string(238) "select * FROM articoli_opac WHERE fonte <> 'ISI' AND fonte='ACNP' AND fasc_anno_pubbl='2006' AND fasc_issn='00029297' order by level desc, fasc_key desc, NULLIF(regexp_replace(pagina_ini, E'\\D', '', 'g'), '')::int asc offset 25 limit 25" ACNP - Italian Periodicals Catalogue
Results: 1-25 | 26-50 | 51-75 | 76-100 | >>    

Articles table of contents

Results : 26-50/126
Polarity and Temporality of High-Resolution Y-Chromosome Distributions in India Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence of Central Asian Pastoralists
Authors: Sengupta, Sanghamitr Zhivotovsky, Lev A. King, Roy Mehdi, S.Q. Edmonds, Christopher A. Chow, Cheryl-Emiliane T Lin, Alice A. Mitra, Mitashree Sil, Samir K. Ramesh, A. Usha Rani, M.V. Thakur, Chitra M. Cavalli-Sforza, Luca L. Majumder, Partha P. Underhill, Peter A.
Journal: American journal of human genetics
Citation: Sengupta, Sanghamitr et al., Polarity and Temporality of High-Resolution Y-Chromosome Distributions in India Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence of Central Asian Pastoralists, American journal of human genetics , 78(2), 2006, pp. 202-221
Evidence That Translation Reinitiation Leads to a Partially Functional Menkes Protein Containing Two Copper-Binding Sites
Authors: Paulsen, Marianne Lund, Connie Akram, Zarqa Winther, Jacob R. Horn, Nina Møller, Lisbeth Birk
Journal: American journal of human genetics
Citation: Paulsen, Marianne et al., Evidence That Translation Reinitiation Leads to a Partially Functional Menkes Protein Containing Two Copper-Binding Sites, American journal of human genetics , 79(2), 2006, pp. 214-229
A Novel Framework for Sib Pair Linkage Analysis
Authors: Poznik, David Adamska, Katarzyna Xu, Xin Krolewski, Andrzej S. Rogus, Jhon J.
Journal: American journal of human genetics
Citation: Poznik, David et al., A Novel Framework for Sib Pair Linkage Analysis, American journal of human genetics , 78(2), 2006, pp. 222-230
A Geographically Explicit Genetic Model of Worldwide Human-Settlement History
Authors: Liu, Hau Prugnolle, Frank Manica, Andrea Balloux, François
Journal: American journal of human genetics
Citation: Liu, Hau et al., A Geographically Explicit Genetic Model of Worldwide Human-Settlement History, American journal of human genetics , 79(2), 2006, pp. 230-237
Regression-Based Association Analysis with Clustered Haplotypes through Use of Genotypes
Authors: Tzeng, Jung-Ying Wang, Chih-Hao Kao, Jau-Tsuen Hsiao, Chuhsing Kate
Journal: American journal of human genetics
Citation: Tzeng, Jung-ying et al., Regression-Based Association Analysis with Clustered Haplotypes through Use of Genotypes, American journal of human genetics , 78(2), 2006, pp. 231-242
Accommodating Chromosome Inversions in Linkage Analysis
Authors: Chen, Gary K. Slaten, Erin Ophoff, Roel A. Lange, Kenneth
Journal: American journal of human genetics
Citation: K. Chen, Gary et al., Accommodating Chromosome Inversions in Linkage Analysis, American journal of human genetics , 79(2), 2006, pp. 238-251
Using Linkage Genome Scans to Improve Power of Association in Genome Scans
Authors: Roeder, Kathryn Bacanu, Silvi-Alin Wasserman, Larry Devlin, B.
Journal: American journal of human genetics
Citation: Roeder, Kathryn et al., Using Linkage Genome Scans to Improve Power of Association in Genome Scans, American journal of human genetics , 78(2), 2006, pp. 243-252
Genomewide Association Analysis of Human Narcolepsy and a New Resistance Gene
Authors: Kawashima, Minae Tamiya, Gen Oka, Akira Hohjoh, Hirohiko Juji, Takeo Ebisawa, Takashi Honda, Yutaka Inoko, Hidetoshi Tokunaga, Katsushi
Journal: American journal of human genetics
Citation: Kawashima, Minae et al., Genomewide Association Analysis of Human Narcolepsy and a New Resistance Gene, American journal of human genetics , 79(2), 2006, pp. 252-263
The SERPINE2 Gene Is Associated with Chronic Obstructive Pulmonary Disease
Authors: DeMeo, Dawn L. Mariani, Thomas J. Lange, Christoph Srisuma, Sorachai Litonjua, Augusto A. Celedón, Juan C. Lake, Stephen L. Reilly, John J. Chapman, Harold A. Mecham, Brigham H Haley, Kathleen J. Sylvia, Jody S. Sparrow, David Spira, Avrum E. Beane, Jennifer Pinto-Plata, Victor Speizer, Frank E. Shapiro, Steven D. Weis, Scott T. Silverman, Edwin K.
Journal: American journal of human genetics
Citation: L. Demeo, Dawn et al., The SERPINE2 Gene Is Associated with Chronic Obstructive Pulmonary Disease, American journal of human genetics , 78(2), 2006, pp. 253-264
Epigenetic Regulation of Human .-Glutamyl Hydrolase Activity in Acute Lymphoblastic Leukemia Cells
Authors: Cheng, Qing Cheng, Cheng Crews, Kristine R. Ribeiro, Raul C. Pui, Ching-Hon Relling, Mary V. Evans, William E.
Journal: American journal of human genetics
Citation: Cheng, Qing et al., Epigenetic Regulation of Human .-Glutamyl Hydrolase Activity in Acute Lymphoblastic Leukemia Cells, American journal of human genetics , 79(2), 2006, pp. 264-274
ZNF674: A New Krüppel-Associated Box.Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation
Authors: Lugtenberg, Dorien Yntema, Helger G. Banning, Martijn J.G. Oudakker, Astrid R. Firth, Helen V. Willatt, Lionel Raynaud, Martine Kleefstra, Tjitske Fryns, Jean-Pierre Ropers, Hans-Hilger Chelly, Jamel Moraine, Claude Gécz, Jozef Van Reeuwijk, Jeroen Nabuurs, Sander B. De Vries, Bert B.A. Hamel,Ben C. J. De Brouwer, Arjan P.M. Van Bokhoven, Hans
Journal: American journal of human genetics
Citation: Lugtenberg, Dorien et al., ZNF674: A New Krüppel-Associated Box.Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation, American journal of human genetics , 78(2), 2006, pp. 265-278
Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human Genome
Authors: Locke, Devin P. Sharp, Andrew J. McCarroll, Steven A. McGrath, Sean D. Newman, Tera L. Cheng, Ze Schwartz, Stuart Albertson, Donna G. Pinkel,Daniel Altshuler, David M. Eichler, Evan E.
Journal: American journal of human genetics
Citation: P. Locke, Devin et al., Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human Genome, American journal of human genetics , 79(2), 2006, pp. 275-290
Diversity and Functional Consequences of Germline and Somatic PTPN11 Mutations in Human Disease
Authors: Tartaglia, Marco Martinelli, Simone Stella, Lorenzo Bocchinfuso, Gianfranco Flex, Elisabetta Cordeddu, Viviana Zampino, Giuseppe Van der Burgt, Ineke Palleschi, Antonio Petrucci, Tamara C. Sorcini, Mariella Schoch, Claudia Foà, Robin Emanuel, Peter D. Gelb, Bruce D.
