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。Intraflagellar-transport A dysfunction causes hyperphagia-induced systemic insulin resistance in a pre-obese state
Damon T. Jacobs et al.
FASEB JOURNAL (2020)
Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in Humans
Ranad Shaheen et al.
HEPATOLOGY (2020)
IFT80 Is Required for Fracture Healing Through Controlling the Regulation of TGF-β Signaling in Chondrocyte Differentiation and Function
Min Liu et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2020)
Primary cilia respond to intermittent low-magnitude, high-frequency vibration and mediate vibration-induced effects in osteoblasts
Yan-Hui Li et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2020)
Testing the role of intraflagellar transport in flagellar length control using length-altering mutants of Chlamydomonas
Kimberly Wemmer et al.
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2020)
Architecture of the IFT ciliary trafficking machinery and interplay between its components
Kazuhisa Nakayama et al.
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY (2020)
Polycystin-1 regulates ARHGAP35-dependent centrosomal RhoA activation and ROCK signaling
Andrew J. Streets et al.
JCI INSIGHT (2020)
Loss of polycystins suppresses deciliation via the activation of the centrosomal integrity pathway
Vasileios Gerakopoulos et al.
LIFE SCIENCE ALLIANCE (2020)
Genetic reduction of cilium length by targeting intraflagellar transport 88 protein impedes kidney and liver cyst formation in mouse models of autosomal polycystic kidney disease
Lina Shao et al.
KIDNEY INTERNATIONAL (2020)
O-GlcNAc transferase regulates centriole behavior and intraflagellar transport to promote ciliogenesis
Fan Yu et al.
PROTEIN & CELL (2020)
YIF1B mutations cause a post-natal neurodevelopmental syndrome associated with Golgi and primary cilium alterations
Jorge Diaz et al.
BRAIN (2020)
Primary cilia mediate early life programming of adiposity through lysosomal regulation in the developing mouse hypothalamus
Chan Hee Lee et al.
NATURE COMMUNICATIONS (2020)
Tulp3 Regulates Renal Cystogenesis by Trafficking of Cystoproteins to Cilia
Sun-Hee Hwang et al.
CURRENT BIOLOGY (2019)
Tulp3 Is a Ciliary Trafficking Gene that Regulates Polycystic Kidney Disease
Emilie Legue et al.
CURRENT BIOLOGY (2019)
Cellular signalling by primary cilia in development, organ function and disease
Zeinab Anvarian et al.
NATURE REVIEWS NEPHROLOGY (2019)
Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis
Sumeda Nandadasa et al.
NATURE COMMUNICATIONS (2019)
Centriolar satellites are required for efficient ciliogenesis and ciliary content regulation
Ezgi Odabasi et al.
EMBO REPORTS (2019)
The cilium as a force sensor-myth versus reality
Rita R. Ferreira et al.
JOURNAL OF CELL SCIENCE (2019)
Primary cilium loss in mammalian cells occurs predominantly by whole-cilium shedding
Mary Mirvis et al.
PLOS BIOLOGY (2019)
Synergistic Genetic Interactions between Pkhd1 and Pkd1 Result in an ARPKD-Like Phenotype in Murine Models
Rory J. Olson et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2019)
Omega-3 Fatty Acids Activate Ciliary FFAR4 to Control Adipogenesis
Keren I. Hilgendorf et al.
CELL (2019)
Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model
Rebecca V. Walker et al.
NATURE COMMUNICATIONS (2019)
Length regulation of multiple flagella that self-assemble from a shared pool of components
Thomas G. Fai et al.
ELIFE (2019)
TULP3 is required for localization of membrane-associated proteins ARL13B and INPP5E to primary cilia
Sarina Han et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2019)
Ciliary defects caused by dysregulation of O-GlcNAc modification are associated with diabetic complications
Fan Yu et al.
CELL RESEARCH (2019)
Personalized Nanotherapy by Specifically Targeting Cell Organelles To Improve Vascular Hypertension
Rajasekharreddy Pala et al.
NANO LETTERS (2019)
Ciliotherapy: Remote Control of Primary Cilia Movement and Function by Magnetic Nanoparticles
Rajasekharreddy Pala et al.
ACS NANO (2019)
Renal epithelial cells retain primary cilia during human acute renal allograft rejection injury
Elizabeth Verghese et al.
