Publication | Closed Access
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5
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Citations
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References
2015
Year
Developmental AnomalyMitophagyDevelopmental BiologyLoss-of-function MutationMendelian DisorderGenetic DisorderGeneticsMolecular GeneticsAutosomal Recessive LissencephalyMedicineCerebellar HypoplasiaNeurogenetics
| Year | Citations | |
|---|---|---|
1995 | 2K | |
Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death. Toshio Ohshima, Jerrold M. Ward, C G Huh, Proceedings of the National Academy of Sciences Developmental BiologySignal TransductionApoptosisExperimental NeuropathologyCdk5 Expression | 1996 | 893 |
2000 | 875 | |
2005 | 562 | |
2000 | 480 | |
2003 | 400 | |
2001 | 379 | |
1933 | 282 | |
2001 | 277 | |
2004 | 227 |
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