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Showing results 1 to 15 of 15
PreviewIssue DateTitleAuthor(s)AdvisorType
2012Jaboticaba peel: Antioxidant compounds, antiproliferative and antimutagenic activitiesLeite-Legatti, AV; Batista, AG; Dragano, NRV; Marques, AC; Malta, LG; Riccio, MF; Eberlin, MN; Machado, ART; de Carvalho-Silva, LB; Ruiz, ALTG; de Carvalho, JE; Pastore, GM; Marostica, MR-Artigo de periódico
1-Nov-2008Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 geneCoeli, Fernanda Borchers; Ferraz, Lúcio Fábio Caldas; Lemos-Marini, Sofia H. V. de; Rigatto, Sumara Zuanazi Pinto; Belangero, Vera Maria Santoro; de-Mello, Maricilda Palandi-Artigo de periódico
2010TP53 mutation profile of esophageal squamous cell carcinomas of patients from Southeastern BrazilRossini, A; Simao, TD; Marques, CB; Soares-Lima, SC; Herbster, S; Rapozo, DCM; Andreollo, NA; Ferreira, MA; El-Jaick, KB; Teixeira, R; Guimaraes, DP; Albano, RM; Pinto, LFR-Artigo de periódico
1-Jan-2003beta-thalassemia intermedia in a Brazilian patient with - 101(C > T) and codon 39 (C > T) mutationsSousa, Sylvia Morais de; Khater, Letícia; Peroni, Luís Antônio; Miranda, Karine; Murai, Marcelo Jun; Albuquerque, Dulcinéia Martins; Arruda, Paulo; Saad, Sara Terezinha Ollala; Costa, Fernando Ferreira-Artigo de periódico
2011Screening for hotspot mutations in PI3K, JAK2, FLT3 and NPM1 in patients with myelodysplastic syndromesMachado-Neto, JA; Traina, F; Lazarini, M; Campos, PD; Borgia, K; Pagnano, B; Lorand-Metze, I; Costa, FF; Saad, STO-Artigo de periódico
2015Ghost Cells In Pilomatrixoma, Craniopharyngioma, And Calcifying Cystic Odontogenic Tumor: Histological, Immunohistochemical, And Ultrastructural StudyRumayor; Alicia; Carlos; Roman; Molina Kirsch; Hernan; Benevenuto de Andrade; Bruno A.; Romanach; Mario J.; de Almeida; Oslei Paes-Artigo de periódico
2015Genomic Variants Revealed By Invariably Missing Genotypes In Nelore Cattleda Silva; Joaquim Manoel; Giachetto; Poliana Fernanda; Campos da Silva; Luiz Otavio; Cintra; Leandro Carrijo; Paiva; Samuel Rezende; Caetano; Alexandre Rodrigues; Beleza Yamagishi; Michel Eduardo-Artigo de periódico
2015Expanding The Molecular And Clinical Phenotype Of Ssr4-cdgNg; Bobby G.; Raymond; Kimiyo; Kircher; Martin; Buckingham; Kati J.; Wood; Tim; Shendure; Jay; Nickerson; Deborah A.; Bamshad; Michael J.; Wong; Jonathan T. S.; Monteiro; Fabiola Paoli; Graham; Brett H.; Jackson; Sheryl; Sparkes; Rebecca; Scheuerle; Angela E.; Cathey; Sara; Kok; Fernando; Gibson; James B.; Freeze; Hudson H.-Artigo de periódico
2015Genotype-phenotype Correlations In Cyp1b1-associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts From India And Brazilde Melo; Monica Barbosa; Mandal; Anil K.; Tavares; Ivan M.; Ali; Mohammed Hasnat; Kabra; Meha; Cabral de Vasconcellos; Jose Paulo; Senthil; Sirisha; Sallum; Juliana M. F.; Kaur; Inderjeet; Betinjane; Alberto J.; Moura; Christiane R.; Paula; Jayter S.; Costa; Karita A.; Sarfarazi; Mansoor; Della Paolera; Mauricio; Finzi; Simone; Ferraz; Victor E. F.; Costa; Vital P.; Belfort; Rubens; Jr.; Chakrabarti; Subhabrata-Artigo de periódico
2015Genetic Diversity Of The Mycobacterium Tuberculosis Beijing Family In Brazil And Mozambique And Relation With Infectivity And Induction Of Necrosis In Thp-1 CellsGomes; Lia Lima; Goncalves Vasconcellos; Sidra Ezidrio; Gomes; Harrison Magdinier; Elias; Atina Ribeiro; Rocha; Adalgiza da Silva; Ribeiro; Simone C. M.; Panunto; Alessandra Costa; Ferrazoli; Lucilaine; da Silva Telles; Maria Alice; Emanuel Ivens de; Araujo Marelo; Kritski; Afranio Lineu; Mokrousov; Igor; Manicheva; Olga A.; Lasunskaia; Elena; Suffys; Philip Noel-Artigo de periódico
2015Single Nucleotide Polymorphisms Of The Gjb2 And Gjb6 Genes Are Associated With Autosomal Recessive Nonsyndromic Hearing LossGrillo; Ana Paula; de Oliveira; Flavia Marcorin; de Carvalho; Gabriela Queila; Vieira Medrano; Ruan Felipe; da Silva-Costa; Sueli Matilde; Sartorato; Edi Lucia; de Oliveira; Camila Andrea-Artigo de periódico
2016A Multicentric Association Study Between 39 Genes And Nonsyndromic Cleft Lip And Palate In A Brazilian Populationde Araujo; Tania Kawasaki; Secolin; Rodrigo; Felix; Temis Maria; de Souza; Liliane Todeschini; Barros Fontes; Marshall Italo; Monlleo; Isabella Lopes; de Souza; Josiane; Fett-Conte; Agnes Cristina; Ribeiro; Erlane Marques; Xavier; Ana Carolina; de Rezende; Adriana Augusto; Simioni; Milena; Campos Ribeiro-dos-Santos; Andrea Kely; Batista dos Santos; Sidney Emanuel; Gil-da-Silva-Lopes; Vera Lucia-Artigo de periódico
2016Extensive Variation In Drug-resistance Mutational Profile Of Brazilian Patients Failing Antiretroviral Therapy In Five Large Brazilian CitiesBrites; Carlos; Pinto-Neto; Lauro; Medeiros; Melissa; Nunes; Estevao; Sprinz; Eduardo; Carvalho; Mariana-Artigo
2013Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuriaGuaragna, MS; Lutaif, ACGB; Piveta, CSC; Belangero, VMS; Maciel-Guerra, AT; Guerra, G; De Mello, MP-Artigo de periódico
2013Two Distinct Wt1 Mutations Identified In Patients And Relatives With Isolated Nephrotic Proteinuria.Guaragna, Mara S; Lutaif, Anna Cristina G B; Piveta, Cristiane S C; Belangero, Vera M S; Maciel-Guerra, Andréa T; Guerra, Gil; De Mello, Maricilda P-Artigo de periódico