Genes and molecular pathways underpinning ciliopathies

Reiter, Jeremy F., Leroux, Michel R.·2017·Nature Reviews Molecular Cell Biology

Cited by (1,001)

Items 501–600 of 1,001

  1. C21ORF2 mutations point towards primary cilia dysfunction in amyotrophic lateral sclerosis
    Mathias De Decker, Pavol Zelina, Thomas G. Moens, Jimmy Beckers, Matilde Contardo, Katarina Stoklund Dittlau, Evelien Van Schoor, Alicja Ronisz, Kristel Eggermont, Matthieu Moisse et al. · 2024 · Brain
  2. Activation of EGFR‐Aurora A induces loss of primary cilia in oral squamous cell carcinoma
    Fengying Yin, Qian Chen, Yujie Shi, Hao Ying Xu, Jie Huang, Maofeng Qing, Zhong Liang, Jing Li, Liang Xie, Xin Ying Zeng · 2021 · Oral Diseases
  3. Identification and characterization of primary cilia‐positive salivary gland tumours exhibiting basaloid/myoepithelial differentiation
    Kazuya Shinmura, Kimihide Kusafuka, Hideya Kawasaki, Hisami Kato, Takahiko Hariyama, Kazuo Tsuchiya, Yuichi Kawanishi, Kazuhito Funai, Kiyoshi Misawa, Hiroyuki Mineta et al. · 2021 · The Journal of Pathology
  4. Using Paramecium as a Model for Ciliopathies
    Megan Smith Valentine, Judith Van Houten · 2021 · Genes
  5. Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via sonic hedgehog signaling
    Hairong Shi, Hongshun Wang, Cheng Zhang, Yajie Lu, Jun Yao, Zhibin Chen, Guangqian Xing, Qinjun Wei, Xin Cao · 2022 · JCI Insight
  6. CPLANE Complex and Ciliopathies
    E. Martin-Salazar, Diana Valverde · 2022 · Biomolecules
  7. A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease
    Hossein Jafari Khamirani, Vivek Reddy Palicharla, Seyed Alireza Dastgheib, Mehdi Dianatpour, Mohammad Hadi Imanieh, Seyed Sajjad Tabei, Whitney Besse, Saikat Mukhopadhyay, Karel F. Liem · 2022 · Frontiers in Genetics
  8. SIRT2 Affects Primary Cilia Formation by Regulating mTOR Signaling in Retinal Pigmented Epithelial Cells
    Jeaho Lim, Juyoung Son, Jaewook Ryu, Ja‐Eun Kim · 2020 · International Journal of Molecular Sciences
  9. Functional Analysis of Hydrolethalus Syndrome Protein HYLS1 in Ciliogenesis and Spermatogenesis in Drosophila
    Yanan Hou, Zhimao Wu, Yingying Zhang, Huicheng Chen, Jinghua Hu, Yi Guo, Ying Peng, Qing Wei · 2020 · Frontiers in Cell and Developmental Biology
  10. Retinal Organoids: Innovative Tools for Understanding Retinal Degeneration
    Nadia Galindo‐Cabello, Estefanía Caballano‐Infantes, Gregorio Benites, Salvador Pastor‐Idoate, Francisco J. Javier Diaz-Corrales, Ricardo Usategui‐Martín · 2025 · International Journal of Molecular Sciences
  11. Mammalian motile cilia: Structure, formation, organization, and function
    Xueliang Zhu · 2025 · Seminars in Cell and Developmental Biology
  12. Primary cilia function as hubs for signal transduction
    Bo Li, Yu‐Ying He, Zeng‐Ming Yang · 2025 · Cell & Bioscience
  13. Centrioles and Cellular Differentiation
    Jaba Tkemaladze · 2026 · Longevity Horizon
  14. The Trp73 Mutant Mice: A Ciliopathy Model That Uncouples Ciliogenesis From Planar Cell Polarity
    Margarita M. Marqués, Javier Villoch-Fernández, Laura Maeso‐Alonso, Sandra Fuertes-Álvarez, María C. Marín · 2019 · Frontiers in Genetics
  15. Case Report: Homozygous Pathogenic Variant P209L in the TTC21B Gene: A Rare Cause of End Stage Renal Disease and Biliary Cirrhosis Requiring Combined Liver-Kidney Transplantation. A Case Report and Literature Review