BMC RESEARCH NOTES (2019)
O-GlcNAcylation Regulates Primary Ciliary Length by Promoting Microtubule Disassembly
Jie L. Tian et al.
ISCIENCE (2019)
Constitutively-active FGFR3 disrupts primary cilium length and IFT20 trafficking in various chondrocyte models of achondroplasia
Ludovic Martin et al.
HUMAN MOLECULAR GENETICS (2018)
Ciliopathy-associated mutations of IFT122 impair ciliary protein trafficking but not ciliogenesis
Mariko Takahara et al.
HUMAN MOLECULAR GENETICS (2018)
The molecular machines that traffic signaling receptors into and out of cilia
Maxence V. Nachury
CURRENT OPINION IN CELL BIOLOGY (2018)
Cilia-localized LKB1 regulates chemokine signaling, macrophage recruitment, and tissue homeostasis in the kidney
Amandine Viau et al.
EMBO JOURNAL (2018)
Regulation of ciliary function by fibroblast growth factor signaling identifies FGFR3-related disorders achondroplasia and thanatophoric dysplasia as ciliopathies
Michaela Kunova Bosakova et al.
HUMAN MOLECULAR GENETICS (2018)
BBSome trains remove activated GPCRs from cilia by enabling passage through the transition zone
Fan Ye et al.
JOURNAL OF CELL BIOLOGY (2018)
Environmental responsiveness of tubulin glutamylation in sensory cilia is regulated by the p38 MAPK pathway
Yoshishige Kimura et al.
SCIENTIFIC REPORTS (2018)
Polycystin-2 is an essential ion channel subunit in the primary cilium of the renal collecting duct epithelium
Xiaowen Liu et al.
ELIFE (2018)
Primary Cilia Are Dysfunctional in Obese Adipose-Derived Mesenchymal Stem Cells
Andreas Ritter et al.
STEM CELL REPORTS (2018)
The regulation of cilium assembly and disassembly in development and disease
Lei Wang et al.
DEVELOPMENT (2018)
Axoneme polyglutamylation regulated by Joubert syndrome protein ARL13B controls ciliary targeting of signaling molecules
Kai He et al.
NATURE COMMUNICATIONS (2018)
Membrane association and remodeling by intraflagellar transport protein IFT172
Qianmin Wang et al.
NATURE COMMUNICATIONS (2018)
Signaling through the Primary Cilium
Gabrielle Wheway et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2018)
Open Sesame: How Transition Fibers and the Transition Zone Control Ciliary Composition
Francesc R. Garcia-Gonzalo et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2017)
A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies
Shalabh Srivastava et al.
HUMAN MOLECULAR GENETICS (2017)
Tubulin glycylation controls primary cilia length
Sudarshan Gadadhar et al.
JOURNAL OF CELL BIOLOGY (2017)
Tubby family proteins are adapters for ciliary trafficking of integral membrane proteins
Hemant B. Badgandi et al.
JOURNAL OF CELL BIOLOGY (2017)
Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein-coupled receptors
Tomoaki Hirano et al.
MOLECULAR BIOLOGY OF THE CELL (2017)
Ciliary entry of KIF17 is dependent on its binding to the IFT-B complex via IFT46-IFT56 as well as on its nuclear localization signal
Teruki Funabashi et al.
MOLECULAR BIOLOGY OF THE CELL (2017)
The Ciliary Transition Zone: Finding the Pieces and Assembling the Gate
Joao Goncalves et al.
MOLECULES AND CELLS (2017)
The Cilium: Cellular Antenna and Central Processing Unit
Jarema J. Malicki et al.
TRENDS IN CELL BIOLOGY (2017)
Functional exploration of the IFT-A complex in intraflagellar transport and ciliogenesis
Bing Zhu et al.
PLOS GENETICS (2017)
Dynamics of the IFT machinery at the ciliary tip
Alexander Chien et al.
ELIFE (2017)
Chronic Hypobaric Hypoxia Modulates Primary Cilia Differently in Adult and Fetal Ovine Kidneys
Kiumars Shamloo et al.
