An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression (English)
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In:
Human molecular genetics
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25
, 17
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3863-
;
2016
- Article (Journal) / Electronic Resource
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Title:An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression
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Contributors:Wyszynski, Asaf ( author ) / Hong, Chi-Chen ( author ) / Lam, Kristin ( author ) / Michailidou, Kyriaki ( author ) / Lytle, Christian ( author ) / Yao, Song ( author ) / Zhang, Yali ( author ) / Bolla, Manjeet K. ( author ) / Wang, Qin ( author ) / Dennis, Joe ( author )
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Published in:Human molecular genetics ; 25, 17 ; 3863-
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Publisher:
- New search for: Oxford University Press
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Publication date:2016-09-01
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 25, Issue 17
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.
- 3647
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Dystrophin contains multiple independent membrane-binding domainsZhao, Junling / Kodippili, Kasun / Yue, Yongping / Hakim, Chady H. / Wasala, Lakmini / Pan, Xiufang / Zhang, Keqing / Yang, Nora N. / Duan, Dongsheng / Lai, Yi et al. | 2016
- 3654
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An enhanced Q175 knock-in mouse model of Huntington disease with higher mutant huntingtin levels and accelerated disease phenotypesSouthwell, Amber L. / Smith-Dijak, Amy / Kay, Chris / Sepers, Marja / Villanueva, Erika B. / Parsons, Matthew P. / Xie, Yuanyun / Anderson, Lisa / Felczak, Boguslaw / Waltl, Sabine et al. | 2016
- 3676
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Molecular disturbance underlies to arrhythmogenic cardiomyopathy induced by transgene content, age and exercise in a truncated PKP2 mouse modelMoncayo-Arlandi, Javier / Guasch, Eduard / Sanz-de la Garza, Maria / Casado, Marta / Garcia, Nahuel Aquiles / Mont, Lluis / Sitges, Marta / Knöll, Ralph / Buyandelger, Byambajav / Campuzano, Oscar et al. | 2016
- 3689
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Sustained expression of FMR1 mRNA from reactivated fragile X syndrome alleles after treatment with small molecules that prevent trimethylation of H3K27Kumari, Daman / Usdin, Karen et al. | 2016
- 3699
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Coordinated movement, neuromuscular synaptogenesis and trans-synaptic signaling defects in Drosophila galactosemia modelsJumbo-Lucioni, Patricia P. / Parkinson, William M. / Kopke, Danielle L. / Broadie, Kendal et al. | 2016
- 3715
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Parent-of-origin tumourigenesis is mediated by an essential imprinted modifier in SDHD-linked paragangliomas: SLC22A18 and CDKN1C are candidate tumour modifiersHoekstra, Attje S / Addie, Ruben D. / Ras, Cor / Seifar, Reza M. / Ruivenkamp, Claudia A. / Briaire-de Bruijn, Inge H. / Hes, Frederik J. / Jansen, Jeroen C. / Corssmit, Eleonora P.M. / Corver, Willem E. et al. | 2016
- 3729
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Calcium dynamics change in degenerating cone photoreceptorsKulkarni, Manoj / Trifunovic, Dragana / Schubert, Timm / Euler, Thomas / Paquet-Durand, Francois et al. | 2016
- 3741
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Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signallingGregianin, Elisa / Pallafacchina, Giorgia / Zanin, Sofia / Crippa, Valeria / Rusmini, Paola / Poletti, Angelo / Fang, Mingyan / Li, Zhouxuan / Diano, Laura / Petrucci, Antonio et al. | 2016
- 3754
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Variant discovery and breakpoint region prediction for studying the human 22q11.2 deletion using BAC clone and whole genome sequencing analysisGuo, Xingyi / Delio, Maria / Haque, Nousin / Castellanos, Raquel / Hestand, Matthew S. / Vermeesch, Joris R. / Morrow, Bernice E. / Zheng, Deyou et al. | 2016
- 3768
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Neuromuscular junctions are pathological but not denervated in two mouse models of spinal bulbar muscular atrophyPoort, Jessica E. / Rheuben, Mary B. / Breedlove, S. Marc / Jordan, Cynthia L. et al. | 2016
- 3784
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Progressive development of renal cysts in glycogen storage disease type IGjorgjieva, Monika / Raffin, Margaux / Duchampt, Adeline / Perry, Ariane / Stefanutti, Anne / Brevet, Marie / Tortereau, Antonin / Dubourg, Laurence / Hubert-Buron, Aurélie / Mabille, Mylène et al. | 2016
- 3798
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Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromesKamaludin, Ain A. / Smolarchuk, Christa / Bischof, Jocelyn M. / Eggert, Rachelle / Greer, John J. / Ren, Jun / Lee, Joshua J. / Yokota, Toshifumi / Berry, Fred B. / Wevrick, Rachel et al. | 2016
- 3810
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Lack of P4H-TM in mice results in age-related retinal and renal alterationsLeinonen, Henri / Rossi, Maarit / Salo, Antti M. / Tiainen, Päivi / Hyvärinen, Jaana / Pitkänen, Marja / Sormunen, Raija / Miinalainen, Ilkka / Zhang, Chi / Soininen, Raija et al. | 2016
- 3824
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SHOC2 subcellular shuttling requires the KEKE motif-rich region and N-terminal leucine-rich repeat domain and impacts on ERK signallingMotta, Marialetizia / Chillemi, Giovanni / Fodale, Valentina / Cecchetti, Serena / Coppola, Simona / Stipo, Silvia / Cordeddu, Viviana / Macioce, Pompeo / Gelb, Bruce D. / Tartaglia, Marco et al. | 2016
- 3836
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The progressive ankylosis protein ANK facilitates clathrin- and adaptor-mediated membrane traffic at the trans-Golgi network-to-endosome interfaceSeifert, Wenke / Posor, York / Schu, Peter / Stenbeck, Gudrun / Mundlos, Stefan / Klaassen, Sabine / Nürnberg, Peter / Haucke, Volker / Kornak, Uwe / Kühnisch, Jirko et al. | 2016
- 3849
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Identification of genetic modifiers of age-at-onset for familial Parkinsons diseaseHill-Burns, Erin M. / Ross, Owen A. / Wissemann, William T. / Soto-Ortolaza, Alexandra I. / Zareparsi, Sepideh / Siuda, Joanna / Lynch, Timothy / Wszolek, Zbigniew K. / Silburn, Peter A. / Mellick, George D. et al. | 2016
- 3863
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An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expressionWyszynski, Asaf / Hong, Chi-Chen / Lam, Kristin / Michailidou, Kyriaki / Lytle, Christian / Yao, Song / Zhang, Yali / Bolla, Manjeet K. / Wang, Qin / Dennis, Joe et al. | 2016
- 3877
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Serum gamma-glutamyl transferase and risk of type 2 diabetes in the general Korean population: a Mendelian randomization studyLee, Youn Sue / Cho, Yoonsu / Burgess, Stephen / Davey Smith, George / Relton, Caroline L. / Shin, So-Youn / Shin, Min-Jeong et al. | 2016
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Front Cover| 2016
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Editorial Board| 2016
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Subscriptions Page| 2016
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Table of Contents| 2016