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A common genetic variant within SCN10A modulates cardiac SCN5A expression.
Published in:
Journal of Clinical Investigation, 2014, v. 124, n. 4, p. 1844, doi. 10.1172/JCI73140
By:
- van den Boogaard, Malou;
- Smemo, Scott;
- Burnicka-Turek, Ozanna;
- Arnolds, David E.;
- van de Werken, Harmen J. G.;
- Klous, Petra;
- McKean, David;
- Muehlschlegel, Jochen D.;
- Moosmann, Julia;
- Okan Toka;
- Xinan H. Yang;
- Koopmann, Tamara T.;
- Adriaens, Michiel E.;
- Bezzina, Connie R.;
- de Laat, Wouter;
- Seidman, Christine;
- Seidman, J. G.;
- Christoffels, Vincent M.;
- Nobrega, Marcelo A.;
- Barnett, Phil
Publication type:
Article
TBX5 drives Scn5a expression to regulate cardiac conduction system function.
Published in:
Journal of Clinical Investigation, 2012, v. 122, n. 7, p. 2509, doi. 10.1172/JCI62617
By:
- Arnolds, David E.;
- Liu, Fang;
- Fahrenbach, John P.;
- Kim, Gene H.;
- Schillinger, Kurt J.;
- Smemo, Scott;
- McNally, Elizabeth M.;
- Nobrega, Marcelo A.;
- Pate, Vickas V.;
- Moskowitz, Ivan P.
Publication type:
Article
Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function.
Published in:
2011
By:
- Tao Shen;
- Aneas, Ivy;
- Sakabe, Noboru;
- Dirschinger, Ralf J.;
- Gang Wang;
- Smemo, Scott;
- Westlund, John M.;
- Cheng, Hongqiang;
- Dalton, Nancy;
- Gu, Yusu;
- Boogerd, Cornelis J.;
- Chen-leng Cai;
- Peterson, Kirk;
- Ju Chen;
- Nobrega, Marcelo A.;
- Evans, Sylvia M.;
- Shen, Tao;
- Wang, Gang;
- Cai, Chen-leng;
- Chen, Ju
Publication type:
journal article
P1-341: Are common variants in APP risk factors for late-onset Alzheimer’s disease?
Published in:
2006
By:
- Nowotny, Petra;
- Simcock, Xavier;
- Hinrichs, Anthony L.;
- Bertelsen, Sarah;
- Smemo, Scott;
- Mayo, Kevin;
- Kauwe, John S.K.;
- Morris, John C.;
- Goate, Alison
Publication type:
Abstract
O2-02-07: Genetic variants on chromosome 9 are associated with late-onset Alzheimer’s disease, variation in allele-specific gene expression, and differential apoptotic response
Published in:
2006
By:
- Li, Yonghong;
- Grupe, Andrew;
- Rowland, Charles;
- Nowotny, Petra;
- Kauwe, John S.K.;
- Smemo, Scott;
- Hinrichs, Anthony;
- Tacey, Kristina;
- Kwok, Shirley;
- Catanese, Joseph;
- Sninsky, John;
- White, Thomas J.;
- Hollingworth, Paul;
- Harris, Sandra L.;
- Levine, Arnold;
- Wavrant-De Vrieze, Fabienne;
- Hardy, John;
- O’Donovan, Michael;
- Lovestone, Simon;
- Morris, John
Publication type:
Abstract
P1-341: Are common variants in APP risk factors for late-onset Alzheimer’s disease?
Published in:
2006
By:
- Nowotny, Petra;
- Simcock, Xavier;
- Hinrichs, Anthony L.;
- Bertelsen, Sarah;
- Smemo, Scott;
- Mayo, Kevin;
- Kauwe, John S.K.;
- Morris, John C.;
- Goate, Alison
Publication type:
Abstract
O2-02-07: Genetic variants on chromosome 9 are associated with late-onset Alzheimer’s disease, variation in allele-specific gene expression, and differential apoptotic response
Published in:
2006
By:
- Li, Yonghong;
- Grupe, Andrew;
- Rowland, Charles;
- Nowotny, Petra;
- Kauwe, John S.K.;
- Smemo, Scott;
- Hinrichs, Anthony;
- Tacey, Kristina;
- Kwok, Shirley;
- Catanese, Joseph;
- Sninsky, John;
- White, Thomas J.;
- Hollingworth, Paul;
- Harris, Sandra L.;
- Levine, Arnold;
- Wavrant-De Vrieze, Fabienne;
- Hardy, John;
- O’Donovan, Michael;
- Lovestone, Simon;
- Morris, John
Publication type:
Abstract
α-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer’s disease.
Published in:
NeuroMolecular Medicine, 2004, v. 5, n. 2, p. 133, doi. 10.1385/NMM:5:2:133
By:
- Busby, Victoria;
- Goossens, Steven;
- Nowotny, Petra;
- Hamilton, Gillian;
- Smemo, Scott;
- Harold, Denise;
- Turic, Dragana;
- Jehu, Luke;
- Myers, Amanda;
- Womick, Meredith;
- Woo, Daniel;
- Compton, Danielle;
- Doil, Lisa;
- Tacey, Kristina;
- Lau, Kit;
- Al-Saraj, Safa;
- Killick, Richard;
- Pickering-Brown, Stuart;
- Moore, Pamela;
- Hollingworth, Paul
Publication type:
Article
FTO-mediated formation of N<sup>6</sup>-hydroxymethyladenosine and N<sup>6</sup>-formyladenosine in mammalian RNA.
