Epigenome-wide association study in the European Prospective Investigation into Cancer and Nutrition (EPIC-Turin) identifies novel genetic loci associated with smoking (English)
- New search for: Shenker, Natalie S.
- New search for: Polidoro, Silvia
- New search for: van Veldhoven, Karin
- New search for: Sacerdote, Carlotta
- New search for: Ricceri, Fulvio
- New search for: Birrell, Mark A.
- New search for: Belvisi, Maria G.
- New search for: Brown, Robert
- New search for: Vineis, Paolo
- New search for: Flanagan, James M.
- New search for: Shenker, Natalie S.
- New search for: Polidoro, Silvia
- New search for: van Veldhoven, Karin
- New search for: Sacerdote, Carlotta
- New search for: Ricceri, Fulvio
- New search for: Birrell, Mark A.
- New search for: Belvisi, Maria G.
- New search for: Brown, Robert
- New search for: Vineis, Paolo
- New search for: Flanagan, James M.
In:
Human molecular genetics
;
22
, 5
;
843-
;
2013
- Article (Journal) / Electronic Resource
-
Title:Epigenome-wide association study in the European Prospective Investigation into Cancer and Nutrition (EPIC-Turin) identifies novel genetic loci associated with smoking
-
Contributors:Shenker, Natalie S. ( author ) / Polidoro, Silvia ( author ) / van Veldhoven, Karin ( author ) / Sacerdote, Carlotta ( author ) / Ricceri, Fulvio ( author ) / Birrell, Mark A. ( author ) / Belvisi, Maria G. ( author ) / Brown, Robert ( author ) / Vineis, Paolo ( author ) / Flanagan, James M. ( author )
-
Published in:Human molecular genetics ; 22, 5 ; 843-
-
Publisher:
- New search for: Oxford University Press
-
Publication date:2013-03-01
-
ISSN:
-
DOI:
-
Type of media:Article (Journal)
-
Type of material:Electronic Resource
-
Language:English
-
Source:
Table of contents – Volume 22, Issue 5
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 843
-
Epigenome-wide association study in the European Prospective Investigation into Cancer and Nutrition (EPIC-Turin) identifies novel genetic loci associated with smokingShenker, Natalie S. / Polidoro, Silvia / van Veldhoven, Karin / Sacerdote, Carlotta / Ricceri, Fulvio / Birrell, Mark A. / Belvisi, Maria G. / Brown, Robert / Vineis, Paolo / Flanagan, James M. et al. | 2013
- 852
-
Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndromeBalemans, Monique C.M. / Nadif Kasri, Nael / Kopanitsa, Maksym V. / Afinowi, Nurudeen O. / Ramakers, Ger / Peters, Theo A. / Beynon, Andy J. / Janssen, Sanne M. / van Summeren, Rik C.J. / Eeftens, Jorine M. et al. | 2013
- 867
-
Loss of cIAP1 attenuates soleus muscle pathology and improves diaphragm function in mdx miceEnwere, Emeka K. / Boudreault, Louise / Holbrook, Janelle / Timusk, Kristen / Earl, Nathalie / LaCasse, Eric / Renaud, Jean-Marc / Korneluk, Robert G. et al. | 2013
- 879
-
Zic3 is required in the extra-cardiac perinodal region of the lateral plate mesoderm for left-right patterning and heart developmentJiang, Zhengxin / Zhu, Lirong / Hu, Lingyun / Slesnick, Timothy C. / Pautler, Robia G. / Justice, Monica J. / Belmont, John W. et al. | 2013
- 890
-
Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7Furrer, Stephanie A. / Waldherr, Sarah M. / Mohanachandran, Mathini S. / Baughn, Travis D. / Nguyen, Kien-Thiet / Sopher, Bryce L. / Damian, Vincent A. / Garden, Gwenn A. / La Spada, Albert R. et al. | 2013
- 904
-
MicroRNA-21 silencing enhances the cytotoxic effect of the antiangiogenic drug sunitinib in glioblastomaCosta, Pedro M. / Cardoso, Ana L. / Nóbrega, Clévio / Pereira de Almeida, Luís F. / Bruce, Jeffrey N. / Canoll, Peter / Pedroso de Lima, Maria C. et al. | 2013
- 919
