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Year Number of Results
2011 1
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15 results

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Page 1
Identification and validation of genes associated with prognosis of cisplatin-resistant ovarian cancer.
Liu D, Li R, Wang Y, Li D, Li L. Liu D, et al. BMC Cancer. 2024 Aug 5;24(1):508. doi: 10.1186/s12885-024-12264-z. BMC Cancer. 2024. PMID: 39103807 Free PMC article.
RESULTS: A total of 132 differential genes were found between cisplatin resistance and control group, and 8 key prognostic genes were selected by analysis, namely VPS13B, PLGRKT, CDKAL1, TBC1D22A, TAP1, PPP3CA, CUX1 and PPP1R15A. The efficacy of the risk assessment model d …
RESULTS: A total of 132 differential genes were found between cisplatin resistance and control group, and 8 key prognostic genes were select …
High Expression of TBC1 Domain Family Member 22A is Related to Poor Prognosis in Ovarian Serous Cystadenocarcinoma.
Lv X, Gong R, Guo L, Wang C. Lv X, et al. Int J Med Sci. 2024 Oct 7;21(13):2603-2612. doi: 10.7150/ijms.99744. eCollection 2024. Int J Med Sci. 2024. PMID: 39439452 Free PMC article.
The research was designed to evaluate the expression and prognostic effect of TBC1D22A in OSC. Methods: TCGA, GTEx, GEO, HPA, and GDSC databases were adopted to explore the oncogenic mechanism of TBC1D22A in OSC, as well as the correlation between TBC1D22A an …
The research was designed to evaluate the expression and prognostic effect of TBC1D22A in OSC. Methods: TCGA, GTEx, GEO, HPA, and GDS …
ACBD3 interaction with TBC1 domain 22 protein is differentially affected by enteroviral and kobuviral 3A protein binding.
Greninger AL, Knudsen GM, Betegon M, Burlingame AL, DeRisi JL. Greninger AL, et al. mBio. 2013 Apr 9;4(2):e00098-13. doi: 10.1128/mBio.00098-13. mBio. 2013. PMID: 23572552 Free PMC article.
Using affinity purification-mass spectrometry, we identified the putative Rab33 GTPase-activating proteins TBC1D22A and TBC1D22B as ACBD3-interacting factors. Fine-scale mapping of binding determinants within ACBD3 revealed that the interaction domains for TBC1D22A/ …
Using affinity purification-mass spectrometry, we identified the putative Rab33 GTPase-activating proteins TBC1D22A and TBC1D22B as A …
New insights into genetics underlying of plumage color.
Davoodi P, Ehsani A, Vaez Torshizi R, Masoudi AA. Davoodi P, et al. Anim Genet. 2022 Feb;53(1):80-93. doi: 10.1111/age.13156. Epub 2021 Dec 1. Anim Genet. 2022. PMID: 34855995
By annotating genes relevant to top SNPs, we have distinguished 18 potential candidate genes comprising HNF4beta, CKMT1B, TBC1D22A, RPL8, CACNA2D1, FZD4, SGMS1, IRF8, OPTN, LOC420362, TRABD, OvoDA1, DAD1, USP6, RBM12B, MIR1772, MIR1709 and MIR6696 and also 89 putative gene …
By annotating genes relevant to top SNPs, we have distinguished 18 potential candidate genes comprising HNF4beta, CKMT1B, TBC1D22A, R …
Four-Generation Pedigree of Monozygotic Female Twins Reveals Genetic Factors in Twinning Process by Whole-Genome Sequencing.
Liu S, Hong Y, Cui K, Guan J, Han L, Chen W, Xu Z, Gong K, Ou Y, Zeng C, Li S, Zhang D, Hu D. Liu S, et al. Twin Res Hum Genet. 2018 Oct;21(5):361-368. doi: 10.1017/thg.2018.41. Epub 2018 Aug 1. Twin Res Hum Genet. 2018. PMID: 30064533
Pathway analysis revealed a significant enrichment of genes carrying novel SNVs in the epithelial adherens junction-signaling pathway (p = .011), contributed by FGFR1, TUBB6, and MYH7B. Meanwhile, TBC1D22A, TRIOBP, and TUBB6, also carrying similar SNVs, were involved in th …
Pathway analysis revealed a significant enrichment of genes carrying novel SNVs in the epithelial adherens junction-signaling pathway (p = . …
Genetic and metabolic profiling of individuals with Phelan-McDermid syndrome presenting with seizures.
Jain L, Oberman LM, Beamer L, Cascio L, May M, Srikanth S, Skinner C, Jones K, Allen B, Rogers C, Phelan K, Kaufmann WE, DuPont B, Sarasua SM, Boccuto L. Jain L, et al. Clin Genet. 2022 Jan;101(1):87-100. doi: 10.1111/cge.14074. Epub 2021 Oct 27. Clin Genet. 2022. PMID: 34664257
Additionally, a 3 Mb genomic region on 22q13.31 containing the gene TBC1D22A, was found to be significantly associated with seizure prevalence. A distinct metabolic profile was identified for individuals with PMS with seizures and suggested among other features a disrupted …
Additionally, a 3 Mb genomic region on 22q13.31 containing the gene TBC1D22A, was found to be significantly associated with seizure p …
Genotype-Phenotype Associations in Phelan-McDermid Syndrome: Insights into Novel Genes Beyond SHANK3.
Nevado J, Escalada B, Muñoz-GªPorrero Y, Adan C, Tenorio-Castaño J, Lapunzina PD. Nevado J, et al. Int J Mol Sci. 2025 May 13;26(10):4653. doi: 10.3390/ijms26104653. Int J Mol Sci. 2025. PMID: 40429797 Free PMC article.
Deletion size within the 22q13.3 region emerged as a major determinant of phenotype, with larger deletions associated with more severe global functional impairment. Furthermore, CERK, TBC1D22A, CELSR1, and GRAMD4 were identified as candidate genes within 22q13.3, potential …
Deletion size within the 22q13.3 region emerged as a major determinant of phenotype, with larger deletions associated with more severe globa …
Genome-wide linkage and regional association study of obesity-related phenotypes: the GenSalt study.
Liu AY, Gu D, Hixson JE, Rao DC, Shimmin LC, Jaquish CE, Liu DP, He J, Kelly TN. Liu AY, et al. Obesity (Silver Spring). 2014 Feb;22(2):545-56. doi: 10.1002/oby.20469. Epub 2013 Jul 2. Obesity (Silver Spring). 2014. PMID: 23526746 Free PMC article.

