Mitochondrial protein transport--a system in search of mutations.

Por Fenton, W A
Publicado em 1995

GroEL-mediated protein folding.

Por Fenton, W. A., Horwich, A. L.
Publicado em 1997

Identification of RNA splicing errors resulting in human ornithine transcarbamylase deficiency.

Por Carstens, R P, Fenton, W A, Rosenberg, L R
Publicado em 1991

The beta subunit of the mitochondrial processing peptidase from rat liver: cloning and sequencing of a cDNA and comparison with a proposed family of metallopeptidases.

Por Paces, V, Rosenberg, L E, Fenton, W A, Kalousek, F
Publicado em 1993

Immunochemical studies on cultured fibroblasts from patients with inherited methylmalonic acidemia.

Por Kolhouse, J F, Utley, C, Fenton, W A, Rosenberg, L E
Publicado em 1981

Immunochemical studies of fibroblasts from patients with methylmalonyl-CoA mutase apoenzyme deficiency: detection of a mutation interfering with mitochondrial import.

Por Fenton, W A, Hack, A M, Kraus, J P, Rosenberg, L E
Publicado em 1987

Identification and application of additional restriction fragment length polymorphisms at the human ornithine transcarbamylase locus.

Por Fox, J E, Hack, A M, Fenton, W A, Rosenberg, L E
Publicado em 1986

Mutation eliminating mitochondrial leader sequence of methylmalonyl-CoA mutase causes muto methylmalonic acidemia.

Por Ledley, F D, Jansen, R, Nham, S U, Fenton, W A, Rosenberg, L E
Publicado em 1990

Mitochondrial import and processing of mutant human ornithine transcarbamylase precursors in cultured cells.

Por Isaya, G, Fenton, W A, Hendrick, J P, Furtak, K, Kalousek, F, Rosenberg, L E
Publicado em 1988

Molecular basis for dysfunction of some mutant forms of methylmalonyl-CoA mutase: deductions from the structure of methionine synthase.

Por Drennan, C L, Matthews, R G, Rosenblatt, D S, Ledley, F D, Fenton, W A, Ludwig, M L
Publicado em 1996