| 257 - 263 |
Experimental infection of mice with Yersinia enterocolitica serotype O9 by oral and parenteral routes: Spreading and enterotropism of virulent yersiniae
Ruiz-Bravo A, Moreno E, Sampedro A, Jimenez-Valera M |
| 264 - 267 |
Distribution of the rubredoxin gene among the Clostridium butyricum species
Gerard P, Amine J, Raval G, Petitdemange H |
| 268 - 272 |
Derivation of extracellular polysaccharide-deficient variants from a serotype a strain of Pasteurella multocida
Champlin FR, Patterson CE, Austin FW, Ryals PE |
| 273 - 278 |
Release of outer membrane vesicles from Bordetella pertussis
Hozbor D, Rodriguez ME, Fernandez J, Lagares A, Guiso N, Yantorno O |
| 279 - 284 |
Selection of vaginal H2O2-generating Lactobacillus species for probiotic use
Ocana VS, Holgado AAPD, Nader-Macias ME |
| 285 - 289 |
Transient production of formate during chemolithotrophic growth of anaerobic microorganisms on hydrogen
Peters V, Janssen PH, Conrad R |
| 290 - 294 |
The Saccharomyces cerevisiae mevalonate diphosphate decarboxylase (Erg19p) forms homodimers in vivo, and a single substitution in a structurally conserved region impairs dimerization
Cordier H, Lacombe C, Karst F, Berges T |
| 295 - 299 |
Two fluorescent markers identify the vacuolar system of Schizophyllum commune
Inselman AL, Gathman AC, Lilly WW |
| 300 - 308 |
Kinetic behavior of some polyphosphate-accumulating bacteria isolates in the presence of nitrate and oxygen
Merzouki M, Bernet N, Delgenes JP, Moletta R, Benlemlih M |
| 309 - 311 |
Buchnera plasmid-associated trpEG probably originated from a chromosomal location between hsIU and fpr
Clark MA, Baumann P, Moran NA |
