Primary cilia proteins: ciliary and extraciliary sites and functions

Intraflagellar transport: mechanisms of motor action, cooperation, and cargo delivery

(2017) Bram Prevo et al.   FEBS Journal

The background puzzle: how identical mutations in the same gene lead to different disease symptoms

(2017) Jan E. Kammenga   FEBS Journal

Tubby proteins prove their adaptability

(2017) Ben Short   JOURNAL OF CELL BIOLOGY

Tubby family proteins are adapters for ciliary trafficking of integral membrane proteins

(2017) Hemant B. Badgandi et al.   JOURNAL OF CELL BIOLOGY

KDM3A coordinates actin dynamics with intraflagellar transport to regulate cilia stability

(2017) Patricia L. Yeyati et al.   JOURNAL OF CELL BIOLOGY

Loss of OCRL increases ciliary PI(4,5)P2in Lowe oculocerebrorenal syndrome

(2017) Philipp P. Prosseda et al.   JOURNAL OF CELL SCIENCE

A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies

(2017) G Banks et al.   MOLECULAR PSYCHIATRY

The Ciliopathy-Associated Cep104 Protein Interacts with Tubulin and Nek1 Kinase

(2017) Caezar Al-Jassar et al.   STRUCTURE

Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models

(2017) Roly Megaw et al.   Nature Communications

The molecular motor Myosin Va interacts with the cilia-centrosomal protein RPGRIP1L

(2017) L. H. P. Assis et al.   Scientific Reports

HypomorphicMKS1mutation in a Pakistani family with mild Joubert syndrome and atypical features: Expanding the phenotypic spectrum ofMKS1-related ciliopathies

(2016) et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Ciliary Extracellular Vesicles: Txt Msg Organelles

(2016) Juan Wang et al.   CELLULAR AND MOLECULAR NEUROBIOLOGY

The intraflagellar transport machinery in ciliary signaling

(2016) André Mourão et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

Functional anatomy of the mammalian sperm flagellum

(2016) Charles B. Lindemann et al.   Cytoskeleton

HDAC2 promotes loss of primary cilia in pancreatic ductal adenocarcinoma

(2016) Tetsuo Kobayashi et al.   EMBO REPORTS

Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome)

(2016) Glen R Monroe et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum

(2016) Ingrid Bader et al.   European Journal of Medical Genetics

Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retina

(2016) Kollu N. Rao et al.   HUMAN MOLECULAR GENETICS

Novel role for the midbody in primary ciliogenesis by polarized epithelial cells

(2016) Miguel Bernabé-Rubio et al.   JOURNAL OF CELL BIOLOGY

Together, the IFT81 and IFT74 N-termini form the main module for intraflagellar transport of tubulin

(2016) Tomohiro Kubo et al.   JOURNAL OF CELL SCIENCE

Motile and non-motile cilia in human pathology: from function to phenotypes

(2016) Hannah M Mitchison et al.   JOURNAL OF PATHOLOGY

IFT88 influences chondrocyte actin organization and biomechanics

(2016) Z. Wang et al.   OSTEOARTHRITIS AND CARTILAGE

Endocytic Control of Cellular Signaling at the Primary Cilium

(2016) Lotte B. Pedersen et al.   TRENDS IN BIOCHEMICAL SCIENCES

The Intraflagellar Transport Machinery

(2016) Michael Taschner et al.   Cold Spring Harbor Perspectives in Biology

A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi

(2016) Corinne Stoetzel et al.   Nature Communications

Loss of MACF1 Abolishes Ciliogenesis and Disrupts Apicobasal Polarity Establishment in the Retina

(2016) Helen L. May-Simera et al.   Cell Reports

Role for the IFT-A Complex in Selective Transport to the Primary Cilium

(2016) Wenxiang Fu et al.   Cell Reports

Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome

(2015) Caroline Alby et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Intrafamilial clinical heterogeneity ofCSPP1-related ciliopathy

(2015) Tawfeg Ben-Omran et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Cilia Dysfunction in Lung Disease

(2015) Ann E. Tilley et al.   Annual Review of Physiology

Myosin heavy chain 10 (MYH10) is required for centriole migration during the biogenesis of primary cilia

(2015) Hyowon Hong et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Formin mDia1, a downstream molecule of FMNL1, regulates Profilin1 for actin assembly and spindle organization during mouse oocyte meiosis

