Regulation of Gene Expression in the Mammalian Eye and Its Relevance to Eye Disease von Scheetz, Todd E., Kim, Kwang-Youn A., Swiderski, Ruth E., Philp, Alisdair R., Braun, Terry A., Knudtson, Kevin L., Dorrance, Anne M., DiBona, Gerald F., Huang, Jian, Casavant, Thomas L., Sheffield, Val C., Stone, Edwin M.

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A Knockin Mouse Model of the Bardet-Biedl Syndrome 1 M390R Mutation Has Cilia Defects, Ventriculomegaly, Retinopathy, and Obesity von Davis, Roger E., Swiderski, Ruth E., Rahmouni, Kamal, Nishimura, Darryl Y., Mullins, Robert F., Agassandian, Khristofor, Philp, Alisdair R., Searby, Charles C., Andrews, Michael P., Thompson, Stewart, Berry, Christopher J., Thedens, Daniel R., Yang, Baoli, Weiss, Robert M., Cassell, Martin D., Stone, Edwin M., Sheffield, Val C.

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Visual Impairment in the Absence of Dystroglycan von Satz, Jakob S, Philp, Alisdair R, Nguyen, Huy, Kusano, Hajime, Lee, Jane, Turk, Rolf, Riker, Megan J, Hernandez, Jasmine, Weiss, Robert M, Anderson, Michael G, Mullins, Robert F, Moore, Steven A, Stone, Edwin M, Campbell, Kevin P

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Identical mutation in a novel retinal gene causes progressive rod–cone degeneration in dogs and retinitis pigmentosa in humans von Zangerl, Barbara, Goldstein, Orly, Philp, Alisdair R., Lindauer, Sarah J.P., Pearce-Kelling, Susan E., Mullins, Robert F., Graphodatsky, Alexander S., Ripoll, Daniel, Felix, Jeanette S., Stone, Edwin M., Acland, Gregory M., Aguirre, Gustavo D.

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Bardet-Biedl syndrome in Denmark--report of 13 novel sequence variations in six genes von Hjortshøj, Tina Duelund, Grønskov, Karen, Philp, Alisdair R, Nishimura, Darryl Y, Riise, Ruth, Sheffield, Val C, Rosenberg, Thomas, Brøndum-Nielsen, Karen

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Visual function testing: A quantifiable visually guided behavior in mice von Thompson, Stewart, Philp, Alisdair R., Stone, Edwin M.

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Divergent Phenotypes of Vision and Accessory Visual Function in Mice with Visual Cycle Dysfunction (Rpe65rd12) or Retinal Degeneration (rd/rd) von Thompson, Stewart, Mullins, Robert F, Philp, Alisdair R, Stone, Edwin M, Mrosovsky, N

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Vertebrate ancient (VA) opsin and extraretinal photoreception in the Atlantic salmon (Salmo salar) von Philp, A R, Garcia-Fernandez, J M, Soni, B G, Lucas, R J, Bellingham, J, Foster, R G

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Novel retinal photoreceptors von Soni, Bobby G, Philp, Alisdair R, Foster, Russell G, Knox, Barry E

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A novel rod-like opsin isolated from the extra-retinal photoreceptors of teleost fish von Philp, Alisdair R., Bellingham, James, Garcia-Fernandez, Josè-M., Foster, Russell G.

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Novel mutations in BBS5 highlight the importance of this gene in non-Caucasian Bardet-Biedl syndrome patients von Hjortshøj, Tina Duelund, Grønskov, Karen, Philp, Alisdair R., Nishimura, Darryl Y., Adeyemo, Adebowale, Rotimi, Charles N., Sheffield, Val C., Rosenberg, Thomas, Brøndum-Nielsen, Karen

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Genetic analysis of oculocutaneous albinism type 1 (OCA1) in Indian families: two novel frameshift mutations in the TYR Gene von Sundaresan, Periasamy, Sil, Asim Kumar, Philp, Alisdair R, Randolph, Mary A, Natchiar, Govindappa, Namperumalsamy, Perumalsamy

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Zebrafish melanopsin: isolation, tissue localisation and phylogenetic position von Bellingham, James, Whitmore, David, Philp, Alisdair R, Wells, Dominic J, Foster, Russell G

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Rod photopigment deficits in albinos are specific to mammals and arise during retinal development von GRANT, SIMON, PATEL, NEHA N., PHILP, ALISDAIR R., GREY, CHARLOTTE N.B., LUCAS, RICHARD D., FOSTER, RUSSELL G., BOWMAKER, JAMES K., JEFFERY, GLEN

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Visual function testing : A quantifiable visually guided behavior in mice: Retinal Degeneration and Gene Therapy von THOMPSON, Stewart, PHILP, Alisdair R, STONE, Edwin M

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Novel mutations in BBS5 highlight the importance of this gene in non-Caucasian BardetaBiedl syndrome patients von HjortshA,j Tina Duelund, GrA, nskov Karen, Philp, Alisdair R, Nishimura, Darryl Y, Adeyemo, Adebowale, Rotimi, Charles N, Sheffield, Val C, Rosenberg, Thomas, BrA, ndum-Nielsen Karen

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Identical Mutation in a Novel Retinal Gene Causes Progressive Rod-Cone Degeneration (prcd) in Dogs and Retinitis Pigmentosa in Man von Zangerl, Barbara, Goldstein, Orly, Philp, Alisdair R., Lindauer, Sarah J.P., Pearce-Kelling, Susan E., Mullins, Robert F., Graphodatsky, Alexander S., Ripoll, Daniel, Felix, Jeanette S., Stone, Edwin M., Acland, Gregory M., Aguirre, Gustavo D.

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Corrigendum to: A novel rod‐like opsin isolated from the extra‐retinal photoreceptors of teleost fish: FEBS Letters 468 (2000) 181–188 von Philp, Alisdair R., Bellingham, James, Garcia-Fernandez, Josè-M., Foster, Russell G.

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Corrigendum to: A novel rod-like opsin isolated from the extra-retinal photoreceptors of teleost fish: [ FEBS Letters 468 (2000) 181–188] von Philp, Alisdair R., Bellingham, James, Garcia-Fernandez, Josè-M., Foster, Russell G.

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Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans von ZANGERL, Barbara, GOLDSTEIN, Orly, ACLAND, Gregory M, AGUIRRE, Gustavo D, PHILP, Alisdair R, LINDAUER, Sarah J. P, PEARCE-KELLING, Susan E, MULLINS, Robert F, GRAPHODATSKY, Alexander S, RIPOLL, Daniel, FELIX, Jeanette S, STONE, Edwin M

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