Renal-retinal ciliopathy gene Sdccag8 regulates DNA damage response signaling (Q34427583)

24722439

2 August 2017

title

Renal-retinal ciliopathy gene Sdccag8 regulates DNA damage response signaling (English)

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2 August 2017

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8

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13 June 2020

Jacob M Schrøder

9

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13 June 2020

Jens S Andersen

11

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13 June 2020

Rachel H Giles

15

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Alessandra Boletta

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13 June 2020

author name string

Rannar Airik

1

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13 June 2020

Gisela G Slaats

2

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13 June 2020

Zhi Guo

3

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13 June 2020

Anna-Carina Weiss

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13 June 2020

Naheed Khan

5

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13 June 2020

Amiya Ghosh

6

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13 June 2020

Toby W Hurd

7

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13 June 2020

Steve J Elledge

10

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13 June 2020

Andreas Kispert

12

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13 June 2020

Maddalena Castelli

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13 June 2020

Friedhelm Hildebrandt

16

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13 June 2020

publication date

10 April 2014

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24722439

Journal of the American Society of Nephrology

2 August 2017

published in

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volume

25

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13 June 2020

issue

11

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13 June 2020

page(s)

2573-2583

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NEK8 links the ATR-regulated replication stress response and S phase CDK activity to renal ciliopathies

13 June 2020

cites work

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CDK inhibitors R-roscovitine and S-CR8 effectively block renal and hepatic cystogenesis in an orthologous model of ADPKD.

6 July 2018

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

6 July 2018

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Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling

6 July 2018

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Selective loss of RPGRIP1-dependent ciliary targeting of NPHP4, RPGR and SDCCAG8 underlies the degeneration of photoreceptor neurons

6 July 2018

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RPGR-associated retinal degeneration in human X-linked RP and a murine model

6 July 2018

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FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair

6 July 2018

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Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15

6 July 2018

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

6 July 2018

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A primary microcephaly protein complex forms a ring around parental centrioles.

6 July 2018

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

6 July 2018

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6 July 2018

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CEP152 is a genome maintenance protein disrupted in Seckel syndrome

6 July 2018

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Mechanisms of Nephronophthisis and Related Ciliopathies

6 July 2018

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Endothelial cells from humans and mice with polycystic kidney disease are characterized by polyploidy and chromosome segregation defects through survivin down-regulation

6 July 2018

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The DNA Damage Response: Making It Safe to Play with Knives

6 July 2018

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

6 July 2018

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Temporal relationship between primary and motile ciliogenesis in airway epithelial cells

6 July 2018

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

6 July 2018

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RPGRIP1 is essential for normal rod photoreceptor outer segment elaboration and morphogenesis

6 July 2018

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A mouse model of ATR-Seckel shows embryonic replicative stress and accelerated aging

6 July 2018

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Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.

6 July 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

6 July 2018

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Deletion of the developmentally essential gene ATR in adult mice leads to age-related phenotypes and stem cell loss

6 July 2018

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Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling

6 July 2018

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Functional characterization of the OFD1 protein reveals a nuclear localization and physical interaction with subunits of a chromatin remodeling complex

6 July 2018

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6 July 2018

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

6 July 2018

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6 July 2018

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A role for rhodopsin in a signal transduction cascade that regulates membrane trafficking and photoreceptor polarity

6 July 2018

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Tbx18 regulates the development of the ureteral mesenchyme

6 July 2018

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Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification

6 July 2018

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6 July 2018

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Identification and characterization of the novel centrosome-associated protein CCCAP

6 July 2018

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Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene

6 July 2018

1 reference

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Expression of the centrosomal colon cancer autoantigen gene during spermatogenesis in the maturing rat testis.

6 July 2018

1 reference

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Long-lasting arrest of murine polycystic kidney disease with CDK inhibitor roscovitine.

27 October 2018

1 reference

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Sustained cell proliferation of renal epithelial cells in mice with inv mutation.

27 October 2018

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Transgenic mouse line with green-fluorescent protein-labeled Centrin 2 allows visualization of the centrosome in living cells

27 October 2018

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Retinopathy induced in mice by targeted disruption of the rhodopsin gene

27 October 2018

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12 December 2020

Isolation and characterization of the lower portion of the thin limb of Henle in primary culture

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12 December 2020

A tale of two tails: ciliary mechanotransduction in ADPKD

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12 December 2020

Juvenile cystic kidneys (jck): a new mouse mutation which causes polycystic kidneys

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12 December 2020

Identifiers

DOI

10.1681/ASN.2013050565

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24722439%20AND%20SRC:MED&resulttype=core&format=json

13 June 2020

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13 June 2020

24722439

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