Ayuso C - Search Results

1

Molecular evidence of field cancerization initiated by diabetes in colon cancer patients.

Del Puerto-Nevado L, Minguez P, Corton M, Solanes-Casado S, Prieto I, Mas S, Sanz AB, Gonzalez-Alonso P, Villaverde C, Portal-Nuñez S, Aguilera O, Gomez-Guerrero C, Esbrit P, Vivanco F, Gonzalez N, Ayuso C, Ortiz A, Rojo F, Egido J, Alvarez-Llamas G, Garcia-Foncillas J; DiabetesCancerConnect Consortium. Del Puerto-Nevado L, et al. Among authors: ayuso c. Mol Oncol. 2019 Apr;13(4):857-872. doi: 10.1002/1878-0261.12438. Epub 2019 Feb 16. Mol Oncol. 2019. PMID: 30628165 Free PMC article.

2

Gene symbol: ABCA4. Disease: Stargardt disease 1.

Riveiro-Alvarez R, Trujillo MJ, Cantalapiedra D, Vallespin E, Villaverde C, Valverde D, Ayuso C. Riveiro-Alvarez R, et al. Among authors: ayuso c. Hum Genet. 2006 Jul;119(6):671. Hum Genet. 2006. PMID: 17128450 No abstract available.

3

Gene symbol: NDP. Disease: Norrie disease.

Riveiro-Alvarez R, Trujillo MJ, Gimenez A, Cantalapiedra D, Vallespin E, Villaverde C, Ayuso C. Riveiro-Alvarez R, et al. Among authors: ayuso c. Hum Genet. 2006 Jul;119(6):675. Hum Genet. 2006. PMID: 17128466 No abstract available.

4

Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hd0510.

Vallespin E, Cantalapiedra D, Garcia-Hoyos M, Riveiro R, Villaverde C, Trujillo-Tiebas MJ, Ayuso C. Vallespin E, et al. Among authors: ayuso c. Hum Genet. 2006 Feb;118(6):774. Hum Genet. 2006. PMID: 17297678 No abstract available.

5

Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0534.

Vallespin E, Cantalapiedra D, Garcia-Hoyos M, Riveiro R, Villaverde C, Trujillo-Tiebas MJ, Ayuso C. Vallespin E, et al. Among authors: ayuso c. Hum Genet. 2006 Feb;118(6):777. Hum Genet. 2006. PMID: 17297689 No abstract available.

6

Novel human pathological mutations. Gene symbol: RS1. Disease: X-linked juvenile retinoschisis.

Riveiro-Alvarez R, Trujillo-Tiebas MJ, Gimenez A, Cantalapiedra D, Vallespin E, Aguirre-Lamban J, Villaverde C, Ayuso C. Riveiro-Alvarez R, et al. Among authors: ayuso c. Hum Genet. 2007 Jun;121(5):647. Hum Genet. 2007. PMID: 17879437 No abstract available.

7

Novel human pathological mutations. Gene symbol: CHM. Disease: choroideraemia.

Villaverde C, Trujillo-Tiebas MJ, Garcia-Hoyos M, Perez N, Narvaiza RC, Guillén E, Ayuso C. Villaverde C, et al. Among authors: ayuso c. Hum Genet. 2007 Jun;121(5):648. Hum Genet. 2007. PMID: 17879443 No abstract available.

8

Novel human pathological mutations. Gene symbol: CHM. Disease: choroideraemia.

Villaverde C, Trujillo-Tiebas MJ, Garcia-Hoyos M, Narvaiza RC, Perez N, Garcia-Sandoval B, Ayuso C. Villaverde C, et al. Among authors: ayuso c. Hum Genet. 2007 Jun;121(5):648. Hum Genet. 2007. PMID: 17879444 No abstract available.

9

Frequency of CEP290 c.2991_1655A>G mutation in 175 Spanish families affected with Leber congenital amaurosis and early-onset retinitis pigmentosa.

Vallespin E, Lopez-Martinez MA, Cantalapiedra D, Riveiro-Alvarez R, Aguirre-Lamban J, Avila-Fernandez A, Villaverde C, Trujillo-Tiebas MJ, Ayuso C. Vallespin E, et al. Among authors: ayuso c. Mol Vis. 2007 Nov 27;13:2160-2. Mol Vis. 2007. PMID: 18079693

10

Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray.

Ávila-Fernández A, Cantalapiedra D, Aller E, Vallespín E, Aguirre-Lambán J, Blanco-Kelly F, Corton M, Riveiro-Álvarez R, Allikmets R, Trujillo-Tiebas MJ, Millán JM, Cremers FP, Ayuso C. Ávila-Fernández A, et al. Among authors: ayuso c. Mol Vis. 2010 Dec 3;16:2550-8. Mol Vis. 2010. PMID: 21151602 Free PMC article.

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