Lista de obras - Rocio Ortiz-Lopez - Dominio Público Uruguay

A Bioactive Cartilage Graft of IGF1-Transduced Adipose Mesenchymal Stem Cells Embedded in an Alginate/Bovine Cartilage Matrix Tridimensional Scaffold

artículo científico publicado en 2019

A New Gene Expression Signature for Triple Negative Breast Cancer Using Frozen Fresh Tissue before Neoadjuvant Chemotherapy.

artículo científico publicado en 2017

A de novo t(10;19)(q22.3;q13.33) leads to ZMIZ1/PRR12 reciprocal fusion transcripts in a girl with intellectual disability and neuropsychiatric alterations

scientific journal article

A potent replicative delta-24 adenoviral vector driven by the promoter of human papillomavirus 16 that is highly selective for associated neoplasms.

artículo científico publicado en 2007

Analyses of chondrogenic induction of adipose mesenchymal stem cells by combined co-stimulation mediated by adenoviral gene transfer

artículo científico publicado en 2013

Ancestry informative markers and admixture proportions in northeastern Mexico.

artículo científico publicado en 2009

Antitumor effect of meclofenamic acid on human androgen-independent prostate cancer: a preclinical evaluation.

artículo científico publicado en 2011

Association between PTPN22 C1858T polymorphism and alopecia areata risk

artículo científico publicado en 2015

Association between genotype and allele frequencies of CYP2A6*12 and rs16969968 in CHRNA5 variants with smoking and body mass index in young subjects from Northeast Mexico

artículo científico publicado en 2015

Association of matrix metalloproteinase-2 gene promoter polymorphism with myocardial infarction susceptibility in a Mexican population

article

CAPN3, DCT, MLANA and TYRP1 are overexpressed in skin of vitiligo vulgaris Mexican patients

artículo científico publicado en 2018

CYP2D6 in Amerindians from Southern Mexico: low variability and higher frequency of functional alleles

artículo científico publicado en 2015

Circulating microRNA expression profile in B-cell acute lymphoblastic leukemia

artículo científico publicado en 2015

Clinical and molecular delineation of duplication 9p24.3q21.11 in a patient with psychotic behavior

artículo científico publicado en 2015

Comparison of specific expression profile in two in vitro hypoxia models.

artículo científico publicado en 2018

Complete Genome Sequence of Streptococcus pneumoniae Serotype 19A, a Blood Clinical Isolate from Northeast Mexico

artículo científico publicado en 2016

Complete genome sequence analysis of Nocardia brasiliensis HUJEG-1 reveals a saprobic lifestyle and the genes needed for human pathogenesis

artículo científico publicado en 2013

Complete genome sequence of Nocardia brasiliensis HUJEG-1.

artículo científico publicado en 2012

Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion

scientific article published on 11 May 2012

Cu/Zn superoxide dismutase (SOD1) induction is implicated in the antioxidative and antiviral activity of acetylsalicylic acid in HCV-expressing cells.

artículo científico publicado en 2012

De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome features

artículo científico publicado en 2013

Del(1)(q23) in a patient with Hutchinson-Gilford progeria

artículo científico publicado en 2002

Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma.

scientific article published on September 2013

Draft Genome Sequence of Actinomadura madurae LIID-AJ290, Isolated from a Human Mycetoma Case

artículo científico

Draft Genome Sequence of an Atypical Strain of Streptococcus pneumoniae Serotype 19A Isolated from Cerebrospinal Fluid

artículo científico publicado en 2016

Drug resistance mutations during structured interruptions of HAART in two HIV-1-infected children.

artículo científico publicado en 2011

Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate

artículo científico publicado en 2012

Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population

artículo científico publicado en 2013

Evaluation of skin expression profiles of patients with vitiligo treated with narrow-band UVB therapy by targeted RNA-seq

scientific article published on 01 November 2018

Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.

artículo científico publicado en 1997

Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1A

artículo científico publicado en 1993

Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability.

artículo científico publicado en 2018

Frequency of Protease and Reverse Transcriptase Drug Resistance Mutations in Naïve HIV-Infected Patients

article

Frequency of S and Z alleles for alpha-1-antitrypsin and tumor necrosis factor alpha -308 promoter polymorphism in northeastern Mexico

artículo científico publicado en 2008

Genetic and molecular aspects of androgenetic alopecia

artículo científico publicado en 2018

Genetic aspects of dilated cardiomyopathy

Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25.

artículo científico publicado en 2010

Genetic structure of Mexican Mestizo women with breast cancer based on three STR loci

artículo científico publicado en 2008

Genetic structure of Mexican Mestizos with type 2 diabetes mellitus based on three STR loci.

