| scholarly article | Q13442814 |
| P50 | author | Bernhard Schermer | Q28321515 |
| Thomas Benzing | Q2422379 | ||
| Max Christoph Liebau | Q47159237 | ||
| Matthias Hammerschmidt | Q71370036 | ||
| P2093 | author name string | Claudia Dafinger | |
| Sandra Habbig | |||
| Julia Hatzold | |||
| Lori Borgal | |||
| Ilinca Sacarea | |||
| P2860 | cites work | The Krüppel-like zinc finger protein Glis2 functions as a negative modulator of the Wnt/beta-catenin signaling pathway | Q24296279 |
| Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling | Q24301800 | ||
| Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways | Q24302034 | ||
| The Hippo pathway regulates Wnt/beta-catenin signaling | Q24307606 | ||
| Identification of c-MYC as a target of the APC pathway | Q24310637 | ||
| Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia | Q24315070 | ||
| Nephrocystin interacts with Pyk2, p130(Cas), and tensin and triggers phosphorylation of Pyk2 | Q24555759 | ||
| Ciliary entry of the kinesin-2 motor KIF17 is regulated by importin-beta2 and RanGTP | Q24621121 | ||
| Jade-1 inhibits Wnt signalling by ubiquitylating beta-catenin and mediates Wnt pathway inhibition by pVHL | Q24634352 | ||
| Scrutinizing ciliopathies by unraveling ciliary interaction networks | Q27025614 | ||
| Wnt/beta-catenin signaling in development and disease | Q27860784 | ||
| MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis | Q28000044 | ||
| Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6 | Q28116478 | ||
| Characterization of the nephrocystin/nephrocystin-4 complex and subcellular localization of nephrocystin-4 to primary cilia and centrosomes | Q28119088 | ||
| Formation of primary cilia in the renal epithelium is regulated by the von Hippel-Lindau tumor suppressor protein | Q28246139 | ||
| Casein kinase 1 gamma couples Wnt receptor activation to cytoplasmic signal transduction | Q28286117 | ||
| Impaired Wnt-beta-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy | Q28506100 | ||
| Proteomic analysis of mammalian primary cilia | Q28512191 | ||
| Glomerulocystic kidney disease in mice with a targeted inactivation of Wwtr1 | Q28513907 | ||
| Wnt-3a utilizes a novel low dose and rapid pathway that does not require casein kinase 1-mediated phosphorylation of Dvl to activate beta-catenin | Q28586720 | ||
| Cystic renal neoplasia following conditional inactivation of apc in mouse renal tubular epithelium | Q28588368 | ||
| A size-exclusion permeability barrier and nucleoporins characterize a ciliary pore complex that regulates transport into cilia | Q29026303 | ||
| When cilia go bad: cilia defects and ciliopathies | Q29547198 | ||
| Effective targeted gene 'knockdown' in zebrafish | Q29547445 | ||
| The vertebrate primary cilium in development, homeostasis, and disease | Q29614609 | ||
| Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms | Q29614613 | ||
| Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways | Q29614619 | ||
| Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response | Q29617051 | ||
| A dual-kinase mechanism for Wnt co-receptor phosphorylation and activation | Q29618700 | ||
| The von Hippel-Lindau tumor suppressor protein controls ciliogenesis by orienting microtubule growth | Q30480543 | ||
| Zebrafish Tsc1 reveals functional interactions between the cilium and the TOR pathway | Q30489319 | ||
| Nephronophthisis: disease mechanisms of a ciliopathy | Q33594278 | ||
| The cell biology of polycystic kidney disease | Q34149966 | ||
| Phosphorylation by casein kinase 2 induces PACS-1 binding of nephrocystin and targeting to cilia | Q34324921 | ||
| Kidney development and disease in the zebrafish | Q34383970 | ||
| Nephronophthisis. | Q34793373 | ||
| Subcellular spatial regulation of canonical Wnt signalling at the primary cilium | Q35022258 | ||
| NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway | Q35196050 | ||
| Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice | Q36119534 | ||
| Urinary concentration defects and mechanisms underlying nephronophthisis | Q37156216 | ||
| The ubiquitin conjugation system is involved in the disassembly of cilia and flagella | Q37323142 | ||
| The canonical Wnt/beta-catenin signalling pathway | Q37355851 | ||
| Ciliary function and Wnt signal modulation | Q37369338 | ||
| Cystic kidney disease: the role of Wnt signaling | Q37767526 | ||
| Zebrafish Kidney Development | Q37812722 | ||
| Inversin, Wnt signaling and primary cilia | Q37972186 | ||
| Polycystin-1 C-terminal tail associates with beta-catenin and inhibits canonical Wnt signaling | Q38289224 | ||
| Control of the Wnt pathways by nephrocystin-4 is required for morphogenesis of the zebrafish pronephros | Q39557728 | ||
| Nephrocystin-4 regulates Pyk2-induced tyrosine phosphorylation of nephrocystin-1 to control targeting to monocilia | Q39584826 | ||
| pVHL and GSK3beta are components of a primary cilium-maintenance signalling network | Q40142798 | ||
| Nephrocystin-4 is required for pronephric duct-dependent cloaca formation in zebrafish | Q47073512 | ||
| Cystic kidney gene seahorse regulates cilia-mediated processes and Wnt pathways | Q47073543 | ||
| A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney | Q47074132 | ||
| Kinase cogs go forward and reverse in the Wnt signaling machine | Q47354687 | ||
| Early development of the zebrafish pronephros and analysis of mutations affecting pronephric function. | Q52182505 | ||
| Early development of polycystic kidney disease in transgenic mice expressing an activated mutant of the beta-catenin gene | Q74604719 | ||
| Linking cilia to Wnts | Q81695265 | ||
| A homozygous mutation in INVS causing juvenile nephronophthisis with abnormal reactivity of the Wnt/beta-catenin pathway | Q84960994 | ||
| P433 | issue | 30 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | negative regulation of canonical Wnt signaling pathway | Q14860027 |
| Jade family PHD finger 1 | Q21113948 | ||
| Nephrocystin 4 | Q21118162 | ||
| Jade family PHD finger 1 | Q29834377 | ||
| P304 | page(s) | 25370–25380 | |
| P577 | publication date | 2012-07-20 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | The ciliary protein nephrocystin-4 translocates the canonical Wnt regulator Jade-1 to the nucleus to negatively regulate β-catenin signaling | |
| P478 | volume | 287 |
| Q35195922 | Bioinformatic analysis of ciliary transition zone proteins reveals insights into the evolution of ciliopathy networks. |
| Q39178607 | CILIA: before and after |
| Q28245461 | Casein kinase 1 α phosphorylates the Wnt regulator Jade-1 and modulates its activity |
| Q91410919 | Cellular signalling by primary cilia in development, organ function and disease |
| Q38171918 | Cilia and coordination of signaling networks during heart development |
| Q34207085 | Ciliopathies: the trafficking connection |
| Q55417331 | Control of Hedgehog Signalling by the Cilia-Regulated Proteasome. |
| Q37668895 | DNA methylation profile associated with rapid decline in kidney function: findings from the CRIC study |
| Q47919079 | Expression profiles of NPHP1 in the germ cells in the semen of men with male factor infertility |
| Q92293141 | FoxH1 represses miR-430 during early embryonic development of zebrafish via non-canonical regulation |
| Q36596124 | HectD1 E3 ligase modifies adenomatous polyposis coli (APC) with polyubiquitin to promote the APC-axin interaction. |
| Q36956926 | Jade-1S phosphorylation induced by CK1α contributes to cell cycle progression |
| Q39339465 | Nuclear roles for cilia-associated proteins |
| Q37618918 | Open Sesame: How Transition Fibers and the Transition Zone Control Ciliary Composition. |
| Q39819105 | Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney |
| Q94463957 | Silencing of microRNA-135b inhibits invasion, migration, and stemness of CD24+CD44+ pancreatic cancer stem cells through JADE-1-dependent AKT/mTOR pathway |
| Q38828242 | Structure, function and regulation of jade family PHD finger 1 (JADE1). |
| Q55616467 | Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalus. |
| Q30540974 | The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity. |
| Q64092333 | The Role of Primary Cilia in the Crosstalk between the Ubiquitin⁻Proteasome System and Autophagy |
| Q90740314 | The ciliary protein Rpgrip1l in development and disease |
| Q45354108 | The ciliopathy disease protein NPHP9 promotes nuclear delivery and activation of the oncogenic transcriptional regulator TAZ. |
| Q34483855 | The novel function of JADE1S in cytokinesis of epithelial cells |
| Q35826045 | The transition zone protein Rpgrip1l regulates proteasomal activity at the primary cilium |
| Q55689509 | Zebrafish as a Model for Drug Screening in Genetic Kidney Diseases. |
| Q35124210 | β-catenin links von Hippel-Lindau to aurora kinase A and loss of primary cilia in renal cell carcinoma |
Search more.