FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies (Q24297877)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

FAM161 centrosomal protein A

1 reference

GOA release 2020-03-11

cilium assembly

1 reference

GOA release 2020-03-11

Family with sequence similarity 161, member A

1 reference

GOA release 2020-03-11

retinitis pigmentosa

1 reference

based on heuristic

inferred from title

Silvio Alessandro Di Gioia

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

9

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Lisette Hetterschijt

5

object named as

Lisette Hetterschijt

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

6

object named as

Dror Sharon

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

author name string

Stef J F Letteboer

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Dikla Bandah-Rozenfeld

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Yvan Arsenijevic

7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Ronald Roepman

8

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

language of work or name

0 references

publication date

1 September 2012

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Human Molecular Genetics

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

21

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

5174-5184

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

23

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

The molecular basis of human retinal and vitreoretinal diseases

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

The retinal ciliopathies.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Modeling human disease in humans: the ciliopathies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

RPGR: role in the photoreceptor cilium, human retinal disease, and gene therapy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

OFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilin

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactyly.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

The proteome of the mouse photoreceptor sensory cilium complex

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Centrin in the photoreceptor cells of mammalian retinae

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

The forkhead-associated domain protein Cep170 interacts with Polo-like kinase 1 and serves as a marker for mature centrioles

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

The PCM-basal body/primary cilium coalition

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

TOPORS, implicated in retinal degeneration, is a cilia-centrosomal protein

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

The retinitis pigmentosa 28 protein FAM161A is a novel ciliary protein involved in intermolecular protein interaction and microtubule association

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Ofd1, a human disease gene, regulates the length and distal structure of centrioles

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Kidney-specific inactivation of Ofd1 leads to renal cystic disease associated with upregulation of the mTOR pathway

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Retinal incorporation and differentiation of neural precursors derived from human embryonic stem cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Versatile screening for binary protein-protein interactions by yeast two-hybrid mating

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

21 January 2018

Protein networks and complexes in photoreceptor cilia.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS368

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1093/HMG/DDS368

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

release_ugnwabw52valfcvylejoa7eb5q

1 reference

https://api.fatcat.wiki/v0/release/ugnwabw52valfcvylejoa7eb5q

24 November 2022

based on heuristic

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22940612%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24297877&oldid=1842357873"