    Giuseppe Gambino, Concetta Catalano, Martina Marangoni, Caroline Geers, Alaín Le Moine, Nathalie Boon, Guillaume Smits, Lidia Ghisdal · 2021 · Frontiers in Medicine
  16. PCD Genes—From Patients to Model Organisms and Back to Humans
    Michał Niziołek, Marta Bicka, Anna Osinka, Zuzanna Samsel, Justyna Sekretarska, Martyna Poprzeczko, Rafał Bazan, Hanna Fabczak, Ewa Joachimiak, Dorota Włoga · 2022 · International Journal of Molecular Sciences
  17. The carboxyl-terminal region of SDCCAG8 comprises a functional module essential for cilia formation as well as organ development and homeostasis
    Ryotaro Tsutsumi, Taro Chaya, Toshinori Tsujii, Takahisa Furukawa · 2022 · Journal of Biological Chemistry
  18. Renal ciliopathies: promising drug targets and prospects for clinical trials
    Laura Alice Devlin, Praveen Dhondurao Sudhindar, John Andrew Sayer · 2023 · Expert Opinion on Therapeutic Targets
  19. The Role of Cilia and the Complex Genetics of Congenital Heart Disease
    George C. Gabriel, Madhavi K. Ganapathiraju, Cecilia W. Lo · 2024 · Annual Review of Genomics and Human Genetics
  20. Molecular and structural perspectives on protein trafficking to the primary cilium membrane
    Vivek Reddy Palicharla, Saikat Mukhopadhyay · 2024 · Biochemical Society Transactions
  21. Simple Method To Characterize the Ciliary Proteome of Multiciliated Cells
    Hyo Jung Sim, Seongmin Yun, Ha Eun Kim, Keun Yeong Kwon, Gun‐Hwa Kim, Sung‐Ho Yun, Byung Gyu Kim, Kyungjae Myung, Tae Joo Park, Taejoon Kwon · 2019 · Journal of Proteome Research
  22. ARL3, a small GTPase with a functionally conserved role in primary cilia and immune synapses
    Laura Powell, Youhani Samarakoon, Shehab Ismail, John Andrew Sayer · 2019 · Small GTPases
  23. Expanding the phenotype and the genotype of Stromme syndrome: A novel variant of the CENPF gene and literature review
    Malak Ali Alghamdi, Waleed H. Alkhamis, Fahad A. Bashiri, Dima Z. Jamjoom, Ghada Al-Nafisah, Asma I. Tahir, Mohamed Abdouelhoda · 2020 · European Journal of Medical Genetics
  24. Dealing with several flagella in the same cell
    Eloïse Bertiaux, Philippe Bastin · 2020 · Cellular Microbiology
  25. Functional Alterations in Ciliogenesis-Associated Kinase 1 (CILK1) that Result from Mutations Linked to Juvenile Myoclonic Epilepsy
    Eric J. Wang, Casey D. Gailey, David L. Brautigan, Zheng Fu · 2020 · Cells
  26. Current understandings of the relationship between extracellular vesicles and cilia
    Koji Ikegami, Faryal Ijaz · 2020 · The Journal of Biochemistry
  27. Imaging phenotype correlation with molecular and molecular pathway defects in malformations of cortical development
    Carolina V. A. Guimaraes, Hisham Dahmoush · 2020 · Pediatric Radiology
  28. ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
    Hyun‐Sook Park, Eirini Papanastasi, Gabriela Blanchard, Elena Chiticariu, Daniel Bachmann, Markus Plomann, Fanny Morice‐Picard, Pierre Vabres, Asma Smahi, Marcel Huber et al. · 2021 · Communications Biology
  29. SCFFbxw5 targets kinesin‐13 proteins to facilitate ciliogenesis
    Jörg Schweiggert, Gregor Habeck, Sandra Hess, Felix Mikus, Roman Beloshistov, Klaus Meese, Shoji Hata, Klaus‐Peter Knobeloch, Frauke Melchior · 2021 · The EMBO Journal
  30. Abnormal ciliogenesis in decidual stromal cells in recurrent miscarriage
    Esraa Hassan, Ryuji Kojima, Fumiko Ozawa, Hiroyuki Yoshihara, Shinobu Goto, Tamao Kitaori, Hiroshi Inagaki, Yoichi Kato, Mayumi Sugiura‐Ogasawara · 2022 · Journal of Reproductive Immunology
