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1. Full Text American Bittern
by Hill, Sean
Callaloo, ISSN 0161-2492, 2016, Volume 39, Issue 1, pp. 44 - 44
Poetry | Arts & Humanities | Literature | Literature, African, Australian, Canadian | Personal narratives | Appreciation | Portrayals | Hill, Sean
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2. Critical issues in peace and conflict studies
: theory, practice, and pedagogy
2011, ISBN 9780739149607, xxviii, 418
Book
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3. Full Text Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations
by Poduri, Annapurna and Evrony, Gilad D and Cai, Xuyu and Elhosary, Princess Christina and Beroukhim, Rameen and Lehtinen, Maria K and Hills, L. Benjamin and Heinzen, Erin L and Hill, Anthony and Hill, R. Sean and Barry, Brenda J and Bourgeois, Blaise F.D and Riviello, James J and Barkovich, A. James and Black, Peter M and Ligon, Keith L and Walsh, Christopher A
Neuron (Cambridge, Mass.), ISSN 0896-6273, 04/2012, Volume 74, Issue 1, pp. 41 - 48
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Humans | Epilepsy - surgery | Malformations of Cortical Development - genetics | Epilepsy - etiology | Malformations of Cortical Development - complications | Proto-Oncogene Proteins c-akt - genetics | Neurogenesis - genetics | Cerebrum - abnormalities | Trisomy - genetics | Cerebrum - growth & development | Chromosomes, Human, Pair 1 - genetics | Malformations of Cortical Development - pathology | Cerebrum - pathology | Epilepsy - pathology | Medical colleges | Neurons | Epilepsy | Genes | Brain | Mutation | Chromosomes | Index Medicus | AKT protein
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4. Dangerous Goods
: poems
by Hill, Sean, 1976
2013, 1st edition., ISBN 1571314571, 114
Lyrik | American poetry | Amerikanisches Englisch | African American authors
Book
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5. The Oxford handbook of music revival
by Hill, Juniper editor of compilation and Bithell, Caroline, 1957- editor of compilation
2014, Oxford handbooks, ISBN 0199765030, x, 701
History and criticism | Music
Book
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6. Full Text Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg Syndrome
by Manzini, M. Chiara and Tambunan, Dimira E and Hill, R. Sean and Yu, Tim W and Maynard, Thomas M and Heinzen, Erin L and Shianna, Kevin V and Stevens, Christine R and Partlow, Jennifer N and Barry, Brenda J and Rodriguez, Jacqueline and Gupta, Vandana A and Al-Qudah, Abdel-Karim and Eyaid, Wafaa M and Friedman, Jan M and Salih, Mustafa A and Clark, Robin and Moroni, Isabella and Mora, Marina and Beggs, Alan H and Gabriel, Stacey B and Walsh, Christopher A
American journal of human genetics, ISSN 0002-9297, 09/2012, Volume 91, Issue 3, pp. 541 - 547
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Neurology | Malformations of the nervous system | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Exome | Walker-Warburg Syndrome - genetics | Glycosyltransferases - genetics | Mutation | Humans | Usage | Gene mutations | Encephalopathy | Analysis | Exome sequencing | Glycosyltransferases | Causes of | Genetic aspects | Glycosylation | Research | Health aspects | Proteins | Zebrafish | Genomes | Gene loci | Genetic disorders | Index Medicus | Report
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7. The future of the brain
: essays by the world's leading neuroscientists
by Freeman, Jeremy Andrew, 1972- editor and Marcus, Gary F. editor. (Gary Fred)
2015, STU - Student edition, ISBN 069116276X, xiii, 284 p., 8 col. plates
Neurosciences | Biological Sciences | Brain | Neuroinformatics
Book
