Cao B - Search Results

1

Genotype-phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus-merzbacher disease.

Duan R, Ji H, Yan H, Wang J, Zhang Y, Zhang Q, Li D, Cao B, Gu Q, Wu Y, Jiang Y, Li M, Wang J. Duan R, et al. Among authors: cao b. Orphanet J Rare Dis. 2022 Mar 28;17(1):137. doi: 10.1186/s13023-022-02267-z. Orphanet J Rare Dis. 2022. PMID: 35346287 Free PMC article.

2

Novel Insight into the Potential Pathogenicity of Mitochondrial Dysfunction Resulting from PLP1 Duplication Mutations in Patients with Pelizaeus-Merzbacher Disease.

Duan R, Li L, Yan H, He M, Gao K, Xing S, Ji H, Wang J, Cao B, Li D, Xie H, Zhao S, Wu Y, Jiang Y, Xiao J, Gu Q, Li M, Zheng X, Chen L, Wang J. Duan R, et al. Among authors: cao b. Neuroscience. 2021 Nov 10;476:60-71. doi: 10.1016/j.neuroscience.2021.08.029. Epub 2021 Sep 9. Neuroscience. 2021. PMID: 34506833 Free article.

3

Targeted next generation sequencing in 112 Chinese patients with intellectual disability/developmental delay: novel mutations and candidate gene.

Yan H, Shi Z, Wu Y, Xiao J, Gu Q, Yang Y, Li M, Gao K, Chen Y, Yang X, Ji H, Cao B, Duan R, Jiang Y, Wang J. Yan H, et al. Among authors: cao b. BMC Med Genet. 2019 May 14;20(1):80. doi: 10.1186/s12881-019-0794-y. BMC Med Genet. 2019. PMID: 31088393 Free PMC article.

4

Epilepsy in children with leukodystrophies.

Zhang J, Ban T, Zhou L, Ji H, Yan H, Shi Z, Cao B, Jiang Y, Wang J, Wu Y. Zhang J, et al. Among authors: cao b. J Neurol. 2020 Sep;267(9):2612-2618. doi: 10.1007/s00415-020-09889-y. Epub 2020 May 9. J Neurol. 2020. PMID: 32388833

5

Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes disease.

Cao B, Yang X, Chen Y, Huang Q, Wu Y, Gu Q, Xiao J, Yang H, Pan H, Chen J, Sun Y, Ren L, Zhao C, Deng Y, Yang Y, Chang X, Yang Z, Zhang Y, Niu Z, Wang J, Wu X, Wang J, Jiang Y. Cao B, et al. Metab Brain Dis. 2017 Aug;32(4):1123-1131. doi: 10.1007/s11011-017-9985-4. Epub 2017 Apr 10. Metab Brain Dis. 2017. PMID: 28397151

6

Ten Novel Mutations in Chinese Patients with Megalencephalic Leukoencephalopathy with Subcortical Cysts and a Long-Term Follow-Up Research.

Cao B, Yan H, Guo M, Xie H, Wu Y, Gu Q, Xiao J, Shang J, Yang Y, Xiong H, Niu Z, Wu X, Jiang Y, Wang J. Cao B, et al. PLoS One. 2016 Jun 20;11(6):e0157258. doi: 10.1371/journal.pone.0157258. eCollection 2016. PLoS One. 2016. PMID: 27322623 Free PMC article.

7

Identification in Chinese patients with GLIALCAM mutations of megalencephalic leukoencephalopathy with subcortical cysts and brain pathological study on Glialcam knock-in mouse models.

Shi Z, Yan HF, Cao BB, Guo MM, Xie H, Gao K, Xiao JX, Yang YL, Xiong H, Gu Q, Li M, Wu Y, Jiang YW, Wang JM. Shi Z, et al. World J Pediatr. 2019 Oct;15(5):454-464. doi: 10.1007/s12519-019-00284-w. Epub 2019 Aug 1. World J Pediatr. 2019. PMID: 31372844 Free PMC article.

8

Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic Leukodystrophy.

Chen L, Yan H, Cao B, Wu Y, Gu Q, Xiao J, Yang Y, Yang H, Shi Z, Yang Z, Pan H, Chang X, Chen J, Sun Y, Zhang Y, Wu X, Jiang Y, Wang J. Chen L, et al. Among authors: cao b. Int J Genomics. 2018 Jul 3;2018:2361068. doi: 10.1155/2018/2361068. eCollection 2018. Int J Genomics. 2018. PMID: 30057904 Free PMC article.

9

[Astrocytic swelling and cysts formation resulting from gene mutation in megalencephalic leukoencephalopathy with subcortical cysts].

Cao BB, Wang JM. Cao BB, et al. Sheng Li Ke Xue Jin Zhan. 2014 Aug;45(4):314-7. Sheng Li Ke Xue Jin Zhan. 2014. PMID: 25434259 Chinese. No abstract available.

10

Cathepsins and cancer risk: a Mendelian randomization study.

Deng T, Lu X, Jia X, Du J, Wang L, Cao B, Yang M, Yin Y, Liu F. Deng T, et al. Among authors: cao b. Front Endocrinol (Lausanne). 2024 May 31;15:1428433. doi: 10.3389/fendo.2024.1428433. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 38883596 Free PMC article.

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