Lista de obras - Donato Gemmati - Dominio Público Uruguay

"Bridging the Gap" Everything that Could Have Been Avoided If We Had Applied Gender Medicine, Pharmacogenetics and Personalized Medicine in the Gender-Omics and Sex-Omics Era

scientific article published on 31 December 2019

A Modified Functional Global Test to Measure Protein C, Protein S Activities and the Activated Protein C-Resistance Phenotype ⬇️

artículo científico publicado el 1 de noviembre de 1998

A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): A risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases

artículo científico publicado en 2001

A novel mutation (Leu817Pro) causing type 2A von Willebrand disease

scientific article published on 01 January 1996

A photometric method for the dosage of factor XIII applied to the study of chronic hepatopathies

artículo científico publicado en 1995

A recurrent missense mutation (Arg----Gln) and a partial deletion in factor VIII gene causing severe haemophilia A.

artículo científico publicado en 1989

Assessment of the interlaboratory variability and robustness of JAK2V617F mutation assays: A study involving a consortium of 19 Italian laboratories

artículo científico publicado en 2017

Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster

artículo científico publicado en 2003

Clinical implications of gene polymorphisms in venous leg ulcer: A model in tissue injury and reparative process

article

Coagulation Factor XIIIA (F13A1): Novel Perspectives in Treatment and Pharmacogenetics.

artículo científico publicado en 2015

Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic family ⬇️

artículo científico publicado el 1 de marzo de 1998

Comparison among natural (Arg304Gln, Arg304Trp) and artificial (Arg290His, Arg290Lys) mutations in coagulation factor VII loops

artículo científico publicado en 2003

Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation

artículo científico publicado en 2019

Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis

artículo científico publicado en 2010

DHFR 19-bp insertion/deletion polymorphism and MTHFR C677T in adult acute lymphoblastic leukaemia: is the risk reduction due to intracellular folate unbalancing?

artículo científico publicado en 2009

DNA-array of gene variants in venous leg ulcers: detection of prognostic indicators.

artículo científico publicado en 2009

Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7)

artículo científico publicado en 1992

Effect of Factor XIII-A G185T Polymorphism on Visual Prognosis after Photodynamic Therapy for Neovascular Macular Degeneration

artículo científico publicado en 2015

Effects of physical stimulation with electromagnetic field and insulin growth factor-I treatment on proteoglycan synthesis of bovine articular cartilage

artículo científico publicado en 2004

Evidence for a factor promoting the conversion of VWF from low and intermediate to high molecular mass polymers on the platelet membrane

scientific article published on 01 June 1989

Factor XIII V34L polymorphism modulates the risk of chronic venous leg ulcer progression and extension

scientific article published on 01 September 2004

Factor XIII contrasts the effects of metalloproteinases in human dermal fibroblast cultured cells

artículo científico publicado en 2004

Factor XIII-A dynamics in acute myocardial infarction: a novel prognostic biomarker?

artículo científico publicado en 2015

Factor XIIIA-V34L and factor XIIIB-H95R gene variants: effects on survival in myocardial infarction patients.

artículo científico publicado en 2007

Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis

artículo científico publicado en 2014

Gene Variant (V34L) and Residual Circulating FXIIIA Levels Predict Short- and Long-Term Mortality in Acute Myocardial Infarction after Coronary Angioplasty

article

Gene polymorphisms in folate metabolizing enzymes in adult acute lymphoblastic leukemia: effects on methotrexate-related toxicity and survival.

artículo científico publicado en 2009

Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases.

artículo científico publicado en 2018

Genetic Hypothesis and Pharmacogenetics Side of Renin-Angiotensin-System in COVID-19

artículo científico publicado en 2020

Genetic Predictors of Response to Photodynamic Therapy ⬇️

artículo científico publicado el 1 de agosto de 2011

Genetic association and altered gene expression of mir-155 in multiple sclerosis patients

artículo científico publicado en 2011

Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration.

artículo científico publicado en 2005

High doses of glucosamine-HCl have detrimental effects on bovine articular cartilage explants cultured in vitro.

