Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways
Top Cited Papers
Open Access
- 13 May 2011
- journal article
- research article
- Published by Elsevier BV in Cell
- Vol. 145 (4), 513-528
- https://doi.org/10.1016/j.cell.2011.04.019
Abstract
No abstract availableThis publication has 91 references indexed in Scilit:
- The role of primary cilia in neuronal functionNeurobiology of Disease, 2010
- CC2D2Amutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlationHuman Mutation, 2009
- Defining the Human Deubiquitinating Enzyme Interaction LandscapeCell, 2009
- CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290American Journal of Human Genetics, 2008
- A Protein Domain-Based Interactome Network for C. elegans Early EmbryogenesisCell, 2008
- Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert SyndromeAmerican Journal of Human Genetics, 2008
- Identification of CC2D2A as a Meckel Syndrome Gene Adds an Important Piece to the Ciliopathy PuzzleAmerican Journal of Human Genetics, 2008
- Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic DysplasiaAmerican Journal of Human Genetics, 2008
- MUSTER: Improving protein sequence profile–profile alignments by using multiple sources of structure informationProteins, 2008
- Disruption of Intraflagellar Transport in Adult Mice Leads to Obesity and Slow-Onset Cystic Kidney DiseaseCurrent Biology, 2007