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Plos One|August 19, 2016
Correction: A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)Markus H Kuehn, Koren A Lipsett, Marilyn Menotti-Raymond, et al.
Human Molecular Genetics|May 5, 2021
Proteomic analysis identifies key differences in the cardiac interactomes of dystrophin and micro-dystrophinHong Wang, Elena Marrosu, Daniel Brayson, et al.
The American Journal of Pathology|May 4, 2019
Choriocapillaris Degeneration in Geographic AtrophyElliott H Sohn, Miles J Flamme-Wiese, S Scott Whitmore, et al.
The Journal of Experimental Medicine|May 16, 2007
RANK signals from CD4(+)3(-) inducer cells regulate development of Aire-expressing epithelial cells in the thymic medullaSimona W Rossi, Mi-Yeon Kim, Andreas Leibbrandt, et al.
Blood Advances|January 4, 2018
<i>ASXL1</i> and <i>BIM</i> germ line variants predict response and identify CML patients with the greatest risk of imatinib failureJustine E Marum, David T Yeung, Leanne Purins, et al.
Scientific Reports|November 3, 2021
Expression of truncated Kir6.2 promotes insertion of functionally inverted ATP-sensitive K<sup>+</sup> channelsBenjamin A Heitz, Robert Bränström, Wei Yang, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromeC G Woods, S Stricker, P Seemann, et al.
Advances in Simulation (London, England)|August 9, 2022
Development of a simulation technical competence curriculum for medical simulation fellowsRami A Ahmed, Dylan Cooper, Chassity L Mays, et al.
Plos One|May 6, 2016
A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)Markus H Kuehn, Koren A Lipsett, Marilyn Menotti-Raymond, et al.
Journal of Analytical Toxicology|June 4, 2021
Recommendations for Toxicological Investigation of Drug-Impaired Driving and Motor Vehicle Fatalities-2021 UpdateAmanda L D'Orazio, Amanda L A Mohr, Ayako Chan-Hosokawa, et al.
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