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PLoS Neglected Tropical Diseases, ISSN 1935-2727, 08/2016, Volume 10, Issue 8, p. e0004885
Journal Article
SAE technical paper series, Volume 2015-36-0296.
Fatigue is the main cause of mechanical failure in aircraft structures, in which aluminum alloys are employed in approximately 70% of their structural... 
Heat treatment | Aluminum alloys | Fatigue
eJournal
by Pedrosa, Fábio O and Monteiro, Rose Adele and Wassem, Roseli and Cruz, Leonardo M and Ayub, Ricardo A and Colauto, Nelson B and Fernandez, Maria Aparecida and Fungaro, Maria Helena P and Grisard, Edmundo C and Hungria, Mariangela and Madeira, Humberto M. F and Nodari, Rubens O and Osaku, Clarice A and Petzl-Erler, Maria Luiza and Terenzi, Hernán and Vieira, Luiz G. E and Steffens, Maria Berenice R and Weiss, Vinicius A and Pereira, Luiz F. P and Almeida, Marina I. M and Alves, Lysangela R and Marin, Anelis and Araujo, Luiza Maria and Balsanelli, Eduardo and Baura, Valter A and Chubatsu, Leda S and Faoro, Helisson and Favetti, Augusto and Friedermann, Geraldo and Glienke, Chirlei and Karp, Susan and Kava-Cordeiro, Vanessa and Raittz, Roberto T and Ramos, Humberto J. O and Ribeiro, Enilze Maria S. F and Rigo, Liu Un and Rocha, Saul N and Schwab, Stefan and Silva, Anilda G and Souza, Eliel M and Tadra-Sfeir, Michelle Z and Torres, Rodrigo A and Dabul, Audrei N. G and Soares, Maria Albertina M and Gasques, Luciano S and Gimenes, Ciela C. T and Valle, Juliana S and Ciferri, Ricardo R and Correa, Luiz C and Murace, Norma K and Pamphile, João A and Patussi, Eliana Valéria and Prioli, Alberto J and Prioli, Sonia Maria A and Rocha, Carmem Lúcia M. S. C and Arantes, Olívia Márcia N and Furlaneto, Márcia Cristina and Godoy, Leandro P and Oliveira, Carlos E. C and Satori, Daniele and Vilas-Boas, Laurival A and Watanabe, Maria Angélica E and Dambros, Bibiana Paula and Guerra, Miguel P and Mathioni, Sandra Marisa and Santos, Karine Louise and Steindel, Mario and Vernal, Javier and Barcellos, Fernando G and Campo, Rubens J and Chueire, Ligia Maria O and Nicolás, Marisa Fabiana and Pereira-Ferrari, Lilian and da Conceição Silva, José L and Gioppo, Nereida M. R and Margarido, Vladimir P and Menck-Soares, Maria Amélia and Pinto, Fabiana Gisele S and de Simão, Rita Cássia G and Takahashi, Elizabete K and Yates, Marshall G and Souza, Eliel M
PLoS Genetics, ISSN 1553-7390, 05/2011, Volume 7, Issue 5, p. e1002064
Journal Article
Journal Article
Saudi Journal of Biological Sciences, ISSN 1319-562X, 01/2018, Volume 25, Issue 1, pp. 101 - 104
Down syndrome (DS) is the most common form of human genetic mental retardation. Several polymorphisms in genes coding folic acid cycle enzymes have been... 
