A miR-1207-5p binding site polymorphism abolishes regulation of HBEGF and is associated with disease severity in CFHR5 nephropathy (Q34154720)

31 July 2017

A miR-1207-5p binding site polymorphism abolishes regulation of HBEGF and is associated with disease severity in CFHR5 nephropathy (English)

1 reference

31 July 2017

1 reference

1 reference

Kamil Erguler

2

0 references

Kyriacos N Felekkis

Kyriacos N Felekkis

9

0 references

Konstantinos Voskarides

Konstantinos Voskarides

4

0 references

Constantinos Deltas

Constantinos Deltas

10

0 references

Yiannis Athanasiou

6

Yiannis Athanasiou

1 reference

31 July 2017

7

Alkis Pierides

1 reference

31 July 2017

3

Harsh Dweep

1 reference

31 July 2017

Gregory Papagregoriou

1

Gregory Papagregoriou

1 reference

31 July 2017

Panayiota Koupepidou

5

1 reference

31 July 2017

Norbert Gretz

8

1 reference

31 July 2017

language of work or name

English

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publication date

2 February 2012

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31 July 2017

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31 July 2017

7

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31 July 2017

2

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31 July 2017

e31021

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Creative Commons Attribution 4.0 International

31 July 2017

start time

2 February 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3271095/fullTextXML

inferred from PubMed Central ID database lookup

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Podocyte-selective deletion of dicer induces proteinuria and glomerulosclerosis

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Analysis of 2 x 2 tables of frequencies: matching test to experimental design

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Allele-specific targeting of hsa-miR-657 to human IGF2R creates a potential mechanism underlying the association of ACAA-insertion/deletion polymorphism with type 2 diabetes

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Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein

5 July 2018

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COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Sequence variants in SLITRK1 are associated with Tourette's syndrome

5 July 2018

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Clinical practice. Microscopic hematuria

5 July 2018

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A conditionally immortalized human podocyte cell line demonstrating nephrin and podocin expression.

5 July 2018

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The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans

5 July 2018

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Chromosome 8 breakpoint far 3' of the c-myc oncogene in a Burkitt's lymphoma 2;8 variant translocation is equivalent to the murine pvt-1 locus

5 July 2018

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Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidn

5 July 2018

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Modifier effect of ENOS in autosomal dominant polycystic kidney disease.

21 January 2018

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Heparin-binding epidermal growth factor-like growth factor downregulates expression of activator protein-1 transcription factor after intestinal ischemia-reperfusion injury.

21 January 2018

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Heparin-binding epidermal growth factor and Src family kinases in proliferation of renal epithelial cells

21 January 2018

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Involvement of HB-EGF and EGF receptor transactivation in TGF-beta-mediated fibronectin expression in mesangial cells

21 January 2018

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21 January 2018

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12 December 2020

An miR-502-binding site single-nucleotide polymorphism in the 3'-untranslated region of the SET8 gene is associated with early age of breast cancer onset

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12 December 2020

SIGNIFICANCE TESTS FOR 2×2 TABLES

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12 December 2020

Heparin binding epidermal growth factor in renal ischaemia/reperfusion injury

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12 December 2020

Heparin-binding EGF-like growth factor is expressed by mesangial cells and is involved in mesangial proliferation in glomerulonephritis

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12 December 2020

Heparin-binding epidermal growth factor-like growth factor is expressed in the adhesive lesions of experimental focal glomerular sclerosis

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Evidence for Association of Endothelial Cell Nitric Oxide Synthase Gene Polymorphism with Earlier Progression to End-Stage Renal Disease in a Cohort of Hellens from Greece and Cyprus

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Polymorphisms in human pre-miRNAs

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12 December 2020

Polymorphic Polymorphic MicroRNA-Target Interactions: A Novel Source of Phenotypic Variation

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12 December 2020

10.1371/JOURNAL.PONE.0031021

Identifiers

DOI

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31 July 2017

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1 reference

31 July 2017

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