Lista de obras -

16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer.

artículo científico publicado en 2012

A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer

scientific article published on 28 January 2017

Amniotic Fluid Stem Cells: A Novel Source for Modeling of Human Genetic Diseases

artículo científico publicado en 2016

Amniotic fluid as a rich source of mesenchymal stromal cells for transplantation therapy

artículo científico publicado en 2010

Amniotic fluid stem cell models: A tool for filling the gaps in knowledge for human genetic diseases

Amniotic fluid stem cells: a promising therapeutic resource for cell-based regenerative therapy

artículo científico publicado en 2012

Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring

artículo científico publicado en 2008

BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 Gene

artículo científico publicado en 2016

C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy

artículo científico publicado en 2002

Calcitonin-induced effects on amniotic fluid-derived mesenchymal stem cells.

artículo científico publicado en 2015

Cardiomyocytes Derived from Human Amniotic Fluids

scientific article published in Scientific Reports

Comparison between CaGene 5.1 and 6.0 for BRCA1/2 mutation prediction: a retrospective study of 150 BRCA1/2 genetic tests in 517 families with breast/ovarian cancer.

artículo científico publicado en 2016

DNMT3B promoter polymorphisms and maternal risk of birth of a child with Down syndrome.

artículo científico publicado en 2012

De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects.

artículo científico publicado en 2013

Epigenetic Features of Human Perinatal Stem Cells Redefine Their Stemness Potential

scientific article published on 24 May 2020

Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime health

artículo científico publicado en 2015

Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits

artículo científico publicado en 2017

Functional interleukin-7/interleukin-7Ralpha, and SDF-1alpha/CXCR4 are expressed by human periodontal ligament derived mesenchymal stem cells

scientific article published on 01 March 2008

Genetic determinants of blood pressure responses to caffeine drinking

scientific article published on 14 December 2011

Genetic determinants of cognitive responses to caffeine drinking identified from a double-blind, randomized, controlled trial.

artículo científico publicado en 2015

Genetic testing in couples undergoing assisted reproduction technique protocols.

artículo científico

Genetics of syndromic and nonsyndromic cleft lip and palate

artículo científico

Human second trimester amniotic fluid cells are able to create embryoid body-like structures in vitro and to show typical expression profiles of embryonic and primordial germ cells

artículo científico publicado en 2014

Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay

artículo científico publicado en 2007

Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene

artículo científico publicado en 2005

Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols

artículo científico publicado en 2010

Impact of lysosomal storage disorders on biology of mesenchymal stem cells: Evidences from in vitro silencing of glucocerebrosidase (GBA) and alpha-galactosidase A (GLA) enzymes.

artículo científico publicado en 2017

Intravenous grafts of amniotic fluid-derived stem cells induce endogenous cell proliferation and attenuate behavioral deficits in ischemic stroke rats

artículo científico publicado en 2012

Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol

artículo científico publicado en 2009

MBL2 and FCN2 gene polymorphisms in a cohort of Italian children with rheumatic fever: A case-control study

artículo científico publicado en 2017

MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting.

artículo científico publicado en 2013

Male factor infertility and lack of openness about infertility as risk factors for depressive symptoms in males undergoing assisted reproductive technology treatment in Italy.

artículo científico publicado en 2017

Molecular and phenotypic characterization of human amniotic fluid-derived cells: a morphological and proteomic approach

artículo científico publicado en 2015

Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson

artículo científico publicado en 2012

Reduced thromboxane biosynthesis in carriers of toll-like receptor 4 polymorphisms in vivo

artículo científico publicado en 2006

Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs

article

Sequence-specific modification of a beta-thalassemia locus by small DNA fragments in human erythroid progenitor cells

artículo científico publicado en 2007

TNF-α gene polymorphisms and juvenile idiopathic arthritis: Influence on disease outcome and therapeutic response

artículo científico publicado en 2015

Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion

artículo científico publicado en 2010

The Impact of Epigenetic Signatures on Amniotic Fluid Stem Cell Fate

scientific article published on 25 November 2018

The MTR 2756A>G polymorphism and maternal risk of birth of a child with Down syndrome: a case-control study and a meta-analysis.

