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01/1981
The purpose of this study was to determine whether home economists in higher education perceived significant others as having played an influential role in... 
Home economics education
Dissertation
Ophthalmic Genetics, ISSN 1381-6810, 1983, Volume 3, Issue 2, pp. 61 - 72
Recent work from our laboratory on the molecular genetics of the lens crystallins is reviewed briefly. Examples of how cDNA and genomic clones have been used... 
eye | hereditary disease | cataract | gene | DNA | crystallins | lens | cloning | Eye | Cataract | Crystallins | Gene | Cloning | Lens | Hereditary disease
Journal Article
Nature, ISSN 0028-0836, 03/1983, Volume 302, Issue 5906, pp. 310 - 315
A 23,000 molecular weight beta-crystallin (beta 23) of the murine eye lens is encoded in a 4.1 +/- 0.3-kilobase gene containing three introns. Each of the four... 
Biological Evolution | Amino Acid Sequence | Animals | Base Sequence | Genes | RNA, Messenger - genetics | Models, Molecular | Protein Conformation | Crystallins - genetics | Mice
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/1986, Volume 83, Issue 5, pp. 1203 - 1207
The isolation and characterization of a cDNA clone for the mRNA of human ornithine aminotransferase (OATase; ornithine--oxo-acid aminotransferase;... 
Enzymes | Messenger RNA | Complementary DNA | RNA | Liver | Antibodies | Retina | Amino acids | Protein precursors | Retinoblastoma
Journal Article
Genomics, ISSN 0888-7543, 1989, Volume 4, Issue 4, pp. 539 - 545
Previous study has shown that the usual DNA marker for Norrie disease, the L1.28 probe which identifies the DXS7 locus, can recombine with the disease locus.... 
GENETICS & HEREDITY | DNA Probes | Transaminases - genetics | Humans | Hybrid Cells | Male | Genetic Markers | Blindness - genetics | Lod Score | Polymorphism, Genetic | Blindness - enzymology | Animals | Polymorphism, Restriction Fragment Length | Recombination, Genetic | DNA | Ornithine-Oxo-Acid Transaminase - genetics | Retina - abnormalities | X Chromosome | Female | Mice
Journal Article
Experimental Eye Research, ISSN 0014-4835, 1990, Volume 50, Issue 6, pp. 759 - 770
Journal Article
Genomics, ISSN 0888-7543, 1990, Volume 6, Issue 1, pp. 123 - 128
A human ornithine aminotransferase (OAT) locus has been mapped to the Xp 11.2, as has the Norrie disease locus. We used a cDNA probe to investigate a... 
Blotting, Southern | Transaminases - genetics | Humans | Retinal Detachment - congenital | Restriction Mapping | Lod Score | Syndrome | Polymorphism, Restriction Fragment Length | Pedigree | Recombination, Genetic | Ornithine-Oxo-Acid Transaminase - genetics | X Chromosome | Intellectual Disability | Hearing Loss | Genetic Linkage
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 07/1992, Volume 51, Issue 1, pp. 81 - 91
A generalized deficiency of the mitochondrial matrix enzyme ornithine aminotransferase (OAT) is the inborn error in gyrate atrophy (GA), an autosomal recessive... 
Amino Acid Sequence | Nucleic Acid Denaturation | Electrophoresis, Polyacrylamide Gel | Humans | Molecular Sequence Data | Gyrate Atrophy - genetics | Male | RNA, Messenger - biosynthesis | Codon | Base Sequence | Ornithine-Oxo-Acid Transaminase - genetics | Polymerase Chain Reaction | Adult | Mutation
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 06/1992, Volume 267, Issue 18, pp. 12950 - 12954
Journal Article
Human Genetics, ISSN 0340-6717, 11/1992, Volume 90, Issue 3, pp. 305 - 307
Gyrate atrophy (GA) is an autosomal recessive eye disease involving a progressive loss of vision due to chorioretinal degeneration in which the mitochondrial... 
MUTATION | DEFECT | GENETICS & HEREDITY | DELTA-AMINOTRANSFERASE | RETINA | VITAMIN-B6 | DEFICIENCY | RNA Splicing | Base Sequence | DNA | Humans | Ornithine-Oxo-Acid Transaminase - genetics | Polymerase Chain Reaction | Adenine | Molecular Sequence Data | Female | Gyrate Atrophy - genetics | Mutation | Guanine
Journal Article
Experimental Cell Research, ISSN 0014-4827, 1993, Volume 204, Issue 2, pp. 311 - 320
A continuous cell line of rat retinal pigment epithelium (RPE), named BPEI-1, has been established and characterized. Sheets of pure RPE cells, uncontaminated... 
LOCALIZATION | ROD OUTER SEGMENTS | PHAGOCYTOSIS | CYTOSKELETON | ONCOLOGY | RPE | FIBROBLAST GROWTH-FACTOR | DNA-SYNTHESIS | BINDING PROTEIN | PLASMA-MEMBRANE | CULTURE | CELL BIOLOGY | Cell Line | Keratins - analysis | Animals | Retina - cytology | Rod Cell Outer Segment - metabolism | Antibodies | Rats | Epithelial Cells | Binding Sites, Antibody | Carrier Proteins - analysis | Rats, Inbred Strains | Phagocytosis
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 1996, Volume 17, Issue 3, pp. 87 - 94
Journal Article
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