Frontiers in Physiology (2017)
IFT54 regulates IFT20 stability but is not essential for tubulin transport during ciliogenesis
Xin Zhu et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2017)
Hepatic ischemia/reperfusion injury disrupts the homeostasis of kidney primary cilia via oxidative stress
Sang Jun Han et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2017)
IFT56 regulates vertebrate developmental patterning by maintaining IFTB complex integrity and ciliary microtubule architecture
Daisy Xin et al.
DEVELOPMENT (2017)
An Actin Network Dispatches Ciliary GPCRs into Extracellular Vesicles to Modulate Signaling
Andrew R. Nager et al.
CELL (2017)
Dynamic Remodeling of Membrane Composition Drives Cell Cycle through Primary Cilia Excision
Siew Cheng Phua et al.
CELL (2017)
Extracellular Vesicles from Trypanosoma brucei Mediate Virulence Factor Transfer and Cause Host Anemia
Anthony J. Szempruch et al.
CELL (2016)
Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia
J. Thevenon et al.
CLINICAL GENETICS (2016)
Comparative Analysis of Ciliary Membranes and Ectosomes
Huan Long et al.
CURRENT BIOLOGY (2016)
Centrosomal protein CP110 controls maturation of the mother centriole during cilia biogenesis
Sharda Prasad Yadav et al.
DEVELOPMENT (2016)
Intraflagellar transport proteins 172, 80, 57, 54, 38, and 20 form a stable tubulin-binding IFT-B2 complex
Michael Taschner et al.
EMBO JOURNAL (2016)
IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome
Wenjuan Zhang et al.
HUMAN MOLECULAR GENETICS (2016)
Reduction of ciliary length through pharmacologic or genetic inhibition of CDK5 attenuates polycystic kidney disease in a model of nephronophthisis
Herve Husson et al.
HUMAN MOLECULAR GENETICS (2016)
Together, the IFT81 and IFT74 N-termini form the main module for intraflagellar transport of tubulin
Tomohiro Kubo et al.
JOURNAL OF CELL SCIENCE (2016)
Primary-cilium-dependent autophagy controls epithelial cell volume in response to fluid flow
Idil Orhon et al.
NATURE CELL BIOLOGY (2016)
Role for the IFT-A Complex in Selective Transport to the Primary Cilium
Wenxiang Fu et al.
CELL REPORTS (2016)
Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome
Ivan Duran et al.
SCIENTIFIC REPORTS (2016)
The primary cilium undergoes dynamic size modifications during adipocyte differentiation of human adipose stem cells
Nicolas Forcioli-Conti et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2015)
Assembly of IFT Trains at the Ciliary Base Depends on IFT74
Jason M. Brown et al.
CURRENT BIOLOGY (2015)
Intraflagellar transport 27 is essential for hedgehog signaling but dispensable for ciliogenesis during hair follicle morphogenesis
Ning Yang et al.
DEVELOPMENT (2015)
A function for the Joubert syndrome protein Arl13b in ciliary membrane extension and ciliary length regulation
Hao Lu et al.
DEVELOPMENTAL BIOLOGY (2015)
IFT46 plays an essential role in cilia development
Mi-Sun Lee et al.
DEVELOPMENTAL BIOLOGY (2015)
Tubulin transport by IFT is upregulated during ciliary growth by a cilium-autonomous mechanism
Julie M. Craft et al.
JOURNAL OF CELL BIOLOGY (2015)
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype
Isabelle Perrault et al.
JOURNAL OF MEDICAL GENETICS (2015)
Dopamine receptors reveal an essential role of IFT-B, KIF17, and Rab23 in delivering specific receptors to primary cilia
Alison Leaf et al.
ELIFE (2015)
Spag17 Deficiency Results in Skeletal Malformations and Bone Abnormalities
Maria Eugenia Teves et al.
PLOS ONE (2015)
C-elegans Ciliated Sensory Neurons Release Extracellular Vesicles that Function in Animal Communication
Juan Wang et al.
CURRENT BIOLOGY (2014)
The Intraflagellar Transport Protein IFT27 Promotes BBSome Exit from Cilia through the GTPase ARL6/BBS3
Gerald M. Liew et al.
DEVELOPMENTAL CELL (2014)
IFT27 Links the BBSome to IFT for Maintenance of the Ciliary Signaling Compartment
Thibaut Eguether et al.