artículo científico publicado en 2013

Genome annotation of a Saccharomyces sp. lager brewer's yeast

artículo científico publicado en 2016

Genomic Changes Associated with the Loss of Nocardia brasiliensis Virulence in Mice after 200 In Vitro Passages

scientific article published on 27 June 2016

Genomic diversity of human papillomavirus-16, 18, 31, and 35 isolates in a Mexican population and relationship to European, African, and Native American variants

artículo científico publicado en 2004

HGH isoforms: cDNA expression, adipogenic activity and production in cell culture

article

Human bone morphogenetic protein 2-transduced mesenchymal stem cells improve bone regeneration in a model of mandible distraction surgery

artículo científico publicado en 2012

Human papillomavirus type 2 associated with pyogenic granuloma in patients without clinical evidence of warts

artículo científico publicado en 2015

Identification of differentially expressed genes associated with prognosis of B acute lymphoblastic leukemia.

artículo científico publicado en 2015

Identification of viral infections in the prostate and evaluation of their association with cancer

artículo científico publicado en 2010

Implant Composed of Demineralized Bone and Mesenchymal Stem Cells Genetically Modified with AdBMP2/AdBMP7 for the Regeneration of Bone Fractures in Ovis aries.

artículo científico publicado en 2016

Induction of virulence factors, apoptosis, and cytokines in precision-cut hamster liver slices infected with Entamoeba histolytica.

artículo científico publicado en 2012

Interethnic relationships of CYP2D6 variants in native and Mestizo populations sharing the same ecosystem.

artículo científico publicado en 2015

Intraprostatic distribution and long-term follow-up after AdV-tk immunotherapy as neoadjuvant to surgery in patients with prostate cancer.

artículo científico publicado en 2013

Ionizing radiation-induced DNA injury and damage detection in patients with breast cancer

artículo científico publicado en 2015

Landscape of Germline Mutations in DNA Repair Genes for Breast Cancer in Latin America: Opportunities for PARP-Like Inhibitors and Immunotherapy

scientific article published on 10 October 2019

Ligneous conjunctivitis in a Mexican patient with a mutation in the plasminogen (PLG) gene.

artículo científico publicado en 2006

Lower than expected cytogenetic and molecular response to imatinib in Mexican patients with chronic myelogenous leukemia

artículo científico publicado en 2013

Maternal overnutrition by hypercaloric diets programs hypothalamic mitochondrial fusion and metabolic dysfunction in rat male offspring.

artículo científico publicado en 2018

Modular organization of a hypocretin gene minimal promoter.

artículo científico publicado en 2017

Molecular characterization of chronic myeloproliferative neoplasias in México

scientific article published on 01 October 2009

Mutations Related to Antiretroviral Resistance Identified by Ultra-Deep Sequencing in HIV-1 Infected Children under Structured Interruptions of HAART

artículo científico publicado en 2016

No association between polymorphisms/haplotypes of the vascular endothelial growth factor gene and preeclampsia

artículo científico publicado en 2011

Papillomavirus subtypes are natural and old taxa: phylogeny of human papillomavirus types 44 and 55 and 68a and -b.

artículo científico publicado en 2005

Polymorphisms -455G/A and -148C/T and Fibrinogen Plasmatic Level as Risk Markers of Coronary Disease and Major Adverse Cardiovascular Events

scientific article published on 01 July 2019

Population based prostate cancer screening in north Mexico reveals a high prevalence of aggressive tumors in detected cases

artículo científico publicado en 2009

Positive association between vascular endothelial growth factor (VEGF) -2578 C/A variant and prostate cancer.

artículo científico publicado en 2013

Prevalence and 3-year persistence of human papillomavirus serotypes in asymptomatic patients in Northern Mexico

artículo científico publicado en 2016

Prevalence and Clinical Significance of FLT3 Mutation Status in Acute Myeloid Leukemia Patients: A Multicenter Study

artículo científico publicado en 2016

Protein tyrosine phosphatase PTPN22 +1858C/T polymorphism is associated with active vitiligo

artículo científico publicado en 2014

Sequencing technology status of BRCA1/2 testing in Latin American Countries

scientific article published on 02 June 2020

Serological Test to Determine Exposure to SARS-CoV-2: ELISA Based on the Receptor-Binding Domain of the Spike Protein (S-RBDN318-V510) Expressed in Escherichia coli

artículo científico publicado en 2021

Spatial Clusters of Children with Cleft Lip and Palate and Their Association with Polluted Zones in the Monterrey Metropolitan Area

artículo científico publicado en 2019

Strong association of variants around FOXE1 and orofacial clefting.

