Lista de obras - África García Orad - Dominio Público Uruguay

A Comprehensive Study of Vesicular and Non-Vesicular miRNAs from a Volume of Cerebrospinal Fluid Compatible with Clinical Practice

artículo científico publicado en 2019

A putative "hepitype" in the ATM gene associated with chronic lymphocytic leukemia risk

artículo científico publicado en 2011

A systematic review and meta-analysis of MDM2 polymorphisms in osteosarcoma susceptibility

artículo científico publicado en 2016

A systematic review and meta-analysis of MTHFR polymorphisms in methotrexate toxicity prediction in pediatric acute lymphoblastic leukemia.

artículo científico

Alpha-1-Antitrypsin Phenotypes among Breast Cancer Patients in the Basque Population

artículo científico publicado en 1994

Alpha2C-adrenoceptor Del322-325 polymorphism and risk of psychiatric disorders: significant association with opiate abuse and dependence

artículo científico publicado en 2016

An update on the implication of physical activity on semen quality: a systematic review and meta-analysis

scientific article published on 22 January 2019

Bcl-2 and BLIMP-1 expression predict worse prognosis in gastric diffuse large B cell lymphoma (DLCBL) while other markers for nodal DLBCL are not useful.

artículo científico publicado en 2012

Biological activity of complexes derived from thiophene-2-carbaldehyde thiosemicarbazone. Crystal structure of [Ni(C(6)H(6)N(3)S(2))(2)].

artículo científico publicado en 2001

Cell-free DNA as a biomarker in diffuse large B-cell lymphoma: A systematic review

artículo científico publicado en 2019

Chromosome instability in lymphocytes of children with coeliac disease.

artículo científico publicado en 2009

Circulating miRNAs as biomarkers in diffuse large B-cell lymphoma: a systematic review.

artículo científico publicado en 2018

Combined fluorescent-chromogenic in situ hybridization for identification and laser microdissection of interphase chromosomes.

artículo científico publicado en 2013

Confirmation of involvement of new variants at CDKN2A/B in pediatric acute lymphoblastic leukemia susceptibility in the Spanish population

artículo científico publicado en 2017

Cytomegalovirus promoter up-regulation is the major cause of increased protein levels of unstable reporter proteins after treatment of living cells with proteasome inhibitors

artículo científico publicado en 2009

Erratum to: Potential relationship between single nucleotide polymorphisms used in forensic genetics and diseases or other traits in European population.

artículo científico publicado en 2015

Errors in the interpretation of copy number variations due to the use of public databases as a reference

artículo científico publicado en 2014

Expression of the DYRK1A gene correlates with its 3D positioning in the interphase nucleus of Down syndrome cells

artículo científico publicado en 2015

Genetic and metabolic determinants of methotrexate-induced mucositis in pediatric acute lymphoblastic leukemia

artículo científico publicado en 2014

Genetic susceptibility in childhood acute lymphoblastic leukemia.

artículo científico publicado en 2017

Genetic typing with HUMTH01, HUMVWA31A and HUMFES/FPS short tandem repeat loci, D1S80 variable number tandem repeat locus and HLA-DQ alpha of recent and from XII-XIII centuries spongy bone.

artículo científico publicado en 1995

Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia

artículo científico publicado en 2008

Genetic variants in miRNA processing genes and pre-miRNAs are associated with the risk of chronic lymphocytic leukemia

artículo científico publicado en 2015

HDAC inhibitors induce cell cycle arrest, activate the apoptotic extrinsic pathway and synergize with a novel PIM inhibitor in Hodgkin lymphoma-derived cell lines.

artículo científico publicado en 2010

High mitochondrial DNA stability in B-cell chronic lymphocytic leukemia

artículo científico publicado en 2009

High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas

artículo científico publicado en 2012

Impact of polymorphisms in apoptosis-related genes on the outcome of childhood acute lymphoblastic leukaemia

article

Intron 3 of the ARID5B gene: a hot spot for acute lymphoblastic leukemia susceptibility.

artículo científico publicado en 2013

Involvement of SNPs in miR-3117 and miR-3689d2 in childhood acute lymphoblastic leukemia risk.

