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Gary Steel

Research Profile

Chemicals & Drugs

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Molecular Sequence Data

Physiology

Disorders

Genes & Molecular Sequences

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Mouse

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Anatomy

Choroid

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Publications

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Pei-Lung Chen; Dimitrios Avramopoulos; Virginia K Lasseter; John A McGrath; MARGARET D FALLIN; Kung-Yee Liang; Gerald Nestadt; Ningping Feng; Gary Steel; Andrew S Cutting; Paula S Wolyniec; Ann E Pulver; David Valle
Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia.
Alecia Willis; Hans Uli Bender; Gary Steel; David Valle
PRODH variants and risk for schizophrenia.
HU CHIEN-AN; Steven P Donald; Jian Yu; Wei-Wen Lin; Zhihe Liu; Gary Steel; Cassandra Obie; David Valle; James M Phang
Overexpression of proline oxidase induces proline-dependent and mitochondria-mediated apoptosis.

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All Publications

2009: Pei-Lung Chen; Dimitrios Avramopoulos; Virginia K Lasseter; John A McGrath; MARGARET D FALLIN; Kung-Yee Liang; Gerald Nestadt; Ningping Feng; Gary Steel; Andrew S Cutting; Paula S Wolyniec; Ann E Pulver; David Valle
Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia.
American journal of human genetics 2009;84(1):21-34.
2008: Alecia Willis; Hans Uli Bender; Gary Steel; David Valle
PRODH variants and risk for schizophrenia.
Amino acids 2008;35(4):673-9.
2007: HU CHIEN-AN; Steven P Donald; Jian Yu; Wei-Wen Lin; Zhihe Liu; Gary Steel; Cassandra Obie; David Valle; James M Phang
Overexpression of proline oxidase induces proline-dependent and mitochondria-mediated apoptosis.
Molecular and cellular biochemistry 2007;295(1-2):85-92.
2005: Sabine Weller; Ivelisse Cajigas; James C Morrell; Cassandra Obie; Gary Steel; Stephen J Gould; David Valle
Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis.
American journal of human genetics 2005;76(6):987-1007.
2005: Hans-Ulrich Bender; Shlomo Almashanu; Gary Steel; HU CHIEN-AN; Wei-Wen Lin; Alecia Willis; Ann E Pulver; David Valle
Functional consequences of PRODH missense mutations.
American journal of human genetics 2005;76(3):409-20.
2002: Nancy Braverman; Li Chen; Paul Lin; Cassandra Obie; Gary Steel; Pamela Douglas; Pranesh K Chakraborty; Joe T R Clarke; Avihu Boneh; Ann B Moser; Hugo Moser; David Valle
Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype.
Human mutation 2002;20(4):284-97.
2000: Matthias R Baumgartner; HU CHIEN-AN; Shlomo Almashanu; Gary Steel; Cassandra Obie; Bernard Aral; Daniel Rabier; Pierre Kamoun; Jean-Marie Saudubray; David Valle
Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding delta(1)-pyrroline-5-carboxylate synthase.
Human molecular genetics 2000;9(19):2853-8.
2000: Tao Wang; Gary Steel; Ann H Milam; David Valle
Correction of ornithine accumulation prevents retinal degeneration in a mouse model of gyrate atrophy of the choroid and retina.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(3):1224-9.
2000: Nancy Braverman; Gary Steel; Paul Lin; Ann B Moser; Hugo Moser; David Valle
PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter.
Genomics 2000;63(2):181-92.
1999: J A Camacho; Cassandra Obie; B Biery; Barbara K Goodman; HU CHIEN-AN; Shlomo Almashanu; Gary Steel; R Casey; M Lambert; G A Mitchell; David Valle
Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter.
Nature genetics 1999;22(2):151-8.
1997: Nancy Braverman; Gary Steel; Cassandra Obie; Ann B Moser; Hugo Moser; Stephen J Gould; David Valle
Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata.
Nature genetics 1997;15(4):369-76.
1996: T Wang; Ann H Milam; Gary Steel; David Valle
A mouse model of gyrate atrophy of the choroid and retina. Early retinal pigment epithelium damage and progressive retinal degeneration.
The Journal of clinical investigation 1996;97(12):2753-62.
1995: T Wang; Ann M Lawler; Gary Steel; I Sipila; Ann H Milam; David Valle
Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degeneration.
Nature genetics 1995;11(2):185-90.
1995: J Michaud; G N Thompson; L C Brody; Gary Steel; Cassandra Obie; G Fontaine; K Schappert; C G Keith; David Valle; Grant A Mitchell
Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226V.
American journal of human genetics 1995;56(3):616-22.
1992: J Michaud; L C Brody; Gary Steel; G Fontaine; L S Martin; David Valle; G Mitchell
Strand-separating conformational polymorphism analysis: efficacy of detection of point mutations in the human ornithine delta-aminotransferase gene.
Genomics 1992;13(2):389-94.
1992: L C Brody; Grant A Mitchell; Cassandra Obie; J Michaud; Gary Steel; G Fontaine; MF Robert; I Sipila; M Kaiser-Kupfer; David Valle
Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences.
The Journal of biological chemistry 1992;267(5):3302-7.
1991: K J Hofman; Gary Steel; Haig Kazazian ; David Valle
Phenylketonuria in U.S. blacks: molecular analysis of the phenylalanine hydroxylase gene.
American journal of human genetics 1991;48(4):791-8.
1991: Grant A Mitchell; D Labuda; G Fontaine; J M Saudubray; J P Bonnefont; S Lyonnet; L C Brody; Gary Steel; Cassandra Obie; David Valle
Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(3):815-9.
1991: J F Engelhardt; Gary Steel; David Valle
Transcriptional analysis of the human ornithine aminotransferase promoter.
The Journal of biological chemistry 1991;266(2):752-8.
1989: Grant A Mitchell; L C Brody; I Sipila; J E Looney; C Wong; J F Engelhardt; A S Patel; Gary Steel; Cassandra Obie; M Kaiser-Kupfer
At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(1):197-201.
1988: Grant A Mitchell; J E Looney; L C Brody; Gary Steel; M Suchanek; J F Engelhardt; H F Willard; David Valle
Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene.
The Journal of biological chemistry 1988;263(28):14288-95.
1988: Grant A Mitchell; L C Brody; J Looney; Gary Steel; M Suchanek; C Dowling; V Der Kaloustian; M Kaiser-Kupfer; David Valle
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.
The Journal of clinical investigation 1988;81(2):630-3.