Cao CY - Search Results

1

Heterozygous Seryl-tRNA Synthetase 1 Variants Cause Charcot-Marie-Tooth Disease.

He J, Liu XX, Ma MM, Lin JJ, Fu J, Chen YK, Xu GR, Xu LQ, Fu ZF, Xu D, Chen WF, Cao CY, Shi Y, Zeng YH, Zhang J, Chen XC, Zhang RX, Wang N, Kennerson M, Fan DS, Chen WJ. He J, et al. Among authors: cao cy. Ann Neurol. 2023 Feb;93(2):244-256. doi: 10.1002/ana.26501. Epub 2022 Sep 28. Ann Neurol. 2023. PMID: 36088542

2

Expanding the phenotype and genotype spectra of PLIN4-associated myopathy with rimmed ubiquitin-positive autophagic vacuolation.

Yang K, Zeng YH, Qiu YS, Lin F, Chen HZ, Jin M, Chen L, Zheng FZ, Ding YL, Cao CY, Lin MT, Chen WJ, Wang ZQ, Wang N. Yang K, et al. Among authors: cao cy. Acta Neuropathol. 2022 Jun;143(6):733-735. doi: 10.1007/s00401-022-02422-7. Epub 2022 May 2. Acta Neuropathol. 2022. PMID: 35499779 No abstract available.

3

GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy.

Zeng YH, Yang K, Du GQ, Chen YK, Cao CY, Qiu YS, He J, Lv HD, Qu QQ, Chen JN, Xu GR, Chen L, Zheng FZ, Zhao M, Lin MT, Chen WJ, Hu J, Wang ZQ, Wang N. Zeng YH, et al. Among authors: cao cy. Ann Neurol. 2022 Sep;92(3):512-526. doi: 10.1002/ana.26436. Epub 2022 Jul 2. Ann Neurol. 2022. PMID: 35700120

4

CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy.

Shi Y, Cao C, Zeng Y, Ding Y, Chen L, Zheng F, Chen X, Zhou F, Yang X, Li J, Xu L, Xu G, Lin M, Ishiura H, Tsuji S, Wang N, Wang Z, Chen WJ, Yang K. Shi Y, et al. J Genet Genomics. 2024 Feb;51(2):184-196. doi: 10.1016/j.jgg.2023.12.009. Epub 2023 Dec 29. J Genet Genomics. 2024. PMID: 38159879

5

Characteristics of tandem repeat inheritance and sympathetic nerve involvement in GAA-FGF14 ataxia.

Zheng ZH, Cao CY, Cheng B, Yuan RY, Zeng YH, Guo ZB, Qiu YS, Lv WQ, Liang H, Li JL, Zhang WX, Fang MK, Sun YH, Lin W, Hong JM, Gan SR, Wang N, Chen WJ, Du GQ, Fang L. Zheng ZH, et al. Among authors: cao cy. J Hum Genet. 2024 Sep;69(9):433-440. doi: 10.1038/s10038-024-01262-5. Epub 2024 Jun 12. J Hum Genet. 2024. PMID: 38866925

6

Case report: A novel mutation of the CAPN3 gene in a Chinese family with limb-girdle muscular dystrophy type 2A.

Feng W, Cao Y, Ren R, Yang X, Cao C, Jiang H, Du G. Feng W, et al. Front Genet. 2024 Aug 12;15:1410727. doi: 10.3389/fgene.2024.1410727. eCollection 2024. Front Genet. 2024. PMID: 39188286 Free PMC article.

7

Congenital paramyotonia.

Cao CY, Yang K, Xu F, Du GQ. Cao CY, et al. QJM. 2024 Sep 1;117(9):659-660. doi: 10.1093/qjmed/hcae078. QJM. 2024. PMID: 38676661 No abstract available.

8

Successful treatment of systemic EBV-positive T-cell lymphoma of childhood using the ruxolitinib combined with L-DEP regimen chemotherapy followed by haploidentical allogeneic hematopoietic stem cell transplantation.

Li J, Cao C, Lu S, Rong L, Kang M, Fang Y. Li J, et al. Ann Hematol. 2023 Oct;102(10):2955-2957. doi: 10.1007/s00277-023-05298-z. Epub 2023 Jul 25. Ann Hematol. 2023. PMID: 37490113 No abstract available.

9

[Applications of chromatography in glycomics].

Zheng Y, Cao CY, Guo ZM, Yan JY, Liang XM. Zheng Y, et al. Among authors: cao cy. Se Pu. 2024 Jul;42(7):646-657. doi: 10.3724/SP.J.1123.2023.12003. Se Pu. 2024. PMID: 38966973 Free PMC article. Review. Chinese.

10

Bottom-Up Assembling Hierarchical Enamel-Like Bulk Materials with Excellent Optical and Mechanical Properties for Tooth Restoration.

Zhang S, Xu W, Wu L, Li X, Liu X, Wu X, Wu G, Zheng S, Cao CY, Zhou Z, Wong HM, Zhang X, Li QL. Zhang S, et al. Among authors: cao cy. Adv Healthc Mater. 2024 Oct;13(26):e2401095. doi: 10.1002/adhm.202401095. Epub 2024 Jun 3. Adv Healthc Mater. 2024. PMID: 38794821

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