Lista de obras - Davide Gentilini - Dominio Público Uruguay

'Here comes the sun': pigmentary traits and sun habits in women with endometriosis.

artículo científico publicado en 2010

A Rare Familial Case of Endometriosis with Very Severe Gynecological and Obstetric Complications: Novel Genetic Variants at a Glance

artículo científico publicado en 2014

A frequent oligogenic involvement in congenital hypothyroidism.

artículo científico publicado en 2017

A meta-analysis on age-associated changes in blood DNA methylation: results from an original analysis pipeline for Infinium 450k data.

artículo científico publicado en 2015

Acceleration of leukocytes' epigenetic age as an early tumor and sex-specific marker of breast and colorectal cancer.

artículo científico publicado en 2017

Acid sensing ion channel 2: A new potential player in the pathophysiology of multiple sclerosis

scientific article published on 19 February 2019

Age-dependent skewing of X chromosome inactivation appears delayed in centenarians' offspring. Is there a role for allelic imbalance in healthy aging and longevity?

artículo científico publicado en 2012

Altered modulation of lamin A/C-HDAC2 interaction and p21 expression during oxidative stress response in HGPS

artículo científico publicado en 2018

Can genetics predict risk for sudden cardiac death? The relentless search for the Holy Grail

artículo científico publicado en 2018

Colorectal cancer early methylation alterations affect the crosstalk between cell and surrounding environment, tracing a biomarker signature specific for this tumor.

artículo científico publicado en 2018

Deregulated human glioma cell motility: inhibitory effect of somatostatin.

artículo científico publicado en 2006

Differences in visceral fat and fat bacterial colonization between ulcerative colitis and Crohn's disease. An in vivo and in vitro study

artículo científico publicado en 2013

Dissecting the Pre-Columbian Genomic Ancestry of Native Americans along the Andes-Amazonia Divide

artículo científico publicado en 2019

Effects of human recombinant type I IFNs (IFN-α2b and IFN-β1a) on growth and migration of primary endometrial stromal cells from women with deeply infiltrating endometriosis: A preliminary study

artículo científico publicado en 2018

Endocannabinoid system regulates migration of endometrial stromal cells via cannabinoid receptor 1 through the activation of PI3K and ERK1/2 pathways.

artículo científico publicado en 2010

Endometrial stromal cells from women with endometriosis reveal peculiar migratory behavior in response to ovarian steroids.

artículo científico publicado en 2008

Endometrial stromal progesterone receptor-A/progesterone receptor-B ratio: no difference between women with and without endometriosis.

artículo científico publicado en 2010

Epigenome-wide association study in hepatocellular carcinoma: Identification of stochastic epigenetic mutations through an innovative statistical approach.

artículo científico publicado en 2017

GENETICS IN ENDOCRINOLOGY: Genetic diagnosis of endocrine diseases by NGS: novel scenarios and unpredictable results and risks

artículo científico publicado en 2018

Gene expression profiling in human corticotroph tumours reveals distinct, neuroendocrine profiles

article

Gene expression profiling of peripheral blood mononuclear cells in endometriosis identifies genes altered in non-gynaecologic chronic inflammatory diseases.

artículo científico publicado en 2011

Genetic evidence of assortative mating in humans

article

Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome

artículo científico publicado en 2017

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

scientific journal article

Heterogeneity of Thyroid Function and Impact of Peripheral Thyroxine Deiodination in Centenarians and Semi-Supercentenarians: Association With Functional Status and Mortality

artículo científico publicado en 2019

Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy.

artículo científico publicado en 2017

Immunomodulatory effects of VEGF: Clinical implications of VEGF-targeted therapy in human cancer

artículo científico publicado en 2010

Integrated DNA methylation analysis identifies topographical and tumoral biomarkers in pilocytic astrocytomas.

artículo científico publicado en 2018

Interferon-inducible genes, TNF-related apoptosis-inducing ligand (TRAIL) and interferon inducible protein 27 (IFI27) are negatively regulated in leiomyomas: implications for a role of the interferon pathway in leiomyoma development.

