del Castillo I - Search Results

1

A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci.

Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, del Castillo I, Chardenoux S, Morais D, Lathrop M, Petit C, Moreno F. Modamio-Høybjør S, et al. Among authors: del castillo i. J Med Genet. 2004 Feb;41(2):e14. doi: 10.1136/jmg.2003.012500. J Med Genet. 2004. PMID: 14757864 Free PMC article. No abstract available.

2

Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome.

del Castillo I, Cohen-Salmon M, Blanchard S, Lutfalla G, Petit C. del Castillo I, et al. Nat Genet. 1992 Dec;2(4):305-10. doi: 10.1038/ng1292-305. Nat Genet. 1992. PMID: 1303284

3

mprA, an Escherichia coli gene that reduces growth-phase-dependent synthesis of microcins B17 and C7 and blocks osmoinduction of proU when cloned on a high-copy-number plasmid.

del Castillo I, Gómez JM, Moreno F. del Castillo I, et al. J Bacteriol. 1990 Jan;172(1):437-45. doi: 10.1128/jb.172.1.437-445.1990. J Bacteriol. 1990. PMID: 2152912 Free PMC article.

4

Characterization of the promoter of the human KAL gene, responsible for the X-chromosome-linked Kallmann syndrome.

Cohen-Salmon M, Tronche F, del Castillo I, Petit C. Cohen-Salmon M, et al. Among authors: del castillo i. Gene. 1995 Oct 27;164(2):235-42. doi: 10.1016/0378-1119(95)00481-k. Gene. 1995. PMID: 7590336

5

Dinucleotide repeat polymorphisms at the D5S1356, D5S1357 and D7S1480 loci.

Velasco E, de la Puente A, Cruces J, Valero MC, García-Patiño E, del Castillo I, Coloma A, Moreno F, Hernández-Chico C. Velasco E, et al. Among authors: del castillo i. Hum Mol Genet. 1994 Aug;3(8):1441. doi: 10.1093/hmg/3.8.1441. Hum Mol Genet. 1994. PMID: 7987335 No abstract available.

6

Isolation and characterization of the gene responsible for the X chromosome-linked Kallmann syndrome.

Legouis R, Cohen-Salmon M, Del Castillo I, Petit C. Legouis R, et al. Among authors: del castillo i. Biomed Pharmacother. 1994;48(5-6):241-6. doi: 10.1016/0753-3322(94)90139-2. Biomed Pharmacother. 1994. PMID: 7999985 Review.

7

A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22.

del Castillo I, Villamar M, Sarduy M, Romero L, Herraiz C, Hernández FJ, Rodríguez M, Borrás I, Montero A, Bellón J, Tapia MC, Moreno F. del Castillo I, et al. Hum Mol Genet. 1996 Sep;5(9):1383-7. doi: 10.1093/hmg/5.9.1383. Hum Mol Genet. 1996. PMID: 8872482

8

Deafness locus DFNB16 is located on chromosome 15q13-q21 within a 5-cM interval flanked by markers D15S994 and D15S132.

Villamar M, del Castillo I, Valle N, Romero L, Moreno F. Villamar M, et al. Among authors: del castillo i. Am J Hum Genet. 1999 Apr;64(4):1238-41. doi: 10.1086/302321. Am J Hum Genet. 1999. PMID: 10090914 Free PMC article. No abstract available.

9

[Non-syndromic familial hearing impairment transmitted by mitochondrial inheritance].

Morales Angulo C, Del Castillo I, Sarduy M, Villamar M, Mazón A, Moreno F. Morales Angulo C, et al. Among authors: del castillo i. Acta Otorrinolaringol Esp. 1999 Mar;50(2):93-9. Acta Otorrinolaringol Esp. 1999. PMID: 10217681 Spanish.

10

Characterization of the genes encoding the SheA haemolysin in Escherichia coli O157:H7 and Shigella flexneri 2a.

del Castillo FJ, Moreno F, del Castillo I. del Castillo FJ, et al. Among authors: del castillo i. Res Microbiol. 2000 Apr;151(3):229-30. doi: 10.1016/s0923-2508(00)00143-1. Res Microbiol. 2000. PMID: 10865950 Free article. No abstract available.

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