artículo científico publicado en 2013

The MTRR 66A>G polymorphism and maternal risk of birth of a child with Down syndrome in Caucasian women: a case–control study and a meta-analysis

article

Therapeutic outcomes of transplantation of amniotic fluid-derived stem cells in experimental ischemic stroke

artículo científico publicado en 2014

Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome

scientific article published on 01 September 2010

Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases.

artículo científico publicado en 2012

Wnt signaling behaves as a "master regulator" in the osteogenic and adipogenic commitment of human amniotic fluid mesenchymal stem cells

artículo científico publicado en 2013

p53 Is Active in Human Amniotic Fluid Stem Cells

scholarly article by Melissa Rodrigues et al published 2 October 2018 in Stem Cells and Development

Lista de obras de

16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer.

A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer

Amniotic Fluid Stem Cells: A Novel Source for Modeling of Human Genetic Diseases

Amniotic fluid as a rich source of mesenchymal stromal cells for transplantation therapy

Amniotic fluid stem cell models: A tool for filling the gaps in knowledge for human genetic diseases

Amniotic fluid stem cells: a promising therapeutic resource for cell-based regenerative therapy

Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring

BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 Gene

C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy

Calcitonin-induced effects on amniotic fluid-derived mesenchymal stem cells.

Cardiomyocytes Derived from Human Amniotic Fluids

Comparison between CaGene 5.1 and 6.0 for BRCA1/2 mutation prediction: a retrospective study of 150 BRCA1/2 genetic tests in 517 families with breast/ovarian cancer.

DNMT3B promoter polymorphisms and maternal risk of birth of a child with Down syndrome.

De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects.

Epigenetic Features of Human Perinatal Stem Cells Redefine Their Stemness Potential

Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime health

Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits

Functional interleukin-7/interleukin-7Ralpha, and SDF-1alpha/CXCR4 are expressed by human periodontal ligament derived mesenchymal stem cells

Genetic determinants of blood pressure responses to caffeine drinking

Genetic determinants of cognitive responses to caffeine drinking identified from a double-blind, randomized, controlled trial.

Genetic testing in couples undergoing assisted reproduction technique protocols.

Genetics of syndromic and nonsyndromic cleft lip and palate

Human second trimester amniotic fluid cells are able to create embryoid body-like structures in vitro and to show typical expression profiles of embryonic and primordial germ cells

Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay

Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene

Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols

Impact of lysosomal storage disorders on biology of mesenchymal stem cells: Evidences from in vitro silencing of glucocerebrosidase (GBA) and alpha-galactosidase A (GLA) enzymes.

Intravenous grafts of amniotic fluid-derived stem cells induce endogenous cell proliferation and attenuate behavioral deficits in ischemic stroke rats

Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol

MBL2 and FCN2 gene polymorphisms in a cohort of Italian children with rheumatic fever: A case-control study

MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting.

Male factor infertility and lack of openness about infertility as risk factors for depressive symptoms in males undergoing assisted reproductive technology treatment in Italy.

Molecular and phenotypic characterization of human amniotic fluid-derived cells: a morphological and proteomic approach

Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson

Reduced thromboxane biosynthesis in carriers of toll-like receptor 4 polymorphisms in vivo

Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs

Sequence-specific modification of a beta-thalassemia locus by small DNA fragments in human erythroid progenitor cells

TNF-α gene polymorphisms and juvenile idiopathic arthritis: Influence on disease outcome and therapeutic response

Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion

The Impact of Epigenetic Signatures on Amniotic Fluid Stem Cell Fate

The MTR 2756A>G polymorphism and maternal risk of birth of a child with Down syndrome: a case-control study and a meta-analysis.

The MTRR 66A>G polymorphism and maternal risk of birth of a child with Down syndrome in Caucasian women: a case–control study and a meta-analysis

Therapeutic outcomes of transplantation of amniotic fluid-derived stem cells in experimental ischemic stroke

Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome

Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases.

Wnt signaling behaves as a "master regulator" in the osteogenic and adipogenic commitment of human amniotic fluid mesenchymal stem cells

p53 Is Active in Human Amniotic Fluid Stem Cells