  31. BROMI/TBC1D32 together with CCRK/CDK20 and FAM149B1/JBTS36 contributes to intraflagellar transport turnaround involving ICK/CILK1
    Yuuki Satoda, Tatsuro Noguchi, Taiju Fujii, Aoi Taniguchi, Yohei Katoh, Kazuhisa Nakayama · 2022 · Molecular Biology of the Cell
  32. Carnitine Protects against MPP+-Induced Neurotoxicity and Inflammation by Promoting Primary Ciliogenesis in SH-SY5Y Cells
    Ji-Eun Bae, Joon Bum Kim, Doo Sin Jo, Na Yeon Park, Yong Hwan Kim, Ha Jung Lee, Seong Hyun Kim, Kim Ys, Mikyung Son, Pansoo Kim et al. · 2022 · Cells
  33. Physiological Condition-Dependent Changes in Ciliary GPCR Localization in the Brain
    Kathryn M. Brewer, Staci E. Engle, Ruchi Bansal, Katlyn K. Brewer, Kalene R. Jasso, Jeremy C. McIntyre, Christian Vaisse, Jeremy F. Reiter, Nicolas F. Berbari · 2023 · eNeuro
  34. Kidney-differentiated cells derived from Lowe Syndrome patient’s iPSCs show ciliogenesis defects and Six2 retention at the Golgi complex
    Wen-Chieh Hsieh, Swetha Ramadesikan, Donna M. Fekete, Ruben Claudio Aguilar · 2018 · PLoS ONE
  35. Setting the dynein motor in motion: New insights from electron tomography
    Danielle Ann Grotjahn, Gabriel C. Lander · 2019 · Journal of Biological Chemistry
  36. Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4
    Junwen Wang, Shiqiang Li, Yi Hua Jiang, Yingwei Wang, Jiamin Ouyang, Zhen Yi, Wenmin Sun, Xiaoyun Jia, Xueshan Xiao, Panfeng Wang et al. · 2023 · American Journal of Ophthalmology
  37. Multicilia dynamically transduce Sonic Hedgehog signaling to regulate choroid plexus functions
    Suifang Mao, Rui Song, Shibo Jin, Song Pang, Aleksandra Jovanović, Adam Zimmerman, Peng Li, Xinying Wu, Michael F. Wendland, Kerry Lin et al. · 2025 · Cell Reports
  38. Intravital visualization of the primary cilium, tubule flow, and innate immune cells in the kidney utilizing an abdominal window imaging approach
    Dustin Z. Revell, Bradley K. Yoder · 2019 · Methods in cell biology
  39. Transient pupillary light reflex in CEP290- or NPHP5-associated Leber congenital amaurosis: Latency as a potential outcome measure of cone function
    Arun K. Krishnan, Samuel G. Jacobson, Alejandro J. Román, Bhavya S. Iyer, Alexandra V. Garafalo, Elise Héon, Artur V. Cideciyan · 2020 · Vision Research
  40. Primary cilia-dependent signaling is involved in regulating mesenchymal stem cell proliferation and pluripotency maintenance
    Zhou-rui Ma, Mingde Qin, Hansi Liang, Ruihua Chen, Shizhong Cai, Zhijian Huang, Guangping Tai · 2020 · Journal of Molecular Histology
  41. Phosphosite T674A mutation in kinesin family member 3A fails to reproduce tissue and ciliary defects characteristic of CILK1 loss of function
    Casey D. Gailey, Eric J. Wang, Li Jin, Sean Ahmadi, David L. Brautigan, Xudong Joshua Li, Wenhao Xu, Michael M. Scott, Zheng Fu · 2020 · Developmental Dynamics
  42. Post-translational modification enzymes as key regulators of ciliary protein trafficking
    Taro Chaya, Takahisa Furukawa · 2021 · The Journal of Biochemistry
  43. Aurora Kinase A proximity map reveals centriolar satellites as regulators of its ciliary function
    Melis D. Arslanhan, Navin Rauniyar, John R. Yates, Elif Nur Firat‐Karalar · 2021 · EMBO Reports
  44. Insights into auto- S -fatty acylation: targets, druggability, and inhibitors
    Lu Hu, Zhipeng Tao, Xu Wu · 2021 · RSC Chemical Biology