artículo científico publicado en 2012

Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci.

artículo científico publicado en 2017

Methylation of ELOVL2 gene as a new epigenetic marker of age

article

Molecular and morphologic characterization of superficial- and deep-subcutaneous adipose tissue subdivisions in human obesity.

artículo científico publicado en 2013

Multifactorial analysis of the stochastic epigenetic variability in cord blood confirmed an impact of common behavioral and environmental factors but not of in vitro conception.

artículo científico publicado en 2018

NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis

scientific article published on 19 September 2019

PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival

scientific article published on 22 March 2019

Pathogenic Variants in STXBP1 and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes

scientific article published on 24 July 2019

Permanence of molecular features of obesity in subcutaneous adipose tissue of ex-obese subjects

artículo científico publicado en 2013

Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations.

artículo científico publicado en 2019

Plasminogen activator inhibitor-1 4G/5G polymorphism and susceptibility to endometriosis in the Italian population

article

Progesterone receptor +331G/A polymorphism in endometriosis and deep-infiltrating endometriosis.

artículo científico publicado en 2008

Pyk2 and Cyr61 at the cross-road of cAMP-dependent signalling in invasiveness and neuroendocrine differentiation of prostate cancer

artículo científico publicado en 2009

Replication and meta-analysis of previous genome-wide association studies confirm vezatin as the locus with the strongest evidence for association with endometriosis.

artículo científico publicado en 2015

Role of epigenetics in human aging and longevity: genome-wide DNA methylation profile in centenarians and centenarians' offspring.

artículo científico publicado en 2012

Soluble EMMPRIN levels discriminate aortic ectasia in Marfan syndrome patients

artículo científico publicado en 2019

Stochastic epigenetic mutations (DNA methylation) increase exponentially in human aging and correlate with X chromosome inactivation skewing in females

artículo científico publicado en 2015

Surgical excision of ovarian endometriomas: Does it truly impair ovarian reserve? Long term anti-Müllerian hormone (AMH) changes after surgery

scientific article published on 30 September 2015

Synergistic activity of everolimus and 5-aza-2'-deoxycytidine in medullary thyroid carcinoma cell lines.

artículo científico publicado en 2017

The endocannabinoid pathway and the female reproductive organs.

artículo científico

The genetic legacy of the Yaghnobis: A witness of an ancient Eurasian ancestry in the historically reshuffled central Asian gene pool

scientific article published on 29 January 2019

The genomic landscape of Nepalese Tibeto-Burmans reveals new insights into the recent peopling of Southern Himalayas.

artículo científico publicado en 2017

Visceral adipocytes: old actors in obesity and new protagonists in Crohn's disease?

artículo científico publicado en 2011

Lista de obras de Davide Gentilini

'Here comes the sun': pigmentary traits and sun habits in women with endometriosis.

A Rare Familial Case of Endometriosis with Very Severe Gynecological and Obstetric Complications: Novel Genetic Variants at a Glance

A frequent oligogenic involvement in congenital hypothyroidism.

A meta-analysis on age-associated changes in blood DNA methylation: results from an original analysis pipeline for Infinium 450k data.

Acceleration of leukocytes' epigenetic age as an early tumor and sex-specific marker of breast and colorectal cancer.

Acid sensing ion channel 2: A new potential player in the pathophysiology of multiple sclerosis

Age-dependent skewing of X chromosome inactivation appears delayed in centenarians' offspring. Is there a role for allelic imbalance in healthy aging and longevity?

Altered modulation of lamin A/C-HDAC2 interaction and p21 expression during oxidative stress response in HGPS

Can genetics predict risk for sudden cardiac death? The relentless search for the Holy Grail

Colorectal cancer early methylation alterations affect the crosstalk between cell and surrounding environment, tracing a biomarker signature specific for this tumor.

Deregulated human glioma cell motility: inhibitory effect of somatostatin.

