Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 26

1.

A unified GMDR method for detecting gene-gene interactions in family and unrelated samples with application to nicotine dependence.

Chen GB, Liu N, Klimentidis YC, Zhu X, Zhi D, Wang X, Lou XY.

Hum Genet. 2014 Feb;133(2):139-50. doi: 10.1007/s00439-013-1361-9. Epub 2013 Sep 21.

PMID:
24057800
[PubMed - indexed for MEDLINE]
2.

Importance of the nicotinic acetylcholine receptor system in the prefrontal cortex.

Wallace TL, Bertrand D.

Biochem Pharmacol. 2013 Jun 15;85(12):1713-20. doi: 10.1016/j.bcp.2013.04.001. Epub 2013 Apr 26. Review.

PMID:
23628449
[PubMed - indexed for MEDLINE]
3.

Relationship between nicotine dependence and the endophenotype-related trait of cognitive function but not acoustic startle reponses in Japanese patients with schizophrenia.

Kishi T, Fukuo Y, Okochi T, Kawashima K, Moriwaki M, Furukawa O, Musso GM, Fujita K, Correll CU, Iwata N.

Hum Psychopharmacol. 2013 May;28(3):220-9. doi: 10.1002/hup.2310. Epub 2013 Apr 4.

PMID:
23553665
[PubMed - indexed for MEDLINE]
4.

Nominal association with CHRNA4 variants and nicotine dependence.

Kamens HM, Corley RP, McQueen MB, Stallings MC, Hopfer CJ, Crowley TJ, Brown SA, Hewitt JK, Ehringer MA.

Genes Brain Behav. 2013 Apr;12(3):297-304. doi: 10.1111/gbb.12021. Epub 2013 Feb 6.

PMID:
23350800
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Resolution of epileptic encephalopathy following treatment with transdermal nicotine.

Zerem A, Nishri D, Yosef Y, Blumkin L, Lev D, Leshinsky-Silver E, Kivity S, Lerman-Sagie T.

Epilepsia. 2013 Jan;54(1):e13-5. doi: 10.1111/j.1528-1167.2012.03715.x. Epub 2012 Oct 12.

PMID:
23061632
[PubMed - indexed for MEDLINE]
6.

Possible association of nicotinic acetylcholine receptor gene (CHRNA4 and CHRNB2) polymorphisms with nicotine dependence in Japanese males: an exploratory study.

Chen HI, Shinkai T, Utsunomiya K, Yamada K, Sakata S, Fukunaka Y, Hwang R, De Luca V, Ohmori O, Kennedy JL, Chuang HY, Nakamura J.

Pharmacopsychiatry. 2013 Mar;46(2):77-82. doi: 10.1055/s-0032-1323678. Epub 2012 Oct 4.

PMID:
23037950
[PubMed - indexed for MEDLINE]
7.

A case of autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) coexisting with pervasive developmental disorder harboring SCN1A mutation in addition to CHRNB2 mutation.

Sone D, Sugawara T, Sakakibara E, Tomioka Y, Taniguchi G, Murata Y, Watanabe M, Kaneko S.

Epilepsy Behav. 2012 Oct;25(2):192-5. doi: 10.1016/j.yebeh.2012.07.027. Epub 2012 Sep 29.

PMID:
23032131
[PubMed - indexed for MEDLINE]
8.

Hippocampal sclerosis worsens autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) phenotype related to CHRNB2 mutation.

Labate A, Mumoli L, Fratto A, Quattrone A, Gambardella A.

Eur J Neurol. 2013 Mar;20(3):591-3. doi: 10.1111/j.1468-1331.2012.03839.x. Epub 2012 Aug 17.

PMID:
22897520
[PubMed - indexed for MEDLINE]
9.

Nicotinic acetylcholine receptor expression and susceptibility to cholinergic immunomodulation in human monocytes of smoking individuals.

van der Zanden EP, Hilbers FW, Verseijden C, van den Wijngaard RM, Skynner M, Lee K, Ulloa L, Boeckxstaens GE, de Jonge WJ.

Neuroimmunomodulation. 2012;19(4):255-65. doi: 10.1159/000335185. Epub 2012 Mar 21.

PMID:
22441542
[PubMed - indexed for MEDLINE]
10.

Repressor element-1 silencing transcription factor (REST)-dependent epigenetic remodeling is critical to ischemia-induced neuronal death.