artículo científico publicado en 2002

Impact of methylenetetrahydrofolate reductase C677T polymorphism on the efficacy of photodynamic therapy in patients with neovascular age-related macular degeneration

scientific article published on 22 February 2019

In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand disease.

artículo científico publicado en 1993

Influence of gene polymorphisms in ulcer healing process after superficial venous surgery.

artículo científico publicado en 2006

Inherited genetic predispositions in F13A1 and F13B genes predict abdominal adhesion formation: identification of gender prognostic indicators

scientific article published in Scientific Reports

Interplay of iron metallobiology, metalloproteinases, and FXIII, and role of their gene variants in venous leg ulcer.

artículo científico publicado en 2010

Investigation of in vitro cytotoxicity of the redox state of ionic iron in neuroblastoma cells

artículo científico publicado en 2012

Karyotype-phenotype correlation in partial trisomies of the short arm of chromosome 6: a family case report and review of the literature.

artículo científico publicado en 2013

Low folate levels and thermolabile methylenetetrahydrofolate reductase as primary determinant of mild hyperhomocystinemia in normal and thromboembolic subjects

artículo científico publicado en 1999

Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes.

artículo científico publicado en 2015

Methylenetetrahydrofolate reductase C677T and A1298C gene variants in adult non-Hodgkin's lymphoma patients: association with toxicity and survival

artículo científico publicado en 2007

Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region.

artículo científico publicado en 1993

Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII

artículo científico publicado en 1994

PCR detection of a repeat polymorphism within the F7 gene

artículo científico publicado en 1991

Pharmacogenetic aspects in therapeutic management of subfoveal choroidal neovascularisation: role of factor XIII-A 185 T-allele.

artículo científico publicado en 2011

Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis

artículo científico publicado en 2012

Predictive role of C677T MTHFR polymorphism in variable efficacy of photodynamic therapy for neovascular age-related macular degeneration.

artículo científico publicado en 2009

Predictive role of coagulation-balance gene polymorphisms in the efficacy of photodynamic therapy with verteporfin for classic choroidal neovascularization secondary to age-related macular degeneration.

artículo científico publicado en 2007

Proteoglycan synthesis in bovine articular cartilage explants exposed to different low-frequency low-energy pulsed electromagnetic fields

artículo científico publicado en 2006

Quantitive evaluation of dentin sialoprotein (DSP) using microbeads - a potential early marker of root resorption

artículo científico publicado en 2016

Rapid detection of a protein C gene mutation present in the asymptomatic and not in the thrombosis-prone lineage.

artículo científico publicado en 1992

Recurrent episodes of spontaneous subconjunctival hemorrhage in patients with factor XIII Val34Leu mutation

artículo científico publicado en 2002

Redox metals homeostasis in multiple sclerosis and amyotrophic lateral sclerosis: a review

artículo científico publicado en 2018

Reference materials (RMs) for analysis of the human factor II (prothrombin) gene G20210A mutation

article

Resistance to activated protein C and low levels of protein S activity in nine thrombophilic families ⬇️

artículo científico publicado el 1 de marzo de 1997

Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls

artículo científico publicado en 2013

Sex/Gender-Specific Imbalance in CVD: Could Physical Activity Help to Improve Clinical Outcome Targeting CVD Molecular Mechanisms in Women?

artículo científico publicado en 2020

Study of a protein S gene polymorphism at DNA and mRNA level in a family with symptomatic protein S deficiency

artículo científico publicado en 1993

Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes: new insights from a case-control study

artículo científico publicado en 2015

Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381 → Ser) in the substrate-binding pocket

artículo científico publicado en 1993

TRAIL, OPG, and TWEAK in kidney disease: biomarkers or therapeutic targets?

artículo científico publicado en 2019

Temporal and Genotype-Driven Variation of Factor VII Levels in Patients With Acute Myocardial Infarction

scientific article published on 01 February 2009

The Active Metabolite of Warfarin (3'-Hydroxywarfarin) and Correlation with INR, Warfarin and Drug Weekly Dosage in Patients under Oral Anticoagulant Therapy: A Pharmacogenetics Study

artículo científico publicado en 2016

The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor X.

