Results 21 to 30 of about 883 (101)

Interplay of RNA m<sup>6</sup>A/m<sup>1</sup>A/m<sup>5</sup>C/m<sup>7</sup>G/ψ Regulators Predicting the Prognosis of Pancreatic Cancer. [PDF]

open access: yesFASEB Bioadv
In this study, we comprehensively analyze the 64 RNA modification regulators, including 24 m6A regulators, 13 m1A regulators, 12 m5C regulators, 9 m7G regulators, and 12 pseudouridine regulators in pancreatic cancer in TCGA, GTEx, and HPA databases. We investigate their RNA and protein expression, their association with patients' clinical significance,
Chen S, Mao J, Xu L, Lu L, Hao Y.
europepmc   +2 more sources

Higher expression of pseudouridine synthase 7 promotes non-small cell lung cancer progression and suggests a poor prognosis

open access: yesJournal of Cardiothoracic Surgery, 2023
Background Lung cancer is currently the second most common cancer, and non-small cell lung cancer accounts for about 85% of cases. NSCLC has not been studied for pseudouridine synthase 7 (PUS), a member of the PUS family that is associated with cancer ...
Guihong Zhang   +6 more
doaj   +1 more source

A novel PUS7 mutation causes intellectual disability with autistic and aggressive behaviors [PDF]

open access: yesNeurology Genetics, 2019
Recently, homozygous PUS7 mutations causing premature stop and truncation of the gene product were identified in 3 independent consanguineous families presenting with intellectual disability (ID), speech delay, short stature, microcephaly, and aggressive behavior.1 PUS7 encodes for a pseudouridine synthase 7 that catalyzes the isomerization of RNA ...
Darvish, Hossein   +7 more
openaire   +2 more sources

Integrative multiomics evaluation reveals the importance of pseudouridine synthases in hepatocellular carcinoma

open access: yesFrontiers in Genetics, 2022
Background: The pseudouridine synthases (PUSs) have been reported to be associated with cancers. However, their involvement in hepatocellular carcinoma (HCC) has not been well documented.
Zhipeng Jin   +6 more
doaj   +1 more source

Integrative Genomic Analysis Reveals Pseudouridine Modification-Related Gene Signatures Associated With Prognosis and Therapeutic Response Patterns in Hepatocellular Carcinoma. [PDF]

open access: yesInt J Genomics
Background Hepatocellular carcinoma (HCC) is a genomically heterogeneous malignancy with substantial variability in prognosis and therapeutic response. Pseudouridine (Ψ) modification is an evolutionarily conserved RNA modification involved in RNA structure stabilization and translational regulation; however, the genomic and functional relevance of ...
Gan Z, Fan T, Wang W, Qiao X, Zhao M.
europepmc   +2 more sources

RNA Modifications in Tumor Microenvironment: A New Dimension for Cancer Treatment. [PDF]

open access: yesMedComm (2020)
Tumor initiation and progression depend on a supportive and highly heterogeneous tumor microenvironment (TME). RNA modifications regulate signaling pathways and cytokine networks that shape TME dynamics, facilitating interactions between cancer cells and noncancerous stromal cells, and ultimately promoting immune evasion and tumor progression ...
Li Q, Sun Y, Lin S, Yuan Q.
europepmc   +2 more sources

Integrated Metabolomic and Transcriptomic Analysis of Modified Nucleosides for Biomarker Discovery in Clear Cell Renal Cell Carcinoma

open access: yesCells, 2023
Clear cell renal cell carcinoma (ccRCC) accounts for ~75% of kidney cancers. The biallelic inactivation of the von Hippel–Lindau tumor suppressor gene (VHL) is the truncal driver mutation of most cases of ccRCC.
Daniel A. Mohl   +10 more
doaj   +1 more source

Deciphering the pseudouridine nucleobase modification in human diseases: From molecular mechanisms to clinical perspectives. [PDF]

open access: yesClin Transl Med
This review discusses the regulatory mechanisms and pathological significance of pseudouridylation in human diseases, with a special emphasis on its involvement in tumourigenesis. Furthermore, the potential therapeutic advantages of targeting pseudouridylation are explored, offering novel strategies for disease treatment. Abstract RNA pseudouridylation,
Jia S   +10 more
europepmc   +2 more sources

PUS7 Deficiency: Phenotypical Expansion of PUS7 ‐Related Neurodevelopmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A
ABSTRACT Pathogenic variants in PUS7 , encoding pseudouridine synthase 7, cause a rare neurodevelopmental disorder marked by intellectual disability, microcephaly, short stature, and behavioral disturbances.
Alice Muda   +5 more
openaire   +1 more source

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