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Laboratory of Molecular Genetics - Faculty of Medical Sciences - Unicamp

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Produção bibliográfica

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Produção bibliográfica
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Barbieri RB, Bufalo NE, Secolin R, Silva AC, Assumpcao LV, Maciel RM, et al. Evidence that polymorphisms in detoxification genes modulate the susceptibility for sporadic medullary thyroid carcinoma. Eur J Endocrinol. 2012 Feb;166(2):241-5. PubMed

Planello AC, Campos MI, Meloto CB, Secolin R, Rizatti-Barbosa CM, Line SR, et al. Association of matrix metalloproteinase gene polymorphism with temporomandibular joint degeneration. Eur J Oral Sci. 2011 Feb;119(1):1-6. PubMed

Pedrazzoli M, Secolin R, Esteves LO, Pereira DS, Koike Bdel V, Louzada FM, et al. Interactions of polymorphisms in different clock genes associated with circadian phenotypes in humans. Genet Mol Biol. 2010 Oct;33(4):627-32. PubMed

Ottman R, Hirose S, Jain S, Lerche H, Lopes-Cendes I, et al. Genetic testing in the epilepsies--report of the ILAE Genetics Commission.Epilepsia. 2010 Apr;51(4):655-670. PubMed 

Secolin R, Banzato CE, Oliveira MC, Bittar MF, Santos ML, Dalgalarrondo P, et al. Family-based association study for bipolar affective disorder. Psychiatr Genet. 2010 Jun;20(3):126-9. PubMed

Secolin R, Maurer-Morelli C, Cendes F, Lopes-Cendes I. Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy. Epilepsia. 2010 Feb;51 Suppl 1:47-50. PubMed

Conte FF, Ribeiro PA, Marchesini RB, Pascoal VD, Silva JM, Oliveira AR, et al.Expression profile and distribution of Efhc1 gene transcript during rodent brain development. J Mol Neurosci. 2009 Sep;39(1-2):69-77. PubMed 

Murai MJ, Sassonia RC, Zamboni AH, Conte FF, Martins-de-Souza D, Aparicio R, et al. Characterization of the C-terminal half of human juvenile myoclonic epilepsy protein EFHC1: dimer formation blocks Ca2+ and Mg2+ binding to its functional EF-hand. Arch Biochem Biophys. 2008 Sep 1;477(1):131-138. PubMed

Pereira TC, Lopes-Cendes I. RNAi-mediated gene silencing as a principle of action of venoms and poisons. Med Hypotheses. 2008 Dec;70(6):1179-81. PubMed

Dogini DB, Ribeiro PA, Rocha C, Pereira TC, Lopes-Cendes I. MicroRNA expression profile in murine central nervous system development. J Mol Neurosci. 2008 Jul;35(3):331-337. PubMed

Ribeiro PA, Sbragia L, Gilioli R, Langone F, Conte FF, Lopes-Cendes I. Expression profile of Lgi1 gene in mouse brain during development. J Mol Neurosci. 2008 Jul;35(3):323-329. PubMed

Secolin R, Rocha CS, Torres FR, Santos ML, Maurer-Morelli CV, Santos NF, et al. LINKGEN: a new algorithm to process data in genetic linkage studies. Genomics. 2008 Jun;91(6):544-7. PubMed

Tsuneda SS, Torres FR, Montenegro MA, Guerreiro MM, Cendes F, Lopes-Cendes I. A new missense mutation found in the FLNA gene in a family with bilateral periventricular nodular heterotopia (BPNH) alters the splicing process. J Mol Neurosci. 2008 Jun;35(2):195-200. PubMed

Santos NF, Secolin R, Brandao-Almeida IL, Silva MS, Torres FR, Tsuneda SS, et al. A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27. Am J Med Genet A. 2008 May 1;146A(9):1151-7. PubMed

dos Santos CO, Zhou S, Secolin R, Wang X, Cunha AF, Higgs DR, et al. Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function. Am J Hematol. 2008 Feb;83(2):103-8. PubMed


Clemente CF, Tornatore TF, Theizen TH, Deckmann AC, Pereira TC, Lopes-Cendes I, et al. Targeting focal adhesion kinase with small interfering RNA prevents and reverses load-induced cardiac hypertrophy in mice. Circ Res. 2007 Dec 7;101(12):1339-48. PubMed

Franca MC, Jr., D'Abreu A, Maurer-Morelli CV, Secolin R, Appenzeller S, Alessio A, et al. Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum. Mov Disord. 2007 Aug 15;22(11):1556-62. PubMed

Maurer-Morelli CV, Marchesini RB, Secolin R, Santos NF, Kobayashi E, Cendes F, et al. Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy. Arq Neuropsiquiatr. 2007 Mar;65(1):20-3. PubMed

Maurer-Morelli CV, Secolin R, Marchesini RB, Santos NF, Kobayashi E, Cendes F, et al. THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy. Epilepsy Res. 2006 Oct;71(2-3):233-6. PubMed

Steiner CE, Guerreiro MM, Marques-de-Faria AP, Lopes-Cendes I. Laboratorial diagnosis of fragile-X syndrome: experience in a sample of individuals with pervasive developmental disorders. Arq Neuropsiquiatr. 2005 Sep;63(3A):564-70. PubMed

Torres FR, Montenegro MA, Marques-De-Faria AP, Guerreiro MM, Cendes F, Lopes-Cendes I. Mutation screening in a cohort of patients with lissencephaly and subcortical band heterotopia. Neurology. 2004 Mar 9;62(5):799-802. PubMed

Kobayashi E, Santos NF, Torres FR, Secolin R, Sardinha LA, Lopez-Cendes I, et al. Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras. Arch Neurol. 2003 Nov;60(11):1546-51. PubMed

Santos NF, Sousa SC, Kobayashi E, Torres FR, Sardinha JA, Cendes F, et al. Clinical and genetic heterogeneity in familial temporal lobe epilepsy. Epilepsia. 2002;43 Suppl 5:136. PubMed


Last Updated on Wednesday, 30 May 2012 08:46  

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