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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Orly Reiner

Department of Molecular Genetics

The Weizmann Institute of Science

Rehovot

Israel

[email]@weizmann.ac.il

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Affiliation

Department of Molecular Genetics, The Weizmann Institute of Science, Rehovot, Israel. 1999 - 2009

References

Polarity regulation in migrating neurons in the cortex. Reiner, O., Sapir, T. Mol. Neurobiol. (2009) [Pubmed]
The evolving doublecortin (DCX) superfamily. Reiner, O., Coquelle, F.M., Peter, B., Levy, T., Kaplan, A., Sapir, T., Orr, I., Barkai, N., Eichele, G., Bergmann, S. BMC. Genomics (2006) [Pubmed]
Lissencephaly 1 linking to multiple diseases: mental retardation, neurodegeneration, schizophrenia, male sterility, and more. Reiner, O., Sapoznik, S., Sapir, T. Neuromolecular Med. (2006) [Pubmed]
Missense mutations resulting in type 1 lissencephaly. Reiner, O., Coquelle, F.M. Cell. Mol. Life Sci. (2005) [Pubmed]
Similarities and differences between the Wnt and reelin pathways in the forming brain. Reiner, O., Sapir, T. Mol. Neurobiol. (2005) [Pubmed]
DCX's phosphorylation by not just another kinase (JNK). Reiner, O., Gdalyahu, A., Ghosh, I., Levy, T., Sapoznik, S., Nir, R., Sapir, T. Cell. Cycle (2004) [Pubmed]
LIS1. let's interact sometimes... (part 1). Reiner, O. Neuron (2000) [Pubmed]
The unfolding story of two lissencephaly genes and brain development. Reiner, O. Mol. Neurobiol. (1999) [Pubmed]