Dong X - Search Results

1

Genomic and Transcriptomic Analyses Reveals ZNF124 as a Critical Regulator in Highly Aggressive Medulloblastomas.

Luo Z, Dong X, Yu J, Xia Y, Berry KP, Rao R, Xu L, Xue P, Chen T, Lin Y, Yu J, Huang G, Li H, Zhou W, Lu QR. Luo Z, et al. Among authors: dong x. Front Cell Dev Biol. 2021 Feb 18;9:634056. doi: 10.3389/fcell.2021.634056. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33681213 Free PMC article.

2

One Novel 2.43Kb Deletion and One Single Nucleotide Mutation of the INSR Gene in a Chinese Neonate with Rabson-Mendenhall Syndrome.

Chen X, Wang H, Wu B, Dong X, Liu B, Chen H, Lu Y, Zhou W, Yang L. Chen X, et al. Among authors: dong x. J Clin Res Pediatr Endocrinol. 2018 Jun 1;10(2):183-187. doi: 10.4274/jcrpe.5080. Epub 2017 Oct 30. J Clin Res Pediatr Endocrinol. 2018. PMID: 29082893 Free PMC article.

3

A histone deacetylase 3-dependent pathway delimits peripheral myelin growth and functional regeneration.

He X, Zhang L, Queme LF, Liu X, Lu A, Waclaw RR, Dong X, Zhou W, Kidd G, Yoon SO, Buonanno A, Rubin JB, Xin M, Nave KA, Trapp BD, Jankowski MP, Lu QR. He X, et al. Among authors: dong x. Nat Med. 2018 Mar;24(3):338-351. doi: 10.1038/nm.4483. Epub 2018 Feb 12. Nat Med. 2018. PMID: 29431744 Free PMC article.

4

Speech and language delay in a patient with WDR4 mutations.

Chen X, Gao Y, Yang L, Wu B, Dong X, Liu B, Lu Y, Zhou W, Wang H. Chen X, et al. Among authors: dong x. Eur J Med Genet. 2018 Aug;61(8):468-472. doi: 10.1016/j.ejmg.2018.03.007. Epub 2018 Mar 26. Eur J Med Genet. 2018. PMID: 29597095

5

Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures.

Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W. Kong Y, et al. Among authors: dong x. Clin Chim Acta. 2018 Aug;483:14-19. doi: 10.1016/j.cca.2018.03.027. Epub 2018 Apr 9. Clin Chim Acta. 2018. PMID: 29649454

6

Dual Requirement of CHD8 for Chromatin Landscape Establishment and Histone Methyltransferase Recruitment to Promote CNS Myelination and Repair.

Zhao C, Dong C, Frah M, Deng Y, Marie C, Zhang F, Xu L, Ma Z, Dong X, Lin Y, Koenig S, Nait-Oumesmar B, Martin DM, Wu LN, Xin M, Zhou W, Parras C, Lu QR. Zhao C, et al. Among authors: dong c, dong x. Dev Cell. 2018 Jun 18;45(6):753-768.e8. doi: 10.1016/j.devcel.2018.05.022. Dev Cell. 2018. PMID: 29920279 Free PMC article.

7

Clinical and genetic spectrum of a large cohort of children with epilepsy in China.

Yang L, Kong Y, Dong X, Hu L, Lin Y, Chen X, Ni Q, Lu Y, Wu B, Wang H, Lu QR, Zhou W. Yang L, et al. Among authors: dong x. Genet Med. 2019 Mar;21(3):564-571. doi: 10.1038/s41436-018-0091-8. Epub 2018 Jun 21. Genet Med. 2019. PMID: 29930392 Free PMC article.

8

Early onset developmental delay and epilepsy in pediatric patients with WDR45 variants.

Chen H, Qian Y, Yu S, Xiao D, Guo X, Wang Q, Hao L, Yan K, Lu Y, Dong X, Zhou W, Wu B, Zhou S, Wang H. Chen H, et al. Among authors: dong x. Eur J Med Genet. 2019 Feb;62(2):149-160. doi: 10.1016/j.ejmg.2018.07.002. Epub 2018 Jul 6. Eur J Med Genet. 2019. PMID: 29981852

9

Early-onset infant epileptic encephalopathy associated with a de novo PPP3CA gene mutation.

Qian Y, Wu B, Lu Y, Dong X, Qin Q, Zhou W, Wang H. Qian Y, et al. Among authors: dong x. Cold Spring Harb Mol Case Stud. 2018 Dec 17;4(6):a002949. doi: 10.1101/mcs.a002949. Print 2018 Dec. Cold Spring Harb Mol Case Stud. 2018. PMID: 30455226 Free PMC article.

10

Data on mutations and Clinical features in SCN1A or SCN2A gene.

Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W. Kong Y, et al. Among authors: dong x. Data Brief. 2018 Aug 30;22:492-501. doi: 10.1016/j.dib.2018.08.122. eCollection 2019 Feb. Data Brief. 2018. PMID: 30619928 Free PMC article.

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