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Duska Sidjanin - Publications

Affiliations: 
Cell Biology, Neurobiology, and Anatomy Medical College of Wisconsin, Milwaukee, WI, United States 
Area:
Genetics, Cell Biology, Molecular Biology
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19 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Handley MT, Carpanini SM, Mali GR, Sidjanin DJ, Aligianis IA, Jackson IJ, FitzPatrick DR. Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation. Open Biology. 5: 150047. PMID 26063829 DOI: 10.1098/Rsob.150047  0.314
2014 Park AK, Liegel RP, Ronchetti A, Ebert AD, Geurts A, Sidjanin DJ. Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice. Bmc Genetics. 15: 135. PMID 25476608 DOI: 10.1186/S12863-014-0135-2  0.809
2014 Liegel RP, Ronchetti A, Sidjanin DJ. Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome. Molecular Genetics and Metabolism Reports. 1: 299-311. PMID 25197626 DOI: 10.1016/J.Ymgmr.2014.06.003  0.786
2013 Liegel RP, Handley MT, Ronchetti A, Brown S, Langemeyer L, Linford A, Chang B, Morris-Rosendahl DJ, Carpanini S, Posmyk R, Harthill V, Sheridan E, Abdel-Salam GM, Terhal PA, Faravelli F, ... Sidjanin DJ, et al. Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans. American Journal of Human Genetics. 93: 1001-14. PMID 24239381 DOI: 10.1016/J.Ajhg.2013.10.011  0.798
2013 Merath K, Ronchetti A, Sidjanin DJ. Functional analysis of HSF4 mutations found in patients with autosomal recessive congenital cataracts. Investigative Ophthalmology & Visual Science. 54: 6646-54. PMID 24045990 DOI: 10.1167/Iovs.13-12283  0.359
2013 Hassemer EL, Endres B, Toonen JA, Ronchetti A, Dubielzig R, Sidjanin DJ. ADAM17 transactivates EGFR signaling during embryonic eyelid closure. Investigative Ophthalmology & Visual Science. 54: 132-40. PMID 23211830 DOI: 10.1167/Iovs.12-11130  0.713
2012 Toonen J, Liang L, Sidjanin DJ. Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene. Bmc Genetics. 13: 76. PMID 22928477 DOI: 10.1186/1471-2156-13-76  0.56
2011 Liang L, Liegel R, Endres B, Ronchetti A, Chang B, Sidjanin DJ. Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice. Molecular Vision. 17: 3062-71. PMID 22162625  0.766
2011 Merath KM, Chang B, Dubielzig R, Jeannotte R, Sidjanin DJ. A spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 (lop13) mouse. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 22: 661-73. PMID 21858719 DOI: 10.1007/S00335-011-9354-2  0.507
2011 Liegel R, Chang B, Dubielzig R, Sidjanin DJ. Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice. Molecular Genetics and Metabolism. 103: 51-9. PMID 21353609 DOI: 10.1016/J.Ymgme.2011.02.002  0.799
2010 Hassemer EL, Le Gall SM, Liegel R, McNally M, Chang B, Zeiss CJ, Dubielzig RD, Horiuchi K, Kimura T, Okada Y, Blobel CP, Sidjanin DJ. The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17. Genetics. 185: 245-55. PMID 20194968 DOI: 10.1534/Genetics.109.113167  0.661
2009 Kim JE, Ruttum MS, Koeberl MJ, Hassemer EL, Sidjanin DJ. Genetic and clinical evaluation of juvenile retinoschisis. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 13: 215-7. PMID 19393523 DOI: 10.1016/J.Jaapos.2008.11.005  0.705
2007 Iannaccone A, Gallaher KT, Buchholz J, Jennings BJ, Neitz M, Sidjanin DJ. Identification of two novel mutations in families with X-linked ocular albinism. Molecular Vision. 13: 1856-61. PMID 17960122  0.41
2007 Hunter LS, Sidjanin DJ, Hijar MV, Johnson JL, Kirkness E, Acland GM, Aguirre GD. Cloning and characterization of canine PAX6 and evaluation as a candidate gene in a canine model of aniridia. Molecular Vision. 13: 431-42. PMID 17417604  0.324
2006 Talamas E, Jackson L, Koeberl M, Jackson T, McElwee JL, Hawes NL, Chang B, Jablonski MM, Sidjanin DJ. Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice. Genomics. 88: 44-51. PMID 16595169 DOI: 10.1016/J.Ygeno.2006.02.012  0.534
2001 Sidjanin DJ, Parker-Wilson DM, Neuhäuser-Klaus A, Pretsch W, Favor J, Deen PM, Ohtaka-Maruyama C, Lu Y, Bragin A, Skach WR, Chepelinsky AB, Grimes PA, Stambolian DE. A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice. Genomics. 74: 313-9. PMID 11414759 DOI: 10.1006/geno.2001.6509  0.489
1997 Sidjanin DJ, Grimes PA, Pretsch W, Neuhäuser-Klaus A, Favor J, Stambolian DE. Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16. Investigative Ophthalmology & Visual Science. 38: 2502-7. PMID 9375568  0.418
1997 Zhou E, Grimes P, Favor J, Koeberlein B, Pretsch W, Neuhauser-Klaus A, Sidjanin D, Stambolian D. Genetic mapping of a mouse ocular malformation locus, Tcm, to Chromosome 4 Mammalian Genome. 8: 178-181. PMID 9069117 DOI: 10.1007/s003359900385  0.513
1995 Stambolian D, Ai Y, Sidjanin D, Nesburn K, Sathe G, Rosenberg M, Bergsma DJ. Cloning of the galactokinase cDNA and identification of mutations in two families with cataracts Nature Genetics. 10: 307-312. PMID 7670469 DOI: 10.1038/ng0795-307  0.419
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