  45. Primary cilia in hard tissue development and diseases
    Sijin Li, Han Zhang, Yao Sun · 2021 · Frontiers of Medicine
  46. The ARF GAPs ELMOD1 and ELMOD3 act at the Golgi and cilia to regulate ciliogenesis and ciliary protein traffic
    Rachel E. Turn, Yihan Hu, Skylar I. Dewees, Narra Devi, Michael P. East, Katherine R. Hardin, Tala Khatib, Joshua Linnert, Uwe Wolfrum, Michael J. Lim et al. · 2021 · Molecular Biology of the Cell
  47. Temporospatial regulation of intraflagellar transport is required for the endochondral ossification in mice
    Hiroyuki Yamaguchi, Megumi Kitami, Karin Harumi Uchima Koecklin, Li He, Jianbo Wang, William R. Lagor, Daniel S. Perrien, Yoshihiro Komatsu · 2021 · Developmental Biology
  48. The ciliary transition zone protein TMEM218 synergistically interacts with the NPHP module and its reduced dosage leads to a wide range of syndromic ciliopathies
    Daniel Epting, Eva Decker, Elisabeth B. Ott, Tobias Eisenberger, Ingrid Bader, Nadine Bachmann, Carsten Bergmann · 2022 · Human Molecular Genetics
  49. Pericentrin interacts with Kinesin-1 to drive centriole motility
    Matthew R. Hannaford, Rong Liu, Neil Billington, Zachary T. Swider, Brian J. Galletta, Carey J. Fagerstrom, Christian A. Combs, James R. Sellers, Nasser M. Rusan · 2022 · The Journal of Cell Biology
  50. Dominantly acting KIF5B variants with pleiotropic cellular consequences cause variable clinical phenotypes
    Elisabetta Flex, Shahad Albadri, Francesca Clementina Radio, Serena Cecchetti, Antonella Lauri, Manuela Priolo, Marta Kissopoulos, Giovanna Carpentieri, Giulia Fasano, Martina Venditti et al. · 2022 · Human Molecular Genetics
  51. Clinical and genetic spectrum from a prototype of ciliopathy: Joubert syndrome
    Tuğçe Aksu Uzunhan, Biray Ertürk, Kürşad Aydın, Akif Ayaz, Umut Altunoğlu, Murat Hakkı Yarar, Alper Gezdirici, Dilara Füsun İçağasıoğlu, Ezgi Gökpınar İli, Bülent Uyanık et al. · 2022 · Clinical Neurology and Neurosurgery
  52. STIL/AURKA axis promotes cell proliferation by influencing primary cilia formation in bladder cancer
    Jingxian Li, Yuanjiong Qi, Bo Li, Yan Liu, Kuo Yang, Zhihong Zhang, Jianqiang Zhu, Eugenie Du · 2023 · Journal of Translational Medicine
  53. Motile cilia defects in diseases other than primary ciliary dyskinesia: The contemporary diagnostic and research role for transmission electron microscopy
    Hannah M. Mitchison, Amelia Shoemark · 2017 · Ultrastructural Pathology
  54. The nucleoside-diphosphate kinase NME3 associates with nephronophthisis proteins and is required for ciliary function during renal development
    Sylvia Hoff, Daniel Epting, Nathalie Falk, Sophie Schroda, Daniela Anne Braun, Jan Halbritter, Friedhelm Hildebrandt, Albrecht G. Kramer-Zucker, Carsten Bergmann, Gerd Walz et al. · 2018 · Journal of Biological Chemistry
  55. BBS5 and INPP5E mutations associated with ciliopathy disorders in families from Pakistan
    Shazia Khan, Siying Lin, Gaurav V. Harlalka, Asmat Ullah, Khadim Shah, Sumbul Khalid, Sarmad Mehmood, Muhammad Jawad Hassan, Wasim Ahmad, Jay Self et al. · 2019 · Annals of Human Genetics
  56. hVFL3/CCDC61 is a component of mother centriole subdistal appendages required for centrosome cohesion and positioning
    Véronique Pizon, Noémie Gaudin, Marion Poteau, Carmen Cifuentes-Díaz, Roland Demdou, Vincent Heyer, Bernardo Reina‐San‐Martin, Juliette Azimzadeh · 2019 · Biology of the Cell
