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Year Number of Results
2004 1
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2009 1
2011 1
2013 1
2014 1
2015 3
2016 2
2017 2
2019 2
2020 2
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2022 3
2023 3
2024 0

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24 results

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Exosome-derived GTF2H2 from Huh7 cells can inhibit endothelial cell viability, migration, tube formation, and permeability.
Li Z, Li Y, Ouyang Q, Li X, Huang J. Li Z, et al. Tissue Cell. 2022 Dec;79:101922. doi: 10.1016/j.tice.2022.101922. Epub 2022 Sep 8. Tissue Cell. 2022. PMID: 36116407 Free article.
Therefore, we hypothesized that GTF2H2 acts as an anti-angiogenesis gene. However, our results showed that GTF2H2 overexpression had no effect on endothelial cell viability, migration, or permeability. ...Our results suggest that overexpressing GTF2H2 had no …
Therefore, we hypothesized that GTF2H2 acts as an anti-angiogenesis gene. However, our results showed that GTF2H2 overexpressi …
TEP linc-GTF2H2-1, RP3-466P17.2, and lnc-ST8SIA4-12 as novel biomarkers for lung cancer diagnosis and progression prediction.
Li X, Liu L, Song X, Wang K, Niu L, Xie L, Song X. Li X, et al. J Cancer Res Clin Oncol. 2021 Jun;147(6):1609-1622. doi: 10.1007/s00432-020-03502-5. Epub 2021 Jan 29. J Cancer Res Clin Oncol. 2021. PMID: 33792796
METHODS: Platelet precipitation was obtained by low-speed centrifugation. TEP linc-GTF2H2-1, RP3-466P17.2, and lnc-ST8SIA4-12 were selected by lncRNA microarray and validated by qPCR in a large cohort of lung cancer patients and healthy donors. ...Notably, their combinatio …
METHODS: Platelet precipitation was obtained by low-speed centrifugation. TEP linc-GTF2H2-1, RP3-466P17.2, and lnc-ST8SIA4-12 were se …
Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.
He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N, Chen WJ. He J, et al. Gene. 2013 Apr 15;518(2):325-9. doi: 10.1016/j.gene.2012.12.109. Epub 2013 Jan 23. Gene. 2013. PMID: 23352792
In this study, we analyzed mutations in SMN1 and quantified the modifying genes, including SMN2, NAIP, GTF2H2, and H4F5 by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), multiplex ligation-dependent probe amplification (MLPA), TA cloning, al …
In this study, we analyzed mutations in SMN1 and quantified the modifying genes, including SMN2, NAIP, GTF2H2, and H4F5 by polymerase …
Genetic findings of Cypriot spinal muscular atrophy patients.
Theodorou L, Nicolaou P, Koutsou P, Georghiou A, Anastasiadou V, Tanteles G, Kyriakides T, Zamba-Papanicolaou E, Christodoulou K. Theodorou L, et al. Neurol Sci. 2015 Oct;36(10):1829-34. doi: 10.1007/s10072-015-2263-5. Epub 2015 May 28. Neurol Sci. 2015. PMID: 26017350
The SMN1 gene is located within an inverted duplication on chromosome 5q13 with the genes SMN2, NAIP and GTF2H2. MLPA analysis of 13 Cypriot SMA patients revealed that, 12 patients carried a homozygous SMN1 gene deletion and one patient carried two copies of the SMN1 gene. …
The SMN1 gene is located within an inverted duplication on chromosome 5q13 with the genes SMN2, NAIP and GTF2H2. MLPA analysis of 13 …
Gene expression signature of human neuropathic pain identified through transcriptome analysis.
Hu L, Yin W, Ma Y, Zhang Q, Xu Q. Hu L, et al. Front Genet. 2023 Feb 3;14:1127167. doi: 10.3389/fgene.2023.1127167. eCollection 2023. Front Genet. 2023. PMID: 36816032 Free PMC article.
Methods: We conducted transcriptome analysis using a training datasetof 202 individuals, including patients with neuropathic pain and healthy controls. Results: Our analysis identified five genes (GTF2H2, KLHL5, LRRC37A4P, PRR24, and MRPL23) that were significantly differe …
Methods: We conducted transcriptome analysis using a training datasetof 202 individuals, including patients with neuropathic pain and health …
Telomeric Region of the Spinal Muscular Atrophy Locus Is Susceptible to Structural Variations.
Noguchi Y, Onishi A, Nakamachi Y, Hayashi N, Harahap NI, Rochmah MA, Shima A, Yanagisawa S, Morisada N, Nakagawa T, Iijima K, Kasagi S, Saegusa J, Kawano S, Shinohara M, Tairaku S, Saito T, Kubo Y, Saito K, Nishio H. Noguchi Y, et al. Pediatr Neurol. 2016 May;58:83-9. doi: 10.1016/j.pediatrneurol.2016.01.019. Epub 2016 Jan 30. Pediatr Neurol. 2016. PMID: 27268759
RESULTS: The SMN2 copy number was shown to vary widely and to correlate with the disease severity of the patients. Interestingly, telomeric NAIP and telomeric GTF2H2 showed similar tendencies. We also noted positive correlations among the copy number of SMN2 and the telome …
RESULTS: The SMN2 copy number was shown to vary widely and to correlate with the disease severity of the patients. Interestingly, telomeric …
Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype.
Zhuri D, Gurkan H, Eker D, Karal Y, Yalcintepe S, Atli E, Demir S, Atli EI. Zhuri D, et al. Glob Med Genet. 2022 Sep 5;9(3):226-236. doi: 10.1055/s-0042-1751302. eCollection 2022 Sep. Glob Med Genet. 2022. PMID: 36071912 Free PMC article.
In this study, we aim to investigate the expression of modifying genes related to the prognosis of SMA like PLS3 , PFN2 , ZPR1 , CORO1C , GTF2H2 , NRN1 , SERF1A , NCALD , NAIP , and TIA1. Methods Seventeen patients, who came to Trakya University, Faculty of Medicine, Medic …
In this study, we aim to investigate the expression of modifying genes related to the prognosis of SMA like PLS3 , PFN2 , ZPR1 , CORO1C , …
Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population.
Gialluisi A, Reccia MG, Tirozzi A, Nutile T, Lombardi A, De Sanctis C; International Parkinson's Disease Genomic Consortium (IPDGC); Varanese S, Pietracupa S, Modugno N, Simeone A, Ciullo M, Esposito T. Gialluisi A, et al. Front Neurol. 2020 Jan 10;10:1362. doi: 10.3389/fneur.2019.01362. eCollection 2019. Front Neurol. 2020. PMID: 31998221 Free PMC article.
Then we ran Exome-Wide Association Scans (EWAS) within sequenced PD cases (N = 113), testing both motor and non-motor PD endophenotypes, as well as their associations with Polygenic Risk Scores (PRS) influencing brain subcortical volumes. We identified a variant associated with P …
Then we ran Exome-Wide Association Scans (EWAS) within sequenced PD cases (N = 113), testing both motor and non-motor PD endophenotypes, as …
ABCC5, ERCC2, XPA and XRCC1 transcript abundance levels correlate with cisplatin chemoresistance in non-small cell lung cancer cell lines.
Weaver DA, Crawford EL, Warner KA, Elkhairi F, Khuder SA, Willey JC. Weaver DA, et al. Mol Cancer. 2005 May 9;4(1):18. doi: 10.1186/1476-4598-4-18. Mol Cancer. 2005. PMID: 15882455 Free PMC article.

