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Items: 31

1.

Genotyping of Single Nucleotide Polymorphisms Using Allele-Specific qPCR Producing Amplicons of Small Sizes Directly from Crude Serum Isolated from Capillary Blood by a Hand-Powered Paper Centrifuge.

Barra GB, Santa Rita TH, Jardim DP, Mesquita PG, Nobre CS, Jácomo RH, Abdalla Nery LF.

Diagnostics (Basel). 2019 Jan 11;9(1). pii: E9. doi: 10.3390/diagnostics9010009.

3.

Noninvasive fetal sex determination by analysis of cell-free fetal DNA in maternal capillary blood obtained by fingertip puncture.

Santa Rita TH, Nobre CS, Jácomo RH, Nery LFA, Barra GB.

Prenat Diagn. 2018 Apr 14. doi: 10.1002/pd.5265. [Epub ahead of print] No abstract available.

PMID:
29655231
4.

Association between suspected Zika virus disease during pregnancy and giving birth to a newborn with congenital microcephaly: a matched case-control study.

Santa Rita TH, Barra RB, Peixoto GP, Mesquita PG, Barra GB.

BMC Res Notes. 2017 Sep 6;10(1):457. doi: 10.1186/s13104-017-2796-1.

5.

Response to Letter by Hahn-Holbrook J., et al.

Zaconeta AM, Amato AA, Barra GB, Casulari da Motta LD, de Souza VC, Karnikowski MG, Casulari LA.

J Clin Endocrinol Metab. 2016 Feb;101(2):L7-8. doi: 10.1210/jc.2015-4186. No abstract available.

PMID:
26840120
6.

Aggressive tumor growth and clinical evolution in a patient with X-linked acro-gigantism syndrome.

Naves LA, Daly AF, Dias LA, Yuan B, Zakir JC, Barra GB, Palmeira L, Villa C, Trivellin G, Júnior AJ, Neto FF, Liu P, Pellegata NS, Stratakis CA, Lupski JR, Beckers A.

Endocrine. 2016 Feb;51(2):236-44. doi: 10.1007/s12020-015-0804-6. Epub 2015 Nov 25.

7.

Prevalence of the rs1801282 single nucleotide polymorphism of the PPARG gene in patients with metabolic syndrome.

Rocha RM, Barra GB, Rosa ÉC, Garcia ÉC, Amato AA, Azevedo MF.

Arch Endocrinol Metab. 2015 Aug;59(4):297-302. doi: 10.1590/2359-3997000000086.

8.

Allele frequencies of 38 insertion/deletion polymorphisms in a population sample from the Federal District (Brazil)--A territory that arose from nothing.

Santa Rita TH, Chianca CF, Nery LFA, Barra GB.

Forensic Sci Int Genet. 2015 Nov;19:79-80. doi: 10.1016/j.fsigen.2015.06.010. Epub 2015 Jul 7. No abstract available.

PMID:
26184901
9.

Cerebrospinal Fluid CRH Levels in Late Pregnancy Are Not Associated With New-Onset Postpartum Depressive Symptoms.

Zaconeta AM, Amato AA, Barra GB, Casulari da Motta LD, de Souza VC, Karnikowski MG, Casulari LA.

J Clin Endocrinol Metab. 2015 Aug;100(8):3159-64. doi: 10.1210/jc.2014-4503. Epub 2015 Jun 12.

PMID:
26066672
10.

EDTA-mediated inhibition of DNases protects circulating cell-free DNA from ex vivo degradation in blood samples.

Barra GB, Santa Rita TH, de Almeida Vasques J, Chianca CF, Nery LF, Santana Soares Costa S.

Clin Biochem. 2015 Oct;48(15):976-81. doi: 10.1016/j.clinbiochem.2015.02.014. Epub 2015 Mar 5.

11.

X-linked acrogigantism syndrome: clinical profile and therapeutic responses.

Beckers A, Lodish MB, Trivellin G, Rostomyan L, Lee M, Faucz FR, Yuan B, Choong CS, Caberg JH, Verrua E, Naves LA, Cheetham TD, Young J, Lysy PA, Petrossians P, Cotterill A, Shah NS, Metzger D, Castermans E, Ambrosio MR, Villa C, Strebkova N, Mazerkina N, Gaillard S, Barra GB, Casulari LA, Neggers SJ, Salvatori R, Jaffrain-Rea ML, Zacharin M, Santamaria BL, Zacharieva S, Lim EM, Mantovani G, Zatelli MC, Collins MT, Bonneville JF, Quezado M, Chittiboina P, Oldfield EH, Bours V, Liu P, W de Herder W, Pellegata N, Lupski JR, Daly AF, Stratakis CA.

