标题
Cilia in cell signaling and human disorders
作者
关键词
-
出版物
Protein & Cell
Volume 1, Issue 8, Pages 726-736
出版商
Springer Nature
发表日期
2010-08-27
DOI
10.1007/s13238-010-0098-7
参考文献
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。- Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation
- (2010) Simon Edvardson et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The Conserved Bardet-Biedl Syndrome Proteins Assemble a Coat that Traffics Membrane Proteins to Cilia
- (2010) Hua Jin et al. CELL
- Primary Cilia Regulate Branching Morphogenesis during Mammary Gland Development
- (2010) Kimberly M. McDermott et al. CURRENT BIOLOGY
- RPGR-containing protein complexes in syndromic and non-syndromic retinal degeneration due to ciliary dysfunction
- (2010) Carlos A. Murga-Zamalloa et al. JOURNAL OF GENETICS
- Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
- (2010) Enza Maria Valente et al. NATURE GENETICS
- AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis
- (2010) Carrie M Louie et al. NATURE GENETICS
- Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait
- (2010) Alan F. Wright et al. NATURE REVIEWS GENETICS
- The cellular and developmental program connecting the centrosome and cilium duplication cycle
- (2010) Tomer Avidor-Reiss SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
- OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin
- (2009) Karlien L.M. Coene et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The PCP Pathway Instructs the Planar Orientation of Ciliated Cells in the Xenopus Larval Skin
- (2009) Brian Mitchell et al. CURRENT BIOLOGY
- Dampened Hedgehog signaling but normal Wnt signaling in zebrafish without cilia
- (2009) P. Huang et al. DEVELOPMENT
- Cilia localization is essential for in vivo functions of the Joubert syndrome protein Arl13b/Scorpion
- (2009) N. A. Duldulao et al. DEVELOPMENT
- Notch signaling controls the balance of ciliated and secretory cell fates in developing airways
- (2009) P.-N. Tsao et al. DEVELOPMENT
- Retrograde Intraflagellar Transport Mutants Identify Complex A Proteins With Multiple Genetic Interactions in Chlamydomonas reinhardtii
- (2009) C. Iomini et al. GENETICS
- Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3
- (2009) Rachaneekorn Tammachote et al. HUMAN MOLECULAR GENETICS
- TheChlamydomonas reinhardtiiBBSome is an IFT cargo required for export of specific signaling proteins from flagella
- (2009) Karl-Ferdinand Lechtreck et al. JOURNAL OF CELL BIOLOGY
- Nephronophthisis: Disease Mechanisms of a Ciliopathy
- (2009) F. Hildebrandt et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse
- (2009) Monique Jacoby et al. NATURE GENETICS
- Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies
- (2009) Stephanie L Bielas et al. NATURE GENETICS
- Rapid Mutation of Endogenous Zebrafish Genes Using Zinc Finger Nucleases Made by Oligomerized Pool ENgineering (OPEN)
- (2009) Jonathan E. Foley et al. PLoS One
- Primary Cilia Are Not Required for Normal Canonical Wnt Signaling in the Mouse Embryo
- (2009) Polloneal Jymmiel R. Ocbina et al. PLoS One
- Motile Cilia of Human Airway Epithelia Are Chemosensory
- (2009) A. S. Shah et al. SCIENCE
- Joubert Syndrome: Insights Into Brain Development, Cilium Biology, and Complex Disease
- (2009) Dan Doherty Seminars in Pediatric Neurology
- Review and update: Current treatment trends for patients with retinitis pigmentosa
- (2009) Kelly Shintani et al. OPTOMETRY
- Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome
- (2008) Vincent Cantagrel et al. AMERICAN JOURNAL OF HUMAN GENETICS
- CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290
- (2008) Nicholas T. Gorden et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Identification of CC2D2A as a Meckel Syndrome Gene Adds an Important Piece to the Ciliopathy Puzzle
- (2008) Jonna Tallila et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Transparent Adult Zebrafish as a Tool for In Vivo Transplantation Analysis
- (2008) Richard Mark White et al. Cell Stem Cell
- Primary cilia are required for cerebellar development and Shh-dependent expansion of progenitor pool
- (2008) N. Spassky et al. DEVELOPMENTAL BIOLOGY
- Defective ciliogenesis, embryonic lethality and severe impairment of the Sonic Hedgehog pathway caused by inactivation of the mouse complex A intraflagellar transport gene Ift122/Wdr10, partially overlapping with the DNA repair gene Med1/Mbd4
- (2008) Salvatore Cortellino et al. DEVELOPMENTAL BIOLOGY
- 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
- Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease
- (2008) Julie A. Jonassen et al. JOURNAL OF CELL BIOLOGY
- An Essential Role for Dermal Primary Cilia in Hair Follicle Morphogenesis
- (2008) Jonathan M. Lehman et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Heritable targeted gene disruption in zebrafish using designed zinc-finger nucleases
- (2008) Yannick Doyon et al. NATURE BIOTECHNOLOGY
- Targeted gene inactivation in zebrafish using engineered zinc-finger nucleases
- (2008) Xiangdong Meng et al. NATURE BIOTECHNOLOGY
- Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells
- (2008) Tae Joo Park et al. NATURE GENETICS
- THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia
- (2008) Pamela V Tran et al. NATURE GENETICS
- 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
- Dishevelled links basal body docking and orientation in ciliated epithelial cells
- (2008) Eszter K. Vladar et al. TRENDS IN CELL BIOLOGY
- Mutations of theCEP290gene encoding a centrosomal protein cause Meckel-Gruber syndrome
- (2007) Valeska Frank et al. HUMAN MUTATION
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started