(2015) Yu Zhang et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

The small GTPase Rab29 is a common regulator of immune synapse assembly and ciliogenesis

(2015) A Onnis et al.   CELL DEATH AND DIFFERENTIATION

NudC regulates actin dynamics and ciliogenesis by stabilizing cofilin 1

(2015) Cheng Zhang et al.   CELL RESEARCH

A novel family of katanin-like 2 protein isoforms (KATNAL2), interacting with nucleotide-binding proteins Nubp1 and Nubp2, are key regulators of different MT-based processes in mammalian cells

(2015) Antonis Ververis et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Bardet Biedl Syndrome

(2015) Amelia Shoemark et al.   CHEST

Mother Centriole Distal Appendages Mediate Centrosome Docking at the Immunological Synapse and Reveal Mechanistic Parallels with Ciliogenesis

(2015) Jane C. Stinchcombe et al.   CURRENT BIOLOGY

RC/BTB2 is essential for formation of primary cilia in mammalian cells

(2015) Ling Zhang et al.   Cytoskeleton

A Phosphoinositide Code for Primary Cilia

(2015) Fubito Nakatsu   DEVELOPMENTAL CELL

Modulation of Ciliary Phosphoinositide Content Regulates Trafficking and Sonic Hedgehog Signaling Output

(2015) Marcelo Chávez et al.   DEVELOPMENTAL CELL

Ins and outs of GPCR signaling in primary cilia

(2015) K. B. Schou et al.   EMBO REPORTS

Bardet-Biedl syndrome: Is it only cilia dysfunction?

(2015) Rossina Novas et al.   FEBS LETTERS

CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies

(2015) Rivka A. Rachel et al.   HUMAN MOLECULAR GENETICS

KIAA0586is Mutated in Joubert Syndrome

(2015) Ruxandra Bachmann-Gagescu et al.   HUMAN MUTATION

Mitotic Protein CSPP1 Interacts with CENP-H Protein to Coordinate Accurate Chromosome Oscillation in Mitosis

(2015) Lijuan Zhu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Human FAM154A (SAXO1) is a microtubule-stabilizing protein specific to cilia and related structures

(2015) D. Dacheux et al.   JOURNAL OF CELL SCIENCE

Mutations in human homologue of chickentalpid3gene (KIAA0586) cause a hybrid ciliopathy with overlapping features of Jeune and Joubert syndromes

(2015) May Christine V Malicdan et al.   JOURNAL OF MEDICAL GENETICS

MKS1 regulates ciliary INPP5E levels in Joubert syndrome

(2015) Gisela G Slaats et al.   JOURNAL OF MEDICAL GENETICS

Crescerin uses a TOG domain array to regulate microtubules in the primary cilium

(2015) Alakananda Das et al.   MOLECULAR BIOLOGY OF THE CELL

Regulation of Vesicular Traffic at the T Cell Immune Synapse: Lessons from the Primary Cilium

(2015) Francesca Finetti et al.   TRAFFIC

IFT–Cargo Interactions and Protein Transport in Cilia

(2015) Karl F. Lechtreck   TRENDS IN BIOCHEMICAL SCIENCES

Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization

(2015) Albane A. Bizet et al.   Nature Communications

Ciliary Phosphoinositide Regulates Ciliary Protein Trafficking in Drosophila

(2015) Jina Park et al.   Cell Reports

TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23)

(2015) Louise A Stephen et al.   eLife

Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome

(2015) Susanne Roosing et al.   eLife

A Cilia Independent Role of Ift88/Polaris during Cell Migration

(2015) Christopher Boehlke et al.   PLoS One

AHI-1: a novel signaling protein and potential therapeutic target in human leukemia and brain disorders

(2015) Sharmin Esmailzadeh et al.   Oncotarget

The formin DIAPH1 (mDia1) regulates megakaryocyte proplatelet formation by remodeling the actin and microtubule cytoskeletons

(2014) J. Pan et al.   BLOOD

Nuclear CSPP1 expression defined subtypes of basal-like breast cancer

(2014) J Sternemalm et al.   BRITISH JOURNAL OF CANCER

Actin Is Required for IFT Regulation in Chlamydomonas reinhardtii

(2014) Prachee Avasthi et al.   CURRENT BIOLOGY

Rab11 Endosomes Contribute to Mitotic Spindle Organization and Orientation

(2014) Heidi Hehnly et al.   DEVELOPMENTAL CELL

MAP4-Dependent Regulation of Microtubule Formation Affects Centrosome, Cilia, and Golgi Architecture as a Central Mechanism in Growth Regulation

