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new member of the frizzled family from Drosophila functions as a wingless receptor

Nature (London), 1996-07, Vol.382 (6588), p.225-230

1996

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Fibroblast Growth Factor (FGF) Homologous Factors: New Members of the FGF Family Implicated in Nervous System Development

Proceedings of the National Academy of Sciences - PNAS, 1996-09, Vol.93 (18), p.9850-9857

1996

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The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons

The Journal of neuroscience, 1995-07, Vol.15 (7), p.4762-4785

1995

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Frizzled-3 Is Required for the Development of Major Fiber Tracts in the Rostral CNS

The Journal of neuroscience, 2002-10, Vol.22 (19), p.8563-8573

2002

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A locus control region adjacent to the human red and green visual pigment genes

Neuron (Cambridge, Mass.), 1992-09, Vol.9 (3), p.429-440

1992

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Saccharomyces cerevisiae PAC2 functions with CIN1, 2 and 4 in a pathway leading to normal microtubule stability

Genetics (Austin), 1997-07, Vol.146 (3), p.849-857

1997

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Screening for amblyopia in preverbal children with photoscreening photographs : Ii. sensitivity and specificity of the mti photoscreener

Ophthalmology (Rochester, Minn.), 2000-09, Vol.107 (9), p.1623-1629

2000

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Human rod photoreceptor cGMP-gated channel: amino acid sequence, gene structure, and functional expression

The Journal of neuroscience, 1992-08, Vol.12 (8), p.3248-3256

1992

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A Large Family of Putative Transmembrane Receptors Homologous to the Product of the Drosophila Tissue Polarity Gene frizzled(∗)

The Journal of biological chemistry, 1996-02, Vol.271 (8), p.4468-4476

1996

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Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa

Investigative ophthalmology & visual science, 1994-04, Vol.35 (5), p.2521-2534

1994

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Sequence variation in the androgen receptor gene is not a common determinant of male sexual orientation

American journal of human genetics, 1993-10, Vol.53 (4), p.844-852

1993

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Individual variation in size of the human red and green visual pigment gene array

Investigative ophthalmology & visual science, 1997-04, Vol.38 (5), p.1040-1043

1997

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Identification of novel rhodopsin mutations responsible for retinitis pigmentosa : implications for the structure and function of rhodopsin

American journal of human genetics, 1993-07, Vol.53 (1), p.80-89

1993

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Screening for amblyopia in preverbal children with photoscreening photographs : Iii. improved grading criteria for hyperopia

Ophthalmology (Rochester, Minn.), 2000-09, Vol.107 (9), p.1630-1636

2000

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Autosomal dominant retinitis pigmentosa in a large family: a clinical and molecular genetic study

Investigative ophthalmology & visual science, 1994-07, Vol.35 (8), p.3134-3144

1994

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Identification and Characterization of a Conserved Family of Protein Serine/Threonine Phosphatases Homologous to Drosophila Retinal Degeneration C (rdgC)

Proceedings of the National Academy of Sciences - PNAS, 1997-10, Vol.94 (21), p.11639-11644

1997

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Mechanisms of Spectral Tuning in the Mouse Green Cone Pigment

Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (16), p.8860-8865

1997

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Saturation mutagenesis of the yeast his3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein

Science (American Association for the Advancement of Science), 1986-10, Vol.234 (4775), p.451-457

1986

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Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347

Human molecular genetics, 1995-04, Vol.4 (4), p.775-776

1995

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Rhodopsin mutation proline super(347)-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347

Human molecular genetics, 1995-01, Vol.4 (4), p.775-776

1995

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Saturation mutagenesis of the yeast his 3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein

Science (American Association for the Advancement of Science), 1986, Vol.234 (4775), p.451-457

1986

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Training deep neural density estimators to identify mechanistic models of neural dynamics

eLife, 2020-09, Vol.9

2020

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The surprising thermal properties of CM carbonaceous chondrites

Meteoritics & planetary science, 2020-08, Vol.55 (8), p.n/a

2020

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HIV-1 Neutralizing Antibody Signatures and Application to Epitope-Targeted Vaccine Design

Cell host & microbe, 2019-01, Vol.25 (1), p.59-72.e8

2019

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new member of the frizzled family from Drosophila functions as a wingless receptor

Fibroblast Growth Factor (FGF) Homologous Factors: New Members of the FGF Family Implicated in Nervous System Development

The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons

Frizzled-3 Is Required for the Development of Major Fiber Tracts in the Rostral CNS

A locus control region adjacent to the human red and green visual pigment genes

Saccharomyces cerevisiae PAC2 functions with CIN1, 2 and 4 in a pathway leading to normal microtubule stability

Screening for amblyopia in preverbal children with photoscreening photographs : Ii. sensitivity and specificity of the mti photoscreener

Human rod photoreceptor cGMP-gated channel: amino acid sequence, gene structure, and functional expression

A Large Family of Putative Transmembrane Receptors Homologous to the Product of the Drosophila Tissue Polarity Gene frizzled(∗)

Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa

Sequence variation in the androgen receptor gene is not a common determinant of male sexual orientation

Individual variation in size of the human red and green visual pigment gene array

Identification of novel rhodopsin mutations responsible for retinitis pigmentosa : implications for the structure and function of rhodopsin

Screening for amblyopia in preverbal children with photoscreening photographs : Iii. improved grading criteria for hyperopia

Autosomal dominant retinitis pigmentosa in a large family: a clinical and molecular genetic study

Identification and Characterization of a Conserved Family of Protein Serine/Threonine Phosphatases Homologous to Drosophila Retinal Degeneration C (rdgC)

Mechanisms of Spectral Tuning in the Mouse Green Cone Pigment

Saturation mutagenesis of the yeast his3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein

cDNA Cloning of a Human Homologue of the Caenorhabditis Elegans Cell Fate-Determining Gene Mab-21: Expression, Chromosomal Localization and Analysis of a Highly Polymorphic (CAG)n Trinucleotide Repeat

Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347

Rhodopsin mutation proline super(347)-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347

Saturation mutagenesis of the yeast his 3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein

Training deep neural density estimators to identify mechanistic models of neural dynamics

The surprising thermal properties of CM carbonaceous chondrites

HIV-1 Neutralizing Antibody Signatures and Application to Epitope-Targeted Vaccine Design

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