Partial amino acid sequences of the murine fourth component of complement (C4): demonstration of homology with human C4 and identification of the amino-terminal subunit in pro-C4.

Por Parker, K L, Shreffler, D C, Capra, J D
Publicado em 1980

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.

Por Amor, M, Parker, K L, Globerman, H, New, M I, White, P C
Publicado em 1988

Nonsense mutation causing steroid 21-hydroxylase deficiency.

Por Globerman, H, Amor, M, Parker, K L, New, M I, White, P C
Publicado em 1988

The orphan nuclear receptor NGFI-B regulates expression of the gene encoding steroid 21-hydroxylase.

Por Wilson, T E, Mouw, A R, Weaver, C A, Milbrandt, J, Parker, K L
Publicado em 1993

Amino acid sequence homologies and glycosylation differences between the fourth component of murine complement and sex-limited protein.

Por Karp, D R, Parker, K L, Shreffler, D C, Slaughter, C, Capra, J D
Publicado em 1982

Nucleotide sequence analysis of murine 21-hydroxylase genes: mutations affecting gene expression.

Por Chaplin, D D, Galbraith, L J, Seidman, J G, White, P C, Parker, K L
Publicado em 1986

Expression of murine 21-hydroxylase in mouse adrenal glands and in transfected Y1 adrenocortical tumor cells.

Por Parker, K L, Chaplin, D D, Wong, M, Seidman, J G, Smith, J A, Schimmer, B P
Publicado em 1985