(Q24302034)

12 December 2016

title

Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways (English)

1 reference

Gene Ontology release 2020-05-02

PubMed

PubMed publication ID

12 December 2016

1 reference

1 reference

GOA release 2020-03-11

RPGRIP1 like

1 reference

GOA release 2020-03-11

Nephrocystin 1

1 reference

GOA release 2020-03-11

1 reference

Friedhelm Hildebrandt

Francesc R Garcia-Gonzalo

30

0 references

Francesc R Garcia-Gonzalo

16

0 references

Diane C Slusarski

Diane C Slusarski

27

0 references

Edgar A. Otto

Edgar A Otto

6

0 references

Rachel H Giles

4

Rachel H Giles

0 references

Kevin C Corbit

3

Kevin C Corbit

0 references

Allen D Seol

17

Allen D Seol

0 references

Jeremy F Reiter

31

Jeremy F Reiter

0 references

author name string

Liyun Sang

1

0 references

Julie J Miller

2

0 references

Matthew J Brauer

5

0 references

Lisa M Baye

7

0 references

Xiaohui Wen

8

0 references

Suzie J Scales

9

0 references

Mandy Kwong

10

0 references

Erik G Huntzicker

11

0 references

Mindan K Sfakianos

12

0 references

Wendy Sandoval

13

0 references

J Fernando Bazan

14

0 references

Priya Kulkarni

15

0 references

John F O'Toole

18

0 references

Susanne Held

19

0 references

Heiko M Reutter

20

0 references

William S Lane

21

0 references

Muhammad Arshad Rafiq

22

0 references

Abdul Noor

23

0 references

Muhammad Ansar

24

0 references

Akella Radha Rama Devi

25

0 references

Val C Sheffield

26

0 references

John B Vincent

28

0 references

Daniel A Doherty

29

0 references

Peter K Jackson

describes a project that uses

32

0 references

language of work or name

English

0 references

publication date

13 May 2011

0 references

published in

Cell

0 references

volume

145

0 references

issue

4

0 references

page(s)

513-28

0 references

Cytoscape

1 reference

Europe PubMed Central

9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

inferred from PubMed Central ID database lookup

cites work

The role of primary cilia in neuronal function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Defining the human deubiquitinating enzyme interaction landscape

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

A systematic approach to mapping recessive disease genes in individuals from outbred populations

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

The human disease network

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Ataxin 10 induces neuritogenesis via interaction with G-protein beta2 subunit

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Cytoscape: a software environment for integrated models of biomolecular interaction networks

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Nephrocystin interacts with Pyk2, p130(Cas), and tensin and triggers phosphorylation of Pyk2

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

High-throughput generation of tagged stable cell lines for proteomic analysis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

The exocyst protein Sec10 is necessary for primary ciliogenesis and cystogenesis in vitro

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Tectonic, a novel regulator of the Hedgehog pathway required for both activation and inhibition.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Vertebrate Smoothened functions at the primary cilium

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Multiprotein complexes of Retinitis Pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked Retinitis Pigmentosa (XLRP).

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Genetic and physical interaction between the NPHP5 and NPHP6 gene products

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Characterization of the nephrocystin/nephrocystin-4 complex and subcellular localization of nephrocystin-4 to primary cilia and centrosomes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

19 March 2017

Intraflagellar transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Crk-associated substrate p130(Cas) interacts with nephrocystin and both proteins localize to cell-cell contacts of polarized epithelial cells

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Hedgehog signalling in the mouse requires intraflagellar transport proteins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Nephronophthisis: disease mechanisms of a ciliopathy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Functional redundancy of the B9 proteins and nephrocystins in Caenorhabditis elegans ciliogenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

The C. elegans homologs of nephrocystin-1 and nephrocystin-4 are cilia transition zone proteins involved in chemosensory perception

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Kupffer's vesicle is a ciliated organ of asymmetry in the zebrafish embryo that initiates left-right development of the brain, heart and gut.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

HNF-3 beta as a regulator of floor plate development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Interaction of ciliary disease protein retinitis pigmentosa GTPase regulator with nephronophthisis-associated proteins in mammalian retinas

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Origin and shaping of the laterality organ in zebrafish.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Joubert syndrome (and related disorders) (OMIM 213300).

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Local modeling of global interactome networks

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383065

Rhodopsin transport in the membrane of the connecting cilium of mammalian photoreceptor cells

29 November 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

MUSTER: Improving protein sequence profile-profile alignments by using multiple sources of structure information

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Cep97 and CP110 suppress a cilia assembly program

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

A protein domain-based interactome network for C. elegans early embryogenesis

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

The emerging complexity of the vertebrate cilium: new functional roles for an ancient organelle

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Pax6 controls progenitor cell identity and neuronal fate in response to graded Shh signaling

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Hedgehog-regulated processing of Gli3 produces an anterior/posterior repressor gradient in the developing vertebrate limb

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Induction of motor neurons by Sonic hedgehog is independent of floor plate differentiation

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Homeobox gene Nkx2.2 and specification of neuronal identity by graded Sonic hedgehog signalling

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Towards a proteome-scale map of the human protein–protein interaction network

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Impaired Wnt-beta-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease?

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Opinion: Building epithelial architecture: insights from three-dimensional culture models

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Nephrocystin-conserved domains involved in targeting to epithelial cell-cell junctions, interaction with filamins, and establishing cell polarity

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

The PSIPRED protein structure prediction server

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Protein homology detection by HMM-HMM comparison

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

SMART 6: recent updates and new developments

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

The renal cell primary cilium functions as a flow sensor

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Kinome siRNA screen identifies regulators of ciliogenesis and hedgehog signal transduction

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Nephrocystin-3 is required for ciliary function in zebrafish embryos

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Small-molecule modulators of Hedgehog signaling: identification and characterization of Smoothened agonists and antagonists

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Pattern formation in the vertebrate neural tube: a sonic hedgehog morphogen-regulated transcriptional network

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

The roles of cilia in developmental disorders and disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

Nephronophthisis-associated ciliopathies

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2011.04.019

7 January 2021

10.1016/J.CELL.2011.04.019

Identifiers

DOI

1 reference

1 reference

1 reference

PubMed publication ID

21565611

1 reference