Xenómica e Biomedicina
XB5
Universitat de Barcelona
Barcelona, EspañaPublicacions en col·laboració amb investigadors/es de Universitat de Barcelona (12)
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
2013
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Potential use of Cytisus scoparius extracts in topical applications for skin protection against oxidative damage
Journal of Photochemistry and Photobiology B: Biology, Vol. 125, pp. 83-89
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
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
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Retinitis pigmentosa in Spain
Clinical Genetics, Vol. 48, Núm. 3, pp. 120-122
1994
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Genetic fine localization of the arrestin (S-antigen) gene 4 c M distal from D2S172
Human Genetics, Vol. 94, Núm. 2, pp. 193-194