(Q28586620)

31 January 2017

title

The ciliary protein Nek8/Nphp9 acts downstream of Inv/Nphp2 during pronephros morphogenesis and left-right establishment in zebrafish (English)

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NIMA (never in mitosis gene a)-related expressed kinase 8

31 January 2017

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Inversin

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NIMA-related kinase 8

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Inversin

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4

Koichi Kawakami

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31 January 2017

Hajime Fukui

1

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31 January 2017

Dai Shiba

series ordinal

2

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31 January 2017

Kazuhide Asakawa

series ordinal

3

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31 January 2017

Takahiko Yokoyama

series ordinal

5

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31 January 2017

language of work or name

English

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publication date

30 July 2012

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31 January 2017

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31 January 2017

volume

586

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31 January 2017

issue

16

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31 January 2017

page(s)

2273–2279

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Ciliogenesis: building the cell's antenna

31 January 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

Comparative genomics: prediction of the ciliary and basal body proteome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

Nephronophthisis: disease mechanisms of a ciliopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

Genetic and physical interaction between the NPHP5 and NPHP6 gene products

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

Nephrocystin-4 is required for pronephric duct-dependent cloaca formation in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

Localization of Inv in a distinctive intraciliary compartment requires the C-terminal ninein-homolog-containing region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

Nek8, a NIMA family kinase member, is overexpressed in primary human breast tumors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

Nephrocystin-3 is required for ciliary function in zebrafish embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

The zebrafish pronephros: a model to study nephron segmentation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

Genetic dissection of neural circuits by Tol2 transposon-mediated Gal4 gene and enhancer trapping in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

The Tol2-mediated Gal4-UAS method for gene and enhancer trapping in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

The zebrafishnodal-related genesouthpawis required for visceral and diencephalic left-right asymmetry

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

The Cerberus/Dan-family protein Charon is a negative regulator of Nodal signaling during left-right patterning in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

Zebrafish pronephros: a model for understanding cystic kidney disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.05.064

10.1016/J.FEBSLET.2012.05.064

21 January 2018

Identifiers

DOI

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31 January 2017

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