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62 results

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Page 1
Nonsyndromic Hypertrophic Cardiomyopathy Overview.
Cirino AL, Channaoui N, Ho C. Cirino AL, et al. 2008 Aug 5 [updated 2025 Mar 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2008 Aug 5 [updated 2025 Mar 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301725 Free Books & Documents. Review.
Knockout of MYOM1 in human cardiomyocytes leads to myocardial atrophy via impairing calcium homeostasis.
Hang C, Song Y, Li Y, Zhang S, Chang Y, Bai R, Saleem A, Jiang M, Lu W, Lan F, Cui M. Hang C, et al. J Cell Mol Med. 2021 Feb;25(3):1661-1676. doi: 10.1111/jcmm.16268. Epub 2021 Jan 15. J Cell Mol Med. 2021. PMID: 33452765 Free PMC article.
Myomesin-1 (encoded by MYOM1 gene) is expressed in almost all cross-striated muscles, whose family (together with myomesin-2 and myomesin-3) helps to cross-link adjacent myosin to form the M-line in myofibrils. ...A better and further understanding of MYOM1 biology …
Myomesin-1 (encoded by MYOM1 gene) is expressed in almost all cross-striated muscles, whose family (together with myomesin-2 and myom …
MiR-135a is highly expressed and aggravates inflammatory response in sepsis by targeting MYOM1.
Chen S, Zhang H, Li H. Chen S, et al. Acta Biochim Pol. 2022 Aug 17;69(3):587-592. doi: 10.18388/abp.2020_5882. Acta Biochim Pol. 2022. PMID: 35977075 Free article.
The association between miR-135a and Myomesin 1 (MYOM1) was speculated bythe predication website and confirmed by the dual-luciferase assay. ...Additionally, the mitigative impact of miR-135a inhibitor on THP-1cells damage triggered by LPS was suppressed by MYOM1 de …
The association between miR-135a and Myomesin 1 (MYOM1) was speculated bythe predication website and confirmed by the dual-luciferase …
Transcriptional landscape of human cancers.
Li M, Sun Q, Wang X. Li M, et al. Oncotarget. 2017 May 23;8(21):34534-34551. doi: 10.18632/oncotarget.15837. Oncotarget. 2017. PMID: 28427185 Free PMC article.
We identified consistently upregulated genes (such as E2F1, EZH2, FOXM1, MYBL2, PLK1, TTK, AURKA/B and BUB1) and consistently downregulated genes (such as SCARA5, MYOM1, NKAPL, PEG3, USP2, SLC5A7 and HMGCLL1) across various cancers. The dysregulation of these genes is like …
We identified consistently upregulated genes (such as E2F1, EZH2, FOXM1, MYBL2, PLK1, TTK, AURKA/B and BUB1) and consistently downregulated …
Pathogenesis of Cardiomyopathy Caused by Variants in ALPK3, an Essential Pseudokinase in the Cardiomyocyte Nucleus and Sarcomere.
Agarwal R, Wakimoto H, Paulo JA, Zhang Q, Reichart D, Toepfer C, Sharma A, Tai AC, Lun M, Gorham J, DePalma SR, Gygi SP, Seidman JG, Seidman CE. Agarwal R, et al. Circulation. 2022 Nov 29;146(22):1674-1693. doi: 10.1161/CIRCULATIONAHA.122.059688. Epub 2022 Nov 2. Circulation. 2022. PMID: 36321451 Free PMC article.
Investigations into alternative functions revealed that ALPK3 colocalized with myomesin proteins (MYOM1, MYOM2) at both the nuclear envelope and the sarcomere M-band. ALPK3 loss-of-function variants caused myomesin proteins to mislocalize and also dysregulated several addi …
Investigations into alternative functions revealed that ALPK3 colocalized with myomesin proteins (MYOM1, MYOM2) at both the nuclear e …
Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation.
Vad OB, Angeli E, Liss M, Ahlberg G, Andreasen L, Christophersen IE, Hansen CC, Møller S, Hellsten Y, Haunsoe S, Tveit A, Svendsen JH, Gotthardt M, Lundegaard PR, Olesen MS. Vad OB, et al. JACC Basic Transl Sci. 2023 Oct 25;9(2):163-180. doi: 10.1016/j.jacbts.2023.08.008. eCollection 2024 Feb. JACC Basic Transl Sci. 2023. PMID: 38510713 Free PMC article.
In a rat model with loss of RBM20, we demonstrated altered splicing of sarcomere genes (NEXN, TTN, TPM1, MYOM1, and LDB3), and differential expression in key cardiac genes. We identified altered sarcomere and mitochondrial structure on electron microscopy imaging and found …
In a rat model with loss of RBM20, we demonstrated altered splicing of sarcomere genes (NEXN, TTN, TPM1, MYOM1, and LDB3), and differ …
Identification of the cytoplasmic DNA-Sensing cGAS-STING pathway-mediated gene signatures and molecular subtypes in prostate cancer.
Yang J, Xu Z, Zheng W, Li Y, Wei Q, Yang L. Yang J, et al. BMC Cancer. 2024 Jun 14;24(1):732. doi: 10.1186/s12885-024-12492-3. BMC Cancer. 2024. PMID: 38877472 Free PMC article.
Among subtype 1 and subtype 2, the top ten mutation genes were MUC5B, DNAH9, SLC5A10, ZNF462, USP31, SIPA1L3, PLEC, HRAS, MYOM1, and ITGB6. Gene set variation analysis revealed a high enrichment of the E2F target in subtype 1, and gene set enrichment analysis showed signif …
Among subtype 1 and subtype 2, the top ten mutation genes were MUC5B, DNAH9, SLC5A10, ZNF462, USP31, SIPA1L3, PLEC, HRAS, MYOM1, and …
Alternative splicing of myomesin 1 gene is aberrantly regulated in myotonic dystrophy type 1.
Koebis M, Ohsawa N, Kino Y, Sasagawa N, Nishino I, Ishiura S. Koebis M, et al. Genes Cells. 2011 Sep;16(9):961-72. doi: 10.1111/j.1365-2443.2011.01542.x. Epub 2011 Jul 28. Genes Cells. 2011. PMID: 21794030 Free article.
Here, by using exon array, we identified aberrant inclusion of myomesin 1 (MYOM1) exon 17a as a novel splicing abnormality in DM1 muscle. A cellular splicing assay with a MYOM1 minigene revealed that not only MBNL1-3 but also CELF1 and 2 decreased the inclusion of …
Here, by using exon array, we identified aberrant inclusion of myomesin 1 (MYOM1) exon 17a as a novel splicing abnormality in DM1 mus …
Dilatative fetal cardiomyopathy followed by a mirror syndrome.
Miletić AI, Stipoljev F, Vičić A, Šerman A, Bekavac Vlatković I. Miletić AI, et al. Wien Med Wochenschr. 2024 Sep;174(11-12):213-216. doi: 10.1007/s10354-024-01041-z. Epub 2024 Jun 5. Wien Med Wochenschr. 2024. PMID: 38836950
Next-generation sequencing panel for pediatric cardiology was performed in the deceased child and parents. Two gene variants were recorded: MYOM1: c.770_771delCA (p.Thr257fs) and TPM1: c.814G>A (p.Glu272Lys). Both variants were classified as variants of uncertain signif …
Next-generation sequencing panel for pediatric cardiology was performed in the deceased child and parents. Two gene variants were recorded: …
62 results