Journal: American journal of human genetics
Citation: Tartaglia, Marco et al., Diversity and Functional Consequences of Germline and Somatic PTPN11 Mutations in Human Disease, American journal of human genetics , 78(2), 2006, pp. 279-290
Single-Nucleotide Polymorphisms in NAGNAG Acceptors Are Highly Predictive for Variations of Alternative Splicing
Authors: Hiller, Michael Huse, Klaus Szafranski, Karol Jahn, Niels Hampe, Jochen Schreiber, Stefan Backofen, Rolf Platzer, Matthias
Journal: American journal of human genetics
Citation: Hiller, Michael et al., Single-Nucleotide Polymorphisms in NAGNAG Acceptors Are Highly Predictive for Variations of Alternative Splicing, American journal of human genetics , 78(2), 2006, pp. 291-302
Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations
Authors: Guan, Min-Xin Yan, Qingfeng Li, Xiaoming Bykhovskaya, Yelena Gallo-Teran, Jaime Hajek, Petr Umeda, Noriko Zhao, Hui Garrido, Gema Mengesha, Embet Suzuki, Tsutomu Del Castillo, Ignacio Peters, Jennifer Lynne Li, Ronghua Qian, Yaping Wang, Xinjian Ballana, Ester Shohat, Mordechai Lu, Jianxin Estivill, Xavier Fischel-Ghodsian, Nathan
Journal: American journal of human genetics
Citation: Guan, Min-xin et al., Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations, American journal of human genetics , 79(2), 2006, pp. 291-302
Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation
Authors: Lalani, Seema R. Safiullah, Arsalan M. Fernbach, Susan D. Harutyunyan, Karine G. Thaller, Christina Peterson, Leif E. McPherson, John D. Gibbs, Richard A. White, Lisa D. Hefner, Margaret Davenport, Sandra L.H. Graham Jr., John M Bacino, Carlos A. Glass, Nancy L. Towbin, Jeffrey A. Craigen, William J Neish, Steven R. Lin, Angela E. Belmont, Jhon W.
Journal: American journal of human genetics
Citation: R. Lalani, Seema et al., Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation, American journal of human genetics , 78(2), 2006, pp. 303-314
Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal . Subunit
Authors: Hoffman, Katrin Müller, Juliane S. Stricker, Sigmar Megarbane, Andre Rajab, Anna Lindner, Tom H. Cohen, Monika Chouery, Eliane Adaimy, Lynn Ghanem, Ismat Delague, Valerie Boltshauser, Eugen Talim, Beril Horvath, Rita Robinson, Peter N. Lochmüller, Hanns Hübner, Christoph Mundlos, Stefan
Journal: American journal of human genetics
Citation: Hoffman, Katrin et al., Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal . Subunit, American journal of human genetics , 79(2), 2006, pp. 303-312
A Coalescence-Guided Hierarchical Bayesian Method for Haplotype Inference
Authors: Zhang, Yu Niu, Tianhua Liu, Jun S.
Journal: American journal of human genetics
Citation: Zhang, Yu et al., A Coalescence-Guided Hierarchical Bayesian Method for Haplotype Inference, American journal of human genetics , 79(2), 2006, pp. 313-322
Genomewide Linkage Scan of 409 European-Ancestry and African American Families with Schizophrenia: Suggestive Evidence of Linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the Combined Sample
Authors: Suarez, Brian K. Duan, Jubao Sanders, Alan R. Hinrichs, Anthony L. Jin, Carol H. Hou,Cuiping Buccola, Nancy G. Hale, Nancy Weilbaecher, Ann N. Nertney, Deborah A Olincy, Ann Green, Susan Schaffer, Arthur W. Smith, Christopher J. Hannah, Dominique E. Rice, John P. Cox, Nancy J. Martinez, Maria Mowry, Bryan J Amin, Farooq Gejman, Pablo V.
Journal: American journal of human genetics
Citation: K. Suarez, Brian et al., Genomewide Linkage Scan of 409 European-Ancestry and African American Families with Schizophrenia: Suggestive Evidence of Linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the Combined Sample, American journal of human genetics , 78(2), 2006, pp. 315-333
Linkage Analysis Using Co-Phenotypes in the BRIGHT Study Reveals Novel Potential Susceptibility Loci for Hypertension
Authors: Wallace, Chris Xue, Ming-Zhan Newhouse, Stephen J. Marçano, Ana Carolina B. Onipinla, Abiodun K. Burke, Beverley Gungadoo, Johannie Dobson, Richard J. Broen, Morris Connell, John M. Dominiczak, Anna Lathrop, G. Mark Webster, Jhon Farrall, Martin Mein, Charles Samani, Nilesh J Caulfield, Mark J. Clayton, David G. Munroe, Patricia B.
