Caputo M - Search Results

1

Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7.

Machiavelli GA, Caputo M, Rivolta CM, Olcese MC, Gruñeiro-Papendieck L, Chiesa A, González-Sarmiento R, Targovnik HM. Machiavelli GA, et al. Among authors: caputo m. Clin Endocrinol (Oxf). 2010 Jan;72(1):112-21. doi: 10.1111/j.1365-2265.2009.03621.x. Epub 2009 May 2. Clin Endocrinol (Oxf). 2010. PMID: 19438905

2

Variable number of tandem repeats of the insulin gene determines susceptibility to latent autoimmune diabetes in adults.

Cerrone GE, Caputo M, Lopez AP, González C, Massa C, Cédola N, Targovnik HM, Frechtel GD. Cerrone GE, et al. Among authors: caputo m. Mol Diagn. 2004;8(1):43-9. doi: 10.1007/BF03260046. Mol Diagn. 2004. PMID: 15230641

3

[HLA DQB1 genotyping in latent autoimmune diabetes of adults (LADA)].

Caputo M, Cerrone GE, Lopez AP, Gonzalez C, Mazza C, Cedola N, Puchulu FM, Targovnik HM, Frechtel GD. Caputo M, et al. Medicina (B Aires). 2005;65(3):235-40. Medicina (B Aires). 2005. PMID: 16042135 Spanish.

4

Cytotoxic T lymphocyte antigen 4 heterozygous codon 49 A/G dimorphism is associated to latent autoimmune diabetes in adults (LADA).

Caputo M, Cerrone GE, López AP, Villalba A, Krochik GA, Cédola FN, Targovnik HM, Frechtel GD. Caputo M, et al. Autoimmunity. 2005 Jun;38(4):277-81. doi: 10.1080/08916930500158203. Autoimmunity. 2005. PMID: 16206510

5

A simple method for the identification of three major haplotypes of the beta2AR.

Cerrone GE, Pérez MS, Caputo M, Targovnik HM, Frechtel GD. Cerrone GE, et al. Among authors: caputo m. Mol Cell Probes. 2007 Jun;21(3):222-5. doi: 10.1016/j.mcp.2006.12.004. Epub 2007 Jan 12. Mol Cell Probes. 2007. PMID: 17303378

6

Congenital hypothyroidism with goitre caused by new mutations in the thyroglobulin gene.

Caputo M, Rivolta CM, Esperante SA, Gruñeiro-Papendieck L, Chiesa A, Pellizas CG, González-Sarmiento R, Targovnik HM. Caputo M, et al. Clin Endocrinol (Oxf). 2007 Sep;67(3):351-7. doi: 10.1111/j.1365-2265.2007.02889.x. Epub 2007 May 28. Clin Endocrinol (Oxf). 2007. PMID: 17532758

7

No evidence of association of CTLA-4 -318 C/T, 159 C/T, 3' STR and SUMO4 163 AG polymorphism with autoimmune diabetes.

Caputo M, Cerrone GE, Mazza C, Cédola N, Targovnik HM, Gustavo DF. Caputo M, et al. Immunol Invest. 2007;36(3):259-70. doi: 10.1080/08820130601109735. Immunol Invest. 2007. PMID: 17558709

8

Recurrence of the p.R277X/p.R1511X compound heterozygous mutation in the thyroglobulin gene in unrelated families with congenital goiter and hypothyroidism: haplotype analysis using intragenic thyroglobulin polymorphisms.

Caputo M, Rivolta CM, Gutnisky VJ, Gruñeiro-Papendieck L, Chiesa A, Medeiros-Neto G, González-Sarmiento R, Targovnik HM. Caputo M, et al. J Endocrinol. 2007 Oct;195(1):167-77. doi: 10.1677/JOE-07-0033. J Endocrinol. 2007. PMID: 17911408

9

Identification and characterization of new variants of three associated SNPs and a microsatellite in the TSH receptor gene which are useful for genetic studies.

Esperante SA, Rivolta CM, Caputo M, González-Sarmiento R, Targovnik HM. Esperante SA, et al. Among authors: caputo m. Mol Cell Probes. 2008 Oct-Dec;22(5-6):281-6. doi: 10.1016/j.mcp.2008.06.003. Epub 2008 Jul 4. Mol Cell Probes. 2008. PMID: 18652889

10

Analysis of thyroglobulin gene polymorphisms in patients with autoimmune thyroiditis.

Caputo M, Rivolta CM, Mories T, Corrales JJ, Galindo P, González-Sarmiento R, Targovnik HM, Miralles-García JM. Caputo M, et al. Endocrine. 2010 Jun;37(3):389-95. doi: 10.1007/s12020-010-9317-5. Epub 2010 Mar 18. Endocrine. 2010. PMID: 20960158

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