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Results: 16

1.

Narcolepsy onset is seasonal and increased following the 2009 H1N1 pandemic in China.

Han F, Lin L, Warby SC, Faraco J, Li J, Dong SX, An P, Zhao L, Wang LH, Li QY, Yan H, Gao ZC, Yuan Y, Strohl KP, Mignot E.

Ann Neurol. 2011 Sep;70(3):410-7. doi: 10.1002/ana.22587. Epub 2011 Aug 22.

PMID:
21866560
[PubMed - indexed for MEDLINE]
2.

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss.

Klein CJ, Botuyan MV, Wu Y, Ward CJ, Nicholson GA, Hammans S, Hojo K, Yamanishi H, Karpf AR, Wallace DC, Simon M, Lander C, Boardman LA, Cunningham JM, Smith GE, Litchy WJ, Boes B, Atkinson EJ, Middha S, B Dyck PJ, Parisi JE, Mer G, Smith DI, Dyck PJ.

Nat Genet. 2011 Jun;43(6):595-600. doi: 10.1038/ng.830. Epub 2011 May 1.

PMID:
21532572
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Structural insight into maintenance methylation by mouse DNA methyltransferase 1 (Dnmt1).

Takeshita K, Suetake I, Yamashita E, Suga M, Narita H, Nakagawa A, Tajima S.

Proc Natl Acad Sci U S A. 2011 May 31;108(22):9055-9. doi: 10.1073/pnas.1019629108. Epub 2011 Apr 25.

PMID:
21518897
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Dnmt1 structure and function.

Svedružić ŽM.

Prog Mol Biol Transl Sci. 2011;101:221-54. doi: 10.1016/B978-0-12-387685-0.00006-8. Review.

PMID:
21507353
[PubMed - indexed for MEDLINE]
5.

Common variants in P2RY11 are associated with narcolepsy.

Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, Winkelmann J, Plazzi G, Nevsimalova S, Hong SC, Honda Y, Honda M, Högl B, Ton TG, Montplaisir J, Bourgin P, Kemlink D, Huang YS, Warby S, Einen M, Eshragh JL, Miyagawa T, Desautels A, Ruppert E, Hesla PE, Poli F, Pizza F, Frauscher B, Jeong JH, Lee SP, Strohl KP, Longstreth WT Jr, Kvale M, Dobrovolna M, Ohayon MM, Nepom GT, Wichmann HE, Rouleau GA, Gieger C, Levinson DF, Gejman PV, Meitinger T, Peppard P, Young T, Jennum P, Steinman L, Tokunaga K, Kwok PY, Risch N, Hallmayer J, Mignot E.

Nat Genet. 2011 Jan;43(1):66-71. doi: 10.1038/ng.734. Epub 2010 Dec 19. Erratum in: Nat Genet. 2011 Oct;43(10):1040.

PMID:
21170044
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

The Sequence Alignment/Map format and SAMtools.

Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R; 1000 Genome Project Data Processing Subgroup.

Bioinformatics. 2009 Aug 15;25(16):2078-9. doi: 10.1093/bioinformatics/btp352. Epub 2009 Jun 8.

PMID:
19505943
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Cutting edge: TCR stimulation is sufficient for induction of Foxp3 expression in the absence of DNA methyltransferase 1.

Josefowicz SZ, Wilson CB, Rudensky AY.

J Immunol. 2009 Jun 1;182(11):6648-52. doi: 10.4049/jimmunol.0803320.

PMID:
19454658
[PubMed - indexed for MEDLINE]
Free Article
8.

Fast and accurate short read alignment with Burrows-Wheeler transform.

Li H, Durbin R.

Bioinformatics. 2009 Jul 15;25(14):1754-60. doi: 10.1093/bioinformatics/btp324. Epub 2009 May 18.

PMID:
19451168
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Narcolepsy is strongly associated with the T-cell receptor alpha locus.

Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SC, Honda Y, Honda M, Högl B, Longstreth WT Jr, Montplaisir J, Kemlink D, Einen M, Chen J, Musone SL, Akana M, Miyagawa T, Duan J, Desautels A, Erhardt C, Hesla PE, Poli F, Frauscher B, Jeong JH, Lee SP, Ton TG, Kvale M, Kolesar L, Dobrovolná M, Nepom GT, Salomon D, Wichmann HE, Rouleau GA, Gieger C, Levinson DF, Gejman PV, Meitinger T, Young T, Peppard P, Tokunaga K, Kwok PY, Risch N, Mignot E.

Nat Genet. 2009 Jun;41(6):708-11. doi: 10.1038/ng.372. Epub 2009 May 3. Erratum in: Nat Genet. 2009 Jul;41(7):859. Hong, Sheng Seung-Chul [corrected to Hong, Seung-Chul].

PMID:
19412176
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Ancora: a web resource for exploring highly conserved noncoding elements and their association with developmental regulatory genes.

Engström PG, Fredman D, Lenhard B.

Genome Biol. 2008;9(2):R34. doi: 10.1186/gb-2008-9-2-r34. Epub 2008 Feb 15.

PMID:
18279518
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Dnmt1 deficiency promotes CAG repeat expansion in the mouse germline.

Dion V, Lin Y, Hubert L Jr, Waterland RA, Wilson JH.

Hum Mol Genet. 2008 May 1;17(9):1306-17. doi: 10.1093/hmg/ddn019. Epub 2008 Feb 5.

PMID:
18252747
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Hypocretin deficiency in familial symptomatic narcolepsy.

Melberg A, Ripley B, Lin L, Hetta J, Mignot E, Nishino S.

Ann Neurol. 2001 Jan;49(1):136-7. No abstract available.

PMID:
11198287
[PubMed - indexed for MEDLINE]
13.

A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains.

Peyron C, Faraco J, Rogers W, Ripley B, Overeem S, Charnay Y, Nevsimalova S, Aldrich M, Reynolds D, Albin R, Li R, Hungs M, Pedrazzoli M, Padigaru M, Kucherlapati M, Fan J, Maki R, Lammers GJ, Bouras C, Kucherlapati R, Nishino S, Mignot E.

Nat Med. 2000 Sep;6(9):991-7.

PMID:
10973318
[PubMed - indexed for MEDLINE]
14.

Hereditary sensory neuropathy with deafness and dementia: a clinical and neuroimaging study.

Hojo K, Imamura T, Takanashi M, Ishii K, Sasaki M, Imura S, Ozono R, Takatsuki Y, Takauchi S, Mori E.

Eur J Neurol. 1999 May;6(3):357-61.

PMID:
10210919
[PubMed - indexed for MEDLINE]
15.

Autosomal dominant cerebellar ataxia deafness and narcolepsy.

Melberg A, Hetta J, Dahl N, Nennesmo I, Bengtsson M, Wibom R, Grant C, Gustavson KH, Lundberg PO.

J Neurol Sci. 1995 Dec;134(1-2):119-29.

PMID:
8747854
[PubMed - indexed for MEDLINE]
16.

Hereditary sensory neuropathy with sensorineural deafness and early-onset dementia.

Wright A, Dyck PJ.

Neurology. 1995 Mar;45(3 Pt 1):560-2.

PMID:
7898717
[PubMed - indexed for MEDLINE]

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