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MicroRNAs in the pathogenesis of cystic kidney disease
scientific article
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instance of
scholarly article
1 reference
stated in
PubMed
review article
1 reference
stated in
Europe PubMed Central
title
MicroRNAs in the pathogenesis of cystic kidney disease
(English)
1 reference
stated in
PubMed
main subject
pathogenesis
1 reference
based on heuristic
inferred from title
microRNA
1 reference
based on heuristic
inferred from title
cystic kidney disease
1 reference
based on heuristic
inferred from title
author name string
Yu Leng Phua
series ordinal
1
1 reference
stated in
Crossref
Jacqueline Ho
series ordinal
2
1 reference
stated in
Crossref
language of work or name
English
1 reference
stated in
PubMed
publication date
April 2015
1 reference
stated in
PubMed
published in
Current Opinion in Pediatrics
1 reference
stated in
PubMed
volume
27
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stated in
PubMed
issue
2
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stated in
PubMed
page(s)
219-26
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stated in
PubMed
cites work
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The RNA-binding protein bicaudal C regulates polycystin 2 in the kidney by antagonizing miR-17 activity
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The miR-17-5p microRNA is a key regulator of the G1/S phase cell cycle transition
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Lin-28 interaction with the Let-7 precursor loop mediates regulated microRNA processing
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Selective blockade of microRNA processing by Lin28
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NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis
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The nuclear RNase III Drosha initiates microRNA processing
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Polycystin-2 is an intracellular calcium release channel
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Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel
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The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains
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c-Myc-regulated microRNAs modulate E2F1 expression
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Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets
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PubMed Central
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MicroRNAs: genomics, biogenesis, mechanism, and function
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A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA
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Dicer functions in RNA interference and in synthesis of small RNA involved in developmental timing in C. elegans
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Distinct sites of renal fibrosis in Crim1 mutant mice arise from multiple cellular origins
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7 April 2017
MicroRNA MiR-17 retards tissue growth and represses fibronectin expression
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PubMed Central
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PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein
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PubMed Central
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Lin28 sustains early renal progenitors and induces Wilms tumor
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Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells
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PubMed Central
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Systems biology approach to identify transcriptome reprogramming and candidate microRNA targets during the progression of polycystic kidney disease
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Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease
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Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella
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The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia
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Somatic mutations in DROSHA and DICER1 impair microRNA biogenesis through distinct mechanisms in Wilms tumours
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Urine microRNA as potential biomarkers of autosomal dominant polycystic kidney disease progression: description of miRNA profiles at baseline
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miR-17~92 miRNA cluster promotes kidney cyst growth in polycystic kidney disease
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DIANA-microT web server v5.0: service integration into miRNA functional analysis workflows
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LIN28 binds messenger RNAs at GGAGA motifs and regulates splicing factor abundance
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Bicc1 links the regulation of cAMP signaling in polycystic kidneys to microRNA-induced gene silencing.
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PKHD1 post-transcriptionally modulated by miR-365-1 inhibits cell-cell adhesion
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MicroRNA-21 promotes fibrosis of the kidney by silencing metabolic pathways
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The long and short of microRNAs in the kidney
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MiR-17/106b seed family regulates p21 in Hodgkin's lymphoma
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The pro-apoptotic protein Bim is a microRNA target in kidney progenitors
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28 September 2017
The inducible deletion of Drosha and microRNAs in mature podocytes results in a collapsing glomerulopathy
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28 September 2017
Dicer regulates the development of nephrogenic and ureteric compartments in the mammalian kidney
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Targeted deletion of Dicer from proximal tubules protects against renal ischemia-reperfusion injury.
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28 September 2017
The microRNA-processing enzyme dicer maintains juxtaglomerular cells
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28 September 2017
Bicaudal C, a novel regulator of Dvl signaling abutting RNA-processing bodies, controls cilia orientation and leftward flow.
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28 September 2017
Lin28 promotes transformation and is associated with advanced human malignancies
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28 September 2017
Systems biology of autosomal dominant polycystic kidney disease (ADPKD): computational identification of gene expression pathways and integrated regulatory networks
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28 September 2017
Aberrant regulation of pVHL levels by microRNA promotes the HIF/VEGF axis in CLL B cells
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28 September 2017
Microarray-based approach identifies microRNAs and their target functional patterns in polycystic kidney disease
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28 September 2017
MicroRNA15a modulates expression of the cell-cycle regulator Cdc25A and affects hepatic cystogenesis in a rat model of polycystic kidney disease
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28 September 2017
Podocyte-specific loss of functional microRNAs leads to rapid glomerular and tubular injury
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28 September 2017
Podocyte-specific deletion of dicer alters cytoskeletal dynamics and causes glomerular disease
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4409326
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28 September 2017
Podocyte-selective deletion of dicer induces proteinuria and glomerulosclerosis
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28 September 2017
Developments in the management of autosomal dominant polycystic kidney disease
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Determinants of microRNA processing inhibition by the developmentally regulated RNA-binding protein Lin28.
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Antagomir-17-5p abolishes the growth of therapy-resistant neuroblastoma through p21 and BIM
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Genotype-phenotype correlations in MYCN-related Feingold syndrome
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28 September 2017
Polycystin-1, STAT6, and P100 function in a pathway that transduces ciliary mechanosensation and is activated in polycystic kidney disease
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28 September 2017
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD).
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28 September 2017
Autosomal dominant polycystic kidney disease (ADPKD, MIM 173900, PKD1 and PKD2 genes, protein products known as polycystin-1 and polycystin-2).
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28 September 2017
Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease
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28 September 2017
cAMP regulates cell proliferation and cyst formation in autosomal polycystic kidney disease cells.
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28 September 2017
Loss of the polycystic kidney disease (PKD1) region of chromosome 16p13 in renal cyst cells supports a loss-of-function model for cyst pathogenesis
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28 September 2017
Apoptosis and loss of renal tissue in polycystic kidney diseases
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28 September 2017
Localized Bicaudal-C RNA encodes a protein containing a KH domain, the RNA binding motif of FMR1.
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28 September 2017
Abnormal sodium pump distribution during renal tubulogenesis in congenital murine polycystic kidney disease
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28 September 2017
Mutations of the VHL tumour suppressor gene in renal carcinoma
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Characterization and deep sequencing analysis of exosomal and non-exosomal miRNA in human urine.
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Genetic analyses reveal a requirement for Dicer1 in the mouse urogenital tract.
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28 November 2018
Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease.
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Multilocular cyst of the kidney (cystic nephroma) and cystic, partially differentiated nephroblastoma. Terminology and criteria for diagnosis
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based on heuristic
inferred from PubMed ID database lookup
Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat. The American PKD1 Consortium (APKD1 Consortium)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25490692
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Progressive renal fibrosis in murine polycystic kidney disease: an immunohistochemical observation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25490692
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1097/MOP.0000000000000168
1 reference
stated in
PubMed
PMCID
4409326
1 reference
stated in
PubMed
PubMed ID
25490692
1 reference
stated in
PubMed
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