A ciliopathy complex at the transition zone protects the cilia as a privileged membrane domain
暂无分享,去创建一个
Ben Chih | Peter S Liu | Yvonne Chinn | Cécile Chalouni | L. Komuves | P. Hass | W. Sandoval | A. Peterson | Peter S. Liu | Cecile Chalouni | Y. Chinn | A. Peterson
[1] D. L. Ringo. FLAGELLAR MOTION AND FINE STRUCTURE OF THE FLAGELLAR APPARATUS IN CHLAMYDOMONAS , 1967, The Journal of cell biology.
[2] S. Sorokin. Reconstructions of centriole formation and ciliogenesis in mammalian lungs. , 1968, Journal of cell science.
[3] N. Gilula,et al. THE CILIARY NECKLACE , 1972, The Journal of cell biology.
[4] W. Snell,et al. Cell body and flagellar agglutinins in Chlamydomonas reinhardtii: the cell body plasma membrane is a reservoir for agglutinins whose migration to the flagella is regulated by a functional barrier , 1990, The Journal of cell biology.
[5] W. Richards,et al. The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination. , 2000, Development.
[6] G. Pazour,et al. Chlamydomonas IFT88 and Its Mouse Homologue, Polycystic Kidney Disease Gene Tg737, Are Required for Assembly of Cilia and Flagella , 2000, The Journal of cell biology.
[7] Lee Niswander,et al. Hedgehog signalling in the mouse requires intraflagellar transport proteins , 2003, Nature.
[8] B. Yoder,et al. An incredible decade for the primary cilium: a look at a once-forgotten organelle. , 2005, American journal of physiology. Renal physiology.
[9] J. Goodship,et al. Cilia and disease. , 2005, Current opinion in genetics & development.
[10] Qian Wang,et al. Cilium-generated signaling and cilia-related disorders , 2005, Laboratory Investigation.
[11] H. Zentgraf,et al. Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia. , 2006, Journal of the American Society of Nephrology : JASN.
[12] K. Gaus,et al. FAPP2, cilium formation, and compartmentalization of the apical membrane in polarized Madin–Darby canine kidney (MDCK) cells , 2006, Proceedings of the National Academy of Sciences.
[13] W. Skarnes,et al. Tectonic, a novel regulator of the Hedgehog pathway required for both activation and inhibition. , 2006, Genes & development.
[14] P. Satir,et al. Overview of structure and function of mammalian cilia. , 2007, Annual review of physiology.
[15] M. Scott,et al. Patched 1 Regulates Hedgehog Signaling at the Primary Cilium , 2022 .
[16] B. Yoder,et al. Functional redundancy of the B9 proteins and nephrocystins in Caenorhabditis elegans ciliogenesis. , 2008, Molecular biology of the cell.
[17] David P. Davis,et al. Kinome siRNA Screen Identifies Regulators of Ciliogenesis and Hedgehog Signal Transduction , 2008, Science Signaling.
[18] Carolyn M Hutter,et al. CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290. , 2008, American journal of human genetics.
[19] M. Nachury. Tandem affinity purification of the BBSome, a critical regulator of Rab8 in ciliogenesis. , 2008, Methods in enzymology.
[20] P. Rakic,et al. The stumpy gene is required for mammalian ciliogenesis , 2008, Proceedings of the National Academy of Sciences.
[21] J. Arellano,et al. Primary cilia regulate hippocampal neurogenesis by mediating sonic hedgehog signaling , 2008, Proceedings of the National Academy of Sciences.
[22] Youngshik Choe,et al. The Rfx4 Transcription Factor Modulates Shh Signaling by Regional Control of Ciliogenesis , 2009, Science Signaling.
[23] K. Anderson,et al. A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling. , 2009, Human molecular genetics.
[24] J. Badano,et al. Ciliary biology: Understanding the cellular and genetic basis of human ciliopathies , 2009, American journal of medical genetics. Part C, Seminars in medical genetics.
[25] Madeline A. Lancaster,et al. Impaired Wnt–β-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy , 2009, Nature Medicine.
[26] Julie J. Miller,et al. High‐throughput generation of tagged stable cell lines for proteomic analysis , 2009, Proteomics.
[27] M. P. Healey,et al. Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins , 2009, Journal of Cell Science.
[28] Madeline A. Lancaster,et al. AHI1 is required for outer segment development and is a modifier for retinal degeneration in nephronophthisis , 2010, Nature Genetics.
[29] B. Yoder,et al. Normal ciliogenesis requires synergy between the cystic kidney disease genes MKS-3 and NPHP-4. , 2010, Journal of the American Society of Nephrology : JASN.
[30] Rajat Rohatgi,et al. The ciliary membrane. , 2010, Current opinion in cell biology.
[31] A. Salic,et al. A mechanism for vertebrate Hedgehog signaling: recruitment to cilia and dissociation of SuFu–Gli protein complexes , 2010, The Journal of cell biology.
[32] Li Li,et al. A mouse knockout library for secreted and transmembrane proteins , 2010, Nature Biotechnology.
[33] J. Rosenbaum,et al. CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content , 2010, The Journal of cell biology.
[34] M. Scott,et al. A Septin Diffusion Barrier at the Base of the Primary Cilium Maintains Ciliary Membrane Protein Distribution , 2010, Science.
[35] Colin A. Johnson,et al. Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes , 2010, Nature Genetics.
[36] J. Naggert,et al. NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development. , 2011, Human molecular genetics.
[37] Matthew J. Brauer,et al. Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways , 2011, Cell.
[38] D. Doherty,et al. The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking , 2011, Human molecular genetics.
[39] Carsten Bergmann,et al. Disruption of a ciliary B9 protein complex causes Meckel syndrome. , 2011, American journal of human genetics.
[40] I. Mellman,et al. Jcb: Article , 2022 .
[41] G. Pazour,et al. Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome , 2010, Disease Models & Mechanisms.
[42] J. García-Verdugo,et al. A Transition Zone Complex Regulates Mammalian Ciliogenesis and Ciliary Membrane Composition , 2011, Nature Genetics.
[43] Nansheng Chen,et al. MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis , 2011, The Journal of cell biology.
[44] V. Torres,et al. B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis. , 2011, Human molecular genetics.