Lista de obras - Anastasios Germenis - Dominio Público Uruguay

A Brief Exposure to Moderate Passive Smoke Increases Metabolism and Thyroid Hormone Secretion

artículo científico publicado en 2006

A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency.

artículo científico publicado en 2014

A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency

scientific article published on 17 January 2020

Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene

scientific article published on 02 December 2009

Acute phase markers for the differentiation of infectious and malignant pleural effusions

artículo científico publicado en 2007

Adiponectin: a new independent predictor of liver steatosis and response to IFN-alpha treatment in chronic hepatitis C.

artículo científico publicado en 2008

Allergy and risk of acute lymphoblastic leukemia among children: a nationwide case control study in Greece

artículo científico publicado en 2012

Alterations of leptin during IFN-alpha therapy in patients with chronic viral hepatitis

scientific article published on 17 February 2006

Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV.

artículo científico publicado en 2007

Anti-cyclic citrullinated peptide-2 (CCP2) autoantibodies and extra-articular manifestations in Greek patients with rheumatoid arthritis

artículo científico publicado en 2008

Anti-survivin antibody responses in lung cancer

artículo científico publicado en 2009

Association of TLR4-T399I polymorphism with chronic obstructive pulmonary disease in smokers.

artículo científico publicado en 2009

Atomic Coordination Reflects Peptide Immunogenicity.

artículo científico publicado en 2015

Baseline levels of CD8+ T cells against survivin and survivin-2B in the blood of lung cancer patients and cancer-free individuals.

artículo científico publicado en 2008

Circulating adhesion molecules levels in type 2 diabetes mellitus and hypertension

artículo científico publicado en 2005

Clinical, functional and biochemical changes during recovery from COPD exacerbations

artículo científico publicado en 2009

Complement: an inflammatory pathway fulfilling multiple roles at the interface of innate immunity and development.

artículo científico publicado en 2005

Cord blood as a source of non-senescent lymphocytes for tumor immunotherapy.

artículo científico publicado en 2010

Cytokine levels in the sera of patients with idiopathic pulmonary fibrosis

artículo científico publicado en 2005

Cytolytic T-cell response against Epstein-Barr virus in lung cancer patients and healthy subjects.

artículo científico publicado en 2010

DHLAS: A web-based information system for statistical genetic analysis of HLA population data.

artículo científico publicado en 2006

Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor

artículo científico publicado en 2020

Deep Intronic SERPING1 Gene Variants: Ending One Odyssey and Starting Another?

artículo científico publicado en 2020

Determinants of cancer immunotherapy success

artículo científico publicado en 2010

Downregulation of serum epidermal growth factor in patients with inflammatory bowel disease. Is there a link with mucosal damage?

artículo científico publicado en 2010

Evaluation of a microsphere-based flow cytometric assay for diagnosis of celiac disease

artículo científico publicado en 2004

Expression patterns of endothelin‐1 and its receptors in colorectal cancer ⬇️

artículo científico publicado el 27 de diciembre de 2011

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

artículo científico publicado en 2015

Foxp3 expression in human cancer cells.

artículo científico

Foxp3 expression in liver correlates with the degree but not the cause of inflammation.

artículo científico publicado en 2011

Function of reticuloendothelial system in splenectomised thalassemics

artículo científico publicado en 1988

Genetic Markers in Renal Adenocarcinoma ⬇️

artículo científico publicado el 1 de julio de 1984

Genetics of Hereditary Angioedema Revisited

artículo científico publicado en 2016

Group-specific component and haptoglobin phenotypes in multiple myeloma

artículo científico publicado en 1983

Hereditary angioedema in Greece: the first results of the greek hereditary angioedema registry.

artículo científico publicado en 2014

Hereditary angioedema in Greek families caused by novel and recurrent mutations

artículo científico publicado en 2009

Hereditary angioedema: molecular and clinical differences among European populations.

artículo científico publicado en 2014

Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia

artículo científico publicado en 2014

Heterozygous alterations of TNFRSF13B/TACI in tonsillar hypertrophy and sarcoidosis.

artículo científico publicado en 2013

Human Cytomegalovirus variant peptides adapt by decreasing their total coordination upon binding to a T cell receptor

artículo científico publicado en 2015

IgA antibodies against deamidated gliadin peptides in patients with chronic liver diseases

artículo científico publicado en 2012

Imbalance of tissue inhibitors of metalloproteinases (TIMP) - 1 and - 4 serum levels, in patients with inflammatory bowel disease

artículo científico publicado en 2008

Impaired degradation and aberrant phagocytosis of necrotic cell debris in the peripheral blood of patients with primary Sjögren's syndrome

artículo científico publicado en 2014

In vivo effect of rhGM-CSF And rhG-CSF on monocyte HLA-DR expression of septic neonates

scientific article published on 01 June 2002

International Consensus on the Use of Genetics in the Management of Hereditary Angioedema

scientific article published on 24 October 2019

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.

