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Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

Nature genetics, 1996-04, Vol.12 (4), p.376-384

1996

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The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase

Nature (London), 1992-07, Vol.358 (6383), p.239-242

1992

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De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis

Nature genetics, 1998-04, Vol.18 (4), p.311-312

1998

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Neto2 is a KCC2 interacting protein required for neuronal Cl⁻ regulation in hippocampal neurons

Proceedings of the National Academy of Sciences - PNAS, 2013-02, Vol.110 (9), p.3561-3566

2013

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Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies

Neuron (Cambridge, Mass.), 1992-06, Vol.8 (6), p.1171-1184

1992

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Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration

Human molecular genetics, 2011-01, Vol.20 (2), p.322-335

2011

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Cloning of the human and murine ROM1 genes: genomic organization and sequence conservation

Human molecular genetics, 1993-04, Vol.2 (4), p.385-391

1993

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A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene

American journal of human genetics, 1998-11, Vol.63 (5), p.1307-1315

1998

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E.coli host strains significantly affect the quality of small scale plasmid DNA preparations used for sequencing

Nucleic acids research, 1993-04, Vol.21 (7), p.1677-1678

1993

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Large Life-Course Cohorts for Characterizing Genetic and Environmental Contributions: The Need for More Thoughtful Designs

Epidemiology (Cambridge, Mass.), 2006-11, Vol.17 (6), p.595-598

2006

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Developmental expression of a novel murine homeobox gene ( Chx10): Evidence for roles in determination of the neuroretina and inner nuclear layer

Neuron (Cambridge, Mass.), 1994-08, Vol.13 (2), p.377-393

1994

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Mutation analysis of the ROM1 gene in retinitis pigmentosa

Human molecular genetics, 1995-12, Vol.4 (12), p.2424-2424

1995

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Hereditary metabolic disease in infancy: new concepts and new disorders

Current opinion in pediatrics, 1992-04, Vol.4 (2), p.228-240

1992

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Use of tetrahydropterins in the treatment of hyperphenylalaninemia due to defective synthesis of tetrahydrobiopterin: evidence that peripherally administered tetrahydropterins enter the brain

Pediatrics (Evanston), 1982-09, Vol.70 (3), p.376-380

1982

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A FILTER PAPER SAMPLING METHOD FOR THE URIC ACID:CREATININE RATIO IN URINE

Pediatrics (Evanston), 1972-03, Vol.49 (3), p.351-351

1972

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A FILTER PAPER SAMPLING METHOD FOR THE URIC ACID:CREATININE RATIO IN URINE

Pediatrics (Evanston), 1972-01, Vol.49 (1), p.80-84

1972

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Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase

De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis

Neto2 is a KCC2 interacting protein required for neuronal Cl⁻ regulation in hippocampal neurons

Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies

Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration

Cloning of the human and murine ROM1 genes: genomic organization and sequence conservation

A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene

E.coli host strains significantly affect the quality of small scale plasmid DNA preparations used for sequencing

Large Life-Course Cohorts for Characterizing Genetic and Environmental Contributions: The Need for More Thoughtful Designs

Developmental expression of a novel murine homeobox gene ( Chx10): Evidence for roles in determination of the neuroretina and inner nuclear layer

Mutation analysis of the ROM1 gene in retinitis pigmentosa

Hereditary metabolic disease in infancy: new concepts and new disorders

Use of tetrahydropterins in the treatment of hyperphenylalaninemia due to defective synthesis of tetrahydrobiopterin: evidence that peripherally administered tetrahydropterins enter the brain

A FILTER PAPER SAMPLING METHOD FOR THE URIC ACID:CREATININE RATIO IN URINE

A FILTER PAPER SAMPLING METHOD FOR THE URIC ACID:CREATININE RATIO IN URINE

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