Identification of novel phytotherapeutic agents for understanding hypertrophic cardiomyopathy via genetic mapping and advanced computational analysis
Abdullahi Tunde Aborode , Onifade Isreal Ayobami , Ammar Usman Danazumi , Christopher Busayo Olowosoke , Haruna Isiyaku Umar , Abraham Osinuga , Aeshah A. Awaji , Fatmah Ali Awaji , Ebenezer Ayomide Omojowolo , Najwa Ahmad Kuthi , Tanveer Shaikh , Babatunde Shuaib Anidu , Athanasios Alexiou , Ridwan Olamilekan Adesola , Zainab Olapade , Awah Favour Matthew , Blessing Ameh , Toluwalope Yinka Oni , Adetolase Azizat Bakre , Godfred Yawson Scott
Genome Instability & Disease ›› : 1 -25.
Identification of novel phytotherapeutic agents for understanding hypertrophic cardiomyopathy via genetic mapping and advanced computational analysis
Hypertrophic cardiomyopathy (HCM) is a monogenic cardiovascular disorder that has been poorly studied at the molecular, genetic, and computational levels. Here, we examined the genetic map of HCM polymorphic targets using a computational approach to identify new phytochemicals with potential therapeutic properties. We demonstrate the range of mutations associated with cardiomyopathies, and identify new associations between genes and phenotypes in this disease category. Specifically, our findings suggest that several genes associated with channelopathies might serve as genetic modifiers, altering the clinical features and severity of cardiomyopathic phenotypes, thus likely impacting disease manifestation.
| [1] |
|
| [2] |
|
| [3] |
|
| [4] |
|
| [5] |
|
| [6] |
|
| [7] |
|
| [8] |
|
| [9] |
|
| [10] |
|
| [11] |
|
| [12] |
|
| [13] |
|
| [14] |
|
| [15] |
|
| [16] |
|
| [17] |
|
| [18] |
|
| [19] |
|
| [20] |
|
| [21] |
|
| [22] |
|
| [23] |
|
| [24] |
|
| [25] |
|
| [26] |
|
| [27] |
|
| [28] |
|
| [29] |
|
| [30] |
|
| [31] |
|
| [32] |
|
| [33] |
|
| [34] |
|
| [35] |
|
| [36] |
|
| [37] |
|
| [38] |
Lindahl, E., Abraham, M., Hess, B., & Spoel, V. D. GROMACS 2019.4 Source code 2019. https://doi.org/10.5281/ZENODO.3460414 |
| [39] |
|
| [40] |
|
| [41] |
|
| [42] |
|
| [43] |
|
| [44] |
|
| [45] |
|
| [46] |
|
| [47] |
|
| [48] |
|
| [49] |
|
| [50] |
|
| [51] |
Ogu, C. C., & Maxa, J. L. (2000). Drug interactions due to cytochrome P450. In: Baylor University medical center proceedings, vol. 13, no. 4. Taylor & Francis, pp. 421–423. https://doi.org/10.1080/08998280.2000.11927719 |
| [52] |
|
| [53] |
|
| [54] |
|
| [55] |
|
| [56] |
|
| [57] |
|
| [58] |
|
| [59] |
|
| [60] |
|
| [61] |
|
| [62] |
|
| [63] |
|
| [64] |
|
| [65] |
|
| [66] |
|
| [67] |
|
| [68] |
|
| [69] |
|
| [70] |
|
| [71] |
|
| [72] |
|
| [73] |
|
| [74] |
|
| [75] |
|
| [76] |
|
| [77] |
|
| [78] |
|
| [79] |
|
| [80] |
|
Shenzhen University School of Medicine; Fondazione Istituto FIRC di Oncologia Molecolare
/
| 〈 |
|
〉 |