FISIOLOGIA, GENETICA Y MICROBIOLOGIA
Department
Centro de Investigación Biomédica en Red sobre Enfermedades Raras
Madrid, EspañaPublications in collaboration with researchers from Centro de Investigación Biomédica en Red sobre Enfermedades Raras (11)
2024
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Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome
Orphanet Journal of Rare Diseases, Vol. 19, Núm. 1
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SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population
Database : the journal of biological databases and curation, Vol. 2024
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Structure and dynamics of the cyanobacterial regulator SipA
Archives of Biochemistry and Biophysics, Vol. 754
2023
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A Slc38a8 Mouse Model of FHONDA Syndrome Faithfully Recapitulates the Visual Deficits of Albinism Without Pigmentation Defects
Investigative ophthalmology & visual science, Vol. 64, Núm. 13, pp. 32
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Identification of the EH CRISPR-Cas9 system on a metagenome and its application to genome engineering
Microbial Biotechnology, Vol. 16, Núm. 7, pp. 1505-1523
2022
2018
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Impairment of photoreceptor ribbon synapses in a novel Pomt1 conditional knockout mouse model of dystroglycanopathy
Scientific Reports, Vol. 8, Núm. 1
2016
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Expanding the cyanobacterial nitrogen regulatory network: The GntR-like regulator PlmA interacts with the PII-PipX complex
Frontiers in Microbiology, Vol. 7, Núm. OCT
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Identification of the photoreceptor transcriptional Co-Repressor SAMD11 as novel cause of autosomal recessive retinitis pigmentosa
Scientific Reports, Vol. 6
2015
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Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations
Human Molecular Genetics, Vol. 24, Núm. 14, pp. 4037-4048
2007
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The crystal structure of the complex of PII and acetylglutamate kinase reveals how PII controls the storage of nitrogen as arginine
Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, Núm. 45, pp. 17644-17649