Genes and mutations causing retinitis pigmentosa von Daiger, S P, Sullivan, L S, Bowne, S J

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis von Daiger, Stephen P, Sohocki, Melanie M, Bowne, Sara J, Sullivan, Lori S, Blackshaw, Seth, Cepko, Constance L, Payne, Annette M, Bhattacharya, Shomi S, Khaliq, Shagufta, Qasim Mehdi, S, Birch, David G, Harrison, Wilbur R, Elder, Frederick F.B, Heckenlively, John R

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A zonal organization of odorant receptor gene expression in the olfactory epithelium von Ressler, Kerry J., Sullivan, Susan L., Buck, Linda B.

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A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene von Sohocki, Melanie M., Sullivan, Lori S., Mintz-Hittner, Helen A., Birch, David, Heckenlively, John R., Freund, Carol L., McInnes, Roderick R., Daiger, Stephen P.

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systematic review and meta‐analysis of the efficacy of furosemide for exercise‐induced pulmonary haemorrhage in Thoroughbred and Standardbred racehorses von Sullivan, S. L., Whittem, T., Morley, P. S., Hinchcliff, K. W.

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Prospective study of the association between exercise‐induced pulmonary haemorrhage and long‐term performance in Thoroughbred racehorses von Sullivan, S. L., Anderson, G. A., Morley, P. S., Hinchcliff, K. W.

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Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa von Sullivan, Lori S, Heckenlively, John R, Bowne, Sara J, Zuo, Jian, Hide, Winston A, Gal, Andreas, Denton, Michael, Inglehearn, Chris F, Blanton, Susan H, Daiger, Stephen P

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The Chromosomal Distribution of Mouse Odorant Receptor Genes von Sullivan, Susan L., Adamson, M. Charlene, Ressler, Kerry J., Kozak, Christine A., Buck, Linda B.

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Characterization of the Human and Mouse Unconventional Myosin XV Genes Responsible for Hereditary Deafness DFNB3 and Shaker 2 von Liang, Yong, Wang, Aihui, Belyantseva, Inna A., Anderson, David W., Probst, Frank J., Barber, Thomas D., Miller, Webb, Touchman, Jeffrey W., Jin, Long, Sullivan, Susan L., Sellers, James R., Camper, Sally A., Lloyd, Ricardo V., Kachar, Bechara, Friedman, Thomas B., Fridell, Robert A.

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Polypoid cystitis as a cause of haematuria in a pony mare von Rosales, C. M., Bamford, N. J., Sullivan, S. L., Bauquier, J. R., Tennent‐Brown, B. S.

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Identification of a novel member of the T1R family of putative taste receptors von Sainz, Eduardo, Korley, Julius N., Battey, James F., Sullivan, Susan L.

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Mutations in the RP1 Gene Causing Autosomal Dominant Retinitis Pigmentosa von Bowne, Sara J., Daiger, Stephen P., Hims, Matthew M., Sohocki, Melanie M., Malone, Kimberly A., McKie, Arthur B., Heckenlively, John R., Birch, David G., Inglehearn, Chris F., Bhattacharya, Shomi S., Bird, Alan, Sullivan, Lori S.

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Information coding in the olfactory system: Evidence for a stereotyped and highly organized epitope map in the olfactory bulb von Ressler, Kerry J., Sullivan, Susan L., Buck, Linda B.

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Spatial patterning and information coding in the olfactory system von Sullivan, Susan L, Ressler, Kerry J, Buck, Linda B

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Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa von BOWNE, Sara J, SULLIVAN, Lori S, BLANTON, Susan H, CEPKO, Constance L, BLACKSHAW, Seth, BIRCH, David G, HUGHBANKS-WHEATON, Dianna, HECKENLIVELY, John R, DAIGER, Stephen P

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Atypical histopathological findings in a 15‐year‐old Warmblood gelding diagnosed with anhidrosis in a temperate climate von Sullivan, S. L., Cudmore, L. A., Bacci, B. B., Tennent‐Brown, B. S.

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Sequence and transcriptional pattern of the essential Escherichia coli secE-nusG operon von Downing, W L, Sullivan, S L, Gottesman, M E, Dennis, P P

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Effect of Escherichia coli nusG function on lambda N-mediated transcription antitermination von SULLIVAN, SL, WARD, DF, GOTTESMAN, ME

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Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies von Sohocki, Melanie M., Daiger, Stephen P., Bowne, Sara J., Rodriquez, Joseph A., Northrup, Hope, Heckenlively, John R., Birch, David G., Mintz-Hittner, Helen, Ruiz, Richard S., Lewis, Richard A., Saperstein, David A., Sullivan, Lori S.

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Linkage Mapping of Thiel–Behnke Corneal Dystrophy (CDB2) to Chromosome 10q23–q24 von Yee, Richard W., Sullivan, Lori S., Lai, Hong T., Stock, E.Lee, Lu, Yuhun, Khan, Mohammed N., Blanton, Susan H., Daiger, Stephen P.

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