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。High prevalence of primary ciliary dyskinesia in a British Asian population
C. O'Callaghan et al.
ARCHIVES OF DISEASE IN CHILDHOOD (2010)
Mutation of Murine Adenylate Kinase 7 Underlies a Primary Ciliary Dyskinesia Phenotype
Angeles Fernandez-Gonzalez et al.
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY (2009)
Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome
Margaret W. Leigh et al.
GENETICS IN MEDICINE (2009)
Polyglutamylation: a fine-regulator of protein function? 'Protein modifications: Beyond the usual suspects' review series
Carsten Janke et al.
EMBO REPORTS (2008)
Glutamylation on α-tubulin is not essential but affects the assembly and functions of a subset of microtubules in Tetrahymena thermophila
Dorota Wloga et al.
EUKARYOTIC CELL (2008)
TTLL10 is a protein polyglycylase that can modify nucleosome assembly protein 1
Koji Ikegami et al.
FEBS LETTERS (2008)
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells
Gwenn M. Hansen et al.
GENOME RESEARCH (2008)
Role of cilia, mucus, and airway surface liquid in mucociliary dysfunction: Lessons from mouse models
Marcus A. Mall
JOURNAL OF AEROSOL MEDICINE AND PULMONARY DRUG DELIVERY (2008)
The cell biological basis of ciliary disease
Wallace F. Marshall
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)
Primary ciliary dyskinesia: current state of the art
Andrew Bush et al.
ARCHIVES OF DISEASE IN CHILDHOOD (2007)
The zebrafish fleer gene encodes an essential regulator of cilia tubulin polyglutamylation
Narendra Pathak et al.
MOLECULAR BIOLOGY OF THE CELL (2007)
Mechanisms of disease - When cilia go bad: cilia defects and ciliopathies
Manfred Fliegauf et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2007)
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 targeted multienzyme mechanism for selective microtubule polyglutamylation
Juliette van Dijk et al.
MOLECULAR CELL (2007)
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
Zhibing Zhang et al.
CELL MOTILITY AND THE CYTOSKELETON (2007)
Molecular architecture of axonemal microtubule doublets revealed by cryo-electron tomography
Haixin Sui et al.
NATURE (2006)
Knockout mouse models of sperm flagellum anomalies
Denise Escalier
HUMAN REPRODUCTION UPDATE (2006)
Piecing together a ciliome
Peter N. Inglis et al.
TRENDS IN GENETICS (2006)
Tubulin polyglutamylase enzymes are members of the TTL domain protein family
C Janke et al.
SCIENCE (2005)
Investigation of the possible role of a novel gene, DPCD, in primary ciliary dyskinesia
M Zariwala et al.
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY (2004)
Central microtubular agenesis causing primary ciliary dyskinesia
W Stannard et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2004)
Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation
I Ibañez-Tallon et al.
HUMAN MOLECULAR GENETICS (2004)
Mice deficient in the axonemal protein Tektin-t exhibit male infertility and immotile-cilium syndrome due to impaired inner arm dynein function
H Tanaka et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Regulation of flagellar dynein activity by a central pair kinesin
R Yokoyama et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Speculations on the evolution of 9+2 organelles and the role of central pair microtubules
DR Mitchell
BIOLOGY OF THE CELL (2004)
Wnk1 kinase deficiency lowers blood pressure in mice: A gene-trap screen to identify potential targets for therapeutic intervention
BP Zambrowicz et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Characterisation of PGs1, a subunit of a protein complex co-purifying with tubulin polyglutamylase
C Regnard et al.
JOURNAL OF CELL SCIENCE (2003)
Predicting drug efficacy: knockouts model pipeline drugs of the pharmaceutical industry
BP Zambrowicz et al.
CURRENT OPINION IN PHARMACOLOGY (2003)
Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene
BE Davy et al.
HUMAN MOLECULAR GENETICS (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)
Differential distribution of glutamylated tubulin Isoforms along the sea urchin sperm axoneme
P Huitorel et al.
MOLECULAR REPRODUCTION AND DEVELOPMENT (2002)
Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus
I Ibañez-Tallon et al.
HUMAN MOLECULAR GENETICS (2002)
The effects of coronavirus on human nasal ciliated respiratory epithelium
MA Chilvers et al.
EUROPEAN RESPIRATORY JOURNAL (2001)
Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency
J Neesen et al.
HUMAN MOLECULAR GENETICS (2001)
Polyglutamylation of nucleosome assembly proteins
C Regnard et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)