xbx-4, a homolog of the Joubert syndrome gene FAM149B1, acts via the CCRK and RCK kinase cascade to regulate cilia morphology

Related articles

1. Dysregulated nuclear Lamin B1 in DYT1 dystonia thickens the nuclear lamina and disrupts 14-3-3 proteins

   This article has 10 authors:

   1. Yuntian Duan
   2. Masood Sepehrimanesh
   3. Md Abir Hosain
   4. Haochen Cui
   5. Jacob Stagray
   6. Xinggui Shen
   7. Ying Xiao
   8. Yuqing Li
   9. Chun-Li Zhang
   10. Baojin Ding

2. The XPF-like domain in SHOC1 required for homologous recombination and safeguarding autosome from meiotic silencing of unsynapsed chromatin

   This article has 27 authors:

   1. Yuxiang Zhang
   2. Qian Sun
   3. Zhiyong Ji
   4. Ren Mo
   5. Yuchuan Zhou
   6. Jingpeng Zhao
   7. Shuai Xu
   8. Na Li
   9. Yifan Sun
   10. Haowei Bai
   11. Erlei Zhi
   12. Sha Han
   13. Huixing Chen
   14. Jing Zhang
   15. Dewei Qian
   16. Xinjie Bu
   17. Yuhua Huang
   18. Ruhui Tian
   19. Ying Guo
   20. Jinxing Lv
   21. Liangyu Zhao
   22. Chao Yang
   23. Fujun Zhao
   24. Peng Li
   25. Zhi Zhou
   26. Zheng Li
   27. Chencheng Yao

3. Glis3 is a modifier of cyst progression in autosomal dominant polycystic kidney disease

   This article has 6 authors:

   1. Zemeng Wei
   2. Jianlei Gu
   3. Xin Tian
   4. Chao Zhang
   5. Hongyu Zhao
   6. Stefan Somlo