Ccdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left–right asymmetry

Cilia Dysfunction in Lung Disease

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

Mutations in CCDC11 , which Encodes a Coiled-Coil Containing Ciliary Protein, Causes Situs Inversus Due to Dysmotility of Monocilia in the Left-Right Organizer

(2015) Vijayashankaranarayanan Narasimhan et al.   HUMAN MUTATION

Global genetic analysis in mice unveils central role for cilia in congenital heart disease

(2015) You Li et al.   NATURE

Centriolar satellites: key mediators of centrosome functions

(2014) Maxim A. X. Tollenaere et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Multiciliated Cells

(2014) Eric R. Brooks et al.   CURRENT BIOLOGY

Proteomic analysis of mammalian sperm cells identifies new components of the centrosome

(2014) E. N. Firat-Karalar et al.   JOURNAL OF CELL SCIENCE

Recent advances in primary ciliary dyskinesia genetics

(2014) Małgorzata Kurkowiak et al.   JOURNAL OF MEDICAL GENETICS

Cilia and ciliopathies: Classic examples linking phenotype and genotype—An overview

(2014) Nicola Powles-Glover   REPRODUCTIVE TOXICOLOGY

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia

(2013) Christina Austin-Tse et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Primary Ciliary Dyskinesia. Recent Advances in Diagnostics, Genetics, and Characterization of Clinical Disease

(2013) Michael R. Knowles et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Rho-Associated Protein Kinase Inhibition Enhances Airway Epithelial Basal-Cell Proliferation and Lentivirus Transduction

(2013) Amjad Horani et al.   AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

The novel centriolar satellite protein SSX2IP targets Cep290 to the ciliary transition zone

(2013) Maren Klinger et al.   MOLECULAR BIOLOGY OF THE CELL

Primary cilia in neurodevelopmental disorders

(2013) Enza Maria Valente et al.   Nature Reviews Neurology

Picking up speed: advances in the genetics of primary ciliary dyskinesia

(2013) Amjad Horani et al.   PEDIATRIC RESEARCH

Transcriptional Program of Ciliated Epithelial Cells Reveals New Cilium and Centrosome Components and Links to Human Disease

(2013) Ramona A. Hoh et al.   PLoS One

Roles of cilia, fluid flow, and Ca2+ signaling in breaking of left–right symmetry

(2013) Satoko Yoshiba et al.   TRENDS IN GENETICS

The role of primary cilia in the development and disease of the retina

(2013) Gabrielle Wheway et al.   Organogenesis

Left-right asymmetry: cilia stir up new surprises in the node

(2013) D. Babu et al.   Open Biology

Acute Versus Chronic Loss of Mammalian Azi1/Cep131 Results in Distinct Ciliary Phenotypes

(2013) Emma A. Hall et al.   PLoS Genetics

A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function

(2012) Muhammad Sajid Hussain et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Cilia, calcium and the basis of left-right asymmetry

(2012) Dominic P Norris   BMC BIOLOGY

High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy

(2012) Nader Nakhleh et al.   CIRCULATION

The centriolar satellite protein Cep131 is important for genome stability

(2012) C. J. Staples et al.   JOURNAL OF CELL SCIENCE

A human laterality disorder associated with recessiveCCDC11mutation

(2012) Zeev Perles et al.   JOURNAL OF MEDICAL GENETICS

The centriolar satellite proteins Cep72 and Cep290 interact and are required for recruitment of BBS proteins to the cilium

(2012) Timothy R. Stowe et al.   MOLECULAR BIOLOGY OF THE CELL

The ciliary transition zone: from morphology and molecules to medicine

(2012) Peter G. Czarnecki et al.   TRENDS IN CELL BIOLOGY

Actin and microtubules drive differential aspects of planar cell polarity in multiciliated cells

(2011) Michael E. Werner et al.   JOURNAL OF CELL BIOLOGY

Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1

(2011) C. A. M. Lopes et al.   JOURNAL OF CELL SCIENCE

Ciliopathies: The Central Role of Cilia in a Spectrum of Pediatric Disorders

(2011) Thomas W. Ferkol et al.   JOURNAL OF PEDIATRICS

A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition

(2011) Francesc R Garcia-Gonzalo et al.   NATURE GENETICS

Centrosomes and cilia in human disease

(2011) Mónica Bettencourt-Dias et al.   TRENDS IN GENETICS

Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4

(2010) Duane L. Guernsey et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Cep120 is asymmetrically localized to the daughter centriole and is essential for centriole assembly

(2010) Moe R. Mahjoub et al.   JOURNAL OF CELL BIOLOGY

Cep152 interacts with Plk4 and is required for centriole duplication

(2010) Emily M. Hatch et al.   JOURNAL OF CELL BIOLOGY

Abnormal respiratory cilia in non-syndromic Leber congenital amaurosis with CEP290 mutations

(2010) J. F. Papon et al.   JOURNAL OF MEDICAL GENETICS

Par6α Interacts with the Dynactin Subunit p150Glued and Is a Critical Regulator of Centrosomal Protein Recruitment

(2010) Andrew Kodani et al.   MOLECULAR BIOLOGY OF THE CELL

Cilia in cell signaling and human disorders

(2010) Neil A. Duldulao et al.   Protein & Cell

Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly

(2009) Arun Kumar et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Centrioles, Centrosomes, and Cilia in Health and Disease

(2009) Erich A. Nigg et al.   CELL

Renal insufficiency, a frequent complication with age in oral-facial-digital syndrome type I

(2009) S Saal et al.   CLINICAL GENETICS

The PCP Pathway Instructs the Planar Orientation of Ciliated Cells in the Xenopus Larval Skin

(2009) Brian Mitchell et al.   CURRENT BIOLOGY

Mutations in zebrafish leucine-rich repeat-containing six-like affect cilia motility and result in pronephric cysts, but have variable effects on left-right patterning

(2009) F. C. Serluca et al.   DEVELOPMENT

Breaking the Code of DNA Binding Specificity of TAL-Type III Effectors

(2009) J. Boch et al.   SCIENCE

A Simple Cipher Governs DNA Recognition by TAL Effectors

(2009) M. J. Moscou et al.   SCIENCE

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations

(2008) Bhagyalaxmi Mohapatra et al.   HUMAN MOLECULAR GENETICS

CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium

(2008) Joon Kim et al.   HUMAN MOLECULAR GENETICS

Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells

(2008) Tae Joo Park et al.   NATURE GENETICS

High-resolution in situ hybridization to whole-mount zebrafish embryos

(2007) Christine Thisse et al.   Nature Protocols