artículo científico publicado en 2014

The genomic landscape of Mexican Indigenous populations brings insights into the peopling of the Americas

artículo científico publicado en 2021

The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.

artículo científico publicado en 2014

The +1858 C/T Polymorphism in the PTPN22 Gene Is Associated with Cystic Fibrosis Patients in Northeast Mexico

artículo científico publicado en 2016

Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer

artículo científico publicado en 2017

Tumor necrosis factor alpha promoter‐308G/A polymorphism in Mexican patients with patchy alopecia areata ⬇️

artículo científico publicado el 1 de mayo de 2012

Tumor necrosis factor-α -308G/A polymorphism is associated with active vitiligo vulgaris in a northeastern Mexican population

artículo científico publicado en 2012

Tyrphostin AG17 inhibits adipocyte differentiation in vivo and in vitro.

artículo científico publicado en 2018

Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies

artículo científico publicado en 2017

Uridine 5'-diphospho-glucronosyltrasferase: Its role in pharmacogenomics and human disease.

artículo científico publicado en 2018

Worldwide genomic diversity of the human papillomaviruses-53, 56, and 66, a group of high-risk HPVs unrelated to HPV-16 and HPV-18.

artículo científico publicado en 2005

[Determination of molecular genetic markers in acute coronary syndromes and their relationship to cardiovascular adverse events].

artículo científico publicado en 2013

Lista de obras de Rocio Ortiz-Lopez

A Bioactive Cartilage Graft of IGF1-Transduced Adipose Mesenchymal Stem Cells Embedded in an Alginate/Bovine Cartilage Matrix Tridimensional Scaffold

A New Gene Expression Signature for Triple Negative Breast Cancer Using Frozen Fresh Tissue before Neoadjuvant Chemotherapy.

A de novo t(10;19)(q22.3;q13.33) leads to ZMIZ1/PRR12 reciprocal fusion transcripts in a girl with intellectual disability and neuropsychiatric alterations

A potent replicative delta-24 adenoviral vector driven by the promoter of human papillomavirus 16 that is highly selective for associated neoplasms.

Analyses of chondrogenic induction of adipose mesenchymal stem cells by combined co-stimulation mediated by adenoviral gene transfer

Ancestry informative markers and admixture proportions in northeastern Mexico.

Antitumor effect of meclofenamic acid on human androgen-independent prostate cancer: a preclinical evaluation.

Association between PTPN22 C1858T polymorphism and alopecia areata risk

Association between genotype and allele frequencies of CYP2A6*12 and rs16969968 in CHRNA5 variants with smoking and body mass index in young subjects from Northeast Mexico

Association of matrix metalloproteinase-2 gene promoter polymorphism with myocardial infarction susceptibility in a Mexican population

CAPN3, DCT, MLANA and TYRP1 are overexpressed in skin of vitiligo vulgaris Mexican patients

CYP2D6 in Amerindians from Southern Mexico: low variability and higher frequency of functional alleles

Circulating microRNA expression profile in B-cell acute lymphoblastic leukemia

Clinical and molecular delineation of duplication 9p24.3q21.11 in a patient with psychotic behavior

Comparison of specific expression profile in two in vitro hypoxia models.

Complete Genome Sequence of Streptococcus pneumoniae Serotype 19A, a Blood Clinical Isolate from Northeast Mexico

Complete genome sequence analysis of Nocardia brasiliensis HUJEG-1 reveals a saprobic lifestyle and the genes needed for human pathogenesis

Complete genome sequence of Nocardia brasiliensis HUJEG-1.

Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion

Cu/Zn superoxide dismutase (SOD1) induction is implicated in the antioxidative and antiviral activity of acetylsalicylic acid in HCV-expressing cells.

De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome features

Del(1)(q23) in a patient with Hutchinson-Gilford progeria

Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma.

Draft Genome Sequence of Actinomadura madurae LIID-AJ290, Isolated from a Human Mycetoma Case

Draft Genome Sequence of an Atypical Strain of Streptococcus pneumoniae Serotype 19A Isolated from Cerebrospinal Fluid

Drug resistance mutations during structured interruptions of HAART in two HIV-1-infected children.

Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate

Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population

Evaluation of skin expression profiles of patients with vitiligo treated with narrow-band UVB therapy by targeted RNA-seq

Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.

Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1A

Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability.