RESULTS: Following validation, single variable models best correlated with chemoresistance (p < 0.001), were ERCC2/XPC, ABCC5/GTF2H2, ERCC2/GTF2H2, XPA/XPC and XRCC1/XPC. All single variable models were examined hierarchically to achieve two variable models. The

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RESULTS: Following validation, single variable models best correlated with chemoresistance (p < 0.001), were ERCC2/XPC, ABCC5/GTF2H2

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New multiplex real-time PCR approach to detect gene mutations for spinal muscular atrophy.
Liu Z, Zhang P, He X, Liu S, Tang S, Zhang R, Wang X, Tan J, Peng B, Jiang L, Hong S, Zou L. Liu Z, et al. BMC Neurol. 2016 Aug 17;16(1):141. doi: 10.1186/s12883-016-0651-y. BMC Neurol. 2016. PMID: 27534852 Free PMC article.
RESULTS: The multiple real-time PCR was established and the accuracy of it to detect the mutations of SMN, NAIP and GTF2H2 was at least 98.8 % comparing with DNA sequencing and MLPA. Among 141 limb movement disorders children, 75 cases were SMA. 71 cases of SMA (94.67 %) w …
RESULTS: The multiple real-time PCR was established and the accuracy of it to detect the mutations of SMN, NAIP and GTF2H2 was at lea …
24 results