The Oak Ridge Polycystic Kidney mouse: modeling ciliopathies of mice and men (Q37118904)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18366137%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

review article

6 references

19 July 2020

28 September 2020

3 December 2020

3 July 2022

27 January 2024

The Oak Ridge Polycystic Kidney mouse: modeling ciliopathies of mice and men (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18366137%20AND%20SRC:MED&resulttype=core&format=json

autosomal dominant polycystic kidney disease

4 January 2020

main subject

9 references

22 April 2019

20 June 2019

24 June 2019

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12 October 2019

22 October 2019

18 December 2019

29 May 2020

19 July 2020

biomedical investigative technique

1 reference

19 September 2019

1 reference

12 October 2019

1 reference

22 October 2019

1 reference

18 December 2019

polycystic kidney disease

2 references

19 July 2020

28 September 2020

1 reference

28 September 2020

1 reference

3 December 2020

Jonathan Merle Lehman

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18366137%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Yesim Aydin-Son

4

1 reference

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4 January 2020

author name string

Edward J Michaud

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18366137%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Trenton R Schoeb

3

1 reference

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4 January 2020

Michael Miller

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18366137%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Bradley K Yoder

6

1 reference

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4 January 2020

publication date

1 August 2008

14 references

22 April 2019

20 June 2019

24 June 2019

19 September 2019

12 October 2019

22 October 2019

18 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18366137%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

29 May 2020

19 July 2020

28 September 2020

3 December 2020

3 July 2022

27 January 2024

Developmental Dynamics

14 references

22 April 2019

20 June 2019

24 June 2019

19 September 2019

12 October 2019

22 October 2019

18 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18366137%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

29 May 2020

19 July 2020

28 September 2020

3 December 2020

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27 January 2024

237

1 reference

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4 January 2020

issue

8

1 reference

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4 January 2020

page(s)

1960-1971

1 reference

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Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms

4 January 2020

cites work

1 reference

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Ciliary proteins link basal body polarization to planar cell polarity regulation

14 September 2017

1 reference

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The primary cilia, a 'Rab-id' transit system for hedgehog signaling

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

A critical developmental switch defines the kinetics of kidney cyst formation after loss of Pkd1

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and function

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Protein networks and complexes in photoreceptor cilia.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

The retinal ciliopathies.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Disruption of intraflagellar transport in adult mice leads to obesity and slow-onset cystic kidney disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Evc is a positive mediator of Ihh-regulated bone growth that localises at the base of chondrocyte cilia

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Patched1 regulates hedgehog signaling at the primary cilium

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Nephronophthisis-associated ciliopathies

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Pathways of signal transduction employed by vertebrate Hedgehogs

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

The intraflagellar transport component IFT88/polaris is a centrosomal protein regulating G1-S transition in non-ciliated cells

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

The Ciliopathies: An Emerging Class of Human Genetic Disorders

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Cilium-generated signaling: a cellular GPS?

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Fat aussie--a new Alström syndrome mouse showing a critical role for ALMS1 in obesity, diabetes, and spermatogenesis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Dissection of epistasis in oligogenic Bardet-Biedl syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

PDGFRalphaalpha signaling is regulated through the primary cilium in fibroblasts

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Indian hedgehog: its roles and regulation in endochondral bone development

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Cilia and Hedgehog responsiveness in the mouse

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Shh controls epithelial proliferation via independent pathways that converge on N-Myc

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Alms1-disrupted mice recapitulate human Alström syndrome

14 September 2017

1 reference

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Mechanoregulation of intracellular Ca2+ concentration is attenuated in collecting duct of monocilium-impaired orpk mice

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Mouse intraflagellar transport proteins regulate both the activator and repressor functions of Gli transcription factors

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

14 September 2017

Cilia-related diseases

1 reference

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Intraflagellar transport and cilia-dependent renal disease: the ciliary hypothesis of polycystic kidney disease.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly

14 September 2017

1 reference

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The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome

14 September 2017

1 reference

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Neuronal primary cilia: a review

14 September 2017

1 reference

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The oligogenic properties of Bardet-Biedl syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Ihh signaling is directly required for the osteoblast lineage in the endochondral skeleton

14 September 2017

1 reference

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Roles of PDGF in animal development

14 September 2017

1 reference

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Loss of the Tg737 protein results in skeletal patterning defects

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Sonic hedgehog-dependent activation of Gli2 is essential for embryonic hair follicle development

14 September 2017

1 reference

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Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Shh and Gli3 are dispensable for limb skeleton formation but regulate digit number and identity

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Phenotypic variations of orpk mutation and chromosomal localization of modifiers influencing kidney phenotype

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis

14 September 2017

1 reference

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Roles for PDGF-A and sonic hedgehog in development of mesenchymal components of the hair follicle

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Sonic hedgehog signaling is essential for hair development

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

A motility in the eukaryotic flagellum unrelated to flagellar beating

14 September 2017

1 reference

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Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice.

14 September 2017

1 reference

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The oviductal cilia and Kartagener's syndrome.

14 September 2017

1 reference

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Removal of the MDCK cell primary cilium abolishes flow sensing

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Bending the MDCK cell primary cilium increases intracellular calcium

14 September 2017

1 reference

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Ciliary motility in the 'immotile cilia syndrome'. First results of microphoto-oscillographic studies.

29 September 2017

1 reference

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Making sense of cilia and flagella

27 June 2018

1 reference

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3 September 2018

1 reference

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SANS (USH1G) expression in developing and mature mammalian retina

3 September 2018

1 reference

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Development of the post-natal growth plate requires intraflagellar transport proteins

3 September 2018

1 reference

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Altered pH(i) regulation and Na(+)/HCO3(-) transporter activity in choroid plexus of cilia-defective Tg737(orpk) mutant mouse

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Intraflagellar transport is essential for endochondral bone formation.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

PDGF isoforms induce and maintain anagen phase of murine hair follicles.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

New neurons follow the flow of cerebrospinal fluid in the adult brain

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cells

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Defective planar cell polarity in polycystic kidney disease

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Heightened epithelial Na+ channel-mediated Na+ absorption in a murine polycystic kidney disease model epithelium lacking apical monocilia

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Disruption of IFT results in both exocrine and endocrine abnormalities in the pancreas of Tg737(orpk) mutant mice

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndrome

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Clinicopathologic reports, case reports, and small case series: usher syndrome type 1 associated with primary ciliary aplasia

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

The C. elegans homolog of the murine cystic kidney disease gene Tg737 functions in a ciliogenic pathway and is disrupted in osm-5 mutant worms

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

WNT signaling in the control of hair growth and structure.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

Evidence of Oligogenic Inheritance in Nephronophthisis

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677030

4 December 2018

1 reference

12 December 2020

Sensenbrenner syndrome: a new member of the hepatorenal fibrocystic family

1 reference

12 December 2020

Somatic inactivation of Pkd2 results in polycystic kidney disease

1 reference

12 December 2020

Renal and retinal involvement in the Sensenbrenner syndrome

1 reference

12 December 2020

Articular cartilage and growth plate defects are associated with chondrocyte cytoskeletal abnormalities in Tg737orpk mice lacking the primary cilia protein polaris

1 reference

12 December 2020

Cilia Proteins Control Cerebellar Morphogenesis by Promoting Expansion of the Granule Progenitor Pool

1 reference

12 December 2020

Identifiers

DOI

10.1002/DVDY.21515

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18366137%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18366137%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

PubMed publication ID

18366137

1 reference