Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3
Sidjanin, Duska J., Lowe, Jennifer K., McElwee, John L., Milne, Bruce S., Phippen, Taryn M., Sargan, David R., Aguirre, Gustavo D., Acland, Gregory M., Ostrander, Elaine A.
Published in Human molecular genetics (01.08.2002)
Published in Human molecular genetics (01.08.2002)
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Journal Article
TBC1D20 mediates autophagy as a key regulator of autophagosome maturation
Sidjanin, D. J., Park, Anna K., Ronchetti, Adam, Martins, Jamaria, Jackson, William T.
Published in Autophagy (02.10.2016)
Published in Autophagy (02.10.2016)
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Journal Article
Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice
Talamas, Elijah, Jackson, Lavinia, Koeberl, Matthew, Jackson, Todd, McElwee, John L., Hawes, Norman L., Chang, Bo, Jablonski, Monica M., Sidjanin, D.J.
Published in Genomics (San Diego, Calif.) (01.07.2006)
Published in Genomics (San Diego, Calif.) (01.07.2006)
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Journal Article
A 76-bp Deletion in the Mip Gene Causes Autosomal Dominant Cataract in Hfi Mice
Sidjanin, D.J., Parker-Wilson, Devonne M., Neuhäuser-Klaus, Angelika, Pretsch, Walter, Favor, Jack, Deen, Peter M.T., Ohtaka-Maruyama, Chiaki, Lu, Yun, Bragin, Alvina, Skach, William R., Chepelinsky, Ana B., Grimes, Patricia A., Stambolian, Dwight E.
Published in Genomics (San Diego, Calif.) (15.06.2001)
Published in Genomics (San Diego, Calif.) (15.06.2001)
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Journal Article
Radiation hybrid map, physical map, and low-pass genomic sequence of the canine prcd region on CFA9 and comparative mapping with the syntenic region on human chromosome 17
Sidjanin, D.J, Miller, B, Kijas, J, McElwee, J, Pillardy, J, Malek, J, Pai, G, Feldblyum, T, Fraser, C, Acland, G, Aguirre, G
Published in Genomics (San Diego, Calif.) (01.02.2003)
Published in Genomics (San Diego, Calif.) (01.02.2003)
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Journal Article
Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice
Liegel, R., Chang, B., Dubielzig, R., Sidjanin, D.J.
Published in Molecular genetics and metabolism (01.05.2011)
Published in Molecular genetics and metabolism (01.05.2011)
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Journal Article
The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17
Hassemer, E L, Le Gall, S M, Liegel, R, McNally, M, Chang, B, Zeiss, C J, Dubielzig, R D, Horiuchi, K, Kimura, T, Okada, Y, Blobel, C P, Sidjanin, D J
Published in Genetics (Austin) (01.05.2010)
Published in Genetics (Austin) (01.05.2010)
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Journal Article
Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice
Liang, Lina, Liegel, Ryan, Endres, Brad, Ronchetti, Adam, Chang, Bo, Sidjanin, D J
Published in Molecular vision (2011)
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Published in Molecular vision (2011)
Journal Article
Genetic and clinical evaluation of juvenile retinoschisis
Kim, Judy E., MD, Ruttum, Mark S., MD, Koeberl, Matthew J., BA, Hassemer, Eryn L., BS, Sidjanin, D.J., PhD
Published in Journal of AAPOS (01.04.2009)
Published in Journal of AAPOS (01.04.2009)
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Journal Article
Cloning of the canine delta tubulin cDNA (TUBD) and mapping to CFA9
Sidjanin, D. J., Zangerl, B., Johnson, J. L., Xue, F., Mellersh, C., Ostrander, E. A., Acland, G., Aguirre, G. D.
Published in Animal genetics (01.04.2002)
Published in Animal genetics (01.04.2002)
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Journal Article
Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16
Sidjanin, DJ, Grimes, PA, Pretsch, W, Neuhauser-Klaus, A, Favor, J, Stambolian, DE
Published in Investigative ophthalmology & visual science (01.11.1997)
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Published in Investigative ophthalmology & visual science (01.11.1997)
Journal Article
Cloning of canine γ-tubulin (TUBG1) cDNA and mapping to CFA9
Sidjanin, D. J., Xue, F., McElwee, J., Johnson, J. L., Holmgren, C., Mellersh, C., Ostrander, E., Acland, G., Aguirre, G. D.
Published in Animal genetics (01.10.2001)
Published in Animal genetics (01.10.2001)
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Journal Article
Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod–cone degeneration interval and identifies ancestral disease-transmitting chromosome
Goldstein, Orly, Zangerl, Barbara, Pearce-Kelling, Sue, Sidjanin, Duska J., Kijas, James W., Felix, Jeanette, Acland, Gregory M., Aguirre, Gustavo D.
Published in Genomics (San Diego, Calif.) (01.11.2006)
Published in Genomics (San Diego, Calif.) (01.11.2006)
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Journal Article
Functional analysis of the Hsf4 super(lop11) allele responsible for cataracts in lop11 mice
Liang, L, Liegel, R, Endres, B, Ronchetti, A, Chang, B, Sidjanin, D J
Published in Molecular vision (01.01.2011)
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Published in Molecular vision (01.01.2011)
Journal Article
Identification of two novel mutations in families with X-linked ocular albinism
Iannaccone, Alessandro, Gallaher, Kevin T, Buchholz, Janda, Jennings, Barbara J, Neitz, Maureen, Sidjanin, D J
Published in Molecular vision (02.10.2007)
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Published in Molecular vision (02.10.2007)
Journal Article