  57. Design principles of ciliary signaling
    Carolyn M. Ott, Jennifer Lippincott‐Schwartz · 2025 · Journal of Cell Science
  58. Biophysical and biochemical properties of Deup1 self-assemblies: a potential driver for deuterosome formation during multiciliogenesis
    Shohei Yamamoto, Ryoichi Yabuki, Daiju Kitagawa · 2021 · Biology Open
  59. Ciliogenesis and autophagy are coordinately regulated by EphA2 in the cornea to maintain proper epithelial architecture
    Nihal Kaplan, Sijia Wang, Junyi Wang, Wending Yang, Rosa Ventrella, Ahmed Majekodunmi, Bethany E. Perez White, Spiro Getsios, Brian J. Mitchell, Han Peng et al. · 2021 · The Ocular Surface
  60. Patient-Patient Similarity-Based Screening of a Clinical Data Warehouse to Support Ciliopathy Diagnosis
    Xiaoyi Chen, Carole Faviez, Marc Vincent, Luis Briseño-Roa, Hassan Faour, Jean‐Philippe Annereau, Stanislas Lyonnet, Mohamad Zaidan, Sophie Saunier, Nicolas Garcelon et al. · 2022 · Frontiers in Pharmacology
  61. Deciphering cilia and ciliopathies using proteomic approaches
    Xiying Chen, Zhouyuanjing Shi, Feng Yang, Tianhua Zhou, Shanshan Xie · 2022 · FEBS Journal
  62. Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla
    Aude Tessier, N. Roux, Lucile Boutaud, Elodie Lunel, Leila Hakkakian, Mélanie Parisot, Meriem Garfa‐Traoré, Amale Ichkou, Nadia Elkhartoufi, Christine Bôle‐Feysot et al. · 2023 · Acta Neuropathologica Communications
  63. The factory, the antenna and the scaffold: the three-way interplay between the Golgi, cilium and extracellular matrix underlying tissue function
    Nicola L. Stevenson · 2023 · Biology Open
  64. Identification of a heterogeneous and dynamic ciliome during embryonic development and cell differentiation
    Kelsey H. Elliott, Sai K. Balchand, Christian Louis Bonatto Paese, Ching‐Fang Chang, Yanfen Yang, Kari M. Brown, Daniel T. Rasicci, Hao He, Konrad Thorner, Praneet Chaturvedi et al. · 2023 · Development
  65. WDR31 displays functional redundancy with GTPase-activating proteins (GAPs) ELMOD and RP2 in regulating IFT complex and recruiting the BBSome to cilium
    Sebiha Cevik, Xiaoyu Peng, Tina Beyer, Mustafa S Pir, Ferhan Yenisert, Franziska Woerz, F. Hoffmann, Betul Altunkaynak, Betul Pir, Karsten Boldt et al. · 2023 · Life Science Alliance
  66. Dysregulated Arginine Metabolism Is Linked to Retinal Degeneration in Cep250 Knockout Mice
    Lue Xiang, Qiaoli Yang, Bintao Xie, Hui-Yi Zeng, Liujun Ding, Feng-Qin Rao, Tong Yan, Fan Lü, Qi Chen, Xiu‐Feng Huang · 2023 · Investigative Ophthalmology & Visual Science
  67. The role of cilia during organogenesis in zebrafish
    Junjun Liu, Haibo Xie, Mengfan Wu, Yidan Hu, Yunsi Kang · 2023 · Open Biology
  68. Postnatal Dynamic Ciliary ARL13B and ADCY3 Localization in the Mouse Brain
    Katlyn K. Brewer, Kathryn M. Brewer, Tiffany T. Terry, Tamara Caspary, Christian Vaisse, Nicolas F. Berbari · 2024 · Cells
  69. Neurons dispose of hyperactive kinesin into glial cells for clearance
    Chao Xie, Guanghan Chen, Ming Li, Peng Huang, Zhe Chen, Kexin Lei, Dong Li, Yuhe Wang, Augustine Cleetus, Mohamed AA Mohamed et al. · 2024 · The EMBO Journal
  70. A review of CDKL: An underestimated protein kinase family
    Chenrui Li, Yan Liu, Shilu Luo, Ming Jun Yang, Li Li, Lin Sun · 2024 · International Journal of Biological Macromolecules
  71. Non-canonical CDK6 activity promotes cilia disassembly by suppressing axoneme polyglutamylation
