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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 2 |
2010 | 2 |
2011 | 1 |
2017 | 1 |
2019 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 8448
7 results
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Page 1
Increased expression of DOC2A in human and rat temporal lobe epilepsy.
Epilepsy Res. 2019 Mar;151:78-84. doi: 10.1016/j.eplepsyres.2019.02.008. Epub 2019 Feb 25.
Epilepsy Res. 2019.
PMID: 30844661
Loss of Doc2-Dependent Spontaneous Neurotransmission Augments Glutamatergic Synaptic Strength.
Ramirez DMO, Crawford DC, Chanaday NL, Trauterman B, Monteggia LM, Kavalali ET.
Ramirez DMO, et al.
J Neurosci. 2017 Jun 28;37(26):6224-6230. doi: 10.1523/JNEUROSCI.0418-17.2017. Epub 2017 May 24.
J Neurosci. 2017.
PMID: 28539418
Free PMC article.
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Doc2 is a Ca2+ sensor required for asynchronous neurotransmitter release.
Yao J, Gaffaney JD, Kwon SE, Chapman ER.
Yao J, et al.
Cell. 2011 Oct 28;147(3):666-77. doi: 10.1016/j.cell.2011.09.046.
Cell. 2011.
PMID: 22036572
Free PMC article.
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An approach based on a genome-wide association study reveals candidate loci for narcolepsy.
Shimada M, Miyagawa T, Kawashima M, Tanaka S, Honda Y, Honda M, Tokunaga K.
Shimada M, et al.
Hum Genet. 2010 Oct;128(4):433-41. doi: 10.1007/s00439-010-0862-z. Epub 2010 Jul 31.
Hum Genet. 2010.
PMID: 20677014
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Strong synaptic transmission impact by copy number variations in schizophrenia.
Glessner JT, Reilly MP, Kim CE, Takahashi N, Albano A, Hou C, Bradfield JP, Zhang H, Sleiman PM, Flory JH, Imielinski M, Frackelton EC, Chiavacci R, Thomas KA, Garris M, Otieno FG, Davidson M, Weiser M, Reichenberg A, Davis KL, Friedman JI, Cappola TP, Margulies KB, Rader DJ, Grant SF, Buxbaum JD, Gur RE, Hakonarson H.
Glessner JT, et al.
Proc Natl Acad Sci U S A. 2010 Jun 8;107(23):10584-9. doi: 10.1073/pnas.1000274107. Epub 2010 May 20.
Proc Natl Acad Sci U S A. 2010.
PMID: 20489179
Free PMC article.
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Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.
Guilmatre A, Dubourg C, Mosca AL, Legallic S, Goldenberg A, Drouin-Garraud V, Layet V, Rosier A, Briault S, Bonnet-Brilhault F, Laumonnier F, Odent S, Le Vacon G, Joly-Helas G, David V, Bendavid C, Pinoit JM, Henry C, Impallomeni C, Germano E, Tortorella G, Di Rosa G, Barthelemy C, Andres C, Faivre L, Frébourg T, Saugier Veber P, Campion D.
Guilmatre A, et al.
Arch Gen Psychiatry. 2009 Sep;66(9):947-56. doi: 10.1001/archgenpsychiatry.2009.80.
Arch Gen Psychiatry. 2009.
PMID: 19736351
Free PMC article.
Review.
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Association and mutation analyses of 16p11.2 autism candidate genes.
Kumar RA, Marshall CR, Badner JA, Babatz TD, Mukamel Z, Aldinger KA, Sudi J, Brune CW, Goh G, Karamohamed S, Sutcliffe JS, Cook EH, Geschwind DH, Dobyns WB, Scherer SW, Christian SL.
Kumar RA, et al.
PLoS One. 2009;4(2):e4582. doi: 10.1371/journal.pone.0004582. Epub 2009 Feb 26.
PLoS One. 2009.
PMID: 19242545
Free PMC article.
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