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Reduced STMN2 and pathogenic TDP-43, two hallmarks of ALS, synergize to accelerate motor decline in mice.
bioRxiv [Preprint]. 2024 Mar 20:2024.03.19.585052. doi: 10.1101/2024.03.19.585052.
bioRxiv. 2024.
PMID: 38562780
Free PMC article.
Preprint.
Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy.
Krus KL, Strickland A, Yamada Y, Devault L, Schmidt RE, Bloom AJ, Milbrandt J, DiAntonio A.
Krus KL, et al.
Cell Rep. 2022 Jun 28;39(13):111001. doi: 10.1016/j.celrep.2022.111001.
Cell Rep. 2022.
PMID: 35767949
Free PMC article.
Item in Clipboard
Synthetic high-density lipoprotein nanoparticles for the treatment of Niemann-Pick diseases.
Schultz ML, Fawaz MV, Azaria RD, Hollon TC, Liu EA, Kunkel TJ, Halseth TA, Krus KL, Ming R, Morin EE, McLoughlin HS, Bushart DD, Paulson HL, Shakkottai VG, Orringer DA, Schwendeman AS, Lieberman AP.
Schultz ML, et al. Among authors: krus kl.
BMC Med. 2019 Nov 11;17(1):200. doi: 10.1186/s12916-019-1423-5.
BMC Med. 2019.
PMID: 31711490
Free PMC article.
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Coordinate regulation of mutant NPC1 degradation by selective ER autophagy and MARCH6-dependent ERAD.
Schultz ML, Krus KL, Kaushik S, Dang D, Chopra R, Qi L, Shakkottai VG, Cuervo AM, Lieberman AP.
Schultz ML, et al. Among authors: krus kl.
Nat Commun. 2018 Sep 10;9(1):3671. doi: 10.1038/s41467-018-06115-2.
Nat Commun. 2018.
PMID: 30202070
Free PMC article.
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Lysosome and endoplasmic reticulum quality control pathways in Niemann-Pick type C disease.
Schultz ML, Krus KL, Lieberman AP.
Schultz ML, et al. Among authors: krus kl.
Brain Res. 2016 Oct 15;1649(Pt B):181-188. doi: 10.1016/j.brainres.2016.03.035. Epub 2016 Mar 26.
Brain Res. 2016.
PMID: 27026653
Free PMC article.
Review.
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