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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 1 |
2012 | 1 |
2015 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 5684
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Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.
J Clin Invest. 2015 Nov 2;125(11):4196-211. doi: 10.1172/JCI81260. Epub 2015 Oct 20.
J Clin Invest. 2015.
PMID: 26524591
Free PMC article.
Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity.
Liu Y, Ramot Y, Torrelo A, Paller AS, Si N, Babay S, Kim PW, Sheikh A, Lee CC, Chen Y, Vera A, Zhang X, Goldbach-Mansky R, Zlotogorski A.
Liu Y, et al.
Arthritis Rheum. 2012 Mar;64(3):895-907. doi: 10.1002/art.33368.
Arthritis Rheum. 2012.
PMID: 21953331
Free PMC article.
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Isolation and characterization of the HC8 subunit gene of the human proteasome.
Akioka H, Forsberg NE, Ishida N, Okumura K, Nogami M, Taguchi H, Noda C, Tanaka K.
Akioka H, et al.
Biochem Biophys Res Commun. 1995 Feb 6;207(1):318-23. doi: 10.1006/bbrc.1995.1190.
Biochem Biophys Res Commun. 1995.
PMID: 7857283
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