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Results: 1-16 |
Results: 16
PROFESSOR VANDERSCHUEREN,EMMANUEL - OBITUARY
Authors: STEEL G
Citation: G. Steel, PROFESSOR VANDERSCHUEREN,EMMANUEL - OBITUARY, European journal of cancer, 34(6), 1998, pp. 761-761
HUMAN PEX7 ENCODES THE PEROXISOMAL PTS2 RECEPTOR AND IS RESPONSIBLE FOR RHIZOMELIC CHONDRODYSPLASIA PUNCTATA
Authors: BRAVERMAN N STEEL G OBIE C MOSER A MOSER H GOULD SJ VALLE D
Citation: N. Braverman et al., HUMAN PEX7 ENCODES THE PEROXISOMAL PTS2 RECEPTOR AND IS RESPONSIBLE FOR RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, Nature genetics, 15(4), 1997, pp. 369-376
A PEROXISOMAL ABC TRANSPORTER EXHIBITS CONTRASTING RELATIONSHIPS WITHDIFFERENT FATTY-ACID ACTIVATORS
Authors: SHANI N STEEL G VALLE D
Citation: N. Shani et al., A PEROXISOMAL ABC TRANSPORTER EXHIBITS CONTRASTING RELATIONSHIPS WITHDIFFERENT FATTY-ACID ACTIVATORS, Molecular biology of the cell, 8, 1997, pp. 665-665
IDENTIFICATION OF A 4TH HALF ABC TRANSPORTER IN THE HUMAN PEROXISOMALMEMBRANE
Authors: SHANI N JIMENEZSANCHEZ G STEEL G DEAN M VALLE D
Citation: N. Shani et al., IDENTIFICATION OF A 4TH HALF ABC TRANSPORTER IN THE HUMAN PEROXISOMALMEMBRANE, Human molecular genetics, 6(11), 1997, pp. 1925-1931
THE YEAST ORTHOLOG OF THE HUMAN ALD PROTEIN EXHIBITS CONTRASTING RELATIONSHIPS WITH DIFFERENT FATTY-ACID ACTIVATORS
Authors: SHANI N STEEL G VALLE D
Citation: N. Shani et al., THE YEAST ORTHOLOG OF THE HUMAN ALD PROTEIN EXHIBITS CONTRASTING RELATIONSHIPS WITH DIFFERENT FATTY-ACID ACTIVATORS, American journal of human genetics, 61(4), 1997, pp. 131-131
GENOMIC STRUCTURE, MUTATION AND HAPLOTYPE ANALYSIS OF PEX7, THE GENE RESPONSIBLE FOR RHIZOMELIC CHONDRODYSPLASIA PUNCTATA (RCDP)
Authors: BRAVERMAN N STEEL G MOSER H MOSER A GOULD SJ VALLE D
Citation: N. Braverman et al., GENOMIC STRUCTURE, MUTATION AND HAPLOTYPE ANALYSIS OF PEX7, THE GENE RESPONSIBLE FOR RHIZOMELIC CHONDRODYSPLASIA PUNCTATA (RCDP), American journal of human genetics, 61(4), 1997, pp. 960-960
HUMAN AND MURINE GENOMES CONTAIN 2 PROLINE OXIDASE HOMOLOGS, ONE OF WHICH MAPS TO DIGEORGE VCFS REGION AND IS DEFICIENT IN THE PRO/RE/
Authors: LIN WW HU CA STEEL G OBIE C STEEL J LUND J REEVES R RUTBERG J GERAGHTY M VALLE D
Citation: Ww. Lin et al., HUMAN AND MURINE GENOMES CONTAIN 2 PROLINE OXIDASE HOMOLOGS, ONE OF WHICH MAPS TO DIGEORGE VCFS REGION AND IS DEFICIENT IN THE PRO/RE/, American journal of human genetics, 61(4), 1997, pp. 1492-1492
PEROXISOMAL ATP BINDING CASSETTE (ABC) TRANSPORTERS HETERODIMERIZE
Authors: SHANI N STEEL G DEAN M VALLE D
Citation: N. Shani et al., PEROXISOMAL ATP BINDING CASSETTE (ABC) TRANSPORTERS HETERODIMERIZE, Molecular biology of the cell, 7, 1996, pp. 2519-2519
