Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene.

Por Melton, D W, Konecki, D S, Brennand, J, Caskey, C T
Publicado em 1984

Direct selection of DNA sequences conserved between species.

Por Sedlacek, Z, Konecki, D S, Siebenhaar, R, Kioschis, P, Poustka, A
Publicado em 1993

Genetic and Physical Mapping of the Locus for Autosomal Dominant Renal Fanconi Syndrome, on Chromosome 15q15.3

Por Lichter-Konecki, U., Broman, K. W., Blau, E. B., Konecki, D. S.
Publicado em 2001

Hypoxanthine-guanine phosphoribosyltransferase genes of mouse and Chinese hamster: construction and sequence analysis of cDNA recombinants.

Por Konecki, D S, Brennand, J, Fuscoe, J C, Caskey, C T, Chinault, A C
Publicado em 1982

Cloned cDNA sequences of the hypoxanthine/guanine phosphoribosyltransferase gene from a mouse neuroblastoma cell line found to have amplified genomic sequences.

Por Brennand, J, Chinault, A C, Konecki, D S, Melton, D W, Caskey, C T
Publicado em 1982

In vitro translation of hypoxanthine/guanine phosphoribosyltransferase mRNA: characterization of a mouse neuroblastoma cell line that has elevated levels of hypoxanthine/guanine ph...

Por Melton, D W, Konecki, D S, Ledbetter, D H, Hejtmancik, J F, Caskey, C T
Publicado em 1981

Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene.

Por Goltsov, A A, Eisensmith, R C, Konecki, D S, Lichter-Konecki, U, Woo, S L
Publicado em 1992

The primary structure of bovine chromogranin A: a representative of a class of acidic secretory proteins common to a variety of peptidergic cells.

Por Benedum, U M, Baeuerle, P A, Konecki, D S, Frank, R, Powell, J, Mallet, J, Huttner, W B
Publicado em 1986

The primary structure of human secretogranin I (chromogranin B): comparison with chromogranin A reveals homologous terminal domains and a large intervening variable region.

Por Benedum, U M, Lamouroux, A, Konecki, D S, Rosa, P, Hille, A, Baeuerle, P A, Frank, R, Lottspeich, F, Mallet, J, Huttner, W B
Publicado em 1987

Multiple origins for phenylketonuria in Europe

Por Eisensmith, R. C., Okano, Y., Dasovich, M., Wang, T., Güttler, F., Lou, H., Guldberg, P., Lichter-Konecki, U., Konecki, D. S., Svensson, E., Hagenfeldt, L., Rey, F., Munnich, A., Lyonnet, S., Cockburn, F., Connor, J. M., Pembrey, M. E., Smith, I., Gitzelmann, R., Steinmann, B., Apold, J., Eiken, H. G., Giovannini, M., Riva, E., Longhi, R., Romano, C., Cerone, R., Naughten, E. R., Mullins, C., Cahalane, S., Özalp, I., Fekete, G., Schuler, D., Berencsi, G. Y., Nász, I., Brdicka, R., Kamaryt, J., Pijackova, A., Cabalska, B., Boszkowa, K., Schwartz, E., Kalinin, V. N., Jin, L., Chakraborty, R., Woo, S. L. C.
Publicado em 1992