Published in:
Nature Communications, 2013, v. 4, n. 4, p. 1798, doi. 10.1038/ncomms2822
By:
- Fu, Ye;
- Jia, Guifang;
- Pang, Xueqin;
- Wang, Richard N.;
- Wang, Xiao;
- Li, Charles J.;
- Smemo, Scott;
- Dai, Qing;
- Bailey, Kathleen A.;
- Nobrega, Marcelo A.;
- Han, Ke-Li;
- Cui, Qiang;
- He, Chuan
Publication type:
Article
Ubiquilin 1 polymorphisms are not associated with late‐onset Alzheimer's disease.
Published in:
Annals of Neurology, 2006, v. 59, n. 1, p. 21, doi. 10.1002/ana.20673
By:
- Scott Smemo;
- Petra Nowotny;
- Anthony L. Hinrichs;
- John S. K. Kauwe;
- Sara Cherny;
- Katherine Erickson;
- Amanda J. Myers;
- Mona Kaleem;
- Lauren Marlowe;
- Alison M. Gibson;
- Paul Hollingworth;
- Michael C. O'Donovan;
- Chris M. Morris;
- Peter Holmans;
- Simon Lovestone;
- John C. Morris;
- Leon Thal;
- Yonghong Li;
- Andrew Grupe;
- John Hardy
Publication type:
Article
Catenin delta-1 (CTNND1) phosphorylation controls the mesenchymal to epithelial transition in astrocytic tumors.
Published in:
Human Molecular Genetics, 2016, v. 25, n. 19, p. 4201, doi. 10.1093/hmg/ddw253
By:
- Yang, Jin;
- Bassuk, Alexander G.;
- Merl-Pham, Juliane;
- Chun-Wei Hsu;
- Colgan, Diana F.;
- Xiaorong Li;
- Kit Sing Au;
- Lijuan Zhang;
- Smemo, Scott;
- Justus, Sally;
- Yasunori Nagahama;
- Grossbach, Andrew J.;
- Howard III, Matthew A.;
- Hiroto Kawasaki;
- Feldstein, Neil A.;
- Dobyns, William B.;
- Northrup, Hope;
- Hauck, Stefanie M.;
- Ueffing, Marius;
- Mahajan, Vinit B.
Publication type:
Article
Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.
Published in:
Human Molecular Genetics, 2012, v. 21, n. 14, p. 3255, doi. 10.1093/hmg/dds165
By:
- Smemo, Scott;
- Campos, Luciene C.;
- Moskowitz, Ivan P.;
- Krieger, José E.;
- Pereira, Alexandre C.;
- Nobrega, Marcelo A.
Publication type:
Article
Obesity-associated variants within FTO form long-range functional connections with IRX3.
Published in:
Nature, 2014, v. 507, n. 7492, p. 371, doi. 10.1038/nature13138
By:
- Smemo, Scott;
- Tena, Juan J.;
- Kim, Kyoung-Han;
- Gamazon, Eric R.;
- Sakabe, Noboru J.;
- Gómez-Marín, Carlos;
- Aneas, Ivy;
- Credidio, Flavia L.;
- Sobreira, Débora R.;
- Wasserman, Nora F.;
- Lee, Ju Hee;
- Puviindran, Vijitha;
- Tam, Davis;
- Shen, Michael;
- Son, Joe Eun;
- Vakili, Niki Alizadeh;
- Sung, Hoon-Ki;
- Naranjo, Silvia;
- Acemel, Rafael D.;
- Manzanares, Miguel
Publication type:
Article
Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1 polymorphisms.
Published in:
Molecular Neurodegeneration, 2007, v. 2, p. 1, doi. 10.1186/1750-1326-2-7
By:
- Wahrle, Suzanne E.;
- Shah, Aarti R.;
- Fagan, Anne M.;
- Smemo, Scott;
- Kauwe, John S. K.;
- Grupe, Andrew;
- Hinrichs, Anthony;
- Mayo, Kevin;
- Hong Jiang;
- Thal, Leon J.;
- Goate, Alison M.;
- Holtzman, David M.
Publication type:
Article
DAPK1 variants are associated with Alzheimer's disease and allele-specific expression.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2560, doi. 10.1093/hmg/ddl178
By:
- Li, Yonghong;
- Grupe, Andrew;
- Rowland, Charles;
- Nowotny, Petra;
- Kauwe, John S.K.;
- Smemo, Scott;
- Hinrichs, Anthony;
- Tacey, Kristina;
- Toombs, Timothy A.;
- Kwok, Shirley;
- Catanese, Joseph;
- White, Thomas J.;
- Maxwell, Taylor J.;
- Hollingworth, Paul;
- Abraham, Richard;
- Rubinsztein, David C.;
- Brayne, Carol;
- Wavrant-De Vrièze, Fabienne;
- Hardy, John;
- O'Donovan, Michael
Publication type:
Article

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