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2003 3
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2010 6
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Page 1
Rare variant contribution to human disease in 281,104 UK Biobank exomes.
Wang Q, Dhindsa RS, Carss K, Harper AR, Nag A, Tachmazidou I, Vitsios D, Deevi SVV, Mackay A, Muthas D, Hühn M, Monkley S, Olsson H; AstraZeneca Genomics Initiative; Wasilewski S, Smith KR, March R, Platt A, Haefliger C, Petrovski S. Wang Q, et al. Nature. 2021 Sep;597(7877):527-532. doi: 10.1038/s41586-021-03855-y. Epub 2021 Aug 10. Nature. 2021. PMID: 34375979 Free PMC article.
Genetics of NO Deficiency.
Leineweber K, Moosmang S, Paulson D. Leineweber K, et al. Among authors: moosmang s. Am J Cardiol. 2017 Oct 15;120(8S):S80-S88. doi: 10.1016/j.amjcard.2017.06.013. Am J Cardiol. 2017. PMID: 29025574 Free article. Review.
Mouse models to study L-type calcium channel function.
Moosmang S, Lenhardt P, Haider N, Hofmann F, Wegener JW. Moosmang S, et al. Pharmacol Ther. 2005 Jun;106(3):347-55. doi: 10.1016/j.pharmthera.2004.12.003. Pharmacol Ther. 2005. PMID: 15922017 Review.
Unbiased kidney-centric molecular categorization of chronic kidney disease as a step towards precision medicine.
Reznichenko A, Nair V, Eddy S, Fermin D, Tomilo M, Slidel T, Ju W, Henry I, Badal SS, Wesley JD, Liles JT, Moosmang S, Williams JM, Quinn CM, Bitzer M, Hodgin JB, Barisoni L, Karihaloo A, Breyer MD, Duffin KL, Patel UD, Magnone MC, Bhat R, Kretzler M. Reznichenko A, et al. Among authors: moosmang s. Kidney Int. 2024 Jan 27:S0085-2538(24)00068-1. doi: 10.1016/j.kint.2024.01.012. Online ahead of print. Kidney Int. 2024. PMID: 38286178 Free article.
36 results