scientific article published on 09 August 2016

Kinetics of heat-damaged homologous erythrocytes. A five-compartmental analysis

artículo científico publicado en 1990

Liver FOXP3 and PD1/PDL1 Expression is Down-Regulated in Chronic HBV Hepatitis on Maintained Remission Related to the Degree of Inflammation

artículo científico publicado en 2013

MBL2 genotypes and their associations with MBL levels and NICU morbidity in a cohort of Greek neonates.

artículo científico publicado en 2015

Morning levels of C-reactive protein in children with obstructive sleep-disordered breathing

artículo científico publicado en 2004

Morning levels of fibrinogen in children with sleep-disordered breathing

artículo científico publicado en 2004

Nationwide collaborative study of HLA class II associations with distinct types of juvenile chronic arthritis (JCA) in Greece

artículo científico publicado en 1999

Naturally occurring tumor-specific CD8+ T-cell precursors in individuals with and without cancer

scientific article published on 09 February 2010

Neutrophil gelatinase-associated lipocalin (NGAL) in inflammatory bowel disease: association with pathophysiology of inflammation, established markers, and disease activity

artículo científico publicado en 2011

Non-indexed medical journals in the Web: new perspectives in the medical literature.

artículo científico publicado en 1997

On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema

artículo científico publicado en 2018

Plasma fibronectin (Fn) study in homozygous beta-thalassemia: relation to splenectomy and transfusion

artículo científico publicado en 1984

Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients

artículo científico publicado en 2020

Prevalence of coeliac disease in the adult population of central Greece

artículo científico publicado en 2007

Rapid detection of MYD88-L265P mutation by PCR-RFLP in B-cell lymphoproliferative disorders.

artículo científico publicado en 2013

Reply to: "SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting"

artículo científico publicado en 2013

SIAE Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies

artículo científico publicado en 2017

SLC40A1-R178G mutation and ferroportin disease

artículo científico publicado en 2011

Serum alpha-1-antitrypsin study in beta-thalassaemic patients

artículo científico publicado en 1982

Serum protein groups (Hp, GC, C3) in patients with gastric carcinoma

artículo científico publicado el 1 de enero de 1992

Soluble adhesion molecules are not involved in the development of retinopathy in type 2 diabetic patients

scientific article published on 01 September 2004

Survivin isoform expression patterns in CML patients correlate with resistance to imatinib and progression, but do not trigger cytolytic responses

artículo científico publicado en 2011

TACI expression and signaling in chronic lymphocytic leukemia

artículo científico publicado en 2015

TLR2 and TLR4 polymorphisms in familial Mediterranean fever.

artículo científico publicado en 2009

TLR4 single nucleotide polymorphisms and thrombosis risk in patients with myeloproliferative disorders

scientific article published on 14 November 2007

TNFRSF13B/TACI alterations in Greek patients with antibody deficiencies

artículo científico publicado en 2011

Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2018

The coordination of unprotonated peptide tertiary structure as a metric of pMHC-TCR functional avidity.

artículo científico publicado en 2015

The immunomodulatory effect of leflunomide in rat cardiac allotransplantation ⬇️

artículo científico publicado el 15 de septiembre de 1995

The quantum chemical causality of pMHC-TCR biological avidity: Peptide atomic coordination data and the electronic state of agonist N termini.

artículo científico publicado en 2015

Toll-like receptor 4 gene (TLR4), but not TLR2, polymorphisms modify the risk of tonsillar disease due to Streptococcus pyogenes and Haemophilus influenzae.

artículo científico publicado en 2010

Lista de obras de Anastasios Germenis

A Brief Exposure to Moderate Passive Smoke Increases Metabolism and Thyroid Hormone Secretion

A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency.

A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency

Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene

Acute phase markers for the differentiation of infectious and malignant pleural effusions

Adiponectin: a new independent predictor of liver steatosis and response to IFN-alpha treatment in chronic hepatitis C.

Allergy and risk of acute lymphoblastic leukemia among children: a nationwide case control study in Greece

Alterations of leptin during IFN-alpha therapy in patients with chronic viral hepatitis

Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV.

Anti-cyclic citrullinated peptide-2 (CCP2) autoantibodies and extra-articular manifestations in Greek patients with rheumatoid arthritis

Anti-survivin antibody responses in lung cancer

Association of TLR4-T399I polymorphism with chronic obstructive pulmonary disease in smokers.

Atomic Coordination Reflects Peptide Immunogenicity.

Baseline levels of CD8+ T cells against survivin and survivin-2B in the blood of lung cancer patients and cancer-free individuals.

