehle, L
Peters, V
Raab, M
Saether, O
Schachter, H
Van Schaftingen, E
Verbert, A
Vilaseca, A
Wevers, R
Yamashita, K
Citation: M. Aebi et al., Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG, GLYCOBIOLOG, 10(6), 2000, pp. III-V
Authors:
Imbach, T
Schenk, B
Schollen, E
Burda, P
Stutz, A
Grunewald, S
Bailie, NM
King, MD
Jaeken, J
Matthijs, G
Berger, EG
Aebi, M
Hennet, T
Citation: T. Imbach et al., Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie, J CLIN INV, 105(2), 2000, pp. 233-239
Citation: A. Stutz et al., Novel fluoride-labile nucleobase-protecting groups for the synthesis of 3 '(2 ')-O-aminoacylated RNA sequences, HELV CHIM A, 83(9), 2000, pp. 2477-2503