Peng Q - Search Results

1

Nar1 deficiency results in shortened lifespan and sensitivity to paraquat that is rescued by increased expression of mitochondrial superoxide dismutase.

Zhao W, Fang BX, Niu YJ, Liu YN, Liu B, Peng Q, Li JB, Wasko BM, Delaney JR, Kennedy BK, Suh Y, Zhou ZJ, Kaeberlein M, Liu XG. Zhao W, et al. Among authors: peng q. Mech Ageing Dev. 2014 Jun;138:53-8. doi: 10.1016/j.mad.2014.01.007. Epub 2014 Jan 31. Mech Ageing Dev. 2014. PMID: 24486555

2

Sir2 deletion prevents lifespan extension in 32 long-lived mutants.

Delaney JR, Sutphin GL, Dulken B, Sim S, Kim JR, Robison B, Schleit J, Murakami CJ, Carr D, An EH, Choi E, Chou A, Fletcher M, Jelic M, Liu B, Lockshon D, Moller RM, Pak DN, Peng Q, Peng ZJ, Pham KM, Sage M, Solanky A, Steffen KK, Tsuchiya M, Tsuchiyama S, Johnson S, Raabe C, Suh Y, Zhou Z, Liu X, Kennedy BK, Kaeberlein M. Delaney JR, et al. Among authors: peng zj, peng q. Aging Cell. 2011 Dec;10(6):1089-91. doi: 10.1111/j.1474-9726.2011.00742.x. Epub 2011 Oct 3. Aging Cell. 2011. PMID: 21902802 Free PMC article.

3

Identification of COMMD1 as a novel lamin A binding partner.

Jiang Z, Chen W, Zhou J, Peng Q, Zheng H, Yuan Y, Cui H, Zhao W, Sun X, Zhou Z, Liu X. Jiang Z, et al. Among authors: peng q. Mol Med Rep. 2019 Aug;20(2):1790-1796. doi: 10.3892/mmr.2019.10419. Epub 2019 Jun 24. Mol Med Rep. 2019. PMID: 31257505 Free PMC article.

4

Large cohort screening of G6PD deficiency and the mutational spectrum in the Dongguan District in Southern China.

Peng Q, Li S, Ma K, Li W, Ma Q, He X, He Y, He T, Lu X. Peng Q, et al. PLoS One. 2015 Mar 16;10(3):e0120683. doi: 10.1371/journal.pone.0120683. eCollection 2015. PLoS One. 2015. PMID: 25775246 Free PMC article.

5

A targeted gene capture next-generation sequencing panel for genetic screening of newborns.

Peng Q, Liu G, Zhu P, Wu C, He X, Li W, Rao C, Li S, Lu X. Peng Q, et al. J Pak Med Assoc. 2020 Oct;70(10):1789-1794. doi: 10.5455/JPMA.28637. J Pak Med Assoc. 2020. PMID: 33159754

6

Case Report: A Novel Intronic Mutation in AIFM1 Associated With Fatal Encephalomyopathy and Mitochondrial Disease in Infant.

Peng Q, Ma K, Wang L, Zhu Y, Zhang Y, Rao C, Luo D, Jiang Z, Lai W, Lu H, Duan C, Zhou Z, Lu X. Peng Q, et al. Front Pediatr. 2022 May 31;10:889089. doi: 10.3389/fped.2022.889089. eCollection 2022. Front Pediatr. 2022. PMID: 35712626 Free PMC article.

7

Candidate single-nucleotide polymorphisms and cerebral palsy: A case-control study.

He XG, Peng QI, Chen YH, He T, Huang H, Ma ZK, Fan XJ, Luo L, Liu SJ, Lu XM. He XG, et al. Among authors: peng qi. Biomed Rep. 2015 Nov;3(6):849-852. doi: 10.3892/br.2015.519. Epub 2015 Sep 25. Biomed Rep. 2015. PMID: 26623029 Free PMC article.

8

Mutational Screening of GLI3, SHH, and SHH ZRS in 78 Chinese Children with Nonsyndromic Polydactyly.

Rao C, Chen J, Peng Q, Mo Q, Xia X, Lu X. Rao C, et al. Among authors: peng q. Genet Test Mol Biomarkers. 2018 Sep;22(9):577-581. doi: 10.1089/gtmb.2018.0096. Genet Test Mol Biomarkers. 2018. PMID: 30235038

9

A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population.

Li S, Peng Q, Liao S, Li W, Ma Q, Lu X. Li S, et al. Among authors: peng q. PLoS One. 2017 May 15;12(5):e0177196. doi: 10.1371/journal.pone.0177196. eCollection 2017. PLoS One. 2017. PMID: 28505178 Free PMC article.

10

A Novel α-Thalassemia Nonsense Mutation on the α2-Globin Gene: HBA2: c.184A>T.

Liang Y, Peng Q, Li M, Li S, Li W, Lu X. Liang Y, et al. Among authors: peng q. Hemoglobin. 2017 Jul-Nov;41(4-6):306-307. doi: 10.1080/03630269.2017.1402027. Epub 2017 Dec 18. Hemoglobin. 2017. PMID: 29251004

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