相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。DNAI2 Mutations Cause Primary Ciliary Dyskinesia with Defects in the Outer Dynein Arm
Niki Tomas Loges et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations
Georg C. Schwabe et al.
HUMAN MUTATION (2008)
Advances in high-capacity extrachromosomal vector technology: Episomal maintenance, vector delivery, and transgene expression
Michele M. P. Lufino et al.
MOLECULAR THERAPY (2008)
Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins
Heymut Omran et al.
NATURE (2008)
Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia
Marcus P. Kennedy et al.
CIRCULATION (2007)
A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia
Benedicte Duriez et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Basal cells of the human adult airway surface epithelium retain transit-amplifying cell properties
Rodolphe Hajj et al.
STEM CELLS (2007)
Targeted retroviral vectors displaying a cleavage site-engineered hemagglutinin (HA) through HA-protease interactions
Judit Szecsi et al.
MOLECULAR THERAPY (2006)
Mutations of DNAI1 in primary ciliary dyskinesia -: Evidence of founder effect in a common mutation
Maimoona A. Zariwala et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2006)
Induction of neutralising antibodies by virus-like particles harbouring surface proteins from highly pathogenic H5N1 and H7N1 influenza viruses
Judit Szecsi et al.
VIROLOGY JOURNAL (2006)
A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome
Bartlomiej Budny et al.
HUMAN GENETICS (2006)
Influenza virus receptor specificity and cell tropism in mouse and human airway epithelial cells
Aida Ibricevic et al.
JOURNAL OF VIROLOGY (2006)
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa
A Moore et al.
JOURNAL OF MEDICAL GENETICS (2006)
Transdifferentiation of ciliated cells during repair of the respiratory epithelium
KS Park et al.
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY (2006)
Lateralization defects and ciliary dyskinesia: lessons from algae
L El Zein et al.
TRENDS IN GENETICS (2003)
Recovery of airway cystic fibrosis transmembrane conductance regulator function in mice with cystic fibrosis after single-dose lentivirus-mediated gene transfer
M Limberis et al.
HUMAN GENE THERAPY (2002)
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia
L Bartoloni et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus
I Ibañez-Tallon et al.
HUMAN MOLECULAR GENETICS (2002)
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right and asymmetry
H Olbrich et al.
NATURE GENETICS (2002)
The effects of coronavirus on human nasal ciliated respiratory epithelium
MA Chilvers et al.
EUROPEAN RESPIRATORY JOURNAL (2001)
Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)
C Guichard et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Characterization of novel safe lentiviral vectors derived from simian immunodeficiency virus (SIVmac251) that efficiently transduce mature human dendritic cells
D Nègre et al.
GENE THERAPY (2000)
Primary ciliary dyskinesia:: a genome-wide linkage analysis reveals extensive locus heterogeneity
JL Blouin et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2000)
分享论文
