Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase lambda-deficient mice: possible implication for the pathogenesis of immotile cilia syndrome.
about
Male infertility, impaired sperm motility, and hydrocephalus in mice deficient in sperm-associated antigen 6Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesiaCFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in miceHuman DNA polymerase lambda functionally and physically interacts with proliferating cell nuclear antigen in normal and translesion DNA synthesisSCO-ping out the mechanisms underlying the etiology of hydrocephalusSibling rivalry: competition between Pol X family members in V(D)J recombination and general double strand break repairSitus inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- miceCongenital hydrocephalus in genetically engineered micePlacenta defects and embryonic lethality resulting from disruption of mouse hydroxysteroid (17-beta) dehydrogenase 2 geneHaploinsufficiency for the murine orthologue of Chlamydomonas PF20 disrupts spermatogenesisInactivation of Chibby affects function of motile airway ciliaPrimary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1.The transcription factor RFX3 directs nodal cilium development and left-right asymmetry specificationCRISPR/Cas9-Mediated Rapid Generation of Multiple Mouse Lines Identified Ccdc63 as Essential for SpermiogenesisNoninvasive real-time measurement of nasal mucociliary clearance in mice by pinhole gamma scintigraphy.Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitisIntracerebroventricular antisense knockdown of G alpha i2 results in ciliary stasis and ventricular dilatation in the rat.Chk2-deficient mice exhibit radioresistance and defective p53-mediated transcriptionStrain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2Lentivector integration sites in ependymal cells from a model of metachromatic leukodystrophy: non-B DNA as a new factor influencing integration.Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.Choosing the right path: does DNA-PK help make the decision?Arabidopsis DNA polymerase lambda mutant is mildly sensitive to DNA double strand breaks but defective in integration of a transgene.Impairment of spermatogenesis leading to infertility.Suffering in silence: the tolerance of DNA damage.Knockout mouse models of sperm flagellum anomalies.Cystic fibrosis and other respiratory diseases of impaired mucus clearance.Mendelian genetics of male infertilityControl of DNA polymerase lambda stability by phosphorylation and ubiquitination during the cell cycle.Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice.Spermiogenesis and DNA repair: a possible etiology of human infertility and genetic disorders.Management of primary ciliary dyskinesia/Kartagener's syndrome in infertile male patients and current progress in defining the underlying genetic mechanism.Primary immunodeficiencies associated with DNA-repair disorders.Polymerases in nonhomologous end joining: building a bridge over broken chromosomes.Mouse models of DNA polymerases.Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy.Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia.A mutation study of sperm head shape and motility in the mouse: lessons for the clinic.A pooling-based genomewide association study identifies genetic variants associated with Staphylococcus aureus colonization in chronic rhinosinusitis patients.A specific loop in human DNA polymerase mu allows switching between creative and DNA-instructed synthesis.
P2860
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P2860
Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase lambda-deficient mice: possible implication for the pathogenesis of immotile cilia syndrome.
description
2002 nî lūn-bûn
@nan
2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@ast
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@en
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@nl
type
label
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@ast
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@en
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@nl
prefLabel
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@ast
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@en
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@nl
P2093
P2860
P1476
Hydrocephalus, situs inversus, ...... is of immotile cilia syndrome.
@en
P2093
Hirofumi Sawa
Hiroshi Suzuki
Hiroyuki Takai
Kazuo Nagashima
Kyoji Ikeda
Makoto Nakanishi
Miho Watanabe
Noboru Motoyama
Yosuke Kawase
Yosuke Kobayashi
P2860
P304
P356
10.1128/MCB.22.8.2769-2776.2002
P407
P577
2002-04-01T00:00:00Z