artículo científico publicado en 2015

The overlapping of local iron overload and HFE mutation in venous leg ulcer pathogenesis.

artículo científico publicado en 2006

The reduced sensitivity of the ProC® Global test in protein S deficient subjects reflects a reduction in the associated thrombotic risk

artículo científico publicado en 2001

The role of the MTHFR 677C>T polymorphism in methotrexate-induced liver toxicity: a meta-analysis in patients with cancer

artículo científico publicado en 2013

Time- and dose-dependent effects of chronic wound fluid on human adult dermal fibroblasts

artículo científico publicado en 2007

Tissue Factor and Coagulation Factor VII Levels During Acute Myocardial Infarction

artículo científico publicado en 2006

Two novel mutations (Pro864His, Val867Glu) causing type 2A von Willebrand disease and affecting a single restriction site in exon 28

artículo científico publicado en 1998

Value of platelet reactivity in predicting response to treatment and clinical outcome in patients undergoing primary coronary intervention: insights into the STRATEGY Study.

artículo científico publicado en 2006

Vision loss after PDT.

artículo científico publicado en 2006

Lista de obras de Donato Gemmati

"Bridging the Gap" Everything that Could Have Been Avoided If We Had Applied Gender Medicine, Pharmacogenetics and Personalized Medicine in the Gender-Omics and Sex-Omics Era

A Modified Functional Global Test to Measure Protein C, Protein S Activities and the Activated Protein C-Resistance Phenotype ⬇️

A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): A risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases

A novel mutation (Leu817Pro) causing type 2A von Willebrand disease

A photometric method for the dosage of factor XIII applied to the study of chronic hepatopathies

A recurrent missense mutation (Arg----Gln) and a partial deletion in factor VIII gene causing severe haemophilia A.

Assessment of the interlaboratory variability and robustness of JAK2V617F mutation assays: A study involving a consortium of 19 Italian laboratories

Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster

Clinical implications of gene polymorphisms in venous leg ulcer: A model in tissue injury and reparative process

Coagulation Factor XIIIA (F13A1): Novel Perspectives in Treatment and Pharmacogenetics.

Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic family ⬇️

Comparison among natural (Arg304Gln, Arg304Trp) and artificial (Arg290His, Arg290Lys) mutations in coagulation factor VII loops

Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation

Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis

DHFR 19-bp insertion/deletion polymorphism and MTHFR C677T in adult acute lymphoblastic leukaemia: is the risk reduction due to intracellular folate unbalancing?

DNA-array of gene variants in venous leg ulcers: detection of prognostic indicators.

Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7)

Effect of Factor XIII-A G185T Polymorphism on Visual Prognosis after Photodynamic Therapy for Neovascular Macular Degeneration

Effects of physical stimulation with electromagnetic field and insulin growth factor-I treatment on proteoglycan synthesis of bovine articular cartilage

Evidence for a factor promoting the conversion of VWF from low and intermediate to high molecular mass polymers on the platelet membrane

Factor XIII V34L polymorphism modulates the risk of chronic venous leg ulcer progression and extension

Factor XIII contrasts the effects of metalloproteinases in human dermal fibroblast cultured cells

Factor XIII-A dynamics in acute myocardial infarction: a novel prognostic biomarker?

Factor XIIIA-V34L and factor XIIIB-H95R gene variants: effects on survival in myocardial infarction patients.

Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis

Gene Variant (V34L) and Residual Circulating FXIIIA Levels Predict Short- and Long-Term Mortality in Acute Myocardial Infarction after Coronary Angioplasty

Gene polymorphisms in folate metabolizing enzymes in adult acute lymphoblastic leukemia: effects on methotrexate-related toxicity and survival.

Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases.

Genetic Hypothesis and Pharmacogenetics Side of Renin-Angiotensin-System in COVID-19

Genetic Predictors of Response to Photodynamic Therapy ⬇️

Genetic association and altered gene expression of mir-155 in multiple sclerosis patients

Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration.