Endocr Relat Cancer. 2015 Jun;22(3):353-67. doi: 10.1530/ERC-15-0038. Epub 2015 Feb 24.

12.

Fetal male lineage determination by analysis of Y-chromosome STR haplotype in maternal plasma.

Barra GB, Santa Rita TH, Chianca CF, Velasco LF, de Sousa CF, Nery LF, Costa SS.

Forensic Sci Int Genet. 2015 Mar;15:105-10. doi: 10.1016/j.fsigen.2014.11.006. Epub 2014 Nov 15.

13.

Low rate of oropharyngeal human papillomavirus infection of women with cervical lesions and their partners: new data from Brazilian population.

Marques AE, Barra GB, de Resende Oyama CN, Guerra EN.

J Oral Pathol Med. 2015 Jul;44(6):453-8. doi: 10.1111/jop.12252. Epub 2014 Sep 12.

PMID:
25212900
14.

Trp28Arg/Ile35Thr LHB gene variants are associated with elevated testosterone levels in women with polycystic ovary syndrome.

Batista MC, Duarte Ede F, Borba MD, Zingler E, Mangussi-Gomes J, dos Santos BT, de Moraes OL, Hayashida SA, Baracat EC, da Rocha Neves Fde A, Maciel GA, Bachega TA, Barra GB, Lofrano-Porto A.

Gene. 2014 Oct 15;550(1):68-73. doi: 10.1016/j.gene.2014.08.017. Epub 2014 Aug 8.

PMID:
25111116
15.

Haplotype diversity of 23 Y-chromosomal STRs in a population sample from the Federal District (Brazil)--a territory that arose from nothing.

Barra GB, Chianca CF, Santa Rita TH, Velasco LF, de Souza CF.

Int J Legal Med. 2014 Nov;128(6):945-7. doi: 10.1007/s00414-013-0960-2. Epub 2014 Jan 5.

PMID:
24390118
16.

Allele frequencies for 15 autosomal STRs in a population sample from the Federal District (Brazil)-a territory that arose from nothing.

Barra GB, Santa Rita TH, Chianca CF, Velasco LF, de Souza CF.

Int J Legal Med. 2014 Sep;128(5):741-2. doi: 10.1007/s00414-013-0866-z. Epub 2013 May 4.

PMID:
23645165
17.

Association of the rs7903146 single nucleotide polymorphism at the Transcription Factor 7-like 2 (TCF7L2) locus with type 2 diabetes in Brazilian subjects.

Barra GB, Dutra LA, Watanabe SC, Costa PG, Cruz PS, Azevedo MF, Amato AA.

Arq Bras Endocrinol Metabol. 2012 Nov;56(8):479-84.

PMID:
23295285
18.

Lack of association between the CC genotype of the rs7903146 polymorphism in the TCF7L2 gene and rheumatoid arthritis.

Mota LM, Rabelo Fde S, Lima FA, Lima RA, Carvalho JF, Barra GB, Amato AA.

Rev Bras Reumatol. 2012 Aug;52(4):523-8. English, Portuguese.

PMID:
22885420
19.

The effect of beta-2 adrenergic receptor haplotype variations on the haemodynamic response following spinal anaesthesia for caesarean delivery.

Daher M, Saito RB, Barra GB, Govêia CS, Magalhães E, Neves FA.

Anaesthesia. 2012 Nov;67(11):1251-9. doi: 10.1111/j.1365-2044.2012.07296.x. Epub 2012 Aug 13.

20.

Helix 12 dynamics and thyroid hormone receptor activity: experimental and molecular dynamics studies of Ile280 mutants.

Souza PC, Barra GB, Velasco LF, Ribeiro IC, Simeoni LA, Togashi M, Webb P, Neves FA, Skaf MS, Martínez L, Polikarpov I.

J Mol Biol. 2011 Oct 7;412(5):882-93. doi: 10.1016/j.jmb.2011.04.014. Epub 2011 Apr 21.

PMID:
21530542
21.

Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: an international collaborative study.