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8. Full Text Synaptic, transcriptional and chromatin genes disrupted in autism
by De Rubeis, Silvia and He, Xin and Goldberg, Arthur P and Poultney, Christopher S and Samocha, Kaitlin and Cicek, A. Ercument and Kou, Yan and Liu, Li and Fromer, Menachem and Walker, Susan and Singh, Tarjinder and Klei, Lambertus and Kosmicki, Jack and Fu, Shih-Chen and Aleksic, Branko and Biscaldi, Monica and Bolton, Patrick F and Brownfeld, Jessica M and Cai, Jinlu and Campbell, Nicholas G and Carracedo, Angel and Chahrour, Maria H and Chiocchetti, Andreas G and Coon, Hilary and Crawford, Emily L and Crooks, Lucy and Curran, Sarah R and Dawson, Geraldine and Duketis, Eftichia and Fernandez, Bridget A and Gallagher, Louise and Geller, Evan and Guter, Stephen J and Hill, R. Sean and Ionita-Laza, Iuliana and Gonzalez, Patricia Jimenez and Kilpinen, Helena and Klauck, Sabine M and Kolevzon, Alexander and Lee, Irene and Lei, Jing and Lehtimäki, Terho and Lin, Chiao-Feng and Ma'ayan, Avi and Marshall, Christian R and McInnes, Alison L and Neale, Benjamin and Owen, Michael J and Ozaki, Norio and Parellada, Mara and Parr, Jeremy R and Purcell, Shaun and Puura, Kaija and Rajagopalan, Deepthi and Rehnström, Karola and Reichenberg, Abraham and Sabo, Aniko and Sachse, Michael and Sanders, Stephan J and Schafer, Chad and Schulte-Rüther, Martin and Skuse, David and Stevens, Christine and Szatmari, Peter and Tammimies, Kristiina and Valladares, Otto and Voran, Annette and Wang, Li-San and Weiss, Lauren A and Willsey, A. Jeremy and Yu, Timothy W and Yuen, Ryan K. C and Cook, Edwin H and Freitag, Christine M and Gill, Michael and Hultman, Christina M and Lehner, Thomas and Palotie, Aarno and Schellenberg, Gerard D and Sklar, Pamela and State, Matthew W and Sutcliffe, James S and Walsh, Christopher A and Scherer, Stephen W and Zwick, Michael E and Barrett, Jeffrey C and Cutler, David J and Roeder, Kathryn and Devlin, Bernie and Daly, Mark J and Buxbaum, Joseph D and Homozygosity Mapping Collaborative and DDD Study and Autism Sequencing Consortium and UK10K Consortium and The Autism Sequencing Consortium and The DDD Study and Homozygosity Mapping Collaborative for Autism
Nature (London), ISSN 0028-0836, 11/2014, Volume 515, Issue 7526, pp. 209 - 215
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Gene mutations | Analysis | Pervasive developmental disorders | Research | Genetic transcription | Nucleotide sequencing | Health aspects | DNA sequencing | Studies | Autism | Neurosciences | Chromatin | Mutation | Genes | Index Medicus | Medicin och hälsovetenskap
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9. Full Text Turbulence measurements using a nanoscale thermal anemometry probe
by BAILEY, SEAN C. C and KUNKEL, GARY J and HULTMARK, MARCUS and VALLIKIVI, MARGIT and HILL, JEFFREY P and MEYER, KARL A and TSAY, CANDICE and ARNOLD, CRAIG B and SMITS, ALEXANDER J
Journal of fluid mechanics, ISSN 0022-1120, 11/2010, Volume 663, pp. 160 - 179
Papers | turbulent flows | MEMS/NEMS | Mechanics | Physical Sciences | Physics, Fluids & Plasmas | Technology | Physics | Science & Technology | Micro- and nanoelectromechanical devices (mems/nems) | Fundamental areas of phenomenology (including applications) | Fluid dynamics | Turbulent flows, convection, and heat transfer | Isotropic turbulence; homogeneous turbulence | Instrumentation for fluid dynamics | Exact sciences and technology | Electronics | Applied sciences | Semiconductor electronics. Microelectronics. Optoelectronics. Solid state devices | Turbulence | Thermal energy | Measurement techniques | Turbulent flow | Nanocomposites | Semiconductors | Fluid flow | Nanomaterials | Nanostructure | Spatial filtering | Anemometry
