Zhang Y - Search Results

1

Gut Dysbiosis Drives Inflammatory Bowel Disease Through the CCL4L2-VSIR Axis in Glycogen Storage Disease.

Lan J, Zhang Y, Jin C, Chen H, Su Z, Wu J, Ma N, Zhang X, Lu Y, Chen Y, Zeng X, Zhang H, Zheng G, Sun Y, Wang C, Hu Y, Wang Y, Liu Y, Zeng Z, Shi L, He J, Cao A, Wang Y, Pan X, Jin G, Wang Y, Jiang X, Shen H, Tang Q, Xie X, Xiao Y, Zhong X, Zhang X, Zeng L, Ye L, Xie J, Geng L, Li Z, Wu X, Wang Y, Mao R, Zhang S, Huang S, Liu S, Zeng H, Xu W, Gong S, Guo Y, Yang M. Lan J, et al. Among authors: zhang s, zhang x, zhang h, zhang y. Adv Sci (Weinh). 2024 Aug;11(30):e2309471. doi: 10.1002/advs.202309471. Epub 2024 Jun 18. Adv Sci (Weinh). 2024. PMID: 38889269 Free PMC article.

2

Diagnosis by metagenomic next-generation sequencing of a Talaromyces marneffei bloodstream infection in an HIV-negative child: A case report.

Yang A, Hu Y, Chen P, Zheng G, Hu X, Zhang J, Wang J, Wang C, Huang Z, Zhang Y, Guo Y. Yang A, et al. Among authors: zhang j, zhang y. Front Pediatr. 2022 Aug 15;10:903617. doi: 10.3389/fped.2022.903617. eCollection 2022. Front Pediatr. 2022. PMID: 36046481 Free PMC article.

3

Exome sequencing identified a novel missense mutation c.464G>A (p.G155D) in Ca²⁺-binding protein 4 (CABP4) in a Chinese pedigree with autosomal dominant nocturnal frontal lobe epilepsy.

Chen ZH, Wang C, Zhuo MQ, Zhai QX, Chen Q, Guo YX, Zhang YX, Gui J, Tang ZH, Zeng XL. Chen ZH, et al. Oncotarget. 2017 Sep 5;8(45):78940-78947. doi: 10.18632/oncotarget.20694. eCollection 2017 Oct 3. Oncotarget. 2017. PMID: 29108277 Free PMC article.

4

Mutational analysis of CHRNB2, CHRNA2 and CHRNA4 genes in Chinese population with autosomal dominant nocturnal frontal lobe epilepsy.

Chen Z, Wang L, Wang C, Chen Q, Zhai Q, Guo Y, Zhang Y. Chen Z, et al. Among authors: zhang y. Int J Clin Exp Med. 2015 Jun 15;8(6):9063-70. eCollection 2015. Int J Clin Exp Med. 2015. PMID: 26309560 Free PMC article.

5

Functional characterization of a KCNAB3 genetic epilepsy with febrile seizures plus adult mouse model.

Ding J, Wang C, Huang GQ, Zhang JW, Zhai QX, Chen ZH, Zhang YX, Guo YX. Ding J, et al. Transl Pediatr. 2022 Oct;11(10):1615-1623. doi: 10.21037/tp-22-436. Transl Pediatr. 2022. PMID: 36345448 Free PMC article.

6

Whole-Exome Sequencing for Identifying Genetic Causes of Intellectual Developmental Disorders.

Guo YX, Ma HX, Zhang YX, Chen ZH, Zhai QX. Guo YX, et al. Int J Gen Med. 2021 Apr 13;14:1275-1282. doi: 10.2147/IJGM.S300775. eCollection 2021. Int J Gen Med. 2021. PMID: 33880059 Free PMC article.

7

A novel missense creatine mutant of CaBP4, c.464G>A (p.G155D), associated with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), reduces the expression of CaBP4.

Guo Y, Miao Q, Zhang Y, Wang C, Liang M, Li X, Qiu W, Shi G, Zhai Q, Chen Z. Guo Y, et al. Among authors: zhang y. Transl Pediatr. 2022 Mar;11(3):396-402. doi: 10.21037/tp-22-54. Transl Pediatr. 2022. PMID: 35378956 Free PMC article.

8

Analysis of the CHRNA7 gene mutation and polymorphism in Southern Han Chinese patients with nocturnal frontal epilepsy.

Chen ZH, Wang C, Wang LG, Zhuo MQ, Tang ZH, Zhai QX, Chen Q, Guo YX, Zhang YX. Chen ZH, et al. Asian Pac J Trop Med. 2015 Apr;8(4):330-3. doi: 10.1016/S1995-7645(14)60340-0. Asian Pac J Trop Med. 2015. PMID: 25975508 Free article.

9

Novel mutations in SCN9A occurring with fever-associated seizures or epilepsy.

Ding J, Zhang JW, Guo YX, Zhang YX, Chen ZH, Zhai QX. Ding J, et al. Seizure. 2019 Oct;71:214-218. doi: 10.1016/j.seizure.2019.06.005. Epub 2019 Jun 7. Seizure. 2019. PMID: 31394368 Free article.

10

[Clinical features and mutation analysis of CHRNA4 gene for families and sporadic cases affected with autosomal dominant nocturnal frontal lobe epilepsy].

Zhai QX, Wang C, Chen Q, Guo YX, Chen ZH, Zhang YX, Gui J, Tang ZH, Zhuo MQ. Zhai QX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Dec;30(6):662-5. doi: 10.3760/cma.j.issn.1003-9406.2013.06.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 24327142 Chinese.

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