scholarly article | Q13442814 |
P50 | author | Tri Q Nguyen | Q42700458 |
Indra A. Shaltiel | Q55458830 | ||
Rachel H Giles | Q63372740 | ||
Marijn F Stokman | Q63867777 | ||
Friedhelm Hildebrandt | Q28050923 | ||
Glenn van de Hoek | Q32421636 | ||
Marianne C. Verhaar | Q40340965 | ||
P2093 | author name string | Amiya K Ghosh | |
Gisela G Slaats | |||
Iain A Drummond | |||
Roel Goldschmeding | |||
Ive Logister | |||
Lucas L Falke | |||
Timothy D Klasson | |||
Stéphanie Le Corre | |||
P2860 | cites work | Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling | Q24294774 |
Defective planar cell polarity in polycystic kidney disease | Q46845250 | ||
Mesenchymal transition in kidney collecting duct epithelial cells. | Q52585581 | ||
The intra-S phase checkpoint targets Dna2 to prevent stalled replication forks from reversing. | Q53163831 | ||
Genome stability, progressive kidney failure and aging | Q84630228 | ||
Cep164, a novel centriole appendage protein required for primary cilium formation | Q24298367 | ||
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways | Q24302034 | ||
Cep164 is a mediator protein required for the maintenance of genomic stability through modulation of MDC1, RPA, and CHK1 | Q24657907 | ||
The role of the cilium in normal and abnormal cell cycles: emphasis on renal cystic pathologies | Q27026481 | ||
Cep164 mediates vesicular docking to the mother centriole during early steps of ciliogenesis | Q28000119 | ||
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination | Q28188363 | ||
Snail activation disrupts tissue homeostasis and induces fibrosis in the adult kidney | Q28505069 | ||
Snail blocks the cell cycle and confers resistance to cell death | Q28572344 | ||
Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis | Q28586772 | ||
The transcription factor snail controls epithelial-mesenchymal transitions by repressing E-cadherin expression | Q28595042 | ||
Visualizing spatiotemporal dynamics of multicellular cell-cycle progression | Q29617610 | ||
In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitro | Q29617927 | ||
Distinct phosphatases antagonize the p53 response in different phases of the cell cycle | Q30578888 | ||
Intrarenal cells, not bone marrow-derived cells, are the major source for regeneration in postischemic kidney | Q33218591 | ||
Live-cell assay for detection of apoptosis by dual-laser flow cytometry using Hoechst 33342 and 7-amino-actinomycin D. | Q33280770 | ||
UV-dependent interaction between Cep164 and XPA mediates localization of Cep164 at sites of DNA damage and UV sensitivity | Q33406218 | ||
tp53 mutant zebrafish develop malignant peripheral nerve sheath tumors | Q33722903 | ||
Origin and function of myofibroblasts in kidney fibrosis | Q33792700 | ||
Murine Joubert syndrome reveals Hedgehog signaling defects as a potential therapeutic target for nephronophthisis | Q33919616 | ||
Epithelial to mesenchymal transition in renal fibrogenesis: pathologic significance, molecular mechanism, and therapeutic intervention | Q35615604 | ||
Renal fibrosis and the origin of the renal fibroblast | Q36556298 | ||
Apoptosis and loss of renal tissue in polycystic kidney diseases | Q36707140 | ||
Phenotypic transitions and fibrosis in diabetic nephropathy | Q36753326 | ||
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy | Q37552382 | ||
Snail and Slug, key regulators of TGF-β-induced EMT, are sufficient for the induction of single-cell invasion | Q39160417 | ||
Chromosome segregation errors as a cause of DNA damage and structural chromosome aberrations | Q39465329 | ||
Snail1 is involved in the renal epithelial-mesenchymal transition. | Q40095313 | ||
Functional aspects of primary cilia in signaling, cell cycle and tumorigenesis | Q40963789 | ||
Bcl-2 overexpression prevents apoptosis-induced Madin-Darby canine kidney simple epithelial cyst formation | Q40979524 | ||
NEK8 links the ATR-regulated replication stress response and S phase CDK activity to renal ciliopathies | Q41883398 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | apoptotic process | Q14599311 |
P304 | page(s) | e1004594 | |
P577 | publication date | 2014-10-01 | |
P1433 | published in | PLOS Genetics | Q1893441 |
P1476 | title | Nephronophthisis-associated CEP164 regulates cell cycle progression, apoptosis and epithelial-to-mesenchymal transition | |
P478 | volume | 10 |
Q47706146 | A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies |
Q34481426 | Autosomal dominant polycystic kidney disease: the changing face of clinical management |
Q26769756 | Cellular Mechanisms of Ciliary Length Control |
Q38650721 | Centrosomes in the DNA damage response--the hub outside the centre |
Q54978155 | Ciliary signalling in cancer. |
Q47290076 | Conditional knockout mice for the distal appendage protein CEP164 reveal its essential roles in airway multiciliated cell differentiation |
Q26771488 | Current topics of functional links between primary cilia and cell cycle |
Q50286581 | EGF receptor kinase suppresses ciliogenesis through activation of USP8 deubiquitinase. |
Q92995595 | Embryonic and foetal expression patterns of the ciliopathy gene CEP164 |
Q38397620 | FUCCI sensors: powerful new tools for analysis of cell proliferation. |
Q41918379 | Germline mutations affecting the histone H4 core cause a developmental syndrome by altering DNA damage response and cell cycle control |
Q42180881 | Inhibition of centrosomal protein 164 sensitizes rhabdomyosarcoma cells to radiotherapy |
Q41611551 | Loss of Glis2/NPHP7 causes kidney epithelial cell senescence and suppresses cyst growth in the Kif3a mouse model of cystic kidney disease. |
Q37054775 | Low expression of centrosomal protein 78 (CEP78) is associated with poor prognosis of colorectal cancer patients |
Q47833085 | Many Genes-One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated Disorders. |
Q38964728 | Mechanisms of ciliogenesis suppression in dividing cells |
Q47674642 | Microtubule stabilization drives 3D centrosome migration to initiate primary ciliogenesis |
Q90647026 | Nek2 kinase displaces distal appendages from the mother centriole prior to mitosis |
Q88539141 | Nephronophthisis: A review of genotype-phenotype correlation |
Q38556258 | Nephronophthisis: should we target cysts or fibrosis? |
Q39231616 | Oral-facial-digital syndrome type I cells exhibit impaired DNA repair; unanticipated consequences of defective OFD1 outside of the cilia network |
Q92763167 | Positioning of the Centrosome and Golgi Complex |
Q37269150 | Rnf25/AO7 positively regulates wnt signaling via disrupting Nkd1-Axin inhibitory complex independent of its ubiquitin ligase activity |
Q38821382 | Screen-based identification and validation of four new ion channels as regulators of renal ciliogenesis |
Q35229307 | The more we know, the more we have to discover: an exciting future for understanding cilia and ciliopathies |
Q91447644 | The role of DNA damage as a therapeutic target in autosomal dominant polycystic kidney disease |
Q64096239 | WDR5, BRCA1, and BARD1 Co-regulate the DNA Damage Response and Modulate the Mesenchymal-to-Epithelial Transition during Early Reprogramming |
Q26750633 | Zebrafish: a vertebrate tool for studying basal body biogenesis, structure, and function |
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