Differences in visceral fat and fat bacterial colonization between ulcerative colitis and Crohn's disease. An in vivo and in vitro study

Dissecting the Pre-Columbian Genomic Ancestry of Native Americans along the Andes-Amazonia Divide

Effects of human recombinant type I IFNs (IFN-α2b and IFN-β1a) on growth and migration of primary endometrial stromal cells from women with deeply infiltrating endometriosis: A preliminary study

Endocannabinoid system regulates migration of endometrial stromal cells via cannabinoid receptor 1 through the activation of PI3K and ERK1/2 pathways.

Endometrial stromal cells from women with endometriosis reveal peculiar migratory behavior in response to ovarian steroids.

Endometrial stromal progesterone receptor-A/progesterone receptor-B ratio: no difference between women with and without endometriosis.

Epigenome-wide association study in hepatocellular carcinoma: Identification of stochastic epigenetic mutations through an innovative statistical approach.

GENETICS IN ENDOCRINOLOGY: Genetic diagnosis of endocrine diseases by NGS: novel scenarios and unpredictable results and risks

Gene expression profiling in human corticotroph tumours reveals distinct, neuroendocrine profiles

Gene expression profiling of peripheral blood mononuclear cells in endometriosis identifies genes altered in non-gynaecologic chronic inflammatory diseases.

Genetic evidence of assortative mating in humans

Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Heterogeneity of Thyroid Function and Impact of Peripheral Thyroxine Deiodination in Centenarians and Semi-Supercentenarians: Association With Functional Status and Mortality

Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy.

Immunomodulatory effects of VEGF: Clinical implications of VEGF-targeted therapy in human cancer

Integrated DNA methylation analysis identifies topographical and tumoral biomarkers in pilocytic astrocytomas.

Interferon-inducible genes, TNF-related apoptosis-inducing ligand (TRAIL) and interferon inducible protein 27 (IFI27) are negatively regulated in leiomyomas: implications for a role of the interferon pathway in leiomyoma development.

Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci.

Methylation of ELOVL2 gene as a new epigenetic marker of age

Molecular and morphologic characterization of superficial- and deep-subcutaneous adipose tissue subdivisions in human obesity.

Multifactorial analysis of the stochastic epigenetic variability in cord blood confirmed an impact of common behavioral and environmental factors but not of in vitro conception.

NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis

PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival

Pathogenic Variants in STXBP1 and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes

Permanence of molecular features of obesity in subcutaneous adipose tissue of ex-obese subjects

Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations.

Plasminogen activator inhibitor-1 4G/5G polymorphism and susceptibility to endometriosis in the Italian population

Progesterone receptor +331G/A polymorphism in endometriosis and deep-infiltrating endometriosis.

Pyk2 and Cyr61 at the cross-road of cAMP-dependent signalling in invasiveness and neuroendocrine differentiation of prostate cancer

Replication and meta-analysis of previous genome-wide association studies confirm vezatin as the locus with the strongest evidence for association with endometriosis.

Role of epigenetics in human aging and longevity: genome-wide DNA methylation profile in centenarians and centenarians' offspring.

Soluble EMMPRIN levels discriminate aortic ectasia in Marfan syndrome patients

Stochastic epigenetic mutations (DNA methylation) increase exponentially in human aging and correlate with X chromosome inactivation skewing in females

Surgical excision of ovarian endometriomas: Does it truly impair ovarian reserve? Long term anti-Müllerian hormone (AMH) changes after surgery

Synergistic activity of everolimus and 5-aza-2'-deoxycytidine in medullary thyroid carcinoma cell lines.

The endocannabinoid pathway and the female reproductive organs.

The genetic legacy of the Yaghnobis: A witness of an ancient Eurasian ancestry in the historically reshuffled central Asian gene pool

The genomic landscape of Nepalese Tibeto-Burmans reveals new insights into the recent peopling of Southern Himalayas.

Visceral adipocytes: old actors in obesity and new protagonists in Crohn's disease?