Publications by authors named "Adam Ronchetti"

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A Disintegrin and Metalloproteinase10 (ADAM10) Regulates NOTCH Signaling during Early Retinal Development.
Joseph A Toonen, Adam Ronchetti, D J Sidjanin

PLoS One· July 2017

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TBC1D20 mediates autophagy as a key regulator of autophagosome maturation.
D J Sidjanin, Anna K Park, Adam Ronchetti, Jamaria Martins, William T Jackson

Autophagy· October 2016

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Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice.
Anna Kyunglim Park, Ryan P Liegel, Adam Ronchetti, Allison D Ebert, Aron Geurts

BMC Genet· December 2014

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Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome.
Ryan P Liegel, Adam Ronchetti, D J Sidjanin

Mol Genet Metab Rep· January 2014

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Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans.
Ryan P Liegel, Mark T Handley, Adam Ronchetti, Stephen Brown, Lars Langemeyer

Am J Hum Genet· December 2013

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Functional analysis of HSF4 mutations found in patients with autosomal recessive congenital cataracts.
Kate Merath, Adam Ronchetti, Duska J Sidjanin

Invest Ophthalmol Vis Sci· October 2013

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ADAM17 transactivates EGFR signaling during embryonic eyelid closure.
Eryn L Hassemer, Bradley Endres, Joseph A Toonen, Adam Ronchetti, Richard Dubielzig

Invest Ophthalmol Vis Sci· January 2013

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Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice.
Lina Liang, Ryan Liegel, Brad Endres, Adam Ronchetti, Bo Chang

Mol Vis· April 2012

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