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	1.	Functional analysis of HSF4 mutations found in patients with autosomal recessive congenital cataracts. [electronic resource] by Merath, Kate Ronchetti, Adam Sidjanin, Duska J Producer: 20131212 In: Investigative ophthalmology & visual science vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome. [electronic resource] by Liegel, Ryan P Ronchetti, Adam Sidjanin, D J Publication details: Molecular genetics and metabolism reports 2014 In: Molecular genetics and metabolism reports vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A Disintegrin and Metalloproteinase10 (ADAM10) Regulates NOTCH Signaling during Early Retinal Development. [electronic resource] by Toonen, Joseph A Ronchetti, Adam Sidjanin, D J Producer: 20170710 In: PloS one vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	TBC1D20 mediates autophagy as a key regulator of autophagosome maturation. [electronic resource] by Sidjanin, D J Park, Anna K Ronchetti, Adam Martins, Jamaria Jackson, William T Producer: 20171113 In: Autophagy vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice. [electronic resource] by Liang, Lina Liegel, Ryan Endres, Brad Ronchetti, Adam Chang, Bo Sidjanin, D J Producer: 20120425 In: Molecular vision vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	6.	ADAM17 transactivates EGFR signaling during embryonic eyelid closure. [electronic resource] by Hassemer, Eryn L Endres, Bradley Toonen, Joseph A Ronchetti, Adam Dubielzig, Richard Sidjanin, Duska J Producer: 20130305 In: Investigative ophthalmology & visual science vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice. [electronic resource] by Park, Anna Kyunglim Liegel, Ryan P Ronchetti, Adam Ebert, Allison D Geurts, Aron Sidjanin, Duska J Producer: 20151002 In: BMC genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans. [electronic resource] by Liegel, Ryan P Handley, Mark T Ronchetti, Adam Brown, Stephen Langemeyer, Lars Linford, Andrea Chang, Bo Morris-Rosendahl, Deborah J Carpanini, Sarah Posmyk, Renata Harthill, Verity Sheridan, Eamonn Abdel-Salam, Ghada M H Terhal, Paulien A Faravelli, Francesca Accorsi, Patrizia Giordano, Lucio Pinelli, Lorenzo Hartmann, Britta Ebert, Allison D Barr, Francis A Aligianis, Irene A Sidjanin, Duska J Producer: 20140212 In: American journal of human genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)