new member of the frizzled family from Drosophila functions as a wingless receptor von Bhanot, P, Brink, M, Samos, C.H, Hsieh, J.C, Wang, Y, Macke, J.P, Andrew, J.P, Andrew, D, Nathans, J, Nusse, R

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Fibroblast Growth Factor (FGF) Homologous Factors: New Members of the FGF Family Implicated in Nervous System Development von Smallwood, Philip M., Munoz-Sanjuan, Ignacio, Tong, Patrick, Macke, Jennifer P., Stewart H. C. Hendry, Gilbert, Debra J., Copeland, Neal G., Jenkins, Nancy A., Nathans, Jeremy

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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 von Xiang, M, Zhou, L, Macke, JP, Yoshioka, T, Hendry, SH, Eddy, RL, Shows, TB, Nathans, J

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Frizzled-3 Is Required for the Development of Major Fiber Tracts in the Rostral CNS von Wang, Yanshu, Thekdi, Nupur, Smallwood, Philip M, Macke, Jennifer P, Nathans, Jeremy

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A locus control region adjacent to the human red and green visual pigment genes von Wang, Yanshu, Macke, Jennifer P., Merbs, Shannath L., Zack, Donald J., Klaunberg, Brenda, Bennett, Jean, Gearhart, John, Nathans, Jeremy

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Saccharomyces cerevisiae PAC2 functions with CIN1, 2 and 4 in a pathway leading to normal microtubule stability von Hoyt, M.A. (The Johns Hopkins University, Baltimore, MD.), Macke, J.P, Tibor Roberts, B, Geiser, J.R

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Screening for amblyopia in preverbal children with photoscreening photographs : Ii. sensitivity and specificity of the mti photoscreener von Tong, Patrick Y, Bassin, Roger E, Enke-Miyazaki, Erinn, Macke, Jennifer P, Tielsch, James M, Stager, David R, Beauchamp, George R, Parks, Marshall M

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Human rod photoreceptor cGMP-gated channel: amino acid sequence, gene structure, and functional expression von Dhallan, RS, Macke, JP, Eddy, RL, Shows, TB, Reed, RR, Yau, KW, Nathans, J

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A Large Family of Putative Transmembrane Receptors Homologous to the Product of the Drosophila Tissue Polarity Gene frizzled(∗) von Wang, Yanshu, Macke, Jennifer P., Abella, Benjamin S., Andreasson, Katrin, Worley, Paul, Gilbert, Debra J., Copeland, Neal G., Jenkins, Nancy A., Nathans, Jeremy

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Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa von Jacobson, SG, Kemp, CM, Cideciyan, AV, Macke, JP, Sung, CH, Nathans, J

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Sequence variation in the androgen receptor gene is not a common determinant of male sexual orientation von MACKE, J. P, NAN HU, HU, S, BAILEY, M, KING, V. L, BROWN, T, HAMER, D, NATHANS, J

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Individual variation in size of the human red and green visual pigment gene array von Macke, JP, Nathans, J

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Identification of novel rhodopsin mutations responsible for retinitis pigmentosa : implications for the structure and function of rhodopsin von MACKE, J. P, DAVENPORT, C. M, GOURAS, P, GOOD, W, NATHANS, J, JACOBSON, S. G, HENNESSEY, J. C, GONZALEZ-FERNANDEZ, F, CONWAY, B. P, HECKENLIVELY, J, PALMER, R, MAUMENEE, I. H, SIEVING, P

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Screening for amblyopia in preverbal children with photoscreening photographs : Iii. improved grading criteria for hyperopia von Tong, Patrick Y, Macke, Jennifer P, Bassin, Roger E, Everett, Mary, Enke-Miyazaki, Erinn, Tielsch, James M, Stager, David R, Parks, Marshall M, Beauchamp, George R

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Autosomal dominant retinitis pigmentosa in a large family: a clinical and molecular genetic study von Rosas, DJ, Roman, AJ, Weissbrod, P, Macke, JP, Nathans, J

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Identification and Characterization of a Conserved Family of Protein Serine/Threonine Phosphatases Homologous to Drosophila Retinal Degeneration C (rdgC) von Sherman, Patti M., Sun, Hui, Macke, Jennifer P., Williams, John, Smallwood, Philip M., Nathans, Jeremy

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Mechanisms of Spectral Tuning in the Mouse Green Cone Pigment von Sun, Hui, Macke, Jennifer P., Nathans, Jeremy

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Saturation mutagenesis of the yeast his3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein von Hill, D.E, Hope, I.A, Macke, J.P, Struhl, K

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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... von Margolis, Russell L., Colin Stine, O., McInnis, Melvin G., Ranen, Neal G., Rubinsztein, David C., Leggo, Jayne, Jones Brando, Lorraine V., Kidwai, Arif S., Loev, Scott J., Breschel, Theresa S., Callahan, Colleen, Simpson, Sylvia G., Raymond DePaulo, J., McMahon, Francis J., Jain, Sanjeev, Paykel, Eugene S., Walsh, Cathy, DeLisi, Lynn E., Crow, Timothy J., Fuller Torrey, E., Ashworth, Roxann G., Macke, Jennifer P., Nathans, Jeremy, Ross, Christopher A.

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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 von Macke, Jennifer P., Hennessey, Jill C., Nathans, Jeremy

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