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    PITX2 paired like homeodomain 2 [ Homo sapiens (human) ]

    Gene ID: 5308, updated on 28-Oct-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    PITX2 functions as a transcription factor for GPX4 and protects pancreatic cancer cells from ferroptosis.

    PITX2 functions as a transcription factor for GPX4 and protects pancreatic cancer cells from ferroptosis.
    Wang Z, Wu D, Zhang Y, Chen W, Yang Y, Yang Y, Zu G, An Y, Yu X, Qin Y, Xu X, Chen X.

    06/13/2024
    Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2.

    Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2.
    Jiang Y, Peng Y, Tian Q, Cheng Z, Feng B, Hu J, Xia L, Guo H, Xia K, Zhou L, Hu Z., Free PMC Article

    05/10/2024
    Exploring the association between PITX2, third molars agenesis and sella turcica morphology : PITX2, third molars agenesis and sella turcica morphology.

    Exploring the association between PITX2, third molars agenesis and sella turcica morphology : PITX2, third molars agenesis and sella turcica morphology.
    Küchler EC, de Melo Teixeira do Brasil J, Madalena IR, Proff P, Baratto-Filho F, Alam MK, Schroder AGD, Lepri CP, Kirschneck C, de Menezes-Oliveira MAH., Free PMC Article

    03/4/2024
    Enamel defects of Axenfeld-Rieger syndrome and the role of PITX2 in its pathogenesis.

    Enamel defects of Axenfeld-Rieger syndrome and the role of PITX2 in its pathogenesis.
    Yang Y, Zhu J, Chiba Y, Fukumoto S, Qin M, Wang X.

    12/15/2023
    Pulmonary Vein Myocardial Sleeve Length and its Association With Sex and 4q25/PITX2 Genotype.

    Pulmonary Vein Myocardial Sleeve Length and its Association With Sex and 4q25/PITX2 Genotype.
    El-Harasis MA, Yoneda ZT, Davogustto GE, Crawford DM, Laws JL, Frye B, Herrmann T, Patel B, Touchton SA Jr, Roden DM, Richardson TD, Saavedra P, Shen ST, Estrada JC, Kanagasundram AN, Montgomery JA, Michaud GF, Crossley GH, Ellis CR, Shoemaker MB.

    07/31/2023
    PITX2 Knockout Induces Key Findings of Electrical Remodeling as Seen in Persistent Atrial Fibrillation.

    PITX2 Knockout Induces Key Findings of Electrical Remodeling as Seen in Persistent Atrial Fibrillation.
    Schulz C, Lemoine MD, Mearini G, Koivumäki J, Sani J, Schwedhelm E, Kirchhof P, Ghalawinji A, Stoll M, Hansen A, Eschenhagen T, Christ T.

    03/27/2023
    PITX2 induction leads to impaired cardiomyocyte function in arrhythmogenic cardiomyopathy.

    PITX2 induction leads to impaired cardiomyocyte function in arrhythmogenic cardiomyopathy.
    van Kampen SJ, Han SJ, van Ham WB, Kyriakopoulou E, Stouthart EW, Goversen B, Monshouwer-Kloots J, Perini I, de Ruiter H, van der Kraak P, Vink A, van Laake LW, Groeneweg JA, de Boer TP, Tsui H, Boogerd CJ, van Veen TAB, van Rooij E., Free PMC Article

    03/22/2023
    Association Between rs2200733 Polymorphism of PITX2 Gene and the Risk of Atrial Fibrillation.

    Association Between rs2200733 Polymorphism of PITX2 Gene and the Risk of Atrial Fibrillation.
    Shen Han Y, Ahmed AM, Chao Z, Jun W, Xiaochen Y., Free PMC Article

    03/6/2023
    Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome.

    Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome.
    Zhou L, Wang X, An J, Zhang Y, He M, Tang L.

    01/21/2023
    Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants.

    Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants.
    Prem Senthil M, Knight LSW, Taranath D, Mackey DA, Ruddle JB, Chiang MY, Siggs OM, Souzeau E, Craig JE., Free PMC Article

    07/23/2022
    Decoding the PITX2-controlled genetic network in atrial fibrillation.

    Decoding the PITX2-controlled genetic network in atrial fibrillation.
    Steimle JD, Grisanti Canozo FJ, Park M, Kadow ZA, Samee MAH, Martin JF., Free PMC Article

    06/18/2022
    Effect of PITX2 genetic variants on the susceptibility to stroke in the Chinese Han population.

    Effect of PITX2 genetic variants on the susceptibility to stroke in the Chinese Han population.
    Zhao W, Hu X, Hao J, Guo L, Zhang W, Liu J, Jin T, Gao D, Zhi J.

    05/14/2022
    Long noncoding RNA PCAT1 sponges miR1343p to regulate PITX2 expression in breast cancer.

    Long non‑coding RNA PCAT1 sponges miR‑134‑3p to regulate PITX2 expression in breast cancer.
    Tang W, Lu G, Ji Y, Xu Y.

    04/2/2022
    Genome-wide association study-based prediction of atrial fibrillation using artificial intelligence.