Frequency of Protease and Reverse Transcriptase Drug Resistance Mutations in Naïve HIV-Infected Patients

Frequency of S and Z alleles for alpha-1-antitrypsin and tumor necrosis factor alpha -308 promoter polymorphism in northeastern Mexico

Genetic and molecular aspects of androgenetic alopecia

Genetic aspects of dilated cardiomyopathy

Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25.

Genetic structure of Mexican Mestizo women with breast cancer based on three STR loci

Genetic structure of Mexican Mestizos with type 2 diabetes mellitus based on three STR loci.

Genome annotation of a Saccharomyces sp. lager brewer's yeast

Genomic Changes Associated with the Loss of Nocardia brasiliensis Virulence in Mice after 200 In Vitro Passages

Genomic diversity of human papillomavirus-16, 18, 31, and 35 isolates in a Mexican population and relationship to European, African, and Native American variants

HGH isoforms: cDNA expression, adipogenic activity and production in cell culture

Human bone morphogenetic protein 2-transduced mesenchymal stem cells improve bone regeneration in a model of mandible distraction surgery

Human papillomavirus type 2 associated with pyogenic granuloma in patients without clinical evidence of warts

Identification of differentially expressed genes associated with prognosis of B acute lymphoblastic leukemia.

Identification of viral infections in the prostate and evaluation of their association with cancer

Implant Composed of Demineralized Bone and Mesenchymal Stem Cells Genetically Modified with AdBMP2/AdBMP7 for the Regeneration of Bone Fractures in Ovis aries.

Induction of virulence factors, apoptosis, and cytokines in precision-cut hamster liver slices infected with Entamoeba histolytica.

Interethnic relationships of CYP2D6 variants in native and Mestizo populations sharing the same ecosystem.

Intraprostatic distribution and long-term follow-up after AdV-tk immunotherapy as neoadjuvant to surgery in patients with prostate cancer.

Ionizing radiation-induced DNA injury and damage detection in patients with breast cancer

Landscape of Germline Mutations in DNA Repair Genes for Breast Cancer in Latin America: Opportunities for PARP-Like Inhibitors and Immunotherapy

Ligneous conjunctivitis in a Mexican patient with a mutation in the plasminogen (PLG) gene.

Lower than expected cytogenetic and molecular response to imatinib in Mexican patients with chronic myelogenous leukemia

Maternal overnutrition by hypercaloric diets programs hypothalamic mitochondrial fusion and metabolic dysfunction in rat male offspring.

Modular organization of a hypocretin gene minimal promoter.

Molecular characterization of chronic myeloproliferative neoplasias in México

Mutations Related to Antiretroviral Resistance Identified by Ultra-Deep Sequencing in HIV-1 Infected Children under Structured Interruptions of HAART

No association between polymorphisms/haplotypes of the vascular endothelial growth factor gene and preeclampsia

Papillomavirus subtypes are natural and old taxa: phylogeny of human papillomavirus types 44 and 55 and 68a and -b.

Polymorphisms -455G/A and -148C/T and Fibrinogen Plasmatic Level as Risk Markers of Coronary Disease and Major Adverse Cardiovascular Events

Population based prostate cancer screening in north Mexico reveals a high prevalence of aggressive tumors in detected cases

Positive association between vascular endothelial growth factor (VEGF) -2578 C/A variant and prostate cancer.

Prevalence and 3-year persistence of human papillomavirus serotypes in asymptomatic patients in Northern Mexico

Prevalence and Clinical Significance of FLT3 Mutation Status in Acute Myeloid Leukemia Patients: A Multicenter Study

Protein tyrosine phosphatase PTPN22 +1858C/T polymorphism is associated with active vitiligo

Sequencing technology status of BRCA1/2 testing in Latin American Countries

Serological Test to Determine Exposure to SARS-CoV-2: ELISA Based on the Receptor-Binding Domain of the Spike Protein (S-RBDN318-V510) Expressed in Escherichia coli

Spatial Clusters of Children with Cleft Lip and Palate and Their Association with Polluted Zones in the Monterrey Metropolitan Area

Strong association of variants around FOXE1 and orofacial clefting.

The genomic landscape of Mexican Indigenous populations brings insights into the peopling of the Americas

The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.

The +1858 C/T Polymorphism in the PTPN22 Gene Is Associated with Cystic Fibrosis Patients in Northeast Mexico

Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer

Tumor necrosis factor alpha promoter‐308G/A polymorphism in Mexican patients with patchy alopecia areata ⬇️

Tumor necrosis factor-α -308G/A polymorphism is associated with active vitiligo vulgaris in a northeastern Mexican population

Tyrphostin AG17 inhibits adipocyte differentiation in vivo and in vitro.

Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies