| P50 | author | Scott D. Weatherbee | Q41879554 |
| | Charles A Greer | Q88239270 |
| P2093 | author name string | Colin A Johnson | |
| | Jennifer L Pluznick | |
| | Michael J Caplan | |
| | Kavita Mistry | |
| | Michael Hull | |
| | Vincent Gattone | |
| | Diego J Rodriguez-Gil | |
| P2860 | cites work | The autosomal recessive polycystic kidney disease protein is localized to primary cilia, with concentration in the basal body area | Q24310842 |
| | Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3 | Q24337720 |
| | The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation | Q24337819 |
| | Ultrastructure of mouse olfactory mucosa | Q28258928 |
| | Mechanical stimuli induce cleavage and nuclear translocation of the polycystin-1 C terminus | Q28506516 |
| | A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling | Q28507443 |
| | Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse | Q28593460 |
| | Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways | Q29614619 |
| | A novel mouse model reveals that polycystin-1 deficiency in ependyma and choroid plexus results in dysfunctional cilia and hydrocephalus. | Q33506091 |
| | The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat. | Q34485086 |
| | Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons | Q36023714 |
| | Polycystic liver and kidney diseases | Q36336546 |
| | Biliary and pancreatic dysgenesis in mice harboring a mutation in Pkhd1. | Q36559697 |
| | Wnt/Frizzled family members mediate olfactory sensory neuron axon extension | Q36943968 |
| | Functional expression of the olfactory signaling system in the kidney | Q37100981 |
| | Olfactory cilia: linking sensory cilia function and human disease | Q37193134 |
| | PACS-1 mediates phosphorylation-dependent ciliary trafficking of the cyclic-nucleotide-gated channel in olfactory sensory neurons | Q37358449 |
| | Molecular genetics and pathogenic mechanisms for the severe ciliopathies: insights into neurodevelopment and pathogenesis of neural tube defects | Q37812586 |
| | Mapping of class I and class II odorant receptors to glomerular domains by two distinct types of olfactory sensory neurons in the mouse | Q38356941 |
| | Development of multiorgan pathology in the wpk rat model of polycystic kidney disease | Q39680116 |
| | Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium | Q40752332 |
| | Overexpression of frequenin, a modulator of phosphatidylinositol 4-kinase, inhibits biosynthetic delivery of an apical protein in polarized madin-darby canine kidney cells | Q40877851 |
| | Ciliated and microvillous structures of rat olfactory and nasal respiratory epithelia. A study using ultra-rapid cryo-fixation followed by freeze-substitution or freeze-etching | Q41636402 |
| | Cytoarchitecture of the normal rat olfactory epithelium: light and scanning electron microscopic studies | Q42468801 |
| | Expression of the neuronal calcium sensor protein NCS-1 in the developing mouse olfactory pathway | Q45196357 |
| | Defective planar cell polarity in polycystic kidney disease | Q46845250 |
| | The expression of tenascin-C along the lamprey olfactory pathway during embryonic development and following axotomy-induced replacement of the olfactory receptor neurons | Q48399770 |
| | A novel embryonic nestin-expressing radial glia-like progenitor gives rise to zonally restricted olfactory and vomeronasal neurons. | Q50638291 |
| | Genesis of cilia and microvilli of rat nasal epithelia during pre-natal development. I. Olfactory epithelium, qualitative studies. | Q53732324 |
| | Mutations of theCEP290gene encoding a centrosomal protein cause Meckel-Gruber syndrome | Q57908821 |
| | Polycystic kidney disease--the ciliary connection | Q73087592 |
| | New rat model that phenotypically resembles autosomal recessive polycystic kidney disease | Q73234904 |
| | Linking cilia to Wnts | Q81695265 |
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | e19694 | |
| P577 | publication date | 2011-01-01 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Renal cystic disease proteins play critical roles in the organization of the olfactory epithelium | |
| P478 | volume | 6 | |