Duska Sidjanin
Affiliations: | Cell Biology, Neurobiology, and Anatomy | Medical College of Wisconsin, Milwaukee, WI, United States |
Area:
Genetics, Cell Biology, Molecular BiologyGoogle:
"Duska Sidjanin"Children
Sign in to add trainee| Eryn L. Hassemer | grad student | 2010 | Medical College of Wisconsin |
| Ryan P. Liegel | grad student | 2013 | Medical College of Wisconsin |
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Publications
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| Handley MT, Carpanini SM, Mali GR, et al. (2015) Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation. Open Biology. 5: 150047 |
| Park AK, Liegel RP, Ronchetti A, et al. (2014) Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice. Bmc Genetics. 15: 135 |
| Liegel RP, Ronchetti A, Sidjanin DJ. (2014) Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome. Molecular Genetics and Metabolism Reports. 1: 299-311 |
| Liegel RP, Handley MT, Ronchetti A, et al. (2013) 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 |
| Merath K, Ronchetti A, Sidjanin DJ. (2013) Functional analysis of HSF4 mutations found in patients with autosomal recessive congenital cataracts. Investigative Ophthalmology & Visual Science. 54: 6646-54 |
| Hassemer EL, Endres B, Toonen JA, et al. (2013) ADAM17 transactivates EGFR signaling during embryonic eyelid closure. Investigative Ophthalmology & Visual Science. 54: 132-40 |
| Toonen J, Liang L, Sidjanin DJ. (2012) 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 |
| Liang L, Liegel R, Endres B, et al. (2011) Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice. Molecular Vision. 17: 3062-71 |
| Merath KM, Chang B, Dubielzig R, et al. (2011) 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 |
| Liegel R, Chang B, Dubielzig R, et al. (2011) Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice. Molecular Genetics and Metabolism. 103: 51-9 |