Results 31 to 40 of about 10,226 (209)

DGCR8-dependent efficient pri-miRNA processing of human pri-miR-9-2

open access: yesJournal of Biological Chemistry, 2021
Microprocessor complex, including DiGeorge syndrome critical region gene 8 (DGCR8) and DROSHA, recognizes and cleaves primary transcripts of microRNAs (pri-miRNAs) in the maturation of canonical miRNAs.
Masahiro Nogami   +2 more
exaly   +2 more sources

HOTTIP suppresses ferroptosis via mediating DGCR8/miR‑214‑3p/GPX4 regulatory axis in osteosarcoma. [PDF]

open access: yesOncol Rep
Osteosarcoma (OS) is the most common primary bone malignancy in children and adolescents and the current typical strategy remains unsatisfactory in clinical practice.
Ding SC   +7 more
europepmc   +2 more sources

Peptidylarginine Deiminase 2 Regulates Expression of DGCR8 Affecting miRNA Biogenesis in Gonadotrope Cells

open access: yesReproduction, 2023
Canonical miRNA biogenesis requires DGCR8 microprocessor complex subunit, which helps cleave pri-miRNAs into pre-miRNAs. Previous studies found that inhibiting peptidylarginine deiminase (PAD) enzyme activity results in increased DGCR8 expression.
Brett A. Ralston   +8 more
semanticscholar   +2 more sources

Expression levels and polymorphisms of the microRNA maturing components; diagnostic values of Drosha, DGCR8 and Dicer in patients with vitiligo. [PDF]

open access: yesAfr Health Sci
Background and Objective Even though the pathogenesis of vitiligo is still unclear, recent studies have suggested that miRNAs can contribute to the occurrence and progression of the disease.
Aşır S   +7 more
europepmc   +2 more sources

Genetic polymorphism in DGCR8 is associated with late onset of preeclampsia [PDF]

open access: yesBMC Medical Genetics, 2019
Background PE (preeclampsia) is a heterogeneous disorder with early onset PE (EOPE) and late onset PE (LOPE) subtypes. Associations between maternal miRNAs biosynthesis genes polymorphisms and risk of PE have been previously observed. However, the impact
Xin Huang   +4 more
doaj   +3 more sources

Prevalence, Molecular Landscape, and Clinical Impact of DICER1 and DGCR8 Mutated Follicular-Patterned Thyroid Nodules

open access: yesJournal of Clinical Endocrinology and Metabolism
Background Mutations in micro-RNA (miRNA) regulators DICER1 and DGCR8 have recently been uncovered, revealing a potential novel mechanism driving thyroid tumor development.
Vincenzo Condello   +2 more
exaly   +2 more sources

The UGU-recognizing mechanism of DGCR8

open access: yes, 2019
Human Microprocessor is a trimeric complex, composed of a RNase Ill - Drosha and the DGCR8 (DiGeorge syndrome chromosomal region 8) dimer, that processes primary microRNAs (pri-miRNAs) to initiate microRNA (miRNA) biogenesis.
Dang, Thi Lieu
core   +3 more sources

Coilin enhances phosphorylation and stability of DGCR8 and promotes miRNA biogenesis [PDF]

open access: yesMolecular Biology of the Cell, 2021
MicroRNAs (miRNAs) are ∼22 nt small noncoding RNAs that control gene expression at the posttranscriptional level through translational inhibition and destabilization of their target mRNAs.
Katheryn E. Lett   +3 more
semanticscholar   +3 more sources

Disrupted miRNA Biogenesis Machinery Reveals Common Molecular Pathways and Diagnostic Potential in MDS and AML [PDF]

open access: yesBiomedicines
Background: Myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) are clonal stem cell disorders in which disrupted post-transcriptional regulation contributes to aberrant hematopoiesis and leukemic transformation.
Kenan Çevik   +5 more
doaj   +2 more sources

Primary MicroRNA Processing Assay Reconstituted Using Recombinant Drosha and DGCR8 [PDF]

open access: yes, 2013
In animals, the Microprocessor complex cleaves primary transcripts of microRNAs (pri-miRNAs) to produce precursor microRNAs in the nucleus. The core components of Microprocessor include the Drosha ribonuclease and its RNA-binding partner protein DiGeorge
Ian Barr   +5 more
core   +8 more sources

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