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Year | Number of Results |
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2022 | 1 |
2023 | 2 |
2024 | 0 |
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Page 1
Systematic gene therapy derived from an investigative study of AAV2/8 vector gene therapy for Fabry disease.
Orphanet J Rare Dis. 2023 Sep 5;18(1):275. doi: 10.1186/s13023-023-02894-0.
Orphanet J Rare Dis. 2023.
PMID: 37670350
Free PMC article.
Development of Lanzyme as the Potential Enzyme Replacement Therapy Drug for Fabry Disease.
Deng M, Zhou H, Liang Z, Li Z, Wang Y, Guo W, Zhao AY, Li F, Mu Y, Zhao AZ.
Deng M, et al. Among authors: zhao ay.
Biomolecules. 2022 Dec 27;13(1):53. doi: 10.3390/biom13010053.
Biomolecules. 2022.
PMID: 36671438
Free PMC article.
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Cyclic adenosine monophosphate potentiates immune checkpoint blockade therapy in acute myeloid leukemia.
Mao P, Feng W, Zhang Z, Huang C, Zhou S, Zhao Z, Mu Y, Zhao AY, Wang L, Li F, Zhao AZ.
Mao P, et al. Among authors: zhao ay.
Clin Transl Med. 2023 Nov;13(11):e1489. doi: 10.1002/ctm2.1489.
Clin Transl Med. 2023.
PMID: 37997561
Free PMC article.
No abstract available.
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