| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/HMG/DDQ031 |
| P698 | PubMed publication ID | 20106870 |
| P50 | author | Paul J. Lockhart | Q42175141 |
| Moira O'Bryan | Q42892639 | ||
| Gary F. Egan | Q44556788 | ||
| Martin Delatycki | Q91487304 | ||
| P2093 | author name string | Philip J Robinson | |
| Hong X Wang | |||
| Gabrielle R Wilson | |||
| P2860 | cites work | Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia | Q24297464 |
| An intronic insertion in KPL2 results in aberrant splicing and causes the immotile short-tail sperm defect in the pig | Q24546353 | ||
| SCO-ping out the mechanisms underlying the etiology of hydrocephalus | Q28241174 | ||
| Ablation of D1 dopamine receptor-expressing cells generates mice with seizures, dystonia, hyperactivity, and impaired oral behavior. | Q28504771 | ||
| Deletion of the Parkin coregulated gene causes male sterility in the quaking(viable) mouse mutant | Q28508054 | ||
| Mutations in Hydin impair ciliary motility in mice | Q28509898 | ||
| Rumpshaker mouse: a new X-linked mutation affecting myelination: evidence for a defect in PLP expression | Q28511941 | ||
| The stumpy gene is required for mammalian ciliogenesis | Q28512591 | ||
| Expression and localization of the Parkin co-regulated gene in mouse CNS suggests a role in ependymal cilia function | Q28587788 | ||
| Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus | Q28588205 | ||
| Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1. | Q28589174 | ||
| Overview of structure and function of mammalian cilia | Q29615164 | ||
| The ciliary proteome database: an integrated community resource for the genetic and functional dissection of cilia | Q29615741 | ||
| A proteomic analysis of human cilia: identification of novel components | Q30841923 | ||
| A contemporary definition and classification of hydrocephalus | Q33438083 | ||
| Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene | Q34193368 | ||
| Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase lambda-deficient mice: possible implication for the pathogenesis of immotile cilia syndrome | Q34277881 | ||
| It's a double knock-out! The quaking mouse is a spontaneous deletion of parkin and parkin co-regulated gene (PACRG). | Q34292476 | ||
| To beat or not to beat: roles of cilia in development and disease | Q34532445 | ||
| Ring chromosome 6 in three fetuses: case reports, literature review, and implications for prenatal diagnosis | Q34540013 | ||
| Genetic defects in ciliary structure and function | Q34576108 | ||
| Rescuing qkV dysmyelination by a single isoform of the selective RNA-binding protein QKI. | Q34578520 | ||
| Parkin Co-Regulated Gene (PACRG) is regulated by the ubiquitin-proteasomal system and is present in the pathological features of Parkinsonian diseases | Q34641555 | ||
| Microtubules containing acetylated alpha-tubulin in mammalian cells in culture | Q36215921 | ||
| Genetics of human hydrocephalus. | Q36506344 | ||
| Piecing together a ciliome | Q36543698 | ||
| Fish and frogs: models for vertebrate cilia signaling | Q36992272 | ||
| Proteomic analysis of isolated chlamydomonas centrioles reveals orthologs of ciliary-disease genes | Q39720851 | ||
| Pathogenesis of mucous cell metaplasia in a murine asthma model | Q41925077 | ||
| Axonemal localization of Chlamydomonas PACRG, a homologue of the human Parkin-coregulated gene product | Q42516432 | ||
| FGFR-1 [corrected] signaling is involved in spermiogenesis and sperm capacitation | Q46849810 | ||
| The Parkin co-regulated gene product, PACRG, is an evolutionarily conserved axonemal protein that functions in outer-doublet microtubule morphogenesis. | Q48113744 | ||
| Cerebral phospholipids in 'quaking' mice | Q48812967 | ||
| P433 | issue | 8 | |
| P921 | main subject | hydrocephalus | Q193003 |
| P304 | page(s) | 1593-1602 | |
| P577 | publication date | 2010-01-27 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse | |
| P478 | volume | 19 |
| Q38289619 | A mutation study of sperm head shape and motility in the mouse: lessons for the clinic |
| Q44357771 | Beating frequency of motile cilia lining the third cerebral ventricle is finely tuned by the hypothalamic peptide MCH |
| Q90387183 | Blood Exposure Causes Ventricular Zone Disruption and Glial Activation In Vitro |
| Q37732663 | Centrin 2 is required for mouse olfactory ciliary trafficking and development of ependymal cilia planar polarity |
| Q22001114 | Ciliary and non-ciliary expression and function of PACRG during vertebrate development. |
| Q50315572 | Clinical phenotype and current diagnostic criteria for primary ciliary dyskinesia |
| Q38649301 | Congenital hydrocephalus and hemivertebrae associated with de novo partial monosomy 6q (6q25.3→qter). |
| Q37470111 | Coordinated genomic control of ciliogenesis and cell movement by RFX2. |
| Q47141354 | Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter Deletion |
| Q28585348 | Disruption of the mouse Jhy gene causes abnormal ciliary microtubule patterning and juvenile hydrocephalus |
| Q47625348 | Functional characterization of tektin-1 in motile cilia and evidence for TEKT1 as a new candidate gene for motile ciliopathies. |
| Q55527707 | Generation and characterisation of a parkin-Pacrg knockout mouse line and a Pacrg knockout mouse line. |
| Q37967602 | Genetic approaches to study glial cells in the rodent brain. |
| Q35617133 | Loss of p53 in quaking viable mice leads to Purkinje cell defects and reduced survival |
| Q45332326 | Microtubule binding protein PACRG plays a role in regulating specific ciliary dyneins during microtubule sliding |
| Q42388111 | Novel childhood asthma genes interact with in utero and early-life tobacco smoke exposure |
| Q92215774 | PACRG and FAP20 form the inner junction of axonemal doublet microtubules and regulate ciliary motility |
| Q37052753 | PACRG, a protein linked to ciliary motility, mediates cellular signaling |
| Q50312477 | PARK2 copy number aberrations in two children presenting with autism spectrum disorder: further support of an association and possible evidence for a new microdeletion/microduplication syndrome |
| Q37697480 | Pathogenic implications of cerebrospinal fluid barrier pathology in neuromyelitis optica. |
| Q27331221 | RAB-like 2 has an essential role in male fertility, sperm intra-flagellar transport, and tail assembly |
| Q30499289 | Regulation of flagellar motility by the conserved flagellar protein CG34110/Ccdc135/FAP50. |
| Q38107881 | Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia |
| Q57476670 | Sequence variant analysis of RNA sequences in severe equine asthma |
| Q92726510 | The inner junction complex of the cilia is an interaction hub that involves tubulin post-translational modifications |
| Q89531715 | The parkin-coregulated gene product PACRG promotes TNF signaling by stabilizing LUBAC |
Search more.