Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1. (Q34339024)

1 August 2017

Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1. (English)

1 reference

1 August 2017

Robert Curtis Hendrickson

4

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Amber K O'Connor

Amber K O'Connor

3

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Luiz F Onuchic

Luiz F Onuchic

9

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Xiangqin Cui

Xiangqin Cui

6

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Peter Igarashi

Peter Igarashi

8

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author name string

Ravindra Boddu

1

1 reference

1 August 2017

Chaozhe Yang

2

1 reference

1 August 2017

Braden Boone

5

1 reference

1 August 2017

Miguel Garcia-Gonzalez

7

1 reference

1 August 2017

Gregory G Germino

10

1 reference

1 August 2017

Lisa M Guay-Woodford

11

1 reference

1 August 2017

3 July 2014

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Journal of Molecular Medicine

1 August 2017

1 reference

1 August 2017

92

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1 August 2017

10

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1 August 2017

1045-1056

1 reference

https://scigraph.springernature.com/pub.10.1007/s00109-014-1185-7

1 August 2017

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cites work

Regulation of splicing by SR proteins and SR protein-specific kinases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Defining the roles and interactions of PTB.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Epitope-tagged Pkhd1 tracks the processing, secretion, and localization of fibrocystin.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Functional consequences of developmentally regulated alternative splicing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Loss of exon identity is a common mechanism of human inherited disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Integrative genomics viewer

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Polysome analysis and RNA purification from sucrose gradients

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Developments in RNA splicing and disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Expansion of the eukaryotic proteome by alternative splicing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

SR proteins and related factors in alternative splicing.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

GUDMAP: the genitourinary developmental molecular anatomy project

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Biliary and pancreatic dysgenesis in mice harboring a mutation in Pkhd1.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Genotype-phenotype correlations in autosomal dominant and autosomal recessive polycystic kidney disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Identification and analysis of alternative splicing events conserved in human and mouse

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Variation in alternative splicing across human tissues

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

The autosomal recessive polycystic kidney disease protein is localized to primary cilia, with concentration in the basal body area

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

ESEfinder: A web resource to identify exonic splicing enhancers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Improved splice site detection in Genie

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Functional analysis of the polypyrimidine tract in pre-mRNA splicing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4197071

Autosomal Recessive Polycystic Kidney Disease: The Clinical Experience in North America

6 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1185-7

Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1185-7

Cellular and subcellular localization of the ARPKD protein; fibrocystin is expressed on primary cilia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1185-7

Increased exon-trapping efficiency through modifications to the pSPL3 splicing vector.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1185-7

Kidney cysts, pancreatic cysts, and biliary disease in a mouse model of autosomal recessive polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1185-7

A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1185-7

Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1185-7

Identification of PKHD1 multiexon deletions using multiplex ligation-dependent probe amplification and quantitative polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1185-7

A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1185-7

10.1007/S00109-014-1185-7

21 January 2018

Identifiers

DOI

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1 August 2017

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1 reference

1 August 2017

1 reference