The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence (English)
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In:
Human molecular genetics
;
16
, 6
;
600-
;
2007
- Article (Journal) / Electronic Resource
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Title:The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence
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Contributors:Mekel-Bobrov, Nitzan ( author ) / Posthuma, Danielle ( author ) / Gilbert, Sandra L. ( author ) / Lind, Penelope ( author ) / Gosso, M. Florencia ( author ) / Luciano, Michelle ( author ) / Harris, Sarah E. ( author ) / Bates, Timothy C. ( author ) / Polderman, Tinca J.C. ( author ) / Whalley, Lawrence J. ( author )
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Published in:Human molecular genetics ; 16, 6 ; 600-
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Publisher:
- New search for: Oxford University Press
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Publication date:2007-03-15
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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 16, Issue 6
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.
- 579
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Association of IRF5 in UK SLE families identifies a variant involved in polyadenylationGraham, Deborah S. Cunninghame / Manku, Harinder / Wagner, Susanne / Reid, Julia / Timms, Kirsten / Gutin, Alexander / Lanchbury, Jerry S. / Vyse, Tim J. et al. | 2007
- 592
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Polymorphisms in pro- and anti-inflammatory cytokine genes and susceptibility to atherosclerosis: a pathological study of 1503 consecutive autopsy casesOda, Kanae / Tanaka, Noriko / Arai, Tomio / Araki, Jungo / Song, Yixuan / Zhang, Ling / Kuchiba, Aya / Hosoi, Takayuki / Shirasawa, Takuji / Muramatsu, Masaaki et al. | 2007
- 600
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The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligenceMekel-Bobrov, Nitzan / Posthuma, Danielle / Gilbert, Sandra L. / Lind, Penelope / Gosso, M. Florencia / Luciano, Michelle / Harris, Sarah E. / Bates, Timothy C. / Polderman, Tinca J.C. / Whalley, Lawrence J. et al. | 2007
- 609
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Glaucoma-causing myocilin mutants require the Peroxisomal targeting signal-1 receptor (PTS1R) to elevate intraocular pressureShepard, Allan R. / Jacobson, Nasreen / Millar, J. Cameron / Pang, Iok-Hou / Steely, H. Thomas / Searby, Charles C. / Sheffield, Val C. / Stone, Edwin M. / Clark, Abbot F. et al. | 2007
- 618
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Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II)Fujita, Eriko / Kouroku, Yoriko / Isoai, Atsushi / Kumagai, Hiromichi / Misutani, Akifumi / Matsuda, Chie / Hayashi, Yukiko K. / Momoi, Takashi et al. | 2007
- 630
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Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarctionHata, Jun / Matsuda, Koichi / Ninomiya, Toshiharu / Yonemoto, Koji / Matsushita, Tomonaga / Ohnishi, Yozo / Saito, Susumu / Kitazono, Takanari / Ibayashi, Setsuro / Iida, Mitsuo et al. | 2007
- 640
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FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null miceDeng, Vivianne / Matagne, Valerie / Banine, Fatima / Frerking, Matthew / Ohliger, Patricia / Budden, Sarojini / Pevsner, Jonathan / Dissen, Gregory A. / Sherman, Larry S. / Ojeda, Sergio R. et al. | 2007
- 651
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Over-expression of alpha-synuclein in human neural progenitors leads to specific changes in fate and differentiationSchneider, Bernard L. / Seehus, Corey R. / Capowski, Elizabeth E. / Aebischer, Patrick / Zhang, Su-Chun / Svendsen, Clive N. et al. | 2007
- 667
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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexiaAnthoni, Heidi / Zucchelli, Marco / Matsson, Hans / Müller-Myhsok, Bertram / Fransson, Ingegerd / Schumacher, Johannes / Massinen, Satu / Onkamo, Päivi / Warnke, Andreas / Griesemann, Heide et al. | 2007
- 678
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Leucine-rich repeat kinase 2 associates with lipid raftsHatano, Taku / Kubo, Shin-ichiro / Imai, Satoshi / Maeda, Masahiro / Ishikawa, Kiyoshi / Mizuno, Yoshikuni / Hattori, Nobutaka et al. | 2007
- 691
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15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disordersHogart, Amber / Nagarajan, Raman P. / Patzel, Katherine A. / Yasui, Dag H. / LaSalle, Janine M. et al. | 2007
- 704
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High density SNP association study of a major autism linkage region on chromosome 17Stone, Jennifer L. / Merriman, Barry / Cantor, Rita M. / Geschwind, Daniel H. / Nelson, Stanley F. et al. | 2007