Bioquímica, xenética e inmunoloxía
Departamento
Universitat de Barcelona
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Universitat de Barcelona (22)
2023
2022
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Evaluation of Blood Soluble CD26 as a Complementary Biomarker for Colorectal Cancer Screening Programs
Cancers, Vol. 14, Núm. 19
2021
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The first wave of the COVID-19 epidemic in Spain was associated with early introductions and fast spread of a dominating genetic variant
Nature Genetics, Vol. 53, Núm. 10, pp. 1405-1414
2018
2017
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Pth4, an ancient parathyroid hormone lost in eutherian mammals, reveals a new brain-to-bone signaling pathway
FASEB Journal, Vol. 31, Núm. 2, pp. 569-583
2009
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Recent data on the distribution of lizards and snakes of the Seychelles
Herpetological Bulletin, pp. 20-32
2008
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Proteomic comparison between two marine snail ecotypes reveals details about the biochemistry of adaptation
Journal of Proteome Research, Vol. 7, Núm. 11, pp. 4926-4934
2006
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Positive selection versus demography: Evolutionary inferences based on an unusual haplotype structure in Drosophila simulans
Molecular Biology and Evolution, Vol. 23, Núm. 9, pp. 1643-1647
2005
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Birth-and-death evolution of the Cecropin multigene family in Drosophila
Journal of Molecular Evolution, Vol. 60, Núm. 1, pp. 1-11
2004
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Phylogeography and speciation of colour morphs in the colonial ascidian Pseudodistoma crucigaster
Molecular Ecology, Vol. 13, Núm. 10, pp. 3125-3136
2003
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Heteroplasmy Suggests Paternal Co-transmission of Multiple Genomes and Pervasive Reversion of Maternally into Paternally Transmitted Genomes of Mussel (Mytilus) Mitochondrial DNA
Journal of Molecular Evolution
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Large-Scale Adaptive Hitchhiking Upon High Recombination in Drosophila simulans
Genetics, Vol. 165, Núm. 2, pp. 895-900
2001
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Cryptic species of Clavelina (Ascidiacea) in two different habitats: Harbours and rocky littoral zones in the northwestern Mediterranean
Marine Biology, Vol. 139, Núm. 3, pp. 455-462
1998
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Identificación de dos mutaciones alélicas en el gen de la subunidad beta de la fosfodiesterasa en una familia española afectada de retinosis pigmentaria autosómica recesiva
Medicina Clinica, Vol. 111, Núm. 11, pp. 420-422
1997
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Putative association of a mutant ROM1 allele with retinitis pigmentosa
Human Genetics, Vol. 99, Núm. 6, pp. 827-830
1996
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A novel mutation in exon 17 of the β-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family
Human Genetics, Vol. 97, Núm. 1, pp. 35-38
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Autosomal recessive retinitis pigmentosa in Spain: Evaluation of four genes and two loci involved in the disease
Clinical Genetics, Vol. 50, Núm. 5, pp. 380-387
1995
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Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families
Human Genetics, Vol. 96, Núm. 1, pp. 89-94
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Homozygous tandem duplication within the gene encoding the β‐subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa
Human Mutation, Vol. 5, Núm. 3, pp. 228-234