Many hypotheses but no replication for the association between PDE4D and strokepp1091 - 1092 Jonathan Rosand, Nick Bayley, Natalia Rost & Paul I W de Bakker doi:10.1038/ng1006-1091 Full text|PDF
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Reply to "Many hypotheses but no replication for the association between PDE4D and stroke"pp1092 - 1093 Jeffrey R Gulcher, Augustine Kong, Solveig Gretarsdottir, Gudmar Thorleifsson & Kari Stefansson doi:10.1038/ng1006-1092 Full text|PDF
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Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataractpp1111 - 1113 Federico Zara, Roberta Biancheri, Claudio Bruno, Laura Bordo, Stefania Assereto, Elisabetta Gazzerro, Federica Sotgia, Xiao Bo Wang, Stefania Gianotti, Silvia Stringara, Marina Pedemonte, Graziella Uziel, Andrea Rossi, Angelo Schenone, Paolo Tortori-Donati, Marjo S van der Knaap, Michael P Lisanti & Carlo Minetti Published online: 03 September 2006|doi:10.1038/ng1870 Abstract|Full text|PDF
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Lamin B1 duplications cause autosomal dominant leukodystrophypp1114 - 1123 Quasar S Padiath, Kazumasa Saigoh, Raphael Schiffmann, Hideaki Asahara, Takeshi Yamada, Anulf Koeppen, Kirk Hogan, Louis J Ptáek & Ying-Hui Fu Published online: 03 September 2006|doi:10.1038/ng1872 Abstract|Full text|PDF
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Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubulepp1124 - 1132 Maria D Lalioti, Junhui Zhang, Heather M Volkman, Kristopher T Kahle, Kristin E Hoffmann, Hakan R Toka, Carol Nelson-Williams, David H Ellison, Richard Flavell, Carmen J Booth, Yin Lu, David S Geller & Richard P Lifton Published online: 10 September 2006|doi:10.1038/ng1877 Abstract|Full text|PDF
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iASPP preferentially binds p53 proline-rich region and modulates apoptotic function of codon 72–polymorphic p53pp1133 - 1141 Daniele Bergamaschi, Yardena Samuels, Alexandra Sullivan, Marketa Zvelebil, Hilde Breyssens, Andrea Bisso, Giannino Del Sal, Nelofer Syed, Paul Smith, Milena Gasco, Tim Crook & Xin Lu Published online: 10 September 2006|doi:10.1038/ng1879 Abstract|Full text|PDF
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Delineation of a Fat tumor suppressor pathwaypp1142 - 1150 Eunjoo Cho, Yongqiang Feng, Cordelia Rauskolb, Sushmita Maitra, Rick Fehon & Kenneth D Irvine Published online: 17 September 2006|doi:10.1038/ng1887 Abstract|Full text|PDF
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Biological function of unannotated transcription during the early development of Drosophila melanogasterpp1151 - 1158 J Robert Manak, Sujit Dike, Victor Sementchenko, Philipp Kapranov, Frederic Biemar, Jeff Long, Jill Cheng, Ian Bell, Srinka Ghosh, Antonio Piccolboni & Thomas R Gingeras Published online: 03 September 2006|doi:10.1038/ng1875 Abstract|Full text|PDF
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Quantitative and predictive model of transcriptional control of the Drosophila melanogaster even skipped genepp1159 - 1165 Hilde Janssens, Shuling Hou, Johannes Jaeger, Ah-Ram Kim, Ekaterina Myasnikova, David Sharp & John Reinitz Published online: 17 September 2006|doi:10.1038/ng1886 Abstract|Full text|PDF
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A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHCpp1166 - 1172 Paul I W de Bakker, Gil McVean, Pardis C Sabeti, Marcos M Miretti, Todd Green, Jonathan Marchini, Xiayi Ke, Alienke J Monsuur, Pamela Whittaker, Marcos Delgado, Jonathan Morrison, Angela Richardson, Emily C Walsh, Xiaojiang Gao, Luana Galver, John Hart, David A Hafler, Margaret Pericak-Vance, John A Todd, Mark J Daly, John Trowsdale, Cisca Wijmenga, Tim J Vyse, Stephan Beck, Sarah Shaw Murray, Mary Carrington, Simon Gregory, Panos Deloukas & John D Rioux Published online: 24 September 2006|doi:10.1038/ng1885 Abstract|Full text|PDF
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A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degenerationpp1173 - 1177 Anne E Hughes, Nick Orr, Hossein Esfandiary, Martha Diaz-Torres, Timothy Goodship & Usha Chakravarthy Published online: 24 September 2006|doi:10.1038/ng1890 Abstract|Full text|PDF
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Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancerpp1178 - 1183 Tsun Leung Chan, Siu Tsan Yuen, Chi Kwan Kong, Yee Wai Chan, Annie SY Chan, Wai Fu Ng, Wai Yin Tsui, Michelle WS Lo, Wing Yip Tam, Vivian SW Li & Suet Yi Leung Published online: 03 September 2006|doi:10.1038/ng1866 Abstract|Full text|PDF
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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPasepp1184 - 1191 Alfredo Ramirez, André Heimbach, Jan Gründemann, Barbara Stiller, Dan Hampshire, L Pablo Cid, Ingrid Goebel, Ammar F Mubaidin, Abdul-Latif Wriekat, Jochen Roeper, Amir Al-Din, Axel M Hillmer, Meliha Karsak, Birgit Liss, C Geoffrey Woods, Maria I Behrens & Christian Kubisch Published online: 10 September 2006|doi:10.1038/ng1884 Abstract|Full text|PDF
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Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi traffickingpp1192 - 1197 Simeon A Boyadjiev, J Christopher Fromme, Jin Ben, Samuel S Chong, Christopher Nauta, David J Hur, George Zhang, Susan Hamamoto, Randy Schekman, Mariella Ravazzola, Lelio Orci & Wafaa Eyaid Published online: 17 September 2006|doi:10.1038/ng1876 Abstract|Full text|PDF
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Secretory COPII coat component Sec23a is essential for craniofacial chondrocyte maturationpp1198 - 1203 Michael R Lang, Lynne A Lapierre, Michael Frotscher, James R Goldenring & Ela W Knapik Published online: 17 September 2006|doi:10.1038/ng1880 Abstract|Full text|PDF
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Indian hedgehog is a major mediator of progesterone signaling in the mouse uteruspp1204 - 1209 Kevin Lee, JaeWook Jeong, Inseok Kwak, Cheng-Tai Yu, Beate Lanske, Desi W Soegiarto, Rune Toftgard, Ming-Jer Tsai, Sophia Tsai, John P Lydon & Francesco J DeMayo Published online: 03 September 2006|doi:10.1038/ng1874 Abstract|Full text|PDF
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Mammalian ultraconserved elements are strongly depleted among segmental duplications and copy number variantspp1216 - 1220 Adnan Derti, Frederick P Roth, George M Church & C-ting Wu Published online: 24 September 2006|doi:10.1038/ng1888 Abstract|Full text|PDF
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ek & Ying-Hui Fu