Follow-up association study of 22q13.31-13.33 revealed an association between the TBC1D22A gene marker rs16996195 and WC (false discovery rate [FDR]-Q < 0.05). In gender-stratified analysis, suggestive linkage signals were attained for WC at 2p24.3-2q12.2 and 22q13.33 a

…
Follow-up association study of 22q13.31-13.33 revealed an association between the TBC1D22A gene marker rs16996195 and WC (false disco …
Network Pharmacology Approaches Used to Identify Therapeutic Molecules for Chronic Venous Disease Based on Potential miRNA Biomarkers.
Barrera-Vázquez OS, Escobar-Ramírez JL, Magos-Guerrero GA. Barrera-Vázquez OS, et al. J Xenobiot. 2024 Oct 15;14(4):1519-1540. doi: 10.3390/jox14040083. J Xenobiot. 2024. PMID: 39449424 Free PMC article.
Previous research identified a functional analysis of seven genes (CDS2, HDAC5, PPP6R2, PRRC2B, TBC1D22A, WNK1, and PABPC3) as targets of miRNAs related to CVD. In this context, miRNAs emerge as essential candidates for CVD diagnosis, representing novel molecular and biolo …
Previous research identified a functional analysis of seven genes (CDS2, HDAC5, PPP6R2, PRRC2B, TBC1D22A, WNK1, and PABPC3) as target …
Gene deletions and amplifications in human hepatocellular carcinomas: correlation with hepatocyte growth regulation.
Nalesnik MA, Tseng G, Ding Y, Xiang GS, Zheng ZL, Yu Y, Marsh JW, Michalopoulos GK, Luo JH. Nalesnik MA, et al. Am J Pathol. 2012 Apr;180(4):1495-508. doi: 10.1016/j.ajpath.2011.12.021. Epub 2012 Feb 8. Am J Pathol. 2012. PMID: 22326833 Free PMC article.
High frequencies of CNV were also seen in PTPRD (21/98), GNB1L (18/98), KIAA1217 (18/98), RP1-1777G6.2 (17/98), ETS1 (11/98), RSU1 (10/98), TBC1D22A (10/98), BAHCC1 (9/98), MAML2 (9/98), RAB1B (9/98), and YIF1A (9/98). The existing literature regarding hepatocytes or other …
High frequencies of CNV were also seen in PTPRD (21/98), GNB1L (18/98), KIAA1217 (18/98), RP1-1777G6.2 (17/98), ETS1 (11/98), RSU1 (10/98), …
15 results