David Valle

An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.

D. Valle, M. Kaiser-Kupfer, G. Mitchell, 1988, The Journal of clinical investigation.

Identification of a fourth half ABC transporter in the human peroxisomal membrane.

D. Valle, G. Jiménez-Sánchez, N. Shani, 1997, Human molecular genetics.

PXA1, a possible Saccharomyces cerevisiae ortholog of the human adrenoleukodystrophy gene.

D. Valle, P. Watkins, N. Shani, 1995, Proceedings of the National Academy of Sciences of the United States of America.

A Saccharomyces cerevisiae homolog of the human adrenoleukodystrophy transporter is a heterodimer of two half ATP-binding cassette transporters.

D. Valle, N. Shani, David Valle, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Colocalization in pericentral hepatocytes in adult mice and similarity in developmental expression pattern of ornithine aminotransferase and glutamine synthetase mRNA.

J E Darnell, D. Valle, J. Darnell, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Selection against lethal alleles in females heterozygous for incontinentia pigmenti.

B. Migeon, J. Axelman, G. Mitchell, 1989, American journal of human genetics.

Phenylketonuria in U.S. blacks: molecular analysis of the phenylalanine hydroxylase gene.

D. Valle, H. Kazazian, G. Steel, 1991, American journal of human genetics.

Hemolytically inactive C4B complement allotype caused by a proline to leucine mutation in the C5-binding site.

D. Valle, B. Julian, R. Wyatt, 1994, The Journal of biological chemistry.