Modelling a ciliopathy: Ahi1 knockdown in model systems reveals an essential role in brain, retinal, and renal development (Q28506685)

24 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959375%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

Modelling a ciliopathy: Ahi1 knockdown in model systems reveals an essential role in brain, retinal, and renal development (English)

2 references

24 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959375%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

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1 reference

GOA release 2020-03-11

1 reference

1 reference

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13 February 2020

Ann Marie Hynes

2 references

24 January 2017

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13 February 2020

Lorraine Eley

2 references

24 January 2017

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13 February 2020

David Inglis

2 references

24 January 2017

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13 February 2020

Bill Chaudhry

2 references

24 January 2017

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13 February 2020

Roslyn J Simms

1 reference

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13 February 2020

Helen R Dawe

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13 February 2020

publication date

29 September 2011

1 reference

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Cellular and Molecular Life Sciences

13 February 2020

published in

2 references

24 January 2017

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13 February 2020

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24 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959375%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

2 references

24 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959375%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

page(s)

993-1009

1 reference

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"Joubert syndrome" revisited: key ocular motor signs with magnetic resonance imaging correlation

13 February 2020

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AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

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AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome

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AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis

21 January 2018

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Jouberin localizes to collecting ducts and interacts with nephrocystin-1

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High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations

21 January 2018

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Species differences in the expression of Ahi1, a protein implicated in the neurodevelopmental disorder Joubert syndrome, with preferential accumulation to stigmoid bodies

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Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function

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21 January 2018

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Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking

21 January 2018

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Decoding cilia function: defining specialized genes required for compartmentalized cilia biogenesis

21 January 2018

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Flagellar motility is required for the viability of the bloodstream trypanosome

21 January 2018

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The Chlorella variabilis NC64A genome reveals adaptation to photosymbiosis, coevolution with viruses, and cryptic sex

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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Cilia localization is essential for in vivo functions of the Joubert syndrome protein Arl13b/Scorpion

21 January 2018

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Cystic kidney gene seahorse regulates cilia-mediated processes and Wnt pathways

21 January 2018

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Mutations in zebrafish leucine-rich repeat-containing six-like affect cilia motility and result in pronephric cysts, but have variable effects on left-right patterning

21 January 2018

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Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants.

21 January 2018

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Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene

21 January 2018

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

21 January 2018

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

21 January 2018

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Left-right pattern of cardiac BMP4 may drive asymmetry of the heart in zebrafish.

21 January 2018

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12 December 2020

Definition of individual components within the cytoskeleton of Trypanosoma brucei by a library of monoclonal antibodies.

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12 December 2020

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12 December 2020

Mutations affecting development of the zebrafish retina

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12 December 2020

10.1007/S00018-011-0826-Z

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Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959375%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

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Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959375%20AND%20SRC:MED&resulttype=core&format=json