Author :

Name  Gleeson JG

7 Publications

First Author Title Year Journal Volume Pages
Kim J Functional genomic screen for modulators of ciliogenesis and cilium length. 2010 Nature 464 1048-51
Tanaka T Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration. 2004 J Cell Biol 165 709-21
Gleeson JG Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. 1998 Cell 92 63-72
Brancati F MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement. 2009 Hum Mutat 30 E432-42
Akizu N Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia. 2013 Am J Hum Genet 92 392-400
Joo K CCDC41 is required for ciliary vesicle docking to the mother centriole. 2013 Proc Natl Acad Sci U S A 110 5987-92
Akizu N AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorder. 2013 Cell 154 505-17

To cite PlanMine, please refer to the following publication:

Rozanski, A., Moon, H., Brandl, H., Martín-Durán, J. M., Grohme, M., Hüttner, K., Bartscherer, K., Henry, I., & Rink, J. C.
PlanMine 3.0—improvements to a mineable resource of flatworm biology and biodiversity
Nucleic Acids Research, gky1070. doi:10.1093/nar/gky1070 (2018)