Coloma A - Search Results

1

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: coloma a. Hum Mol Genet. 1994 Aug;3(8):1441. doi: 10.1093/hmg/3.8.1441. Hum Mol Genet. 1994. PMID: 7987335 No abstract available.

2

Isolation of microsatellites from the spinal muscular atrophy (SMA) candidate region on chromosome 5q and linkage analysis in Spanish SMA families.

Velasco E, Valero C, García E, de la Puente A, Cruces J, San Millán JL, del Castillo I, Coloma A, Moreno F, Hernández-Chico C. Velasco E, et al. Among authors: coloma a. Eur J Hum Genet. 1995;3(2):96-101. doi: 10.1159/000472282. Eur J Hum Genet. 1995. PMID: 7552147

3

A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK.

Pérez Jurado LA, Wang YK, Peoples R, Coloma A, Cruces J, Francke U. Pérez Jurado LA, et al. Among authors: coloma a. Hum Mol Genet. 1998 Mar;7(3):325-34. doi: 10.1093/hmg/7.3.325. Hum Mol Genet. 1998. PMID: 9466987

4

Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1.

Jurado LA, Coloma A, Cruces J. Jurado LA, et al. Among authors: coloma a. Genomics. 1999 Jun 1;58(2):171-80. doi: 10.1006/geno.1999.5819. Genomics. 1999. PMID: 10366449

5

Factor IXMadrid 2: a deletion/insertion in factor IX gene which abolishes the sequence of the donor junction at the exon IV-intron d splice site.

Solera J, Magallón M, Martin-Villar J, Coloma A. Solera J, et al. Among authors: coloma a. Am J Hum Genet. 1992 Feb;50(2):434-7. Am J Hum Genet. 1992. PMID: 1346483 Free PMC article.

6

Gallus gallus orthologous to human alpha-dystroglycanopathies candidate genes: Gene expression and characterization during chicken embryogenesis.

Izquierdo-Lahuerta A, de Luis O, Gómez-Esquer F, Cruces J, Coloma A. Izquierdo-Lahuerta A, et al. Among authors: coloma a. Biochem Biophys Res Commun. 2016 Sep 23;478(3):1043-8. doi: 10.1016/j.bbrc.2016.08.027. Epub 2016 Aug 20. Biochem Biophys Res Commun. 2016. PMID: 27553274

7

Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality.

Willer T, Prados B, Falcón-Pérez JM, Renner-Müller I, Przemeck GK, Lommel M, Coloma A, Valero MC, de Angelis MH, Tanner W, Wolf E, Strahl S, Cruces J. Willer T, et al. Among authors: coloma a. Proc Natl Acad Sci U S A. 2004 Sep 28;101(39):14126-31. doi: 10.1073/pnas.0405899101. Epub 2004 Sep 21. Proc Natl Acad Sci U S A. 2004. PMID: 15383666 Free PMC article.

8

Structure, organization, and chromosomal mapping of the human neurogranin gene (NRGN).

Martínez de Arrieta C, Pérez Jurado L, Bernal J, Coloma A. Martínez de Arrieta C, et al. Among authors: coloma a. Genomics. 1997 Apr 15;41(2):243-9. doi: 10.1006/geno.1997.4622. Genomics. 1997. PMID: 9143500

9

Identification of a new haemophilia BM case produced by a mutation located at the carboxy terminal cleavage site of activation peptide.

Solera J, Magallón M, Martin-Villar J, Coloma A. Solera J, et al. Among authors: coloma a. Br J Haematol. 1991 Jul;78(3):385-9. doi: 10.1111/j.1365-2141.1991.tb04452.x. Br J Haematol. 1991. PMID: 1651755

10

Entraining synthetic genetic oscillators.

Wagemakers A, Buldú JM, Sanjuán MA, de Luis O, Izquierdo A, Coloma A. Wagemakers A, et al. Among authors: coloma a. Chaos. 2009 Sep;19(3):033139. doi: 10.1063/1.3231089. Chaos. 2009. PMID: 19792019

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