(2014) Diana Zahnleiter et al.   HUMAN MUTATION

Arl13b and the non-muscle myosin heavy chain IIA are required for circular dorsal ruffle formation and cell migration

(2014) C. Casalou et al.   JOURNAL OF CELL SCIENCE

Complexité génétique des ciliopathies et identification de nouveaux gènes

(2014) Ruxandra Bachmann-Gagescu   M S-MEDECINE SCIENCES

The Ca2+-activated Cl− channel ANO1/TMEM16A regulates primary ciliogenesis

(2014) Chelsey Chandler Ruppersburg et al.   MOLECULAR BIOLOGY OF THE CELL

Casein kinase 1δ functions at the centrosome and Golgi to promote ciliogenesis

(2014) Yoshimi Endo Greer et al.   MOLECULAR BIOLOGY OF THE CELL

Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number

(2014) Wen F. Hu et al.   NEURON

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

(2014) Marta Romani et al.   Orphanet Journal of Rare Diseases

Lack of Dopaminergic Inputs Elongates the Primary Cilia of Striatal Neurons

(2014) Ko Miyoshi et al.   PLoS One

A Mec17-Myosin II Effector Axis Coordinates Microtubule Acetylation and Actin Dynamics to Control Primary Cilium Biogenesis

(2014) Yanhua Rao et al.   PLoS One

Ciliopathies: The Trafficking Connection

(2014) Kayalvizhi Madhivanan et al.   TRAFFIC

The Cellular and Physiological Functions of the Lowe Syndrome Protein OCRL1

(2014) Zenobia B. Mehta et al.   TRAFFIC

Mutations in CSPP1 Lead to Classical Joubert Syndrome

(2013) Naiara Akizu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in CSPP1 Cause Primary Cilia Abnormalities and Joubert Syndrome with or without Jeune Asphyxiating Thoracic Dystrophy

(2013) Karina Tuz et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in CSPP1, Encoding a Core Centrosomal Protein, Cause a Range of Ciliopathy Phenotypes in Humans

(2013) Ranad Shaheen et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Distinct localization of septin proteins to ciliary sub-compartments in airway epithelial cells

(2013) Manfred Fliegauf et al.   BIOLOGICAL CHEMISTRY

Hedgehog signaling from the primary cilium to the nucleus: an emerging picture of ciliary localization, trafficking and transduction

(2013) Yoko Inès Nozawa et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Bardet–Biedl syndrome proteins control the cilia length through regulation of actin polymerization

(2013) Victor Hernandez-Hernandez et al.   HUMAN MOLECULAR GENETICS

BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking

(2013) Q. Zhang et al.   JOURNAL OF CELL SCIENCE

Septins 2, 7 and 9 and MAP4 colocalize along the axoneme in the primary cilium and control ciliary length

(2013) R. Ghossoub et al.   JOURNAL OF CELL SCIENCE

Riding the wave of ependymal cilia: Genetic susceptibility to hydrocephalus in primary ciliary dyskinesia

(2013) Lance Lee   JOURNAL OF NEUROSCIENCE RESEARCH

Joubert syndrome: congenital cerebellar ataxia with the molar tooth

(2013) Marta Romani et al.   LANCET NEUROLOGY

Neuronal Primary Cilia: An Underappreciated Signaling and Sensory Organelle in the Brain

(2013) Jill A Green et al.   NEUROPSYCHOPHARMACOLOGY

CCDC41 is required for ciliary vesicle docking to the mother centriole

(2013) K. Joo et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Identification of Cilia Genes That Affect Cell-Cycle Progression Using Whole-Genome Transcriptome Analysis in Chlamydomonas reinhardtti

(2013) Alison J. Albee et al.   G3-Genes Genomes Genetics

Ciliary disorder of the skeleton

(2012) Celine Huber et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Branched F-actin as a negative regulator of cilia formation

(2012) Xiumin Yan et al.   EXPERIMENTAL CELL RESEARCH

The Lowe syndrome protein OCRL1 is involved in primary cilia assembly

(2012) Brian G. Coon et al.   HUMAN MOLECULAR GENETICS

OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome

(2012) Na Luo et al.   HUMAN MOLECULAR GENETICS

Compartmentalization of signaling by vesicular trafficking: a shared building design for the immune synapse and the primary cilium

