Hu P - Search Results

1

The Cation Channel TMEM63B Is an Osmosensor Required for Hearing.

Du H, Ye C, Wu D, Zang YY, Zhang L, Chen C, He XY, Yang JJ, Hu P, Xu Z, Wan G, Shi YS. Du H, et al. Among authors: hu p. Cell Rep. 2020 May 5;31(5):107596. doi: 10.1016/j.celrep.2020.107596. Cell Rep. 2020. PMID: 32375046 Free article.

2

A novel LGI1 mutation causing autosomal dominant lateral temporal lobe epilepsy confirmed by a precise knock-in mouse model.

Hu P, Wu D, Zang YY, Wang Y, Zhou YP, Qiao F, Teng XY, Chen J, Li QQ, Sun JH, Liu T, Feng HY, Zhou QG, Shi YS, Xu Z. Hu P, et al. CNS Neurosci Ther. 2022 Feb;28(2):237-246. doi: 10.1111/cns.13761. Epub 2021 Nov 12. CNS Neurosci Ther. 2022. PMID: 34767694 Free PMC article.

3

Proline-rich transmembrane protein 2 specifically binds to GluA1 but has no effect on AMPA receptor-mediated synaptic transmission.

Feng HY, Qiao F, Tan J, Zhang X, Hu P, Shi YS, Xu Z. Feng HY, et al. Among authors: hu p. J Clin Lab Anal. 2022 Feb;36(2):e24196. doi: 10.1002/jcla.24196. Epub 2022 Jan 8. J Clin Lab Anal. 2022. PMID: 34997978 Free PMC article.

4

Enhancing GluN2A-type NMDA receptors impairs long-term synaptic plasticity and learning and memory.

Li QQ, Chen J, Hu P, Jia M, Sun JH, Feng HY, Qiao FC, Zang YY, Shi YY, Chen G, Sheng N, Xu Y, Yang JJ, Xu Z, Shi YS. Li QQ, et al. Among authors: hu p. Mol Psychiatry. 2022 Aug;27(8):3468-3478. doi: 10.1038/s41380-022-01579-7. Epub 2022 Apr 28. Mol Psychiatry. 2022. PMID: 35484243

5

A novel Lgi1 mutation causes white matter abnormalities and impairs motor coordination in mice.

Teng XY, Hu P, Chen Y, Zang Y, Ye X, Ou J, Chen G, Shi YS. Teng XY, et al. Among authors: hu p. FASEB J. 2022 Mar;36(3):e22212. doi: 10.1096/fj.202101652R. FASEB J. 2022. PMID: 35167164

6

Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis.

Ma D, Zhang J, Luo C, Lin Y, Ji X, Hu P, Xu Z. Ma D, et al. Among authors: hu p. Mol Med Rep. 2016 Mar;13(3):1967-74. doi: 10.3892/mmr.2016.4769. Epub 2016 Jan 13. Mol Med Rep. 2016. PMID: 26783197 Free PMC article.

7

Copy number variations and fetal ventriculomegaly.

Wang Y, Hu P, Xu Z. Wang Y, et al. Among authors: hu p. Curr Opin Obstet Gynecol. 2018 Apr;30(2):104-110. doi: 10.1097/GCO.0000000000000439. Curr Opin Obstet Gynecol. 2018. PMID: 29356709 Review.

8

Generation of MERRF patient-derived induced pluripotent stem cell line iMERRF-C7.

Liang D, Hu H, Xu T, Wang Y, Hu P, Xu Z. Liang D, et al. Among authors: hu h, hu p. Stem Cell Res. 2016 Nov;17(3):616-618. doi: 10.1016/j.scr.2016.11.008. Epub 2016 Nov 5. Stem Cell Res. 2016. PMID: 27934592 Free article.

9

Application of next-generation sequencing for the diagnosis of fetuses with congenital heart defects.

Qiao F, Hu P, Xu Z. Qiao F, et al. Among authors: hu p. Curr Opin Obstet Gynecol. 2019 Apr;31(2):132-138. doi: 10.1097/GCO.0000000000000520. Curr Opin Obstet Gynecol. 2019. PMID: 30608255 Review.

10

Application of fetal cell-free DNA enrichment in non-invasive prenatal screening: experience from a single center in Eastern China.

Lin Y, Liang D, Hu P, Li H, Luo CY, Xu ZF. Lin Y, et al. Among authors: hu p. Chin Med J (Engl). 2020 Sep 30;134(1):104-106. doi: 10.1097/CM9.0000000000001112. Chin Med J (Engl). 2020. PMID: 33009030 Free PMC article. No abstract available.

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