화학공학소재연구정보센터
검색결과 : 15건
No. Article
1 Structural and functional characterization of TgpA, a critical protein for the viability of Pseudomonas aeruginosa
Uruburu M, Mastrangelo E, Bolognesi M, Ferrara S, Bertoni G, Milani M
Journal of Structural Biology, 205(3), 18, 2019
2 Group III alcohol dehydrogenase from Pectobacterium atrosepticum: insights into enzymatic activity and organization of the metal ion-containing region
Elleuche S, Fodor K, von der Heyde A, Klippel B, Wilmanns M, Antranikian G
Applied Microbiology and Biotechnology, 98(9), 4041, 2014
3 On the structural affinity of macromolecules with different biological properties: Molecular dynamics simulations of a series of TEM-1 mutants
Di Giampaolo A, Mazza F, Daidone I, Amicosante G, Perilli M, Aschi M
Biochemical and Biophysical Research Communications, 436(4), 666, 2013
4 Biochemical basis for retinol deficiency induced by the I41N and G75D mutations in human plasma retinol-binding protein
Folli C, Viglione S, Busconi M, Berni R
Biochemical and Biophysical Research Communications, 336(4), 1017, 2005
5 Ab initio study of the prototropic tautomerism of cytosine and guanine and their contribution to spontaneous point mutations
Podolyan Y, Gorb L, Leszczynski J
International Journal of Molecular Sciences, 4(7), 410, 2003
6 Peptide probe study of the critical regulatory domain of the cardiac ryanodine receptor
Yamamoto T, Ikemoto N
Biochemical and Biophysical Research Communications, 291(4), 1102, 2002
7 Recent progress in DNA analysis by capillary electrophoresis
Righetti PG, Gelfi C, D'Acunto MR
Electrophoresis, 23(10), 1361, 2002
8 Single-strand conformation polymorphism for p53 mutation by a combination of neutral pH buffer and temperature gradient in capillary electrophoresis
Gelfi C, Vigano A, De Palma S, Righetti PG, Righetti SC, Corna E, Zunino F
Electrophoresis, 23(10), 1517, 2002
9 Identification of post-translationally modified proteins in proteome studies
Sickmann A, Marcus K, Schafer H, Butt-Dorje E, Lehr S, Herkner A, Suer S, Bahr I, Meyer HE
Electrophoresis, 22(9), 1669, 2001
10 Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome
Perucca-Lostanlen D, Narbonne H, Hernandez JB, Staccini P, Saunieres A, Paquis-Flucklinger V, Vialettes B, Desnuelle C
Biochemical and Biophysical Research Communications, 277(3), 771, 2000