Daly AF, Tichomirowa MA, Petrossians P, Heliövaara E, Jaffrain-Rea ML, Barlier A, Naves LA, Ebeling T, Karhu A, Raappana A, Cazabat L, De Menis E, Montañana CF, Raverot G, Weil RJ, Sane T, Maiter D, Neggers S, Yaneva M, Tabarin A, Verrua E, Eloranta E, Murat A, Vierimaa O, Salmela PI, Emy P, Toledo RA, Sabaté MI, Villa C, Popelier M, Salvatori R, Jennings J, Longás AF, Labarta Aizpún JI, Georgitsi M, Paschke R, Ronchi C, Valimaki M, Saloranta C, De Herder W, Cozzi R, Guitelman M, Magri F, Lagonigro MS, Halaby G, Corman V, Hagelstein MT, Vanbellinghen JF, Barra GB, Gimenez-Roqueplo AP, Cameron FJ, Borson-Chazot F, Holdaway I, Toledo SP, Stalla GK, Spada A, Zacharieva S, Bertherat J, Brue T, Bours V, Chanson P, Aaltonen LA, Beckers A.

J Clin Endocrinol Metab. 2010 Nov;95(11):E373-83. doi: 10.1210/jc.2009-2556. Epub 2010 Aug 4.

22.
23.

Selenoprotein-related disease in a young girl caused by nonsense mutations in the SBP2 gene.

Azevedo MF, Barra GB, Naves LA, Ribeiro Velasco LF, Godoy Garcia Castro P, de Castro LC, Amato AA, Miniard A, Driscoll D, Schomburg L, de Assis Rocha Neves F.

J Clin Endocrinol Metab. 2010 Aug;95(8):4066-71. doi: 10.1210/jc.2009-2611. Epub 2010 May 25.

PMID:
20501692
24.

The Wnt signaling pathway and rheumatoid arthritis.

Rabelo Fde S, da Mota LM, Lima RA, Lima FA, Barra GB, de Carvalho JF, Amato AA.

Autoimmun Rev. 2010 Feb;9(4):207-10. doi: 10.1016/j.autrev.2009.08.003. Epub 2009 Aug 13. Review.

PMID:
19683077
25.

Allele-specific PCR assay to genotype SNP rs7903146 in TCF7L2 gene for rapid screening of diabetes susceptibility.

Dutra LA, Costa PG, Velasco LF, Amato AA, Barra GB.

Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1362-6.

PMID:
19169495
26.

A novel mutation of thyroid hormone receptor beta (I431V) impairs corepressor release, and induces thyroid hormone resistance syndrome.

Ferreira Azevedo M, Barra GB, Medeiros LD, Simeoni LA, Naves LA, Neves Fde A.

Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1304-12.

PMID:
19169485
27.

Pendred syndrome in a large consanguineous Brazilian family caused by a homozygous mutation in the SLC26A4 gene.

Lofrano-Porto A, Barra GB, Nascimento PP, Costa PG, Garcia EC, Vaz RF, Batista AR, Freitas AC, Cherulli BL, Bahmad F Jr, Figueiredo LG, Neves FA, Casulari LA.

Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1296-303.

PMID:
19169484
28.

Luteinizing hormone beta mutation and hypogonadism in men and women.

Lofrano-Porto A, Barra GB, Giacomini LA, Nascimento PP, Latronico AC, Casulari LA, da Rocha Neves Fde A.

N Engl J Med. 2007 Aug 30;357(9):897-904.

29.

Thyroid hormone response element organization dictates the composition of active receptor.

Velasco LF, Togashi M, Walfish PG, Pessanha RP, Moura FN, Barra GB, Nguyen P, Rebong R, Yuan C, Simeoni LA, Ribeiro RC, Baxter JD, Webb P, Neves FA.

J Biol Chem. 2007 Apr 27;282(17):12458-66. Epub 2007 Feb 20.

30.

Negative regulation of superoxide dismutase-1 promoter by thyroid hormone.

Santos GM, Afonso V, Barra GB, Togashi M, Webb P, Neves FA, Lomri N, Lomri A.

Mol Pharmacol. 2006 Sep;70(3):793-800. Epub 2006 May 31.

PMID:
16738222
31.

[Molecular mechanism of thyroid hormone action].

Barra GB, Velasco LF, Pessanha RP, Campos AM, Moura FN, Dias SM, Polikarpov I, Ribeiro RC, Simeoni LA, Neves FA.

Arq Bras Endocrinol Metabol. 2004 Feb;48(1):25-39. Epub 2004 Jun 1. Review. Portuguese.

PMID:
15611816

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