DEVELOPMENTAL CELL (2014)
Nedd9 restrains renal cystogenesis in Pkd1-/- mice
Anna S. Nikonova et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Roles of dopamine receptor on chennosensory and mechanosensory primary cilia in renal epithelial cells
Viralkumar S. Upadhyay et al.
FRONTIERS IN PHYSIOLOGY (2014)
Novel IFT122 mutation associated with impaired ciliogenesis and cranioectodermal dysplasia
Anas M. Alazami et al.
MOLECULAR GENETICS & GENOMIC MEDICINE (2014)
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans
Jan Halbritter et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Asymmetric Inheritance of Centrosome-Associated Primary Cilium Membrane Directs Ciliogenesis after Cell Division
Judith T. M. L. Paridaen et al.
CELL (2013)
The Ciliary G-Protein-Coupled Receptor Gpr161 Negatively Regulates the Sonic Hedgehog Pathway via cAMP Signaling
Saikat Mukhopadhyay et al.
CELL (2013)
The role of the cilium in normal and abnormal cell cycles: emphasis on renal cystic pathologies
Junmin Pan et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2013)
A Differential Cargo-Loading Model of Ciliary Length Regulation by IFT
Kathryne N. Wren et al.
CURRENT BIOLOGY (2013)
The Cilium Secretes Bioactive Ectosomes
Christopher R. Wood et al.
CURRENT BIOLOGY (2013)
Cluap1 localizes preferentially to the base and tip of cilia and is required for ciliogenesis in the mouse embryo
Yanick Botilde et al.
DEVELOPMENTAL BIOLOGY (2013)
Functional interaction between autophagy and ciliogenesis
Olatz Pampliega et al.
NATURE (2013)
Loss of cilia suppresses cyst growth in genetic models of autosomal dominant polycystic kidney disease
Ming Ma et al.
NATURE GENETICS (2013)
Molecular Basis of Tubulin Transport Within the Cilium by IFT74 and IFT81
Sagar Bhogaraju et al.
SCIENCE (2013)
TGF-β Signaling Is Associated with Endocytosis at the Pocket Region of the Primary Cilium
Christian Alexandro Clement et al.
CELL REPORTS (2013)
Cauli: A Mouse Strain with an Ift140 Mutation That Results in a Skeletal Ciliopathy Modelling Jeune Syndrome
Kerry A. Miller et al.
PLOS GENETICS (2013)
Reduction of oxidative stress during recovery accelerates normalization of primary cilia length that is altered after ischemic injury in murine kidneys
Jee In Kim et al.
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY (2013)
The intraflagellar transport protein IFT80 is required for cilia formation and osteogenesis
Shuying Yang et al.
BONE (2012)
Dopamine, the Kidney, and Hypertension
Raymond C. Harris et al.
CURRENT HYPERTENSION REPORTS (2012)
IFT25 Links the Signal-Dependent Movement of Hedgehog Components to Intraflagellar Transport
Brian T. Keady et al.
DEVELOPMENTAL CELL (2012)
The IFT-A complex regulates Shh signaling through cilia structure and membrane protein trafficking
Karel F. Liem et al.
JOURNAL OF CELL BIOLOGY (2012)
Ciliogenesis in normal human kidney development and post-natal life
Mirna Saraga-Babic et al.
PEDIATRIC NEPHROLOGY (2012)
Ciliopathies with Skeletal Anomalies and Renal Insufficiency due to Mutations in the IFT-A Gene WDR19
Cecilie Bredrup et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Cross Talk Between O-GlcNAcylation and Phosphorylation: Roles in Signaling, Transcription, and Chronic Disease
Gerald W. Hart et al.
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 80 (2011)
A Role for the Primary Cilium in Notch Signaling and Epidermal Differentiation during Skin Development
Ellen J. Ezratty et al.
CELL (2011)
The Tubulin Deglutamylase CCPP-1 Regulates the Function and Stability of Sensory Cilia in C. elegans
Robert O'Hagan et al.
CURRENT BIOLOGY (2011)
Mutations in Traf3ip1 reveal defects in ciliogenesis, embryonic development, and altered cell size regulation
Nicolas F. Berbari et al.
