![Foto de MARIA ISABEL](/img/nophoto.png)
MARIA ISABEL
ARRIETA SAEZ
Investigador/a en el periodo 1989-2017
Publicaciones (25) Publicaciones de MARIA ISABEL ARRIETA SAEZ
2016
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Study of the genetic etiology of primary ovarian insufficiency: FMR1 gene
Genes, Vol. 7, Núm. 12
2015
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Evaluation of genotoxic effects of antihypertensive drugs: Angiotensin II receptor blockers
Antihypertensive Drugs: Pharmacology, Medical Uses and Potential Side Effects (Nova Science Publishers, Inc.), pp. 55-78
2014
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Genotoxic evaluation of five Angiotesin II receptor blockers: In vivo and in vitro micronucleus assay
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, Vol. 767, pp. 1-7
2013
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Allelic and genotypic frequencies of platelet glycoprotein polymorphisms in a Portuguese population
Revista Portuguesa de Cardiologia, Vol. 32, Núm. 2, pp. 111-115
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Study of FMR1 gene association with ovarian dysfunction in a sample from the Basque Country
Gene, Vol. 521, Núm. 1, pp. 145-149
2012
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Single Nucleotide Polymorphism and FMR1 CGG Repeat Instability in Two Basque Valleys
Annals of Human Genetics, Vol. 76, Núm. 2, pp. 110-120
2010
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Assessment of the genotoxicity of atenolol in human peripheral blood lymphocytes: Correlation between chromosomal fragility and content of micronuclei
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, Vol. 695, Núm. 1-2, pp. 46-54
2008
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Fragile X gene stability in Basque valleys: Prevalence of premutation and intermediate alleles
Human Biology, Vol. 80, Núm. 6, pp. 593-600
2004
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A new insight into fragile X syndrome among Basque population
American Journal of Medical Genetics, Vol. 128 A, Núm. 3, pp. 250-255
2003
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Dermatoglyphic variation in Spanish Basque populations
Human Biology, Vol. 75, Núm. 2, pp. 265-291
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Haplotypes in the Dystrophin DNA Segment Point to a Mosaic Origin of Modern Human Diversity
American Journal of Human Genetics, Vol. 73, Núm. 5, pp. 994-1015
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The FMR1 CGG repeat and linked microsatellite markers in two Basque valleys
Heredity, Vol. 90, Núm. 3, pp. 206-211
2002
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Chromosomal fragility in a behavioral disorder
Behavior Genetics, Vol. 32, Núm. 6, pp. 397-412
2001
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Determination of the β-blocker atenolol in plasma by capillary zone electrophoresis
Journal of Chromatography A
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Evaluation of the cytogenetic damage induced by the antihypertensive drug nimodipine in human lymphocytes
Mutagenesis, Vol. 16, Núm. 4, pp. 345-351
2000
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In vitro and in vivo evaluation of the antihypertensive drug atenolol in cultured human lymphocytes: Effects of long-term therapy
Mutagenesis, Vol. 15, Núm. 3, pp. 195-202
1999
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A survey of fragile X syndrome in a sample from Spanish Basque country
Annales de Genetique, Vol. 42, Núm. 4, pp. 197-201
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Stability of the FMR1 CGG repeat in a Basque sample
Human Biology, Vol. 71, Núm. 1, pp. 55-68
1997
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Angelman syndrome caused by loss of a marker chromosome: Cytogenetic and fluorescence in situ hybridization analysis
Psychiatric Genetics, Vol. 7, Núm. 4, pp. 153-158
1996
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A case of Prader-Willi syndrome associated with mosaicism: Cytogenetic and FISH study
Genes and Genetic Systems, Vol. 71, Núm. 1, pp. 31-36