Items where Subject is "codon processing"

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Jump to: A | B | F | G | N
Number of items at this level: 6.

A

Atkins, J. F., Gesteland, R. F. (August 1975) The synthetase gene of the RNA phages R17, MS2 and f2 has a single UAG terminator codon. Mol Gen Genet, 139 (1). pp. 19-31.

B

Brown, P., Cervenáková, L., Goldfarb, L. G., McCombie, W. R., Rubenstein, R., Will, R. G., Pocchiari, M., Martinez-Lage, J. F., Scalici, C., Masullo, C., Graupera, G., Ligan, J., Gajdusek, D. C. (1994) Iatrogenic Creutzfeldt-Jakob disease: An example of the interplay between ancient genes and modern medicine. Neurology, 44 (2). pp. 291-293. ISSN 00283878 (ISSN)

F

Futcher, B., Latter, G. I., Monardo, P., McLaughlin, C. S., Garrels, J. I. (November 1999) A sampling of the yeast proteome. Molecular and Cellular Biology, 19 (11). pp. 7357-68. ISSN 0270-7306 (Print)

G

Gesteland, R. F., Wolfner, M., Grisafi, P., Fink, G., Botstein, D., Roth, J. R. (March 1976) Yeast suppressors of UAA and UAG nonsense codons work efficiently in vitro via tRNA. Cell, 7 (3). pp. 381-90.

Goldfarb, L. G., Brown, P., Haltia, M., Cathala, F., McCombie, W. R., Kovanen, J., Červeňáková, L., Goldin, L., Nieto, A., Godec, M. S., Asher, D. M., Gajdusek, D. C. (1992) Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin. Annals of neurology, 31 (3). pp. 274-281. ISSN 03645134 (ISSN)

N

Nieto, A., Goldfarb, L. G., Brown, P., McCombie, W. R., Trapp, S., Asher, D. M., Gajdusek, D. C. (1991) Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families [29]. Lancet, 337 (8741). pp. 622-623. ISSN 01406736 (ISSN)

This list was generated on Sat Nov 30 21:08:40 2024 EST.