artículo científico publicado en 2018

Involvement of miRNA polymorphism in mucositis development in childhood acute lymphoblastic leukemia treatment

scientific article published on 01 December 2018

Lack of association between deficient mismatch repair expression and outcome in endometrial carcinomas of the endometrioid type.

artículo científico publicado en 2014

Lack of association of the CEP72 rs924607 TT genotype with vincristine-related peripheral neuropathy during the early phase of pediatric acute lymphoblastic leukemia treatment in a Spanish population

artículo científico publicado en 2015

Letter regarding Wang et al. entitled "Effects of murine double minute 2 polymorphisms on the risk and survival of osteosarcoma: a systematic review and meta-analysis".

artículo científico publicado en 2014

MTHFR 677TT genotype and toxicity of methotrexate: controversial results

article

MTHFR polymorphisms in childhood acute lymphoblastic leukemia: influence on methotrexate therapy.

artículo científico publicado en 2017

Methylation of CpG sites in BCL2 major breakpoint region and the increase of BCL2/JH translocation with aging

artículo científico publicado en 2015

Methylation of the nonhomologous end joining repair pathway genes does not explain the increase of translocations with aging.

artículo científico publicado en 2014

MiR-pharmacogenetics of methotrexate in childhood B-cell acute lymphoblastic leukemia

artículo científico publicado en 2016

Mir-pharmacogenetics of Vincristine and peripheral neurotoxicity in childhood B-cell acute lymphoblastic leukemia.

artículo científico publicado en 2017

Newborn genetic identification: a protocol using microsatellite DNA as an alternative to footprinting

artículo científico publicado en 1997

No Evidence for an Association between Glyoxalase I and Haptoglobin in Nine Spanish Populations

article

Noncoding RNA-related polymorphisms in pediatric acute lymphoblastic leukemia susceptibility.

artículo científico publicado en 2014

PNPLA3 rs738409 and Hepatotoxicity in Children With B-cell Acute Lymphoblastic Leukemia: A Validation Study in a Spanish Cohort.

artículo científico publicado en 2017

Pharmacoepigenetics in childhood acute lymphoblastic leukemia: involvement of miRNA polymorphisms in hepatotoxicity

scientific article published on 23 March 2018

Pharmacogenetics of childhood acute lymphoblastic leukemia.

artículo científico publicado en 2014

Pharmacogenetics of microRNAs and microRNAs biogenesis machinery in pediatric acute lymphoblastic leukemia

artículo científico publicado en 2014

Polymorphisms in miRNA processing genes and their role in osteosarcoma risk.

artículo científico publicado en 2015

Polymorphisms in the methotrexate transport pathway: a new tool for MTX plasma level prediction in pediatric acute lymphoblastic leukemia

artículo científico publicado en 2013

Polymorphisms of the SLCO1B1 gene predict methotrexate-related toxicity in childhood acute lymphoblastic leukemia.

artículo científico publicado en 2011

Population study of 3 STR loci in the Basque Country (northern Spain)

article

Re: novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations

artículo científico publicado en 2013

Recurrent loss of heterozygosity in 1p36 associated with TNFRSF14 mutations in IRF4 translocation negative pediatric follicular lymphomas

artículo científico publicado en 2013

Research commentary regarding Savage et al. entitled "Genome-wide association study identifies two susceptibility loci for osteosarcoma".

artículo científico publicado en 2015

Review of pharmacogenetics studies of L-asparaginase hypersensitivity in acute lymphoblastic leukemia points to variants in the GRIA1 gene

artículo científico publicado en 2017

Role of miRNAs in treatment response and toxicity of childhood acute lymphoblastic leukemia.

artículo científico publicado en 2018

Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia

artículo científico publicado en 2020

S-Adenosylmethionine increases circulating very-low density lipoprotein clearance in non-alcoholic fatty liver disease.

artículo científico publicado en 2014

SLC19A1 hot spot for MTX plasma concentration.

artículo científico publicado en 2014

Synthesis and spectroscopic properties of copper(II) complexes derived from thiophene-2-carbaldehyde thiosemicarbazone. Structure and biological activity of [Cu(C6H6N3S2)2]

artículo científico publicado en 1999

Systematic Review of the Potential of MicroRNAs in Diffuse Large B Cell Lymphoma

article

The (8-thiotheophyllinate) (triphenylphosphine) gold (1), (tTAUP): a new gold complex as an anticancer agent

artículo científico publicado en 1993

The N251K functional polymorphism in the alpha(2A)-adrenoceptor gene is not associated with depression: a study in suicide completers

artículo científico publicado en 2005

The miR-1206 microRNA variant is associated with methotrexate-induced oral mucositis in pediatric acute lymphoblastic leukemia.

