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Camila Andréa de Oliveira
Camila Andréa de Oliveira
Docente do Centro Universitário Hermínio Ometto - UNIARARAS
Verified email at fho.edu.br
Title
Cited by
Cited by
Year
A novel deletion involving the connexin-30 gene, del (GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing …
FJ Del Castillo, M Rodriguez-Ballesteros, A Alvarez, T Hutchin, ...
Journal of medical genetics 42 (7), 588-594, 2005
3732005
Guidelines for the tetra-primer ARMS–PCR technique development
RFV Medrano, CA De Oliveira
Molecular biotechnology 56, 599-608, 2014
2482014
Early cytotoxic and genotoxic effects of atrazine on Wistar rat liver: A morphological, immunohistochemical, biochemical, and molecular study
FD Campos-Pereira, CA Oliveira, AA Pigoso, E Silva-Zacarin, R Barbieri, ...
Ecotoxicology and Environmental Safety, 2012
1082012
Epidemiological study of HPV in oral mucosa through PCR
W Tristão, RMP Ribeiro, CA Oliveira, JC Betiol, JSR Bettini
Brazilian journal of otorhinolaryngology 78, 66-70, 2012
592012
Determination of the frequency of the 35delG allele in Brazilian neonates
EL Sartorato, E Gottardi, CA De Oliveira, LA Magna, ...
Clinical Genetics 58 (4), 339-340, 2000
582000
Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients
CA Oliveira, AT Maciel‐Guerra, EL Sartorato
Clinical genetics 61 (5), 354-358, 2002
572002
Newborn hearing screening and genetic testing in 8974 Brazilian neonates
K de AB Nivoloni, SM da Silva-Costa, MCA Pomílio, T Pereira, KC Lopes, ...
International journal of pediatric otorhinolaryngology 74 (8), 926-929, 2010
422010
Molecular genetics of non-syndromic deafness
VB Piatto, ECT Nascimento, F Alexandrino, CA Oliveira, ACP Lopes, ...
Revista Brasileira de Otorrinolaringologia 71, 216-223, 2005
412005
Molecular genetics study of deafness in Brazil: 8‐year experience
CA de Oliveira, F Alexandrino, TV Christiani, CE Steiner, JLR Cunha, ...
American Journal of Medical Genetics Part A 143 (14), 1574-1579, 2007
392007
Frequency of the 35delG Mutation in the GJB2 Gene in Samples of European, Asian, and African Brazilians
CA Oliveira, F Alexandrino, K Abe-Sandes, WA Silva
Human biology 76, 2, 2004
382004
Immune response mediated by Th1/IL-17/caspase-9 promotes evolution of periodontal disease
MEL Sommer, RA Dalia, AVB Nogueira, JA Cirelli, MAR Vinolo, JL Fachi, ...
Archives of oral biology 97, 77-84, 2019
332019
Allelic frequencies of the 35delG mutation of the GJB2 gene in different Brazilian regions
CA Oliveira, CJ Pimpinati, F Alexandrino, LA Magna, AT Maciel-Guerra, ...
Genetic testing 11 (1), 1-3, 2007
322007
Evolution of periodontal disease: immune response and RANK/RANKL/OPG system
F Gibertoni, MEL Sommer, MAM Esquisatto, MEC Amaral, CA Oliveira, ...
Brazilian Dental Journal 28, 679-687, 2017
292017
Screening for mutations in the GJB3 gene in Brazilian patients with nonsyndromic deafness
F Alexandrino, CA Oliveira, FC Reis, AT Maciel-Guerra, EL Sartorato
Journal of Applied Genetics 45 (2), 249-254, 2004
282004
Genotoxic effect and rat hepatocyte death occurred after oxidative stress induction and antioxidant gene downregulation caused by long term fluoride exposure
FD Campos-Pereira, L Lopes-Aguiar, FL Renosto, GAS Nogueira, ...
Chemico-biological interactions 264, 25-33, 2017
252017
Perspectivas para triagem da deficiência auditiva genética: rastreamento da mutação 35delG em neonatos
VB Piatto, CA Oliveira, F Alexandrino, CJ Pimpinati, EL Sartorato
Jornal de Pediatria 81, 139-142, 2005
222005
Castration methods do not affect weight gain and have diverse impacts on the welfare of water buffalo males
LT Martins, MC Gonçalves, KCS Tavares, S Gaudêncio, PCS Neto, ...
Livestock Science 140 (1-3), 171-176, 2011
212011
Single Nucleotide Polymorphisms of the GJB2 and GJB6 Genes Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss
ANAP GRILLO, FM DE OLIVEIRA, GQ DE CARVALHO, RFV MEDRANO, ...
BioMed Research International 2015, 8, 2015
202015
Connexin mutations in Brazilian patients with skin disorders with or without hearing loss
F Alexandrino, CA de Oliveira, RF Magalhaes, MEB Florence, ...
American Journal of Medical Genetics Part A 149 (4), 681-684, 2009
192009
Genética molecular da deficiência auditiva não-sindrômica
VB Piatto, ECT Nascimento, F Alexandrino, CA Oliveira, ACP Lopes, ...
Revista Brasileira de Otorrinolaringologia 71, 216-223, 2005
192005
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