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10. Full Text Study: Virus To Keep Spreading For Up To Two Years Until 60 Percent To 70 Percent Of Population Has Been Infected; Gov. Newsom: "Days, Not Weeks" Away From Lifting Some Stay-At-Home Restrictions; Sean Penn's Organization Offers Free Testing For Essential Workers. Aired 9-10p ET
by Anderson Cooper and Erica Hill and Sanjay Gupta and Randi Kaye
05/2020
COVID-19 | Pandemics | Disease transmission | Shelter in place | Fatalities | Essential workers | Vaccines | Coronaviruses | Governors
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11. Full Text G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex
by Xianhua Piao and R. Sean Hill and Adria Bodell and Bernard S. Chang and Lina Basel-Vanagaite and Rachel Straussberg and William B. Dobyns and Bassam Qasrawi and Robin M. Winter and A. Micheil Innes and Thomas Voit and M. Elizabeth Ross and Jacques L. Michaud and Jean-Claude Déscarie and A. James Barkovich and Christopher A. Walsh
Science (American Association for the Advancement of Science), ISSN 0036-8075, 3/2004, Volume 303, Issue 5666, pp. 2033 - 2036
Proteins | Brain | Cerebral cortex | Splicing | Neurons | Exons | Cousins | Amino acids | Reports | Genetic mutation | Progenitor cells | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Vertebrates: nervous system and sense organs | Biological and medical sciences | Development. Senescence. Regeneration. Transplantation | Antisense Elements (Genetics) | Sequence Deletion | Frameshift Mutation | Receptors, G-Protein-Coupled - metabolism | Humans | Male | Mutation, Missense | Body Patterning | Neurons - physiology | Female | Cerebral Ventricles - embryology | Cerebral Cortex - abnormalities | Gene Order | Receptors, G-Protein-Coupled - physiology | Signal Transduction | Parietal Lobe - abnormalities | Parietal Lobe - embryology | Biological Evolution | Sequence Homology, Amino Acid | Animals | Cerebral Cortex - embryology | Ligands | Stem Cells - physiology | Frontal Lobe - abnormalities | Mice | Receptors, G-Protein-Coupled - genetics | Cerebral Ventricles - cytology | Frontal Lobe - embryology | Receptors, G-Protein-Coupled - chemistry | Amino Acid Substitution | Genetic aspects | Anatomy & physiology | Mutation | Genes | Cells | bilateral frontoparietal polymicrogyria | GPR56 protein | Index Medicus
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12. Full Text Mutations in QARS, Encoding Glutaminyl-tRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures
by Zhang, Xiaochang and Ling, Jiqiang and Barcia, Giulia and Jing, Lili and Wu, Jiang and Barry, Brenda J and Mochida, Ganeshwaran H and Hill, R. Sean and Weimer, Jill M and Stein, Quinn and Poduri, Annapurna and Partlow, Jennifer N and Ville, Dorothée and Dulac, Olivier and Yu, Tim W and Lam, Anh-Thu N and Servattalab, Sarah and Rodriguez, Jacqueline and Boddaert, Nathalie and Munnich, Arnold and Colleaux, Laurence and Zon, Leonard I and Söll, Dieter and Walsh, Christopher A and Nabbout, Rima
American journal of human genetics, ISSN 0002-9297, 04/2014, Volume 94, Issue 4, pp. 547 - 558
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Amino Acyl-tRNA Synthetases - genetics | Aminoacylation | Genetic Predisposition to Disease | Microcephaly - genetics | Seizures - genetics | Humans | Brain Diseases - genetics | Child, Preschool | Male | Zebrafish | Magnetic Resonance Imaging | Animals | Pedigree | Microcephaly - pathology | Female | Mutation | Atrophy | Gene mutations | Ligases | Causes of | Genetic aspects | Seizures (Medicine) | Microcephaly | Health aspects | Brain | Survival analysis | Convulsions & seizures | Neurons | Genes | Amino acids | Transfer RNA | Index Medicus | Life Sciences | Genetics | Human genetics
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