artículo científico publicado en 2017

Variability in Cerebrospinal Fluid MicroRNAs Through Life

scientific article published on 16 July 2020

Variants in the 14q32 miRNA cluster are associated with osteosarcoma risk in the Spanish population

artículo científico publicado en 2018

Variants in vincristine pharmacodynamic genes involved in neurotoxicity at induction phase in the therapy of pediatric acute lymphoblastic leukemia

scientific article published on 06 February 2019

Vincristine pharmacokinetics pathway and neurotoxicity during early phases of treatment in pediatric acute lymphoblastic leukemia.

artículo científico publicado en 2016

miRNA deregulation in childhood acute lymphoblastic leukemia: a systematic review

scientific article published on 13 December 2019

Lista de obras de África García Orad

A Comprehensive Study of Vesicular and Non-Vesicular miRNAs from a Volume of Cerebrospinal Fluid Compatible with Clinical Practice

A putative "hepitype" in the ATM gene associated with chronic lymphocytic leukemia risk

A systematic review and meta-analysis of MDM2 polymorphisms in osteosarcoma susceptibility

A systematic review and meta-analysis of MTHFR polymorphisms in methotrexate toxicity prediction in pediatric acute lymphoblastic leukemia.

Alpha-1-Antitrypsin Phenotypes among Breast Cancer Patients in the Basque Population

Alpha2C-adrenoceptor Del322-325 polymorphism and risk of psychiatric disorders: significant association with opiate abuse and dependence

An update on the implication of physical activity on semen quality: a systematic review and meta-analysis

Bcl-2 and BLIMP-1 expression predict worse prognosis in gastric diffuse large B cell lymphoma (DLCBL) while other markers for nodal DLBCL are not useful.

Biological activity of complexes derived from thiophene-2-carbaldehyde thiosemicarbazone. Crystal structure of [Ni(C(6)H(6)N(3)S(2))(2)].

Cell-free DNA as a biomarker in diffuse large B-cell lymphoma: A systematic review

Chromosome instability in lymphocytes of children with coeliac disease.

Circulating miRNAs as biomarkers in diffuse large B-cell lymphoma: a systematic review.

Combined fluorescent-chromogenic in situ hybridization for identification and laser microdissection of interphase chromosomes.

Confirmation of involvement of new variants at CDKN2A/B in pediatric acute lymphoblastic leukemia susceptibility in the Spanish population

Cytomegalovirus promoter up-regulation is the major cause of increased protein levels of unstable reporter proteins after treatment of living cells with proteasome inhibitors

Erratum to: Potential relationship between single nucleotide polymorphisms used in forensic genetics and diseases or other traits in European population.

Errors in the interpretation of copy number variations due to the use of public databases as a reference

Expression of the DYRK1A gene correlates with its 3D positioning in the interphase nucleus of Down syndrome cells

Genetic and metabolic determinants of methotrexate-induced mucositis in pediatric acute lymphoblastic leukemia

Genetic susceptibility in childhood acute lymphoblastic leukemia.

Genetic typing with HUMTH01, HUMVWA31A and HUMFES/FPS short tandem repeat loci, D1S80 variable number tandem repeat locus and HLA-DQ alpha of recent and from XII-XIII centuries spongy bone.

Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia

Genetic variants in miRNA processing genes and pre-miRNAs are associated with the risk of chronic lymphocytic leukemia

HDAC inhibitors induce cell cycle arrest, activate the apoptotic extrinsic pathway and synergize with a novel PIM inhibitor in Hodgkin lymphoma-derived cell lines.

High mitochondrial DNA stability in B-cell chronic lymphocytic leukemia

High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas

Impact of polymorphisms in apoptosis-related genes on the outcome of childhood acute lymphoblastic leukaemia

Intron 3 of the ARID5B gene: a hot spot for acute lymphoblastic leukemia susceptibility.

Involvement of SNPs in miR-3117 and miR-3689d2 in childhood acute lymphoblastic leukemia risk.