    Kai He, Xiaobo Sun, Chuan Chen, San Luc, Jielu Hao, Yingyi Zhang, Yan Huang, Biyun Ji, Pei-I Ku, Radhika Subramanian et al. · 2024 · The Journal of Cell Biology
  72. Clinical Spectrum and Prognosis of Atypical Autosomal Dominant Polycystic Kidney Disease Caused by Monoallelic Pathogenic Variants of IFT140
    Nikola Zagorec, Alizée Calamel, Margaux Delaporte, Eric Gregory Olinger, Sarah E. Orr, John Andrew Sayer, Vignesh-Guru Pillay, Anne‐Sophie Denommé‐Pichon, Frédéric Tran Mau‐Them, Sophie Nambot et al. · 2024 · American Journal of Kidney Diseases
  73. Apical PtdIns(4,5)P 2 is required for ciliogenesis and suppression of polycystic kidney disease
    Wenyan Xu, Miaomiao Jin, Weilai Huang, Hong Wang, Ruikun Hu, Jingyu Li, Ying Cao · 2018 · The FASEB Journal
  74. Dissecting the Vesicular Trafficking Function of IFT Subunits
    Huihui Yang, Kaiyao Huang · 2020 · Frontiers in Cell and Developmental Biology
  75. Physiological and Pathophysiological Aspects of Primary Cilia—A Literature Review with View on Functional and Structural Relationships in Cartilage
    Friedrich Barsch, Tanja Niedermair, Andreas Mamilos, Volker H. Schmitt, David Grevenstein, Maximilian Babel, Thomas Burgoyne, Amelia Shoemark, Christoph Brochhausen · 2020 · International Journal of Molecular Sciences
  76. Non-ciliary Roles of IFT Proteins in Cell Division and Polycystic Kidney Diseases
    Benjamin Vitre, Audrey Guesdon, Bénédicte Delaval · 2020 · Frontiers in Cell and Developmental Biology
  77. Differentiation of ciliated human midbrain-derived LUHMES neurons
    Gilbert Lauter, Andrea Coschiera, Masahito Yoshihara, Debora Sugiaman‐Trapman, Sini Ezer, Shalini Sethurathinam, Shintaro Katayama, Juha Kere, Peter Swoboda · 2020 · Journal of Cell Science
  78. Differential requirement of NPHP1 for compartmentalized protein localization during photoreceptor outer segment development and maintenance
    Poppy Datta, J. Thomas Cribbs, Seongjin Seo · 2021 · PLoS ONE
  79. Deletion of kif3a in CK19 positive cells leads to primary cilia loss, biliary cell proliferation and cystic liver lesions in TAA-treated mice
    Jinbiao Chen, Ngan Ching Cheng, Jade A Boland, Ken Liu, James G. Kench, D. Neil Watkins, Sofía Ferreira-González, Stuart John Forbes, Geoffrey William McCaughan · 2021 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  80. Combinations of deletion and missense variations of the dynein-2 DYNC2LI1 subunit found in skeletal ciliopathies cause ciliary defects
    Hantian Qiu, Yuta Tsurumi, Yohei Katoh, Kazuhisa Nakayama · 2022 · Scientific Reports
  81. Zebrafish models of inherited retinal dystrophies
    Brian D. Perkins · 2022 · Journal of Translational Genetics and Genomics
  82. Cytoskeletal networks in primary cilia: Current knowledge and perspectives
    Ruixin Ge, Minghui Cao, Miao Chen, Min Liu, Songbo Xie · 2022 · Journal of Cellular Physiology
  83. Assembly and stability of IFT-B complex and its function in BBSome trafficking
    Jieling Wang, Xin Zhu, Zhengmao Wang, Xuecheng Li, Hui Tao, Junmin Pan · 2022 · iScience
  84. TMEM67 is required for the gating function of the transition zone that controls entry of membrane-associated proteins ARL13B and INPP5E into primary cilia
    Zhuoma Yinsheng, Ko Miyoshi, Yuanyuan Qin, Yuuki Fujiwara, Takeshi Yoshimura, Taiichi Katayama · 2022 · Biochemical and Biophysical Research Communications
  85. Coordination of Cilia Movements in Multi-Ciliated Cells
