about
Identification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesiaA common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesiaDNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armUnderstanding ciliated epithelia: the power of XenopusMucociliary clearance: pathophysiological aspectsMutations in Hydin impair ciliary motility in miceTubulin tyrosine ligase-like 1 deficiency results in chronic rhinosinusitis and abnormal development of spermatid flagella in miceInactivation of Chibby affects function of motile airway ciliaPrimary ciliary dyskinesia caused by homozygous mutation in DNAL1, encoding dynein light chain 1.Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitisTargeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects.A proteomic analysis of human cilia: identification of novel components.Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesia.Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.Freeze fracture study of airway epithelium from patients with primary ciliary dyskinesia.Primary ciliary dyskinesia: clinical presentation, diagnosis and genetics.Mouse models for genes involved in impaired spermatogenesis.Cystic fibrosis and other respiratory diseases of impaired mucus clearance.Management of primary ciliary dyskinesia/Kartagener's syndrome in infertile male patients and current progress in defining the underlying genetic mechanism.In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases.Primary ciliary dyskinesia: overlooked and undertreated in children.Modeling the lung: Design and development of tissue engineered macro- and micro-physiologic lung models for research use.Nasal versus tracheobronchial biopsies to diagnose primary ciliary dyskinesia: A meta-analysis.Wheezing in infancy.Mechanosensitive ATP release maintains proper mucus hydration of airwaysSuccessful treatment of persistent hypoxemia by nasal suctioning in a neonate with primary ciliary dyskinesia.Primary Ciliary Dyskinesia: An Update on New Diagnostic Modalities and Review of the Literature.Nasal nitric oxide to diagnose primary ciliary dyskinesia in newborns.Identification of predicted human outer dynein arm genes: candidates for primary ciliary dyskinesia genes.Investigation of the possible role of a novel gene, DPCD, in primary ciliary dyskinesia.Compound Heterozygous Variants in the Coiled-Coil Domain Containing 40 Gene in a Chinese Family with Primary Ciliary Dyskinesia Cause Extreme Phenotypic Diversity in Cilia Ultrastructure.Clinical analysis of patients with primary ciliary dyskinesia in mainland China.Primary ciliary dyskinesia: diagnostic and phenotypic features.Primary ciliary dyskinesia as a cause of neonatal respiratory distress: implications for the neonatologist.Nephronophthisis and retinal degeneration in tmem218-/- mice: a novel mouse model for Senior-Løken syndrome?
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Primary ciliary dyskinesia (PCD).
@ast
Primary ciliary dyskinesia (PCD).
@en
type
label
Primary ciliary dyskinesia (PCD).
@ast
Primary ciliary dyskinesia (PCD).
@en
prefLabel
Primary ciliary dyskinesia (PCD).
@ast
Primary ciliary dyskinesia (PCD).
@en
P2860
P1476
Primary ciliary dyskinesia (PCD).
@en
P2860
P304
P356
10.1002/(SICI)1099-0496(200004)29:4<307::AID-PPUL11>3.0.CO;2-2
P577
2000-04-01T00:00:00Z