| Q38289619 | A mutation study of sperm head shape and motility in the mouse: lessons for the clinic |
| Q39034026 | A pooling-based genomewide association study identifies genetic variants associated with Staphylococcus aureus colonization in chronic rhinosinusitis patients |
| Q48414762 | A simple method to obtain pure cultures of multiciliated ependymal cells from adult rodents |
| Q39113544 | A specific loop in human DNA polymerase mu allows switching between creative and DNA-instructed synthesis |
| Q44927419 | Accelerated mortality from hydrocephalus and pneumonia in mice with a combined deficiency of SPAG6 and SPAG16L reveals a functional interrelationship between the two central apparatus proteins |
| Q45213360 | Adult ependymal cells are postmitotic and are derived from radial glial cells during embryogenesis. |
| Q35650249 | Arabidopsis DNA polymerase lambda mutant is mildly sensitive to DNA double strand breaks but defective in integration of a transgene |
| Q27306183 | CFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in mice |
| Q28592641 | CRISPR/Cas9-Mediated Rapid Generation of Multiple Mouse Lines Identified Ccdc63 as Essential for Spermiogenesis |
| Q34149479 | Chk2-deficient mice exhibit radioresistance and defective p53-mediated transcription |
| Q35029335 | Choosing the right path: does DNA-PK help make the decision? |
| Q34609964 | Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome |
| Q48222348 | Computer reconstruction of the three-dimensional structure of mouse cerebral ventricles |
| Q30495744 | Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitis |
| Q28506486 | Congenital hydrocephalus in genetically engineered mice |
| Q47614597 | Constitutive and regulated expression of the mouse Dinb (Polkappa) gene encoding DNA polymerase kappa. |
| Q36946963 | Control of DNA polymerase lambda stability by phosphorylation and ubiquitination during the cell cycle |
| Q36746482 | Cystic fibrosis and other respiratory diseases of impaired mucus clearance |
| Q55129602 | DNA damage checkpoint pathway modulates the regulation of skeletal growth and osteoblastic bone formation by parathyroid hormone-related peptide. |
| Q40400659 | DNA polymerase lambda protects mouse fibroblasts against oxidative DNA damage and is recruited to sites of DNA damage/repair |
| Q79773213 | DNA polymerases for translesion DNA synthesis: enzyme purification and mouse models for studying their function |
| Q48331130 | Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse |
| Q35582961 | Error-Prone DNA Polymerases: When Making a Mistake is the Only Way to Get Ahead |
| Q28585662 | Haploinsufficiency for the murine orthologue of Chlamydomonas PF20 disrupts spermatogenesis |
| Q46927548 | Heat shock transcription factor 1 is required for maintenance of ciliary beating in mice. |
| Q28205678 | Human DNA polymerase lambda functionally and physically interacts with proliferating cell nuclear antigen in normal and translesion DNA synthesis |
| Q73234169 | Human DNA polymerase lambda possesses terminal deoxyribonucleotidyl transferase activity and can elongate RNA primers: implications for novel functions |
| Q50739578 | Hydrodynamic phase locking in mouse node cilia. |
| Q35903958 | Impairment of spermatogenesis leading to infertility |
| Q28585930 | Inactivation of Chibby affects function of motile airway cilia |
| Q28255797 | Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice |
| Q48248516 | Inflammatory demyelination induces ependymal modifications concomitant to activation of adult (SVZ) stem cell proliferation. |
| Q33281960 | Intracerebroventricular antisense knockdown of G alpha i2 results in ciliary stasis and ventricular dilatation in the rat. |
| Q48219291 | Investigation of the possible role of a novel gene, DPCD, in primary ciliary dyskinesia |
| Q40136379 | Involvement of DNA polymerase mu in the repair of a specific subset of DNA double-strand breaks in mammalian cells. |
| Q36431990 | Knockout mouse models of sperm flagellum anomalies |
| Q36423913 | Left-right asymmetry in the vertebrate embryo: from early information to higher-level integration |
| Q34459397 | Lentivector integration sites in ependymal cells from a model of metachromatic leukodystrophy: non-B DNA as a new factor influencing integration |
| Q24635321 | Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia |
| Q24537766 | Male infertility, impaired sperm motility, and hydrocephalus in mice deficient in sperm-associated antigen 6 |
| Q37514946 | Management of primary ciliary dyskinesia/Kartagener's syndrome in infertile male patients and current progress in defining the underlying genetic mechanism. |
| Q37812789 | Mechanisms of mammalian ciliary motility: Insights from primary ciliary dyskinesia genetics |
| Q36846121 | Mendelian genetics of male infertility |
| Q38045848 | Mouse models of DNA polymerases. |
| Q51642463 | Mucociliary transport determined by in vivo microdialysis in the airways of normal and CF mice. |
| Q37163023 | Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice. |
| Q30494863 | Noninvasive real-time measurement of nasal mucociliary clearance in mice by pinhole gamma scintigraphy |
| Q28507425 | Placenta defects and embryonic lethality resulting from disruption of mouse hydroxysteroid (17-beta) dehydrogenase 2 gene |
| Q37774662 | Polymerases in nonhomologous end joining: building a bridge over broken chromosomes |
| Q28589174 | Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1. |
| Q38066984 | Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy |
| Q37713997 | Primary immunodeficiencies associated with DNA-repair disorders |
| Q38107881 | Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia |
| Q36687824 | Roles of DNA polymerases in replication, repair, and recombination in eukaryotes. |
| Q28241174 | SCO-ping out the mechanisms underlying the etiology of hydrocephalus |
| Q28270934 | Sibling rivalry: competition between Pol X family members in V(D)J recombination and general double strand break repair |
| Q28505979 | Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice |
| Q47171971 | Sperm dysfunction and ciliopathy. |
| Q37187725 | Spermiogenesis and DNA repair: a possible etiology of human infertility and genetic disorders |
| Q52159624 | Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCD |
| Q34183826 | Strain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2 |
| Q36337954 | Suffering in silence: the tolerance of DNA damage |
| Q42061406 | The DNA polymerase lambda is required for the repair of non-compatible DNA double strand breaks by NHEJ in mammalian cells |
| Q28592361 | The transcription factor RFX3 directs nodal cilium development and left-right asymmetry specification |
| Q34660648 | Two rotating cilia in the node cavity are sufficient to break left-right symmetry in the mouse embryo. |
| Q83288895 | Up-regulation of the fidelity of human DNA polymerase lambda by its non-enzymatic proline-rich domain |