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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 1
2006 3
2008 3
2010 2
2011 1
2012 2
2013 2
2014 1
2016 2
2018 3
2019 4
2021 3
2023 1
2024 0

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27 results

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Page 1
Cardiolipin metabolism regulates expression of muscle transcription factor MyoD1 and muscle development.
Vo L, Schmidtke MW, Da Rosa-Junior NT, Ren M, Schlame M, Greenberg ML. Vo L, et al. J Biol Chem. 2023 Mar;299(3):102978. doi: 10.1016/j.jbc.2023.102978. Epub 2023 Feb 4. J Biol Chem. 2023. PMID: 36739949 Free PMC article.
Our data suggest that MyoD1 repression is caused by upregulation of the MyoD1 negative regulator, homeobox protein Mohawk, and decreased Wnt signaling. Our findings reveal, for the first time, that CL metabolism regulates muscle differentiation through MyoD1 …
Our data suggest that MyoD1 repression is caused by upregulation of the MyoD1 negative regulator, homeobox protein Mohawk, and …
FOXF1 is required for the oncogenic properties of PAX3-FOXO1 in rhabdomyosarcoma.
Milewski D, Shukla S, Gryder BE, Pradhan A, Donovan J, Sudha P, Vallabh S, Pyros A, Xu Y, Barski A, Szabo S, Turpin B, Pressey JG, Millay DP, Khan J, Kalinichenko VV, Kalin TV. Milewski D, et al. Oncogene. 2021 Mar;40(12):2182-2199. doi: 10.1038/s41388-021-01694-9. Epub 2021 Feb 24. Oncogene. 2021. PMID: 33627785 Free PMC article.
FOXF1 cooperates with PAX3-FOXO1 and E-box transcription factors MYOD1 and MYOG to regulate FP-RMS-specific gene expression. Altogether, FOXF1 functions downstream of PAX3-FOXO1 to promote FP-RMS tumorigenesis....
FOXF1 cooperates with PAX3-FOXO1 and E-box transcription factors MYOD1 and MYOG to regulate FP-RMS-specific gene expression. Altogeth …
Combined Sclerosing and Spindle Cell Rhabdomyosarcoma in Previous Craniotomy Site: A Case Report and a Review of the Literature.
Gui H, Lhospital E, Staddon AP, Nagda SN, Zager EL, Zhang PJL, Brooks JS. Gui H, et al. Int J Surg Pathol. 2019 May;27(3):328-335. doi: 10.1177/1066896918802030. Epub 2018 Oct 1. Int J Surg Pathol. 2019. PMID: 30270691 Review.
Our review documents the following: sclerosing RMS occurs in both childhood and adult populations, has a predilection for the head and neck areas, and has a worse prognosis in adults. Sclerosing RMS harbors a high frequency of MYOD1 mutations, conferring a poor clinical ou …
Our review documents the following: sclerosing RMS occurs in both childhood and adult populations, has a predilection for the head and neck …
Long non-coding RNA MALAT1 promotes cardiac remodeling in hypertensive rats by inhibiting the transcription of MyoD.
Li D, Zhang C, Li J, Che J, Yang X, Xian Y, Li X, Cao C. Li D, et al. Aging (Albany NY). 2019 Oct 15;11(20):8792-8809. doi: 10.18632/aging.102265. Epub 2019 Oct 15. Aging (Albany NY). 2019. PMID: 31619581 Free PMC article.
Although long non-coding RNA (lncRNA) metastasis associated lung adenocarcinoma transcript 1 (MALAT1) has been identified to play important roles in the development of cardiovascular diseases, the regulatory function of lncRNA MALAT1 in hypertension remains poorly u …
Although long non-coding RNA (lncRNA) metastasis associated lung adenocarcinoma transcript 1 (MALAT1) has been identified to play important …
Genomewide linkage and peakwide association analyses of carotid plaque in Caribbean Hispanics.
Dong C, Beecham A, Slifer S, Wang L, Blanton SH, Wright CB, Rundek T, Sacco RL. Dong C, et al. Stroke. 2010 Dec;41(12):2750-6. doi: 10.1161/STROKEAHA.110.596981. Epub 2010 Oct 21. Stroke. 2010. PMID: 20966410 Free PMC article.
BACKGROUND AND PURPOSE: Atherosclerosis is a complex subclinical cardiovascular disorder with a substantial genetic component. This study sought to identify genetic loci influencing carotid plaque in 2 independent samples. ...In the association analysis of the 4 linkage pe …
BACKGROUND AND PURPOSE: Atherosclerosis is a complex subclinical cardiovascular disorder with a substantial genetic component. This s …
Association of ventricular noncompaction and histiocytoid cardiomyopathy: case report and review of the literature.
Planas S, Ferreres JC, Balcells J, Garrido M, Ramón Y Cajal S, Torán N. Planas S, et al. Pediatr Dev Pathol. 2012 Sep-Oct;15(5):397-402. doi: 10.2350/12-05-1193-CR.1. Epub 2012 Jul 3. Pediatr Dev Pathol. 2012. PMID: 22758650 Review.
In our case, the histiocytoid cells showed strong cytoplasmic expression for the skeletal muscle transcription factor MyoD1, which could be attributed to cross reactivity with an undetermined cytoplasmic antigen....
In our case, the histiocytoid cells showed strong cytoplasmic expression for the skeletal muscle transcription factor MyoD1, which co …
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome.
Clayton P, Chatelain P, Tatò L, Yoo HW, Ambler GR, Belgorosky A, Quinteiro S, Deal C, Stevens A, Raelson J, Croteau P, Destenaves B, Olivier C. Clayton P, et al. Eur J Endocrinol. 2013 Jul 29;169(3):277-89. doi: 10.1530/EJE-13-0069. Print 2013 Sep. Eur J Endocrinol. 2013. PMID: 23761422 Free PMC article. Clinical Trial.
Differences in expression were identified for one of the growth response-associated genes in GHD (AKT1) and for two in TS (KRAS and MYOD1). CONCLUSIONS: Carriage of specific growth-related genetic markers is associated with growth response in GHD and TS. ...
Differences in expression were identified for one of the growth response-associated genes in GHD (AKT1) and for two in TS (KRAS and MYOD1 …
27 results