    Genome-wide association study-based prediction of atrial fibrillation using artificial intelligence.
    Kwon OS, Hong M, Kim TH, Hwang I, Shim J, Choi EK, Lim HE, Yu HT, Uhm JS, Joung B, Oh S, Lee MH, Kim YH, Pak HN., Free PMC Article

    03/12/2022
    Paired-like homeodomain transcription factor 2 affects endometrial cell function and embryo implantation through the Wnt/beta-catenin pathway.

    Paired-like homeodomain transcription factor 2 affects endometrial cell function and embryo implantation through the Wnt/β-catenin pathway.
    Zhang H, Qi J, Guo J, Wang Y, Guan Y, Fan J, Sui L, Xu Y, Kong L, Yan B, Kong Y.

    01/15/2022
    In Silico Assessment of Class I Antiarrhythmic Drug Effects on Pitx2-Induced Atrial Fibrillation: Insights from Populations of Electrophysiological Models of Human Atrial Cells and Tissues.

    In Silico Assessment of Class I Antiarrhythmic Drug Effects on Pitx2-Induced Atrial Fibrillation: Insights from Populations of Electrophysiological Models of Human Atrial Cells and Tissues.
    Bai J, Zhu Y, Lo A, Gao M, Lu Y, Zhao J, Zhang H., Free PMC Article

    09/11/2021
    Understanding PITX2-Dependent Atrial Fibrillation Mechanisms through Computational Models.

    Understanding PITX2-Dependent Atrial Fibrillation Mechanisms through Computational Models.
    Bai J, Lu Y, Zhu Y, Wang H, Yin D, Zhang H, Franco D, Zhao J., Free PMC Article

    08/7/2021
    Gene-specific facial dysmorphism in Axenfeld-Rieger syndrome caused by FOXC1 and PITX2 variants.

    Gene-specific facial dysmorphism in Axenfeld-Rieger syndrome caused by FOXC1 and PITX2 variants.
    Souzeau E, Siggs OM, Pasutto F, Knight LSW, Perez-Jurado LA, McGregor L, Le Blanc S, Barnett CP, Liebelt J, Craig JE., Free PMC Article

    07/10/2021
    Differential DNA methylation patterns in human Schlemm's canal endothelial cells with glaucoma.

    Differential DNA methylation patterns in human Schlemm's canal endothelial cells with glaucoma.
    Cai J, Drewry MD, Perkumas K, Dismuke WM, Hauser MA, Stamer WD, Liu Y., Free PMC Article

    07/3/2021
    A PITX2 splice-site mutation in a family with Axenfeld-Rieger syndrome leads to decreased expression of nuclear PITX2 protein.

    A PITX2 splice-site mutation in a family with Axenfeld-Rieger syndrome leads to decreased expression of nuclear PITX2 protein.
    Zhang F, Zhang L, He L, Cao M, Yang Y, Duan X, Shi J, Liu K., Free PMC Article

    07/3/2021
    Reduced left atrial cardiomyocyte PITX2 and elevated circulating BMP10 predict atrial fibrillation after ablation.

    Reduced left atrial cardiomyocyte PITX2 and elevated circulating BMP10 predict atrial fibrillation after ablation.
    Reyat JS, Chua W, Cardoso VR, Witten A, Kastner PM, Kabir SN, Sinner MF, Wesselink R, Holmes AP, Pavlovic D, Stoll M, Kääb S, Gkoutos GV, de Groot JR, Kirchhof P, Fabritz L., Free PMC Article

    06/12/2021
    Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld-Rieger syndrome.

    Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld-Rieger syndrome.
    Lo Faro V, Siddiqui SN, Khan MI, Villanueva-Mendoza C, Cortés-González V, Jansonius N, Bergen AAB, Micheal S., Free PMC Article

    05/1/2021
    The diagnosis and phacoemulsification in combination with intraocular lens implantation for an Axenfeld-Rieger syndrome patient with small cornea: a case report.

    The diagnosis and phacoemulsification in combination with intraocular lens implantation for an Axenfeld-Rieger syndrome patient with small cornea: a case report.
    Ma Y, Wu X, Ni S, Chen X, He S, Xu W., Free PMC Article

    03/6/2021
    In Silico Assessment of Genetic Variation in PITX2 Reveals the Molecular Mechanisms of Calcium-Mediated Cellular Triggered Activity in Atrial Fibrillation(.)

    In Silico Assessment of Genetic Variation in PITX2 Reveals the Molecular Mechanisms of Calcium-Mediated Cellular Triggered Activity in Atrial Fibrillation().
    Bai J, Zhu Y, Lo A, Lu Y, Zhao J.

    10/31/2020
    Findings suggest that downregulation of Pitx2c may regulate atrial fibrosis through modulating calcium homeostasis, which may contribute to its role in anti-atrial fibrosis, and Pitx2c downregulation may change the atrial electrophysiology and atrial fibrillation occurrence through modulating fibroblast activity.

    Pitx2c inhibition increases atrial fibroblast activity: Implications in atrial arrhythmogenesis.
    Kao YH, Chung CC, Cheng WL, Lkhagva B, Chen YJ.

    06/6/2020
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