Involvement of miRNA polymorphism in mucositis development in childhood acute lymphoblastic leukemia treatment

Lack of association between deficient mismatch repair expression and outcome in endometrial carcinomas of the endometrioid type.

Lack of association of the CEP72 rs924607 TT genotype with vincristine-related peripheral neuropathy during the early phase of pediatric acute lymphoblastic leukemia treatment in a Spanish population

Letter regarding Wang et al. entitled "Effects of murine double minute 2 polymorphisms on the risk and survival of osteosarcoma: a systematic review and meta-analysis".

MTHFR 677TT genotype and toxicity of methotrexate: controversial results

MTHFR polymorphisms in childhood acute lymphoblastic leukemia: influence on methotrexate therapy.

Methylation of CpG sites in BCL2 major breakpoint region and the increase of BCL2/JH translocation with aging

Methylation of the nonhomologous end joining repair pathway genes does not explain the increase of translocations with aging.

MiR-pharmacogenetics of methotrexate in childhood B-cell acute lymphoblastic leukemia

Mir-pharmacogenetics of Vincristine and peripheral neurotoxicity in childhood B-cell acute lymphoblastic leukemia.

Newborn genetic identification: a protocol using microsatellite DNA as an alternative to footprinting

No Evidence for an Association between Glyoxalase I and Haptoglobin in Nine Spanish Populations

Noncoding RNA-related polymorphisms in pediatric acute lymphoblastic leukemia susceptibility.

PNPLA3 rs738409 and Hepatotoxicity in Children With B-cell Acute Lymphoblastic Leukemia: A Validation Study in a Spanish Cohort.

Pharmacoepigenetics in childhood acute lymphoblastic leukemia: involvement of miRNA polymorphisms in hepatotoxicity

Pharmacogenetics of childhood acute lymphoblastic leukemia.

Pharmacogenetics of microRNAs and microRNAs biogenesis machinery in pediatric acute lymphoblastic leukemia

Polymorphisms in miRNA processing genes and their role in osteosarcoma risk.

Polymorphisms in the methotrexate transport pathway: a new tool for MTX plasma level prediction in pediatric acute lymphoblastic leukemia

Polymorphisms of the SLCO1B1 gene predict methotrexate-related toxicity in childhood acute lymphoblastic leukemia.

Population study of 3 STR loci in the Basque Country (northern Spain)

Re: novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations

Recurrent loss of heterozygosity in 1p36 associated with TNFRSF14 mutations in IRF4 translocation negative pediatric follicular lymphomas

Research commentary regarding Savage et al. entitled "Genome-wide association study identifies two susceptibility loci for osteosarcoma".

Review of pharmacogenetics studies of L-asparaginase hypersensitivity in acute lymphoblastic leukemia points to variants in the GRIA1 gene

Role of miRNAs in treatment response and toxicity of childhood acute lymphoblastic leukemia.

Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia

S-Adenosylmethionine increases circulating very-low density lipoprotein clearance in non-alcoholic fatty liver disease.

SLC19A1 hot spot for MTX plasma concentration.

Synthesis and spectroscopic properties of copper(II) complexes derived from thiophene-2-carbaldehyde thiosemicarbazone. Structure and biological activity of [Cu(C6H6N3S2)2]

Systematic Review of the Potential of MicroRNAs in Diffuse Large B Cell Lymphoma

The (8-thiotheophyllinate) (triphenylphosphine) gold (1), (tTAUP): a new gold complex as an anticancer agent

The N251K functional polymorphism in the alpha(2A)-adrenoceptor gene is not associated with depression: a study in suicide completers

The miR-1206 microRNA variant is associated with methotrexate-induced oral mucositis in pediatric acute lymphoblastic leukemia.

Variability in Cerebrospinal Fluid MicroRNAs Through Life

Variants in the 14q32 miRNA cluster are associated with osteosarcoma risk in the Spanish population

Variants in vincristine pharmacodynamic genes involved in neurotoxicity at induction phase in the therapy of pediatric acute lymphoblastic leukemia

Vincristine pharmacokinetics pathway and neurotoxicity during early phases of treatment in pediatric acute lymphoblastic leukemia.

miRNA deregulation in childhood acute lymphoblastic leukemia: a systematic review