DNMT3B | Rs2424913 | De novo methylation | Down syndrome | 149C > T | Folic acid metabolism | MATERNAL RISK | C46359T | ORIGIN | GENE | METHYLTRANSFERASES | BIOLOGY | PROMOTER | EXPRESSION | AGE | 149C > T
Journal Article
Journal Article
by Grilo, Clara and Coimbra, Michely R and Cerqueira, Rafaela C and Barbosa, Priscilla and Dornas, Rubem A. P and Gonçalves, Larissa O and Teixeira, Fernanda Z and Coelho, Igor Pfeifer and Schmidt, Brenda R and Pacheco, Diana L. K and Schuck, Gabriela and Esperando, Isadora B and Anza, Juan A and Beduschi, Júlia and Oliveira, Nicole R and Pinheiro, Paula F and Bager, Alex and Secco, Helio and Guerreiro, Marcello and Carvalho, Carine F and Veloso, Aline C and Custódio, Ana E. I and Marçal, Oswaldo and Ciocheti, Giordano and Assis, Julia and Ribeiro, Milton Cezar and Francisco, Beatriz S. S and Cherem, Jorge J and Trigo, Tatiane C and Jardim, Márcia M. A and Franceschi, Ingridi C and Espinosa, Caroline and Tirelli, Flávia P and Rocha, Vlamir J and Sekiama, Margareth L and Barbosa, Gedimar P and Rossi, Helen R and Moreira, Tainah C and Cervini, Marcelo and Rosa, Clarissa Alves and Silva, Lucas Gonçalves and Ferreira, Claudia M. M and César, Augusto and Casella, Janaina and Mendes, Sérgio L and Zina, Juliana and Bastos, Deivson F. O and Souza, Ricardo A. T and Hartmann, Paulo A and Deffaci, Angela C. G and Mulinari, Jéssica and Luzzi, Siane C and Rezzadori, Tiago and Kolcenti, Cassiane and Reis, Tiago Xavier and Fonseca, Vanessa S. C and Giorgi, Camilo F and Migliorini, Raissa P and Kasper, Carlos Benhur and Bueno, Cecília and Sobanski, Marcela and Pereira, Ana P. F. G and Andrade, Fernanda A. G and Fernandes, Marcus E. B and Corrêa, Luiz L. C and Nepomuceno, Adriana and Banhos, Aureo and Hannibal, Wellington and Fonseca, Rogério and Costa, Lizit A and Medici, Emilia P and Croce, Aline and Werther, Karin and Oliveira, Juliana P and Ribeiro, Julia M and Santi, Mariele and Kawanami, Aline E and Perles, Livia and Couto, Caroline and Figueiró, Daniela S and Eizirik, Eduardo and Correia, Antonio A and Corrêa, Fabio M and Queirolo, Diego and Quagliatto, André L and Saranholi, Bruno H and Galetti, Pedro M and Rodriguez‐Castro, Karen G and Braz, Vivian S and França, Frederico G. R and Buss, Gerson and Rezini, Josias A and Lion, Marília B and Cheida, Carolina C and Lacerda, Ana C. R and Freitas, Carlos Henrique and Venâncio, Fernando and Adania, Cristina H and Batisteli, Augusto F and Hegel, Carla G. Z and ...
Ecology, ISSN 0012-9658, 11/2018, Volume 99, Issue 11, pp. 2625 - 2625
Journal Article
Rodriguésia, ISSN 0370-6583, 2018, Volume 69, Issue 4, pp. 1513 - 1527
The Global Strategy for Plant Conservation (GSPC) was established by the conference of Parties in 2002 to decrease the loss of plant diversity, reduce poverty... 
database | diversity | 2 International | Taxonomy | hotspots | Database | Diversity | Hotspots | taxonomy
Journal Article
Ciencia e Saude Coletiva, ISSN 1413-8123, 01/2015, Volume 20, Issue 1, pp. 57 - 63
A deficiência auditiva é doença prevalente e justifica a necessidade de regulamentação das Leis e suas execuções através das Portarias de Atenção à Saúde... 
Deafness | Hearing screening | Hearing | Health Policy & Services
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 5, pp. 644 - 651
Oligophrenin-1 (OPHN1) is one of at least seven genes located on chromosome X that take part in Rho GTPase-dependent signaling pathways involved in X-linked... 
cerebellar hypoplasia | Oligophrenin-1 | BAR domain | X-linked intellectual disability | hippocampus | Rho GTPase | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROTEIN OLIGOPHRENIN-1 | GRAF FAMILY | ENDOCYTOSIS | REPLICATION | LINKED MENTAL-RETARDATION | GENE | RHOGAP | GENETICS & HEREDITY | VENTRICULAR ENLARGEMENT | MUTATIONS | Sequence Deletion | Cytoskeletal Proteins - genetics | Humans | Middle Aged | Male | Reading Frames | Intellectual Disability - genetics | Brain - metabolism | Young Adult | DNA Mutational Analysis | Protein Interaction Domains and Motifs - genetics | Facies | Adult | Female | Nuclear Proteins - genetics | Child | Hippocampus - pathology | Cytoskeletal Proteins - chemistry | GTPase-Activating Proteins - chemistry | Nuclear Proteins - chemistry | Hippocampus - metabolism | Magnetic Resonance Imaging | Phenotype | Comparative Genomic Hybridization | Pedigree | Intellectual Disability - diagnosis | Adolescent | GTPase-Activating Proteins - genetics | X Chromosome Inactivation | Cerebellum | Neuroimaging | Neonates | Transcription | Intellectual disabilities | Hyperactivity | Cognitive ability | Males | Gene deletion | Atrophy | Signal transduction | Clonal deletion | Nose | Ventricle (lateral) | Hypoplasia | Brain architecture | Strabismus | Splicing | Anatomy | Intolerance | Magnetic resonance imaging | Skull | Mutation | Frustration | Hippocampus | Guanosinetriphosphatase
Journal Article
14.