Search Results - "Abad, Maria M"

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    Uranium removal from complex mining waters by alginate beads doped with cells of Stenotrophomonas sp. Br8: Novel perspectives for metal bioremediation by Sánchez-Castro, Iván, Martínez-Rodríguez, Pablo, Abad, María M., Descostes, Michael, Merroun, Mohamed Larbi

    Published in Journal of environmental management (15-10-2021)
    “…Uranium-containing effluents generated by nuclear energy industry must be efficiently remediated before release to the environment. Currently, numerous…”
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    Effect of different phosphate sources on uranium biomineralization by the Microbacterium sp. Be9 strain: A multidisciplinary approach study by Martínez-Rodríguez, Pablo, Sánchez-Castro, Iván, Ojeda, Jesús J, Abad, María M, Descostes, Michael, Merroun, Mohamed Larbi

    Published in Frontiers in microbiology (09-01-2023)
    “…Industrial activities related with the uranium industry are known to generate hazardous waste which must be managed adequately. Amongst the remediation…”
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    IL2RA/CD25 gene polymorphisms: uneven association with multiple sclerosis (MS) and type 1 diabetes (T1D) by Alcina, Antonio, Fedetz, María, Ndagire, Dorothy, Fernández, Oscar, Leyva, Laura, Guerrero, Miguel, Abad-Grau, María M, Arnal, Carmen, Delgado, Concepción, Lucas, Miguel, Izquierdo, Guillermo, Matesanz, Fuencisla

    Published in PloS one (2009)
    “…IL-2 receptor (IL2R) alpha is the specific component of the high affinity IL2R system involved in the immune response and in the control of autoimmunity. Here…”
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    Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test by Abad-Grau, María M, Medina-Medina, Nuria, Montes-Soldado, Rosana, Moreno-Ortega, José, Matesanz, Fuencisla

    Published in Human genetics (01-09-2010)
    “…Multimarker transmission/disequilibrium tests (TDTs) are powerful association and linkage tests used to perform genome-wide filtering in the search for disease…”
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    A network model to predict the risk of death in sickle cell disease by Sebastiani, Paola, Nolan, Vikki G., Baldwin, Clinton T., Abad-Grau, Maria M., Wang, Ling, Adewoye, Adeboye H., McMahon, Lillian C., Farrer, Lindsay A., Taylor, James G., Kato, Gregory J., Gladwin, Mark T., Steinberg, Martin H.

    Published in Blood (01-10-2007)
    “…Modeling the complexity of sickle cell disease pathophysiology and severity is difficult. Using data from 3380 patients accounting for all common genotypes of…”
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    Operations strategy and flexibility: modeling with Bayesian classifiers by AbadGrau, Mara M., AriasAranda, Daniel

    Published in Industrial management + data systems (01-01-2006)
    “…Purpose - Information analysis tools enhance the possibilities of firm competition in terms of knowledge management. However, the generalization of decision…”
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    Building chromosome-wide LD maps by Abad-Grau, María M., Montes, Rosana, Sebastiani, Paola

    Published in Bioinformatics (15-08-2006)
    “…BMapBuilder builds maps of pairwise linkage disequilibrium (LD) in either two or three dimensions. The optimized resolution allows for graphical display of LD…”
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    Robust Transmission/Disequilibrium Test for Incomplete Family Genotypes by Sebastiani, Paola, Abad, Maria M, Alpargu, Gulhan, Ramoni, Marco F

    Published in Genetics (Austin) (01-12-2004)
    “…Several solutions have been proposed to extend the transmission disequilibrium test (TDT) to include cases with missing parental genotype. However, completion…”
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    GeneOnEarth: Fitting Genetic PC Plots on the Globe by Torres-Sanchez, Sergio, Medina-Medina, Nuria, Gignoux, Chris, Abad-Grau, Maria M., Gonzalez-Burchard, Esteban

    “…Principal component (PC) plots have become widely used to summarize genetic variation of individuals in a sample. The similarity between genetic distance in PC…”
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    Evolution and challenges in the design of computational systems for triage assistance by Abad-Grau, María M., Ierache, Jorge, Cervino, Claudio, Sebastiani, Paola

    Published in Journal of biomedical informatics (01-06-2008)
    “…Compared with expert systems for specific disease diagnosis, knowledge-based systems to assist decision making in triage usually try to cover a much wider…”
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    Increasing power by using haplotype similarity in a multimarker transmission/disequilibrium test by Abad-Grau, María M, Medina-Medina, Nuria, Moral, Serafín, Montes-Soldado, Rosana, Torres-Sánchez, Sergio, Matesanz, Fuencisla

    “…It is already known that power in multimarker transmission/disequilibrium tests may improve with the number of markers as some associations may require several…”
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    Bayesian estimates of linkage disequilibrium by Sebastiani, Paola, Abad-Grau, María M

    Published in BMC genetics (25-06-2007)
    “…The maximum likelihood estimator of D'--a standard measure of linkage disequilibrium--is biased toward disequilibrium, and the bias is particularly evident in…”
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    RNA Silencing in Aspergillus nidulans Is Independent of RNA-Dependent RNA Polymerases by Hammond, T. M, Keller, N. P

    Published in Genetics (Austin) (01-02-2005)
    “…The versatility of RNA-dependent RNA polymerases (RDRPs) in eukaryotic gene silencing is perhaps best illustrated in the kingdom Fungi. Biochemical and genetic…”
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    Fetal Hemoglobin (HbF) in Sickle Cell Anemia: Genome-Wide Association Studies Using Pooled DNA Samples Can Reveal Genetic Associations with HbF Concentration by Sebastiani, Paola, Abad-Grau, Maria M., Riva, Alberto A., Nolan, Vikki G., Melista, Efthimia, Steinberg, Martin H., Baldwin, Clinton T.

    Published in Blood (16-11-2006)
    “…The complex regulatory environment controlling HbF levels provides ample opportunity for modulating expression of this key modifier of sickle cell anemia…”
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    Severity of Sickle Cell Disease: Modeling Interrelationships among Hemolysis, Pulmonary Hypertension and Risk of Death by Sebastiani, Paola, Nolan, Vikki G., Baldwin, Clinton T., Abad-Grau, Maria M., Wang, Ling, Adewoye, Adeboye H., McMahon, Lillian C., Farrer, Lindsay A., Taylor, James G., Kato, Gregory J., Gladwin, Mark T., Steinberg, Martin H.

    Published in Blood (16-11-2006)
    “…A single point mutation in the β hemoglobin gene causes sickle cell disease (SCD), but patients have extremely variable phenotypes. Hemolysis-related…”
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    Immunohistochemical expression of p53 in breast carcinoma is associated with the intron 1 BglII polymorphism of the p53 gene by Trejo-Becerril, C, Sarmiento, R G, Abad, M M, Ichaso, N, Delgado, R, Cruz, J J, Dueñas-González, A

    Published in Mutation research (18-09-2000)
    “…Breast carcinoma is a public health problem worldwide. It is known that both genetic and environmental factors are important for breast carcinogenesis and that…”
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