From modulation of cellular plasticity to potentiation of therapeutic resistance: new and emerging roles of MYB transcription factors in human malignancies

S Anand, KS Vikramdeo, SK Sudan, A Sharma… - Cancer and Metastasis …, 2024 - Springer
MYB transcription factors are encoded by a large family of highly conserved genes from
plants to vertebrates. There are three members of the MYB gene family in human, namely …

Analyzing the effects of single nucleotide polymorphisms on hnRNPA2/B1 protein stability and function: insights for anticancer therapeutic design

K Dutta, V Kravtsov, K Oleynikova, A Ruzov… - ACS …, 2024 - ACS Publications
Heterogeneous nuclear ribonucleoprotein A2/B1 (hnRNPA2/B1) is a pivotal player in m6A
recognition, RNA metabolism, and antiviral responses. In the context of cancer …

In-Silico Analysis of Deleterious SNPs of FGF4 Gene and Their Impacts on Protein Structure, Function and Bladder Cancer Prognosis

EC Lim, SW Lim, KJK Tan, M Sathiya, WH Cheng… - Life, 2022 - mdpi.com
Dysregulation of fibroblast growth factors is linked to the pathogenesis of bladder cancer.
The role of FGF1 and FGF3 is evident in bladder cancer; however, the role of FGF4 is vague …

An in-silico analysis predicting the impact of coding single nucleotide polymorphisms (SNPs) in the human multidrug pump ABCG2

S Bora, R Kukreti, Y Hasija - Human Gene, 2023 - Elsevier
Abstract ATP-Binding Cassette transporter G2 (ABCG2) is a multidrug resistance pump
involved in pathophysiology and pharmacoresistance in various neurological, and …

Computational screening of pathogenic missense nsSNPs in heme oxygenase 1 (HMOX1) gene and their structural and functional consequences

AK Yadav, TPK Murthy, G Divyashri… - Journal of …, 2024 - Taylor & Francis
Abstract Heme Oxygenase 1 (HMOX1) is a cytoprotective enzyme, exhibiting the highest
activity in the spleen, catalyzing the heme ring breakdown into products of biological …

In-silico identification of deleterious non-synonymous SNPs of TBX1 gene: Functional and structural impact towards 22q11.2DS

M Almakhari, Y Chen, ASY Kong, D Moradigaravand… - Plos one, 2024 - journals.plos.org
The TBX1 gene plays a critical role in the development of 22q11. 2 deletion syndrome
(22q11. 2DS), a complex genetic disorder associated with various phenotypic …

[HTML][HTML] Preliminary insights on the mutational spectrum of BRCA1 and BRCA2 genes in Pakhtun ethnicity breast cancer patients from Khyber Pakhtunkhwa (KP) …

H Ahmad, A Ali, R Ali, AT Khalil, I Khan, MM Khan… - Neoplasia, 2024 - Elsevier
Gene mutations are a source of genetic instability which fuels the progression of cancer.
Mutations in BRCA1 and BRCA2 are considered as major drivers in the progression of …

An integrated computational analysis of high-risk SNPs in angiopoietin-like proteins (ANGPTL3 and ANGPTL8) reveals perturbed protein dynamics associated with …

S Iqbal, F Begum, DW Nyamai, N Jalal, P Shaw - Molecules, 2023 - mdpi.com
Angiopoietin-like proteins (ANGPTL) constitute a family of eight proteins (1–8) which play a
pivotal role in the regulation of various pathophysiological processes. The current study …

Genome-Wide Identification and Expression Analysis of the MYB Transcription Factor Family in Salvia nemorosa

H Yang, C Chen, L Han, X Zhang, M Yue - Genes, 2024 - mdpi.com
The MYB transcription factor gene family is among the most extensive superfamilies of
transcription factors in plants and is involved in various essential functions, such as plant …

Expression pattern and clinical value of Key RNA methylation modification regulators in ischemic stroke

X Zhang, Y Wang, B Dong, Y Jiang, D Liu, K Xie… - Frontiers in …, 2022 - frontiersin.org
Ischemic stroke (IS) is one of the major causes of death and disability worldwide, and
effective diagnosis and treatment methods are lacking. RNA methylation, a common …