Pages that link to "Q28274803"
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The following pages link to LIS2, gene and pseudogene, homologous to LIS1 (lissencephaly 1), located on the short and long arms of chromosome 2 (Q28274803):
Displaying 12 items.
- Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome (Q24336051) (← links)
- Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis. (Q24539086) (← links)
- Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE (Q26690426) (← links)
- Cytoplasmic LEK1 is a regulator of microtubule function through its interaction with the LIS1 pathway (Q28508499) (← links)
- In silico discovery and experimental validation of new protein-protein interactions (Q28842760) (← links)
- Characterization and chromosomal mapping of two pseudogenes of the mouse Pafaha/Lis1 gene: retrointegration hotspots in the mouse genome (Q32026644) (← links)
- The unfolding story of two lissencephaly genes and brain development. (Q34019154) (← links)
- Role of subcortical structures in the pathogenesis of infantile spasms: what are possible subcortical mediators? (Q34663321) (← links)
- Brain malformations associated with cell migration (Q36523314) (← links)
- Microcephaly with simplified gyral pattern in six related children (Q41925745) (← links)
- The LIS1-related protein NUDF of Aspergillus nidulans and its interaction partner NUDE bind directly to specific subunits of dynein and dynactin and to alpha- and gamma-tubulin (Q56765523) (← links)
- Models of temporal processing and language development (Q58064575) (← links)