    Masaki Arata, Fumiko Matsukawa Usami, Toshihiko Fujimori · 2022 · Journal of Developmental Biology
  86. Primary Cilia: The New Face of Craniofacial Research
    Emily R. Moore · 2022 · Biomolecules
  87. Primary cilia suppress Ripk3-mediated necroptosis
    Emilia Kieckhöfer, Gisela G.G. Slaats, Lena K. Ebert, Marie‐Christine Albert, Claudia Dafinger, Hamid Kashkar, Thomas R. Benzing, Bernhard Schermer · 2022 · Cell Death Discovery
  88. Drosophila transition fibers are essential for IFT-dependent ciliary elongation but not basal body docking and ciliary budding
    Yanan Hou, Shirui Zheng, Zhimao Wu, Céline Augière, Véronique Morel, Elisabeth Cortier, Jean-Luc Duteyrat, Yingying Zhang, Huicheng Chen, Ying Peng et al. · 2023 · Current Biology
  89. Ocular Ciliopathies: Genetic and Mechanistic Insights into Developing Therapies
    Mahesh Shivanna, Manisha Anand, Subhabrata Chakrabarti, Hemant Khanna · 2018 · Current Medicinal Chemistry
  90. DYRK1B regulates Hedgehog-induced microtubule acetylation
    Rajeev Kumar Singh, Philipp Simon Holz, Katrin Sabine Roth, Anna Hupfer, Wolfgang Meißner, Rolf Müller, Malte Buchholz, Thomas Mathias Gress, Hans‐Peter Elsässer, Ralf Jacob et al. · 2018 · Cellular and Molecular Life Sciences
  91. Extraciliary roles of the ciliopathy protein JBTS17 in mitosis and neurogenesis
    Hyowon Hong, Kwangsic Joo, Sang Min Park, Jimyung Seo, Min Hwan Kim, Eunbie Shin, Hae Il Cheong, Jeong Ho Lee, Joon Kim · 2019 · Annals of Neurology
  92. Biallelic mutations in the TOGARAM1 gene cause a novel primary ciliopathy
    Valeria Morbidoni, Emanuele Agolini, Kevin C. Slep, Luca Pannone, Daniela Zuccarello, Matteo Cassina, Enrico Grosso, Giorgia Gai, Leonardo Salviati, Bruno Dallapiccola et al. · 2020 · Journal of Medical Genetics
  93. Oncogenic FGFR Fusions Produce Centrosome and Cilia Defects by Ectopic Signaling
    Alexandru Niţă, Sara P. Abraham, Pavel Krejčı́, Michaela Kunova Bosakova · 2021 · Cells
  94. A Synthesis Concerning Conservation and Divergence of Cell Types across Epithelia
    Daniel T. Montoro, Adam L. Haber, Jennifer Rood, Aviv Regev, Jayaraj Rajagopal · 2020 · Cold Spring Harbor Perspectives in Biology
  95. Retinal Degeneration Animal Models in Bardet–Biedl Syndrome and Related Ciliopathies
    Clarisse Delvallée, Hélène Dollfus · 2023 · Cold Spring Harbor Perspectives in Medicine
  96. High-throughput tracking enables systematic phenotyping and drug repurposing in C. elegans disease models
    Thomas James O’Brien, Ida L. Barlow, Luigi Feriani, André EX Brown · 2023 · eLife
  97. The primary cilia are associated with the axon initial segment in neurons
    Wang, Han, Li, Yu, Li, Xin, Sun, Zehui, Yu, Fengdan, Pashang, Abolghasem, Kulasiri, Don, Li, Hung Wing, Chen, Huan, Hou, Hongwei et al. · 2025 · Advanced Science
  98. The Desert Hedgehog Signalling Pathway in Human Gonadal Development and Differences of Sex Development
    Svenja Pachernegg, Elizabeth Georges, Katie L. Ayers · 2021 · Sexual Development
  99. Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components
    Friederike Hantel, Huaize Liu, Lisa Fechtner, Herbert Neuhaus, Jie Ding, Danilo Arlt, Peter Walentek, Pablo Villavicencio‐Lorini, Christoph Gerhardt, Thomas Hollemann et al. · 2022 · Journal of Cell Science
  100. The flagellar length control system: exploring the physical biology of organelle size
    Wallace F. Marshall · 2023 · Physical Biology