Circulating adhesion molecules levels in type 2 diabetes mellitus and hypertension

Clinical, functional and biochemical changes during recovery from COPD exacerbations

Complement: an inflammatory pathway fulfilling multiple roles at the interface of innate immunity and development.

Cord blood as a source of non-senescent lymphocytes for tumor immunotherapy.

Cytokine levels in the sera of patients with idiopathic pulmonary fibrosis

Cytolytic T-cell response against Epstein-Barr virus in lung cancer patients and healthy subjects.

DHLAS: A web-based information system for statistical genetic analysis of HLA population data.

Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor

Deep Intronic SERPING1 Gene Variants: Ending One Odyssey and Starting Another?

Determinants of cancer immunotherapy success

Downregulation of serum epidermal growth factor in patients with inflammatory bowel disease. Is there a link with mucosal damage?

Evaluation of a microsphere-based flow cytometric assay for diagnosis of celiac disease

Expression patterns of endothelin‐1 and its receptors in colorectal cancer ⬇️

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

Foxp3 expression in human cancer cells.

Foxp3 expression in liver correlates with the degree but not the cause of inflammation.

Function of reticuloendothelial system in splenectomised thalassemics

Genetic Markers in Renal Adenocarcinoma ⬇️

Genetics of Hereditary Angioedema Revisited

Group-specific component and haptoglobin phenotypes in multiple myeloma

Hereditary angioedema in Greece: the first results of the greek hereditary angioedema registry.

Hereditary angioedema in Greek families caused by novel and recurrent mutations

Hereditary angioedema: molecular and clinical differences among European populations.

Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia

Heterozygous alterations of TNFRSF13B/TACI in tonsillar hypertrophy and sarcoidosis.

Human Cytomegalovirus variant peptides adapt by decreasing their total coordination upon binding to a T cell receptor

IgA antibodies against deamidated gliadin peptides in patients with chronic liver diseases

Imbalance of tissue inhibitors of metalloproteinases (TIMP) - 1 and - 4 serum levels, in patients with inflammatory bowel disease

Impaired degradation and aberrant phagocytosis of necrotic cell debris in the peripheral blood of patients with primary Sjögren's syndrome

In vivo effect of rhGM-CSF And rhG-CSF on monocyte HLA-DR expression of septic neonates

International Consensus on the Use of Genetics in the Management of Hereditary Angioedema

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.

Kinetics of heat-damaged homologous erythrocytes. A five-compartmental analysis

Liver FOXP3 and PD1/PDL1 Expression is Down-Regulated in Chronic HBV Hepatitis on Maintained Remission Related to the Degree of Inflammation

MBL2 genotypes and their associations with MBL levels and NICU morbidity in a cohort of Greek neonates.

Morning levels of C-reactive protein in children with obstructive sleep-disordered breathing

Morning levels of fibrinogen in children with sleep-disordered breathing

Nationwide collaborative study of HLA class II associations with distinct types of juvenile chronic arthritis (JCA) in Greece

Naturally occurring tumor-specific CD8+ T-cell precursors in individuals with and without cancer

Neutrophil gelatinase-associated lipocalin (NGAL) in inflammatory bowel disease: association with pathophysiology of inflammation, established markers, and disease activity

Non-indexed medical journals in the Web: new perspectives in the medical literature.

On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema

Plasma fibronectin (Fn) study in homozygous beta-thalassemia: relation to splenectomy and transfusion

Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients

Prevalence of coeliac disease in the adult population of central Greece

Rapid detection of MYD88-L265P mutation by PCR-RFLP in B-cell lymphoproliferative disorders.

Reply to: "SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting"

SIAE Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies

SLC40A1-R178G mutation and ferroportin disease

Serum alpha-1-antitrypsin study in beta-thalassaemic patients

Serum protein groups (Hp, GC, C3) in patients with gastric carcinoma

Soluble adhesion molecules are not involved in the development of retinopathy in type 2 diabetic patients

Survivin isoform expression patterns in CML patients correlate with resistance to imatinib and progression, but do not trigger cytolytic responses

TACI expression and signaling in chronic lymphocytic leukemia

TLR2 and TLR4 polymorphisms in familial Mediterranean fever.

TLR4 single nucleotide polymorphisms and thrombosis risk in patients with myeloproliferative disorders

TNFRSF13B/TACI alterations in Greek patients with antibody deficiencies

Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency

The coordination of unprotonated peptide tertiary structure as a metric of pMHC-TCR functional avidity.

The immunomodulatory effect of leflunomide in rat cardiac allotransplantation ⬇️

The quantum chemical causality of pMHC-TCR biological avidity: Peptide atomic coordination data and the electronic state of agonist N termini.

Toll-like receptor 4 gene (TLR4), but not TLR2, polymorphisms modify the risk of tonsillar disease due to Streptococcus pyogenes and Haemophilus influenzae.