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。Formation of the transition zone by Mks5/Rpgrip1L establishes a ciliary zone of exclusion (CIZE) that compartmentalises ciliary signalling proteins and controls PIP2 ciliary abundance
Victor Jensen et al.
EMBO JOURNAL (2015)
TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone
Elle C. Roberson et al.
JOURNAL OF CELL BIOLOGY (2015)
The TOPCONS web server for consensus prediction of membrane protein topology and signal peptides
Konstantinos D. Tsirigos et al.
NUCLEIC ACIDS RESEARCH (2015)
JPred4: a protein secondary structure prediction server
Alexey Drozdetskiy et al.
NUCLEIC ACIDS RESEARCH (2015)
Single-molecule imaging of Hedgehog pathway protein Smoothened in primary cilia reveals binding events regulated by Patched1
Ljiljana Milenkovic et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone
T. Tony Yang et al.
SCIENTIFIC REPORTS (2015)
Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling
Laura E. Yee et al.
PLOS GENETICS (2015)
Hypomorphism for RPGRIP1L, a Ciliary Gene Vicinal to the FTO Locus, Causes Increased Adiposity in Mice
George Stratigopoulos et al.
CELL METABOLISM (2014)
The Awesome Power of Dikaryons for Studying Flagella and Basal Bodies in Chlamydomonas reinhardtii
Susan K. Dutcher
CYTOSKELETON (2014)
NPHP4 controls ciliary trafficking of membrane proteins and large soluble proteins at the transition zone
Junya Awata et al.
JOURNAL OF CELL SCIENCE (2014)
ModBase, a database of annotated comparative protein structure models and associated resources
Ursula Pieper et al.
NUCLEIC ACIDS RESEARCH (2014)
Murine Joubert syndrome reveals Hedgehog signaling defects as a potential therapeutic target for nephronophthisis
Ann Marie Hynes et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Unraveling the genetics of Joubert and Meckel-Gruber syndromes
Katarzyna Szymanska et al.
JOURNAL OF PEDIATRIC GENETICS (2014)
Nuclear Pore Scaffold Structure Analyzed by Super-Resolution Microscopy and Particle Averaging
Anna Szymborska et al.
SCIENCE (2013)
STED Microscopy with Optimized Labeling Density Reveals 9-Fold Arrangement of a Centriole Protein
Lana Lau et al.
BIOPHYSICAL JOURNAL (2012)
The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization
Jeremy F. Reiter et al.
EMBO REPORTS (2012)
Scoring a backstage pass: Mechanisms of ciliogenesis and ciliary access
Francesc R. Garcia-Gonzalo et al.
JOURNAL OF CELL BIOLOGY (2012)
Mutations in TMEM231 cause Joubert syndrome in French Canadians
Myriam Srour et al.
JOURNAL OF MEDICAL GENETICS (2012)
A ciliopathy complex at the transition zone protects the cilia as a privileged membrane domain
Ben Chih et al.
NATURE CELL BIOLOGY (2012)
Subdiffraction-resolution fluorescence microscopy reveals a domain of the centrosome critical for pericentriolar material organization
V. Mennella et al.
NATURE CELL BIOLOGY (2012)
Subdiffraction imaging of centrosomes reveals higher-order organizational features of pericentriolar material
Steffen Lawo et al.
NATURE CELL BIOLOGY (2012)
NIH Image to ImageJ: 25 years of image analysis
Caroline A. Schneider et al.
NATURE METHODS (2012)
Disruption of a Ciliary B9 Protein Complex Causes Meckel Syndrome
William E. Dowdle et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways
Liyun Sang et al.
CELL (2011)
B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis
Katharina Hopp et al.
HUMAN MOLECULAR GENETICS (2011)
MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis
Corey L. Williams et al.
JOURNAL OF CELL BIOLOGY (2011)
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics
Claudia Dafinger et al.
JOURNAL OF CLINICAL INVESTIGATION (2011)
A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition
Francesc R. Garcia-Gonzalo et al.
NATURE GENETICS (2011)
CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content
Branch Craige et al.
JOURNAL OF CELL BIOLOGY (2010)
Nanoscale architecture of integrin-based cell adhesions
Pakorn Kanchanawong et al.
NATURE (2010)
The primary cilium: a signalling centre during vertebrate development
Sarah C. Goetz et al.
NATURE REVIEWS GENETICS (2010)
Superresolution Imaging of Chemical Synapses in the Brain
Adish Dani et al.
NEURON (2010)
Adenylate cyclase regulates elongation of mammalian primary cilia
Young Ou et al.
EXPERIMENTAL CELL RESEARCH (2009)
Adult Type 3 Adenylyl Cyclase-Deficient Mice Are Obese
Zhenshan Wang et al.
PLOS ONE (2009)
Basal Body Assembly in Ciliates: The Power of Numbers
Chad G. Pearson et al.
TRAFFIC (2009)
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome
Vincent Cantagrel et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Multicolor far-field fluorescence nanoscopy through isolated detection of distinct molecular species
Mariano Bossi et al.
NANO LETTERS (2008)
Efficient subpixel image registration algorithms
Manuel Guizar-Sicairos et al.
OPTICS LETTERS (2008)
Three-dimensional super-resolution imaging by stochastic optical reconstruction microscopy
Bo Huang et al.
SCIENCE (2008)
Type III adenylyl cyclase localizes to primary cilia throughout the adult mouse brain
Georgia A. Bishop et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2007)
Vitamin D levels and early mortality among incident hemodialysis patients
M. Wolf et al.
KIDNEY INTERNATIONAL (2007)
Multicolor super-resolution imaging with photo-switchable fluorescent probes
Mark Bates et al.
SCIENCE (2007)
Patched1 regulates Hedgehog signaling at the primary cilium
Rajat Rohatgi et al.
SCIENCE (2007)
Ftm is a novel basal body protein of cilia involved in Shh signalling
Jeanette Vierkotten et al.
DEVELOPMENT (2007)
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
Heleen H. Arts et al.
NATURE GENETICS (2007)
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
Marion Delous et al.
NATURE GENETICS (2007)
Vertebrate Smoothened functions at the primary cilium
KC Corbit et al.
NATURE (2005)
Inactivation of the mouse adenylyl cyclase 3 gene disrupts male fertility and spermatozoon function
G Livera et al.
MOLECULAR ENDOCRINOLOGY (2005)
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome
RJ Ferland et al.
NATURE GENETICS (2004)
The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome
MA Parisi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Mutations in the AHI1 gene, encoding Jouberin, cause Joubert syndrome with cortical polymicrogyria
T Dixon-Salazar et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution
E Otto et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Small molecule modulation of Smoothened activity
JK Chen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Localization of intraflagellar transport protein IFT52 identifies basal body transitional fibers as the docking site for IFT particles
JA Deane et al.
CURRENT BIOLOGY (2001)
Disruption of the type III adenylyl cyclase gene leads to peripheral and behavioral anosmia in transgenic mice
ST Wong et al.
NEURON (2000)