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。Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry
Heike Olbrich et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Computer-assisted image analysis of human cilia and Chlamydomonas flagella reveals both similarities and differences in axoneme structure
Eileen T. O'Toole et al.
CYTOSKELETON (2012)
Analyses of functional domains within the PF6 protein of the central apparatus reveal a role for PF6 sub-complex members in regulating flagellar beat frequency
Daniel J. Goduti et al.
CYTOSKELETON (2012)
Static respiratory cilia associated with mutations in Dnahc11/DNAH11: A mouse model of PCD
Jane S. Lucas et al.
HUMAN MUTATION (2012)
Lung Oxidative Damage by Hypoxia
O. F. Araneda et al.
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY (2012)
Mutations in Radial Spoke Head Genes and Ultrastructural Cilia Defects in East-European Cohort of Primary Ciliary Dyskinesia Patients
Ewa Zietkiewicz et al.
PLOS ONE (2012)
Mechanisms of mammalian ciliary motility: Insights from primary ciliary dyskinesia genetics
Lance Lee
GENE (2011)
Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: Implications for application to clinical testing
Jonathan S. Berg et al.
GENETICS IN MEDICINE (2011)
Sperm flagella: comparative and phylogenetic perspectives of protein components
Kazuo Inaba
MOLECULAR HUMAN REPRODUCTION (2011)
Ciliogenesis: building the cell's antenna
Hiroaki Ishikawa et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2011)
Mutations in Radial Spoke Head Protein Genes RSPH9 and RSPH4A Cause Primary Ciliary Dyskinesia with Central-Microtubular-Pair Abnormalities
Victoria H. Castleman et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome
Margaret W. Leigh et al.
GENETICS IN MEDICINE (2009)
Interpreting Neonatal Lethal Phenotypes in Mouse Mutants: Insights Into Gene Function and Human Diseases
Benjamin Turgeon et al.
PHYSIOLOGICAL REVIEWS (2009)
Mutations in Hydin impair ciliary motility in mice
Karl-Ferdinand Lechtreck et al.
JOURNAL OF CELL BIOLOGY (2008)
Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1
Lance Lee et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axoneme
Zhibing Zhang et al.
BIOLOGY OF REPRODUCTION (2007)
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
ZB Zhang et al.
BIOLOGY OF REPRODUCTION (2006)
Calmodulin and PF6 are components of a complex that localizes to the C1 microtubule of the flagellar central apparatus
MJ Wargo et al.
JOURNAL OF CELL SCIENCE (2005)
Dissecting the axoneme interactome -: The mammalian orthologue of Chlamydomonas PF6 interacts with sperm-associated antigen 6, the mammalian orthologue of chlamydomonas PF16
ZB Zhang et al.
MOLECULAR & CELLULAR PROTEOMICS (2005)
Haploinsufficiency for the murine orthologue of Chlamydomonas PF20 disrupts spermatogenesis
ZB Zhang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
The vertebrate primary cilium is a sensory organelle
GJ Pazour et al.
CURRENT OPINION IN CELL BIOLOGY (2003)
Male infertility, impaired sperm motility, and hydrocephalus in mice deficient in sperm-associated antigen 6
R Sapiro et al.
MOLECULAR AND CELLULAR BIOLOGY (2002)
Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus
I Ibañez-Tallon et al.
HUMAN MOLECULAR GENETICS (2002)
The Chlamydomonas PF6 locus encodes a large alanine/proline-rich polypeptide that is required for assembly of a central pair projection and regulates flagellar motility
G Rupp et al.
MOLECULAR BIOLOGY OF THE CELL (2001)
Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice
SL Brody et al.
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY (2000)
分享论文