(2012) Francesca Finetti et al.   IMMUNOLOGICAL REVIEWS

Cell cycle regulation by the NEK family of protein kinases

(2012) A. M. Fry et al.   JOURNAL OF CELL SCIENCE

Microtubule-severing enzymes at the cutting edge

(2012) D. J. Sharp et al.   JOURNAL OF CELL SCIENCE

HDAC2 overexpression confers oncogenic potential to human lung cancer cells by deregulating expression of apoptosis and cell cycle proteins

(2012) Kwang Hwa Jung et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

Tg737 signaling is required for hypoxia-enhanced invasion and migration of hepatoma cells

(2012) Nan You et al.   JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH

Actin-capping protein promotes microtubule stability by antagonizing the actin activity of mDia1

(2012) Francesca Bartolini et al.   MOLECULAR BIOLOGY OF THE CELL

miR-129-3p controls cilia assembly by regulating CP110 and actin dynamics

(2012) Jingli Cao et al.   NATURE CELL BIOLOGY

Septins: the fourth component of the cytoskeleton

(2012) Serge Mostowy et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

RPGRmutations might cause reduced orientation of respiratory cilia

(2012) Zuzanna Bukowy-Bieryłło et al.   PEDIATRIC PULMONOLOGY

IFT Proteins Accumulate during Cell Division and Localize to the Cleavage Furrow in Chlamydomonas

(2012) Christopher R. Wood et al.   PLoS One

Arl13b regulates endocytic recycling traffic

(2012) D. C. Barral et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

OCRL1 Modulates Cilia Length in Renal Epithelial Cells

(2012) Youssef Rbaibi et al.   TRAFFIC

Primary cilia and graded Sonic Hedgehog signaling

(2012) Noriaki Sasai et al.   Wiley Interdisciplinary Reviews-Developmental Biology

Assembly and function of the archaeal flagellum

(2011) Abhrajyoti Ghosh et al.   BIOCHEMICAL SOCIETY TRANSACTIONS

Ultrastructure of cilia and flagella - back to the future!

(2011) Cathy Fisch et al.   BIOLOGY OF THE CELL

Rab8 GTPase as a regulator of cell shape

(2011) Johan Peränen   Cytoskeleton

Stages of ciliogenesis and regulation of ciliary length

(2011) Prachee Avasthi et al.   DIFFERENTIATION

The role of RPGR in cilia formation and actin stability

(2011) Milica Gakovic et al.   HUMAN MOLECULAR GENETICS

Tracing the origins of centrioles, cilia, and flagella

(2011) Zita Carvalho-Santos et al.   JOURNAL OF CELL BIOLOGY

Spindle positioning in human cells relies on proper centriole formation and on the microcephaly proteins CPAP and STIL

(2011) D. Kitagawa et al.   JOURNAL OF CELL SCIENCE

Primary cilia regulates the directional migration and barrier integrity of endothelial cells through the modulation of Hsp27 dependent actin cytoskeletal organization

(2011) Thomas J. Jones et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics

(2011) Claudia Dafinger et al.   JOURNAL OF CLINICAL INVESTIGATION

Hook2 is involved in the morphogenesis of the primary cilium

(2011) Carole L. Baron Gaillard et al.   MOLECULAR BIOLOGY OF THE CELL

The cilia protein IFT88 is required for spindle orientation in mitosis

(2011) Benedicte Delaval et al.   NATURE CELL BIOLOGY

Ciliogenesis: building the cell's antenna

(2011) Hiroaki Ishikawa et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Ciliopathies

(2011) Friedhelm Hildebrandt et al.   NEW ENGLAND JOURNAL OF MEDICINE

Ciliopathies: an expanding disease spectrum

(2011) Aoife M. Waters et al.   PEDIATRIC NEPHROLOGY

Intraflagellar transport: a new player at the immune synapse

(2011) Francesca Finetti et al.   TRENDS IN IMMUNOLOGY

The Golgin Coiled-Coil Proteins of the Golgi Apparatus

(2011) S. Munro   Cold Spring Harbor Perspectives in Biology

The tubby family proteins

(2011) Saikat Mukhopadhyay et al.   GENOME BIOLOGY

The ciliary membrane

(2010) Rajat Rohatgi et al.   CURRENT OPINION IN CELL BIOLOGY

The actin nucleator Cordon-bleu is required for development of motile cilia in zebrafish

