Solans A - Search Results

1

Comprehensive screening procedure for detection of stimulants, narcotics, adrenergic drugs, and their metabolites in human urine.

Solans A, Carnicero M, de la Torre R, Segura J. Solans A, et al. J Anal Toxicol. 1995 Mar-Apr;19(2):104-14. doi: 10.1093/jat/19.2.104. J Anal Toxicol. 1995. PMID: 7769779

2

Determination of morphine and codeine in urine by gas chromatography-mass spectrometry.

Solans A, de la Torre R, Segura J. Solans A, et al. J Pharm Biomed Anal. 1990;8(8-12):905-9. doi: 10.1016/0731-7085(90)80140-k. J Pharm Biomed Anal. 1990. PMID: 2100640

3

Simultaneous detection of methylphenidate and its main metabolite, ritalinic acid, in doping control.

Solans A, Carnicero M, De La Torre R, Segura J. Solans A, et al. J Chromatogr B Biomed Appl. 1994 Aug 19;658(2):380-4. doi: 10.1016/0378-4347(94)00234-7. J Chromatogr B Biomed Appl. 1994. PMID: 7820267

4

CYP1A2-catalyzed conversion of dietary heterocyclic amines to their proximate carcinogens is their major route of metabolism in humans.

Boobis AR, Lynch AM, Murray S, de la Torre R, Solans A, Farré M, Segura J, Gooderham NJ, Davies DS. Boobis AR, et al. Among authors: solans a. Cancer Res. 1994 Jan 1;54(1):89-94. Cancer Res. 1994. PMID: 8261468 Clinical Trial.

5

The 9-bp deletion in region V of mitochondrial DNA: evidence of mutation recurrence.

Barrientos A, Casademont J, Solans A, Moral P, Cardellach F, Urbano-Márquez A, Estivill X, Nunes V. Barrientos A, et al. Among authors: solans a. Hum Genet. 1995 Aug;96(2):225-8. doi: 10.1007/BF00207385. Hum Genet. 1995. PMID: 7635476

6

A human homologue of Drosophila minibrain (MNB) is expressed in the neuronal regions affected in Down syndrome and maps to the critical region.

Guimerá J, Casas C, Pucharcòs C, Solans A, Domènech A, Planas AM, Ashley J, Lovett M, Estivill X, Pritchard MA. Guimerá J, et al. Among authors: solans a. Hum Mol Genet. 1996 Sep;5(9):1305-10. doi: 10.1093/hmg/5.9.1305. Hum Mol Genet. 1996. PMID: 8872470

7

Cloning and characterization of human FTCD on 21q22.3, a candidate gene for glutamate formiminotransferase deficiency.

Solans A, Estivill X, de la Luna S. Solans A, et al. Cytogenet Cell Genet. 2000;88(1-2):43-9. doi: 10.1159/000015483. Cytogenet Cell Genet. 2000. PMID: 10773664

8

A new aspartyl protease on 21q22.3, BACE2, is highly similar to Alzheimer's amyloid precursor protein beta-secretase.

Solans A, Estivill X, de La Luna S. Solans A, et al. Cytogenet Cell Genet. 2000;89(3-4):177-84. doi: 10.1159/000015608. Cytogenet Cell Genet. 2000. PMID: 10965118

9

Cytotoxicity of a mutant huntingtin fragment in yeast involves early alterations in mitochondrial OXPHOS complexes II and III.

Solans A, Zambrano A, Rodríguez M, Barrientos A. Solans A, et al. Hum Mol Genet. 2006 Oct 15;15(20):3063-81. doi: 10.1093/hmg/ddl248. Epub 2006 Sep 12. Hum Mol Genet. 2006. PMID: 16968735

10

Cosmid contig and transcriptional map of three regions of human chromosome 21q22: identification of 37 novel transcripts by direct selection.

Guimera J, Pucharcós C, Domènech A, Casas C, Solans A, Gallardo T, Ashley J, Lovett M, Estivill X, Pritchard M. Guimera J, et al. Among authors: solans a. Genomics. 1997 Oct 1;45(1):59-67. doi: 10.1006/geno.1997.4861. Genomics. 1997. PMID: 9339361

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