| 321 |
|
Role and location of the unusual redox-active cysteines in the hydrophobic domain of the transmembrane electron transporter DsbD/
|
Katzen, F
|
National Academy of Sciences [etc.]
|
2003
|
|
|
|
| 322 |
|
Role for Bcl-x~L as an inhibitor of cytosolic cytochrome C accumulation in DNA damage-induced apoptosis
|
Kharbanda, S
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 323 |
|
Role for cells in the presupplementary motor area in updating motor plans
|
Shima, K
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 324 |
|
Role for the class A macrophage scavenger receptor in the phagocytosis of apoptotic thymocytes in vitro
|
Platt, N
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 325 |
|
Role of backbone solvation and electrostatics in generating preferred peptide backbone conformations: Distributions of phi/
|
Avbelj, F
|
National Academy of Sciences [etc.]
|
2003
|
|
|
|
| 326 |
|
Role of B cells in antigen presentation of the hepatitis B core
|
Milichi, D. R
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 327 |
|
Role of cortical N-methyl-D-aspartate receptors in auditory sensory memory and mismatch negativity generation: Implications for schizophrenia
|
Javitt, D. C
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 328 |
|
Role of guanine nucleotide-binding proteins-ras-family or trimeric proteins or both-in Ca^2^+ sensitization of smooth muscle
|
Ming Cui Gong
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 329 |
|
Role of human Pso4 in mammalian DNA repair and association with terminal deoxynucleotidyl transferase/
|
Mahajan, K. N
|
National Academy of Sciences [etc.]
|
2003
|
|
|
|
| 330 |
|
Role of hydrophobic interactions and desolvation in determining the structural properties of a model 褻 peptide
|
Butcher, D. J
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 331 |
|
Role of intrinsic synaptic circuitry in collicular sensorimotor integration
|
Lee, P. H
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 332 |
|
Role of left inferior prefrontal cortex in retrieval of semantic knowledge: A reevaluation
|
Thompson-Schill, S. L
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 333 |
|
Role of leptin in hypothalamic-pituitary function
|
Yu, W. H
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 334 |
|
Role of lipid polymorphism in G protein-membrane interactions: Nonlamellar-prone phospholipids and peripheral protein binding to membranes
|
Escriba, P. V
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 335 |
|
Role of neuronal nitric oxide in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced dopaminergic neurotoxicity
|
Przedborski, S
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 336 |
|
Role of oxidation in the neurotoxic effects of intrastriatal dopamine injections
|
Hastings, T. G
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 337 |
|
Role of p300-family proteins in E1A oncogene induction of cytolytic susceptibility and tumor cell rejection
|
Cook, J. L
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 338 |
|
Role of recombination enzymes in mammalian cell survival
|
Edelmann, W
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
| 339 |
|
Role of residual structure in the unfolded state of a thermophilic protein/
|
Robic, S
|
National Academy of Sciences [etc.]
|
2003
|
|
|
|
| 340 |
|
Role of Saccharomyces cerevisiae Msh2 and Msh3 repair proteins in double-strand break-induced recombination
|
Sugawara, N
|
National Academy of Sciences[etc.]
|
1980
|
|
|
|