(2010) Andrew M. Ravanelli et al.   DEVELOPMENTAL BIOLOGY

MIM and Cortactin Antagonism Regulates Ciliogenesis and Hedgehog Signaling

(2010) Marina Bershteyn et al.   DEVELOPMENTAL CELL

Tubby and tubby-like protein 1 are new MerTK ligands for phagocytosis

(2010) Nora B Caberoy et al.   EMBO JOURNAL

TBCCD1, a new centrosomal protein, is required for centrosome and Golgi apparatus positioning

(2010) João Gonçalves et al.   EMBO REPORTS

TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia

(2010) S. Mukhopadhyay et al.   GENES & DEVELOPMENT

The retinitis pigmentosa protein RP2 links pericentriolar vesicle transport between the Golgi and the primary cilium

(2010) R. Jane Evans et al.   HUMAN MOLECULAR GENETICS

CSPP Is a Ciliary Protein Interacting with Nephrocystin 8 and Required for Cilia Formation

(2010) Sebastian Patzke et al.   MOLECULAR BIOLOGY OF THE CELL

Functional genomic screen for modulators of ciliogenesis and cilium length

(2010) Joon Kim et al.   NATURE

Joubert Syndrome and related disorders

(2010) Francesco Brancati et al.   Orphanet Journal of Rare Diseases

A New Organellar Complex in Rat Sympathetic Neurons

(2010) Matt S. Ramer et al.   PLoS One

Coordination of Rab8 and Rab11 in primary ciliogenesis

(2010) A. Knodler et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Ciliary biology: Understanding the cellular and genetic basis of human ciliopathies

(2009) Magdalena Cardenas-Rodriguez et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Identification of tyrosine kinase, HCK, and tumor suppressor, BIN1, as potential mediators ofAHI-1oncogene in primary and transformed CTCL cells

(2009) Erin Kennah et al.   BLOOD

Olfactory Cilia: Linking Sensory Cilia Function and Human Disease

(2009) P. M. Jenkins et al.   CHEMICAL SENSES

The Primary Cilium as a Complex Signaling Center

(2009) Nicolas F. Berbari et al.   CURRENT BIOLOGY

The Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formation

(2009) Y. Yin et al.   DEVELOPMENT

Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking

(2009) Yi-Chun Hsiao et al.   HUMAN MOLECULAR GENETICS

Centrosome/Spindle Pole–associated Protein Regulates Cytokinesis via Promoting the Recruitment of MyoGEF to the Central Spindle

(2009) Michael Asiedu et al.   MOLECULAR BIOLOGY OF THE CELL

Intraflagellar transport is required for polarized recycling of the TCR/CD3 complex to the immune synapse

(2009) Francesca Finetti et al.   NATURE CELL BIOLOGY

Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies

(2009) Stephanie L Bielas et al.   NATURE GENETICS

Absence of decussation of the superior cerebellar peduncles in patients with Joubert syndrome

(2008) M. Vittoria Spampinato et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Building it up and taking it down: The regulation of vertebrate ciliogenesis

(2008) Nicole Santos et al.   DEVELOPMENTAL DYNAMICS

The mammalian Nek1 kinase is involved in primary cilium formation

(2008) Ohad Shalom et al.   FEBS LETTERS

Structure and function of mammalian cilia

(2008) Peter Satir et al.   HISTOCHEMISTRY AND CELL BIOLOGY

Species differences in the expression of Ahi1, a protein implicated in the neurodevelopmental disorder Joubert syndrome, with preferential accumulation to stigmoid bodies

(2008) Jennifer E. Doering et al.   JOURNAL OF COMPARATIVE NEUROLOGY

AHI-1 interacts with BCR-ABL and modulates BCR-ABL transforming activity and imatinib response of CML stem/progenitor cells

(2008) Liang L. Zhou et al.   JOURNAL OF EXPERIMENTAL MEDICINE

Monitoring changes in membrane phosphatidylinositol 4,5-bisphosphate in living cells using a domain from the transcription factor tubby

(2008) Kathryn V. Quinn et al.   JOURNAL OF PHYSIOLOGY-LONDON

Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia

(2008) A. S. Shah et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia

(2008) N. F. Berbari et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The Golgin GMAP210/TRIP11 Anchors IFT20 to the Golgi Complex

(2008) John A. Follit et al.   PLoS Genetics