Journal: American journal of human genetics
Citation: Wallace, Chris et al., Linkage Analysis Using Co-Phenotypes in the BRIGHT Study Reveals Novel Potential Susceptibility Loci for Hypertension, American journal of human genetics , 79(2), 2006, pp. 323-331
Submicroscopic Deletion in Patients with Williams-Beuren Syndrome Influences Expression Levels of the Nonhemizygous Flanking Genes
Authors: Merla, Giuseppe Howald, Cédric Henrichsen, Charlotte N. Lyle, Robert Wyss, Carine Zabot, Marie-Thérèse Antonarakis, Stylianos E. Reymond, Alexandre
Journal: American journal of human genetics
Citation: Merla, Giuseppe et al., Submicroscopic Deletion in Patients with Williams-Beuren Syndrome Influences Expression Levels of the Nonhemizygous Flanking Genes, American journal of human genetics , 79(2), 2006, pp. 332-341
Increased Sensitivity of the Neuronal Nicotinic Receptor .2 Subunit Causes Familial Epilepsy with Nocturnal Wandering and Ictal Fear
Authors: Aridon, Paolo Marini, Carla Di Resta, Chiara Brilli, Elisa De Fusco, Maurizio Politi, Fausta Parrini, Elena Manfredi, Irene Pisano, Tiziana Pruna, Dario Curia, Giulia Cianchetti, Carlo Pasqualetti, Massimo Bacchetti, Andrea Guerrini, Renzo Casari, Giorgio
Journal: American journal of human genetics
Citation: Aridon, Paolo et al., Increased Sensitivity of the Neuronal Nicotinic Receptor .2 Subunit Causes Familial Epilepsy with Nocturnal Wandering and Ictal Fear, American journal of human genetics , 79(2), 2006, pp. 342-350
A Genomewide Search Finds Major Susceptibility Loci for Gallbladder Disease on Chromosome 1 in Mexican Americans
Authors: Puppala, Sobha Dodd, Gerald D. Fowler, Sharon Arya, Rector Schneider, Jennifer Farook, Vidya S. Granato, Richard Dyer, Thomas D. Almasy, Laura Jenkinson, Christopher P. Diehl, Andrew K. Stern, Michael P Blangero, John Duggirala, Ravindranath
Journal: American journal of human genetics
Citation: Puppala, Sobha et al., A Genomewide Search Finds Major Susceptibility Loci for Gallbladder Disease on Chromosome 1 in Mexican Americans, American journal of human genetics , 78(3), 2006, pp. 377-392
An Ancient Balanced Polymorphism in a Regulatory Region of Human Major Histocompatibility Complex Is Retained in Chinese Minorities but Lost Worldwide
Authors: Liu, Xiaoyi Fu, Yonggui Liu, Zehuan Lin, Bin Xi, Yi Liu, Yin Xu, Yunpin Lin, Jianghai Fan, Xinlan Dong, Meiling Zeng, Kai Wu, Chung-l Xu, Anlong
Journal: American journal of human genetics
Citation: Liu, Xiaoyi et al., An Ancient Balanced Polymorphism in a Regulatory Region of Human Major Histocompatibility Complex Is Retained in Chinese Minorities but Lost Worldwide, American journal of human genetics , 78(3), 2006, pp. 393-400
Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of Metabolism
Authors: Sass, Jörn Oliver Mohr, Verena Olbrich, Heike Engelke, Udo Horvath, Judit Fliegauf, Manfred Loges, Niki Tomas Schweitzer-Krantz, Susanne Moebus, Ralf Weiler, Polly Kispert, Andreas Superti-Furga, Andrea Wevers, Ron A. Omran, Heymut
Journal: American journal of human genetics
Citation: Sass, Jörn Oliver et al., Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of Metabolism, American journal of human genetics , 78(3), 2006, pp. 401-409
Results: 1-25 | 26-50 | 51-75 | 76-100 | >>