-
Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial cleftsVogelaar, Ingrid P. / Figueiredo, Joana / van Rooij, Iris A.L.M. / Simões-Correia, Joana / van der Post, Rachel S. / Melo, Soraia / Seruca, Raquel / Carels, Carine E.L. / Ligtenberg, Marjolijn J.L. / Hoogerbrugge, Nicoline et al. | 2013
- 927
-
GLRB is the third major gene of effect in hyperekplexiaChung, Seo-Kyung / Bode, Anna / Cushion, Thomas D. / Thomas, Rhys H. / Hunt, Charlotte / Wood, Sian-Elin / Pickrell, William O. / Drew, Cheney J.G. / Yamashita, Sumimasa / Shiang, Rita et al. | 2013
- 941
-
X-linked dystonia parkinsonism syndrome (XDP, lubag): disease-specific sequence change DSC3 in TAF1/DYT3 affects genes in vesicular transport and dopamine metabolismHerzfeld, Thilo / Nolte, Dagmar / Grznarova, Maria / Hofmann, Andrea / Schultze, Joachim L. / Müller, Ulrich et al. | 2013
- 952
-
LKB1-regulated adaptive mechanisms are essential for neuronal survival following mitochondrial dysfunctionGermain, Marc / Nguyen, Angela P. / Khacho, Mireille / Patten, David A. / Screaton, Robert A. / Park, David S. / Slack, Ruth S. et al. | 2013
- 963
-
Functional characterization of Klippel-Trenaunay syndrome gene AGGF1 identifies a novel angiogenic signaling pathway for specification of vein differentiation and angiogenesis during embryogenesisChen, Di / Li, Lei / Tu, Xin / Yin, Zhan / Wang, Qing et al. | 2013
- 977
-
Heterozygous inactivation of the Nf1 gene in myeloid cells enhances neointima formation via a rosuvastatin-sensitive cellular pathwayStansfield, Brian K. / Bessler, Waylan K. / Mali, Raghuveer / Mund, Julie A. / Downing, Brandon / Li, Fang / Sarchet, Kara N. / DiStasi, Matthew R. / Conway, Simon J. / Kapur, Reuben et al. | 2013
- 989
-
Defective mitochondrial disulfide relay system, altered mitochondrial morphology and function in Huntington's diseaseNapoli, Eleonora / Wong, Sarah / Hung, Connie / Ross-Inta, Catherine / Bomdica, Prithvi / Giulivi, Cecilia et al. | 2013
- 1005
-
Hedgehog regulates Norrie disease protein to drive neural progenitor self-renewalMcNeill, Brian / Mazerolle, Chantal / Bassett, Erin A. / Mears, Alan J. / Ringuette, Randy / Lagali, Pamela / Picketts, David J. / Paes, Kim / Rice, Dennis / Wallace, Valerie A. et al. | 2013
- 1017
-
Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenanceHumble, Margaret M. / Young, Matthew J. / Foley, Julie F. / Pandiri, Arun R. / Travlos, Greg S. / Copeland, William C. et al. | 2013
- 1026
-
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and miceBeck, Tyler F. / Veenma, Danielle / Shchelochkov, Oleg A. / Yu, Zhiyin / Kim, Bum Jun / Zaveri, Hitisha P. / van Bever, Yolande / Choi, Sunju / Douben, Hannie / Bertin, Terry K. et al. | 2013
- 1039
-
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's diseaseHolmans, Peter / Moskvina, Valentina / Jones, Lesley / Sharma, Manu / The International Parkinson's Disease Genomics Consortium (IPDGC), / Vedernikov, Alexey / Buchel, Finja / Sadd, Mohamad / Bras, Jose M. / Bettella, Francesco et al. | 2013
- 1050
-
FTO, obesity and the adolescent brainMelka, Melkaye G. / Gillis, Jesse / Bernard, Manon / Abrahamowicz, Michal / Chakravarty, M. Mallar / Leonard, Gabriel T. / Perron, Michel / Richer, Louis / Veillette, Suzanne / Banaschewski, Tobias et al. | 2013
- 1059
-
Interleukin-1 alpha blockade prevents hyperkeratosis in an in vitro model of lamellar ichthyosisO'Shaughnessy, Ryan F.L. / Chaudhury, Ishaan / Harper, John I. et al. | 2013
- NP-c
-
Subscription Page| 2013
- NP
-
Contents Page| 2013
- NP-b
-
Editorial Board| 2013
- NP-a
-
Cover Page| 2013