Noh KM, Hwang JY, Follenzi A, Athanasiadou R, Miyawaki T, Greally JM, Bennett MV, Zukin RS.

Proc Natl Acad Sci U S A. 2012 Apr 17;109(16):E962-71. doi: 10.1073/pnas.1121568109. Epub 2012 Feb 27.

PMID:
22371606
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Smoking cessation pharmacogenetics: analysis of varenicline and bupropion in placebo-controlled clinical trials.

King DP, Paciga S, Pickering E, Benowitz NL, Bierut LJ, Conti DV, Kaprio J, Lerman C, Park PW.

Neuropsychopharmacology. 2012 Feb;37(3):641-50. doi: 10.1038/npp.2011.232. Epub 2011 Nov 2.

PMID:
22048466
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Mutations in familial nocturnal frontal lobe epilepsy might be associated with distinct neurological phenotypes.

Steinlein OK, Hoda JC, Bertrand S, Bertrand D.

Seizure. 2012 Mar;21(2):118-23. doi: 10.1016/j.seizure.2011.10.003. Epub 2011 Oct 28.

PMID:
22036597
[PubMed - indexed for MEDLINE]
Free Article
13.

Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses.

Chen CP, Lin SP, Chen M, Su YN, Chern SR, Wang TY, Liu YP, Tsai FJ, Lee CC, Chen YJ, Wang W.

Genet Couns. 2011;22(3):273-80.

PMID:
22029168
[PubMed - indexed for MEDLINE]
14.

Autosomal dominant nocturnal frontal lobe epilepsy: a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation.

Hwang SK, Makita Y, Kurahashi H, Cho YW, Hirose S.

J Hum Genet. 2011 Aug;56(8):609-12. doi: 10.1038/jhg.2011.69. Epub 2011 Jul 14.

PMID:
21753767
[PubMed - indexed for MEDLINE]
15.

Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes.

Swan GE, Javitz HS, Jack LM, Wessel J, Michel M, Hinds DA, Stokowksi RP, McClure JB, Catz SL, Richards J, Zbikowski SM, Deprey M, McAfee T, Conti DV, Bergen AW.

Pharmacogenomics J. 2012 Aug;12(4):349-58. doi: 10.1038/tpj.2011.19. Epub 2011 May 24.

PMID:
21606948
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Associations of nicotine intake measures with CHRN genes in Finnish smokers.

Keskitalo-Vuokko K, Pitkäniemi J, Broms U, Heliövaara M, Aromaa A, Perola M, Ripatti S, Salminen O, Salomaa V, Loukola A, Kaprio J.

Nicotine Tob Res. 2011 Aug;13(8):686-90. doi: 10.1093/ntr/ntr059. Epub 2011 Apr 16.

PMID:
21498873
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsy.

Liu H, Lu C, Li Z, Zhou S, Li X, Ji L, Lu Q, Lv R, Wu L, Ma X.

Epilepsy Res. 2011 Jun;95(1-2):94-9. doi: 10.1016/j.eplepsyres.2011.03.002. Epub 2011 Apr 16.

PMID:
21497487
[PubMed - indexed for MEDLINE]
18.

A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy.

Muhle H, Steinich I, von Spiczak S, Franke A, Weber Y, Lerche H, Wittig M, Heidemann S, Suls A, de Jonghe P, Marini C, Guerrini R, Scheffer IE, Berkovic SF, Stephani U, Siebert R, Sander T, Helbig I, Tönnies H.

Epilepsia. 2010 Dec;51(12):2453-6. doi: 10.1111/j.1528-1167.2010.02712.x. Epub 2010 Sep 24.

PMID:
21204805
[PubMed - indexed for MEDLINE]
19.

CHRNB2 promoter region: association with subjective effects to nicotine and gene expression differences.

Hoft NR, Stitzel JA, Hutchison KE, Ehringer MA.

Genes Brain Behav. 2011 Mar;10(2):176-85. doi: 10.1111/j.1601-183X.2010.00650.x. Epub 2010 Nov 4.

PMID:
20854418
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Advances on the genetics of Mendelian idiopathic epilepsies.

Baulac S, Baulac M.

Clin Lab Med. 2010 Dec;30(4):911-29. doi: 10.1016/j.cll.2010.07.008. Review.

PMID:
20832659
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk