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Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility

By Daniela Formicola, Andrea Aloia, Simone Sampaolo, Olimpia Farina, Daria Diodato, Lyn R Griffiths, Fernando Gianfrancesco, Giuseppe Di Iorio and Teresa Esposito
Topics: Research Article
Publisher: BioMed Central
OAI identifier: oai:pubmedcentral.nih.gov:2909201
Provided by: PubMed Central

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Citations

  1. (2006). Animal models of migraine: looking at the component parts of a complex disorder.
  2. (2009). den Maagdenberg AMJM: Molecular genetics of migraine. Hum Genet
  3. (2009). Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice. Neuron
  4. (2000). Familial typical migraine: significant linkage and localization of a gene to Xq24-28. Hum Genet
  5. (2003). Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat Genet
  6. (2004). Headache Classification Committee of the International Headache Society: The International Classification of Headache Disorders, 2nd Edition. Cephalalgia
  7. (1988). HF: A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res
  8. (2007). LR: The search for migraine genes: an overview of current knowledge. Cell Mol Life Sci
  9. (2002). MD: Calcium channel mutations and migraine. Curr Opin Neurol
  10. (2005). Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. Lancet
  11. (2003). The link between glutamate and migraine.
  12. (2002). The structure of haplotype blocks in the human genome. Science