PRODUCTION AND CHARACTERIZATION OF A MOUSE MODEL OF GYRATE ATROPHY OFTHE CHOROID AND RETINA
Authors: WANG T MILAM AH LAWLER A STEEL G VALLE D
Citation: T. Wang et al., PRODUCTION AND CHARACTERIZATION OF A MOUSE MODEL OF GYRATE ATROPHY OFTHE CHOROID AND RETINA, Investigative ophthalmology & visual science, 37(3), 1996, pp. 4788-4788
PRODUCTION AND CHARACTERIZATION OF A MOUSE MODEL OF GYRATE ATROPHY OFTHE CHOROID AND RETINA
Authors: WANG T MILAM AH LAWLER A STEEL G VALLE D
Citation: T. Wang et al., PRODUCTION AND CHARACTERIZATION OF A MOUSE MODEL OF GYRATE ATROPHY OFTHE CHOROID AND RETINA, Pediatric research, 39(4), 1996, pp. 879-879
A MOUSE MODEL OF GYRATE ATROPHY OF THE CHOROID AND RETINA - EARLY RETINAL-PIGMENT EPITHELIUM DAMAGE AND PROGRESSIVE RETINAL DEGENERATION
Authors: WANG T MILAM AH STEEL G VALLE D
Citation: T. Wang et al., 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, 97(12), 1996, pp. 2753-2762
MICE LACKING ORNITHINE-DELTA-AMINO-TRANSFERASE HAVE PARADOXICAL NEONATAL HYPOORNITHINAEMIA AND RETINAL DEGENERATION
Authors: WANG T LAWLER AM STEEL G SIPILA I MILAM AH VALLE D
Citation: T. Wang et al., MICE LACKING ORNITHINE-DELTA-AMINO-TRANSFERASE HAVE PARADOXICAL NEONATAL HYPOORNITHINAEMIA AND RETINAL DEGENERATION, Nature genetics, 11(2), 1995, pp. 185-190
MOUSE MODEL OF GYRATE ATROPHY OF THE CHORIOD AND RETINA
Authors: WANG T MILAM AH STEEL G VALLE D
Citation: T. Wang et al., MOUSE MODEL OF GYRATE ATROPHY OF THE CHORIOD AND RETINA, American journal of human genetics, 57(4), 1995, pp. 273-273
PYRIDOXINE-RESPONSIVE GYRATE ATROPHY OF THE CHOROID AND RETINA - CLINICAL AND BIOCHEMICAL CORRELATES OF THE MUTATION A226V
Authors: MICHAUD J THOMPSON GN BRODY LC STEEL G OBIE C FONTAINE G SCHAPPERT K KEITH CG VALLE D MITCHELL GA
Citation: J. Michaud et al., PYRIDOXINE-RESPONSIVE GYRATE ATROPHY OF THE CHOROID AND RETINA - CLINICAL AND BIOCHEMICAL CORRELATES OF THE MUTATION A226V, American journal of human genetics, 56(3), 1995, pp. 616-622
TARGETED DISRUPTION OF MURINE ORNITHINE AMINOTRANSFERASE GENE - SURPRISING NEONATAL LETHALITY RESCUED BY ARGININE THERAPY AND POSSIBLE MOUSE MODEL FOR GYRATE ATROPHY
Authors: WANG T LAWLER AM STEEL G VALLE E
Citation: T. Wang et al., TARGETED DISRUPTION OF MURINE ORNITHINE AMINOTRANSFERASE GENE - SURPRISING NEONATAL LETHALITY RESCUED BY ARGININE THERAPY AND POSSIBLE MOUSE MODEL FOR GYRATE ATROPHY, American journal of human genetics, 55(3), 1994, pp. 10000004-10000004
TELEPHONE ACCESS TO A UNIVERSITY HIV AIDS CLINIC
Authors: MORRISON RE STEEL G ARHEART KL SARGENT SJ DORKO CS
Citation: Re. Morrison et al., TELEPHONE ACCESS TO A UNIVERSITY HIV AIDS CLINIC, Clinical research, 41(4), 1993, pp. 10000751-10000751
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