Acosta AX - Search Results

1

Prevalence of the CCR5Delta32 mutation in Brazilian populations and cell susceptibility to HIV-1 infection.

Grimaldi R, Shindo N, Acosta AX, Dourado I, Brites C, de Melo Carvalho O, Brito I, Bou-Habib DC, Galvão-Castro B. Grimaldi R, et al. Among authors: acosta ax. Hum Genet. 2002 Jul;111(1):102-4. doi: 10.1007/s00439-002-0747-x. Epub 2002 Jun 13. Hum Genet. 2002. PMID: 12136242

2

Low frequency of the deltaAF508 mutation of the CFTR gene in a highly admixed population in Bahia, Brazil.

Moura Costa FM, Santana MA, Lemos AC, Galvão-Castro B, Acosta AX. Moura Costa FM, et al. Among authors: acosta ax. Hum Biol. 2007 Jun;79(3):293-7. doi: 10.1353/hub.2007.0040. Hum Biol. 2007. PMID: 18078202

3

Correlation between polymorphisms at interleukin-6 but not at interleukin-10 promoter and the risk of human T lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis in Brazilian individuals.

Gadelha SR, Junior Alcântara LC, Costa GC, Acosta AX, Rios D, Kashima S, Covas DT, Galvão-Castro B. Gadelha SR, et al. Among authors: acosta ax. J Med Virol. 2008 Dec;80(12):2141-6. doi: 10.1002/jmv.21341. J Med Virol. 2008. PMID: 19040291

4

Distribution of SDF1-3'A polymorphisms in three different ethnic groups from Brazil.

Grimaldi R, Acosta AX, Machado TM, Bomfim TF, Galvão-Castro B. Grimaldi R, et al. Among authors: acosta ax. Braz J Infect Dis. 2010 Mar-Apr;14(2):197-200. Braz J Infect Dis. 2010. PMID: 20563451 Free article.

5

HLA-Bw4-B*57 and Cw*18 alleles are associated with plasma viral load modulation in HIV-1 infected individuals in Salvador, Brazil.

Silva EM, Acosta AX, Santos EJ, Netto EM, Lemaire DC, Oliveira AS, Barbosa CM, Bendicho MT, Galvão-Castro B, Brites C. Silva EM, et al. Among authors: acosta ax. Braz J Infect Dis. 2010 Sep-Oct;14(5):468-75. Braz J Infect Dis. 2010. PMID: 21221475 Free article.

6

Ten novel mutations in the phenylalanine hydroxylase gene (PAH) observed in Brazilian patients with phenylketonuria.

Acosta AX, Silva WA Jr, Carvalho TM, Zago MA. Acosta AX, et al. Hum Mutat. 2001;17(1):77. doi: 10.1002/1098-1004(2001)17:1<77::AID-HUMU19>3.0.CO;2-S. Hum Mutat. 2001. PMID: 11139255

7

Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil.

Manzoli GN, Bademci G, Acosta AX, Félix TM, Cengiz FB, Foster J 2nd, Da Silva DS, Menendez I, Sanchez-Pena I, Tekin D, Blanton SH, Abe-Sandes K, Liu XZ, Tekin M. Manzoli GN, et al. Among authors: acosta ax. Ann Hum Genet. 2016 Nov;80(6):327-331. doi: 10.1111/ahg.12177. Ann Hum Genet. 2016. PMID: 27870113 Free PMC article.

8

Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria.

Acosta A, Silva W Jr, Carvalho T, Gomes M, Zago M. Acosta A, et al. Hum Mutat. 2001 Feb;17(2):122-30. doi: 10.1002/1098-1004(200102)17:2<122::AID-HUMU4>3.0.CO;2-C. Hum Mutat. 2001. PMID: 11180595

9

Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis.

Cerqueira TLO, Ramos YR, Strappa GB, Jesus MS, Santos JG, Sousa C, Carvalho G, Fernandes V, Boa-Sorte N, Amorim T, Silva TM, Ladeia AMT, Acosta AX, Ramos HE. Cerqueira TLO, et al. Among authors: acosta ax. Arch Endocrinol Metab. 2018 Aug;62(4):466-471. doi: 10.20945/2359-3997000000065. Arch Endocrinol Metab. 2018. PMID: 30304112 Free PMC article.

10

Population medical genetics: translating science to the community.

Giugliani R, Bender F, Couto R, Bochernitsan A, Brusius-Facchin AC, Burin M, Amorim T, Acosta AX, Purificação A, Leistner-Segal S, Saraiva-Pereira ML, Jardim LB, Matte U, Riegel M, Cardoso-Dos-Santos AC, Rodrigues G, Oliveira MZ, Tagliani-Ribeiro A, Heck S, Dresch V, Schuler-Faccini L, Kubaski F. Giugliani R, et al. Among authors: acosta ax. Genet Mol Biol. 2019;42(1 suppl 1):312-320. doi: 10.1590/1678-4685-GMB-2018-0096. Epub 2019 Apr 11. Genet Mol Biol. 2019. PMID: 30985854 Free PMC article.

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