High doses of glucosamine-HCl have detrimental effects on bovine articular cartilage explants cultured in vitro.

Impact of methylenetetrahydrofolate reductase C677T polymorphism on the efficacy of photodynamic therapy in patients with neovascular age-related macular degeneration

In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand disease.

Influence of gene polymorphisms in ulcer healing process after superficial venous surgery.

Inherited genetic predispositions in F13A1 and F13B genes predict abdominal adhesion formation: identification of gender prognostic indicators

Interplay of iron metallobiology, metalloproteinases, and FXIII, and role of their gene variants in venous leg ulcer.

Investigation of in vitro cytotoxicity of the redox state of ionic iron in neuroblastoma cells

Karyotype-phenotype correlation in partial trisomies of the short arm of chromosome 6: a family case report and review of the literature.

Low folate levels and thermolabile methylenetetrahydrofolate reductase as primary determinant of mild hyperhomocystinemia in normal and thromboembolic subjects

Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes.

Methylenetetrahydrofolate reductase C677T and A1298C gene variants in adult non-Hodgkin's lymphoma patients: association with toxicity and survival

Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region.

Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII

PCR detection of a repeat polymorphism within the F7 gene

Pharmacogenetic aspects in therapeutic management of subfoveal choroidal neovascularisation: role of factor XIII-A 185 T-allele.

Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis

Predictive role of C677T MTHFR polymorphism in variable efficacy of photodynamic therapy for neovascular age-related macular degeneration.

Predictive role of coagulation-balance gene polymorphisms in the efficacy of photodynamic therapy with verteporfin for classic choroidal neovascularization secondary to age-related macular degeneration.

Proteoglycan synthesis in bovine articular cartilage explants exposed to different low-frequency low-energy pulsed electromagnetic fields

Quantitive evaluation of dentin sialoprotein (DSP) using microbeads - a potential early marker of root resorption

Rapid detection of a protein C gene mutation present in the asymptomatic and not in the thrombosis-prone lineage.

Recurrent episodes of spontaneous subconjunctival hemorrhage in patients with factor XIII Val34Leu mutation

Redox metals homeostasis in multiple sclerosis and amyotrophic lateral sclerosis: a review

Reference materials (RMs) for analysis of the human factor II (prothrombin) gene G20210A mutation

Resistance to activated protein C and low levels of protein S activity in nine thrombophilic families ⬇️

Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls

Sex/Gender-Specific Imbalance in CVD: Could Physical Activity Help to Improve Clinical Outcome Targeting CVD Molecular Mechanisms in Women?

Study of a protein S gene polymorphism at DNA and mRNA level in a family with symptomatic protein S deficiency

Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes: new insights from a case-control study

Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381 → Ser) in the substrate-binding pocket

TRAIL, OPG, and TWEAK in kidney disease: biomarkers or therapeutic targets?

Temporal and Genotype-Driven Variation of Factor VII Levels in Patients With Acute Myocardial Infarction

The Active Metabolite of Warfarin (3'-Hydroxywarfarin) and Correlation with INR, Warfarin and Drug Weekly Dosage in Patients under Oral Anticoagulant Therapy: A Pharmacogenetics Study

The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor X.

The overlapping of local iron overload and HFE mutation in venous leg ulcer pathogenesis.

The reduced sensitivity of the ProC® Global test in protein S deficient subjects reflects a reduction in the associated thrombotic risk

The role of the MTHFR 677C>T polymorphism in methotrexate-induced liver toxicity: a meta-analysis in patients with cancer

Time- and dose-dependent effects of chronic wound fluid on human adult dermal fibroblasts

Tissue Factor and Coagulation Factor VII Levels During Acute Myocardial Infarction

Two novel mutations (Pro864His, Val867Glu) causing type 2A von Willebrand disease and affecting a single restriction site in exon 28

Value of platelet reactivity in predicting response to treatment and clinical outcome in patients undergoing primary coronary intervention: insights into the STRATEGY Study.

Vision loss after PDT.