DEVELOPMENTAL BIOLOGY (2011)
An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia
Suzanne Rix 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)
The centrosome cycle: Centriole biogenesis, duplication and inherent asymmetries
Erich A. Nigg et al.
NATURE CELL BIOLOGY (2011)
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
Erica E. Davis et al.
NATURE GENETICS (2011)
A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition
Francesc R. Garcia-Gonzalo et al.
NATURE GENETICS (2011)
Complex interactions between genes controlling trafficking in primary cilia
Polloneal Jymmiel R. Ocbina et al.
NATURE GENETICS (2011)
Intraflagellar transport protein 122 antagonizes Sonic Hedgehog signaling and controls ciliary localization of pathway components
Jian Qin et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Primary cilia membrane assembly is initiated by Rab11 and transport protein particle II (TRAPPII) complex-dependent trafficking of Rabin8 to the centrosome
Christopher J. Westlake et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Hepato-Renal Pathology in Pkd2WS25/- Mice, an Animal Model of Autosomal Dominant Polycystic Kidney Disease
Angela Stroope et al.
AMERICAN JOURNAL OF PATHOLOGY (2010)
Identification of Signaling Pathways Regulating Primary Cilium Length and Flow-Mediated Adaptation
Tatiana Y. Besschetnova et al.
CURRENT BIOLOGY (2010)
TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia
Saikat Mukhopadhyay et al.
GENES & DEVELOPMENT (2010)
The major α-tubulin K40 acetyltransferase αTAT1 promotes rapid ciliogenesis and efficient mechanosensation
Toshinobu Shida et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Intraflagellar transport protein 172 is essential for primary cilia formation and plays a vital role in patterning the mammalian brain
Marat Gorivodsky et al.
DEVELOPMENTAL BIOLOGY (2009)
The ubiquitin conjugation system is involved in the disassembly of cilia and flagella
Kaiyao Huang et al.
JOURNAL OF CELL BIOLOGY (2009)
Renal Primary Cilia Lengthen after Acute Tubular Necrosis
Elizabeth Verghese et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2009)
Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia
Vishal Patel et al.
HUMAN MOLECULAR GENETICS (2008)
Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease
Julie A. Jonassen et al.
JOURNAL OF CELL BIOLOGY (2008)
THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia
Pamela V. Tran et al.
NATURE GENETICS (2008)
Renal cilia display length alterations following tubular injury and are present early in epithelial repair
Elizabeth Verghese et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION (2008)
Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms
Kevin C. Corbit et al.
NATURE CELL BIOLOGY (2008)
An essential quality control mechanism at the eukaryotic basal body prior to intraflagellar transport
Angela Stephan et al.
TRAFFIC (2007)
HEF1-Dependent aurora a activation induces disassembly of the primary cilium
Elena N. Pugacheva et al.
CELL (2007)
Intraflagellar transport is essential for endochondral bone formation
Courtney J. Haycraft et al.
DEVELOPMENT (2007)
The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly
John A. Follit et al.
MOLECULAR BIOLOGY OF THE CELL (2006)
PDGFRαα signaling is regulated through the primary cilium in fibroblasts
L Schneider et al.
CURRENT BIOLOGY (2005)
Flagellar length control system: Testing a simple model based on intraflagellar transport and turnover
WF Marshall et al.
MOLECULAR BIOLOGY OF THE CELL (2005)
Hedgehog signalling in the mouse requires intraflagellar transport proteins
DW Huangfu et al.
NATURE (2003)
Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells
SM Nauli et al.
NATURE GENETICS (2003)
Removal of the MDCK cell primary cilium abolishes flow sensing
HA Praetorius et al.
JOURNAL OF MEMBRANE BIOLOGY (2003)
Intraflagellar transport
JL Rosenbaum et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2002)
Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium
BK Yoder et al.
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY (2002)
Bending the MDCK cell primary cilium increases intracellular calcium
HA Praetorius et al.
JOURNAL OF MEMBRANE BIOLOGY (2001)
Intraflagellar transport balances continuous turnover of outer doublet microtubules: implications for flagellar length control
WF Marshall et al.
JOURNAL OF CELL BIOLOGY (2001)
Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene Tg737, are required for assembly of cilia and flagella
GJ Pazour et al.
JOURNAL OF CELL BIOLOGY (2000)
分享论文
