Figuera LE - Search Results

1

SOD2 Gene Variants (rs4880 and rs5746136) and Their Association with Breast Cancer Risk.

Gallegos-Arreola MP, Ramírez-Patiño R, Sánchez-López JY, Zúñiga-González GM, Figuera LE, Delgado-Saucedo JI, Gómez-Meda BC, Rosales-Reynoso MA, Puebla-Pérez AM, Lemus-Varela ML, Garibaldi-Ríos AF, Marín-Domínguez NA, Pacheco-Verduzco DP, Mohamed-Flores EA. Gallegos-Arreola MP, et al. Among authors: figuera le. Curr Issues Mol Biol. 2022 Oct 26;44(11):5221-5233. doi: 10.3390/cimb44110355. Curr Issues Mol Biol. 2022. PMID: 36354667 Free PMC article.

2

Heteroallelic monozygotic twins and triplets.

Cantú JM, Díaz-Gallardo MY, Barros-Núñez P, Figuera LE. Cantú JM, et al. Among authors: figuera le. Am J Med Genet. 1998 May 1;77(2):166-7. Am J Med Genet. 1998. PMID: 9605292 No abstract available.

3

Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1.

Figuera LE, Pandolfo M, Dunne PW, Cantú JM, Patel PI. Figuera LE, et al. Nat Genet. 1995 Jun;10(2):202-7. doi: 10.1038/ng0695-202. Nat Genet. 1995. PMID: 7663516

4

Geleophysic dysplasia vs. Myhre syndrome.

Figuera LE. Figuera LE. Am J Med Genet. 1996 Nov 11;65(4):361-2. doi: 10.1002/(SICI)1096-8628(19961111)65:4<361::AID-AJMG25>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8923952 No abstract available.

5

Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions.

Yang SP, Bidichandani SI, Figuera LE, Juyal RC, Saxon PJ, Baldini A, Patel PI. Yang SP, et al. Among authors: figuera le. Am J Hum Genet. 1997 May;60(5):1184-93. Am J Hum Genet. 1997. PMID: 9150166 Free PMC article.

6

Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum.

Struk B, Cai L, Zäch S, Ji W, Chung J, Lumsden A, Stumm M, Huber M, Schaen L, Kim CA, Goldsmith LA, Viljoen D, Figuera LE, Fuchs W, Munier F, Ramesar R, Hohl D, Richards R, Neldner KH, Lindpaintner K. Struk B, et al. Among authors: figuera le. J Mol Med (Berl). 2000;78(5):282-6. doi: 10.1007/s001090000114. J Mol Med (Berl). 2000. PMID: 10954200

7

Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients.

Juyal RC, Figuera LE, Hauge X, Elsea SH, Lupski JR, Greenberg F, Baldini A, Patel PI. Juyal RC, et al. Among authors: figuera le. Am J Hum Genet. 1996 May;58(5):998-1007. Am J Hum Genet. 1996. PMID: 8651284 Free PMC article.

8

Virtual molecular medicine in developing countries: the Mexican initiative.

Cantu JM, Figuera LE. Cantu JM, et al. Among authors: figuera le. Mol Med Today. 2000 May;6(5):190-2. doi: 10.1016/s1357-4310(00)01682-8. Mol Med Today. 2000. PMID: 10782065

9

Effects of enzyme replacement therapy in Fabry disease--a comprehensive review of the medical literature.

Lidove O, West ML, Pintos-Morell G, Reisin R, Nicholls K, Figuera LE, Parini R, Carvalho LR, Kampmann C, Pastores GM, Mehta A. Lidove O, et al. Among authors: figuera le. Genet Med. 2010 Nov;12(11):668-79. doi: 10.1097/GIM.0b013e3181f13b75. Genet Med. 2010. PMID: 20962662 Free article. Review.

10

Ambral syndrome and congenital generalized hypertrichosis.

Figuera LE, Cantu JM. Figuera LE, et al. Clin Genet. 1994 Nov;46(5):384. doi: 10.1111/j.1399-0004.1994.tb04186.x. Clin Genet. 1994. PMID: 7889653 No abstract available.

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