Lista de obras - Federica Sangiuolo - Dominio Público Uruguay

108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands

artículo científico publicado en 2003

3'-UTR OLR1/LOX-1 gene polymorphism and endothelial dysfunction: molecular and vascular data in never-treated hypertensive patients

artículo científico publicado en 2012

A Perturbed MicroRNA Expression Pattern Characterizes Embryonic Neural Stem Cells Derived from a Severe Mouse Model of Spinal Muscular Atrophy (SMA).

artículo científico publicado en 2015

A new method for direct analysis of polymerase chain reaction-amplified human papillomavirus using DNA enzyme immunoassay

artículo científico publicado en 1994

A pilot beta-thalassaemia screening program in the Albanian population for a health planning program.

artículo científico publicado en 2009

A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis

article

An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene

scientific article published on 02 June 2020

Analysis of 14 cystic fibrosis mutations in five South European populations

article

Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies

artículo científico publicado en 2003

Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian population.

artículo científico publicado en 1995

Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery

artículo científico publicado en 2020

Application of Next Generation Sequencing for personalized medicine for sudden cardiac death

artículo científico publicado en 2015

Carrier frequency of CFTR variants in the non-Caucasian populations by genome aggregation database (gnomAD)-based analysis

scientific article published on 02 June 2020

Cellular genetic therapy.

artículo científico publicado en 2005

Cftr gene targeting in mouse embryonic stem cells mediated by Small Fragment Homologous Replacement (SFHR)

artículo científico publicado en 2008

Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes

article

Comparative analysis between saliva and buccal swabs as source of DNA: lesson from HLA-B*57:01 testing.

artículo científico publicado en 2015

Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?

artículo científico publicado en 2015

Delta F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish families.

artículo científico publicado en 1990

Diagnostic CFTR mutation analysis.

artículo científico publicado en 2008

Effects of Simulated Microgravity on Wild Type and Marfan hiPSCs-Derived Embryoid Bodies

scientific article published on 07 June 2021

Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study

article

Exclusion of the elastin gene in the pathogenesis of Costello syndrome

article

Expression analysis and protein localization of the human HPC-1/syntaxin 1A, a gene deleted in Williams syndrome.

artículo científico publicado en 1999

Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues

artículo científico publicado en 2004

FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation.

artículo científico publicado en 2015

Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms

scientific article published on 01 January 1991

Gene transfection efficiency of tracheal epithelial cells by DC-chol-DOPE/DNA complexes.

artículo científico publicado en 1999

Generation of Human Induced Pluripotent Stem Cells from Extraembryonic Tissues of Fetuses Affected by Monogenic Diseases.

artículo científico publicado en 2015

IPLEX Administration Improves Motor Neuron Survival and Ameliorates Motor Functions in a Severe Mouse Model of Spinal Muscular Atrophy ⬇️

artículo científico publicado el 25 de septiembre de 2012

In Vitro Restoration of Functional SMN Protein in Human Trophoblast Cells Affected by Spinal Muscular Atrophy by Small Fragment Homologous Replacement

scientific article published on 01 July 2005

In vitro correction of cystic fibrosis epithelial cell lines by small fragment homologous replacement (SFHR) technique.

artículo científico publicado en 2002

In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction

artículo científico publicado en 2005

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

artículo científico publicado en 2002

Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.

artículo científico publicado en 2001

MicroRNA genetic variations: association with type 2 diabetes

artículo científico publicado en 2013

Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy

artículo científico publicado en 2004

Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience

artículo científico publicado en 2019

Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome

artículo científico publicado en 2011

Polymorphic DNA haplotypes and ΔF508 deletion in 212 Italian CF families

article

Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy

artículo científico publicado en 2004

Recessive congenital myotonia resulting from maternal isodisomy of chromosome 7: a case report

artículo científico publicado en 2009

Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cells

artículo científico publicado en 2011

Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism.

artículo científico publicado en 2015

SARS-COV-2 and infectivity: Possible increase in infectivity associated to integrin motif expression

scientific article published on 04 April 2020

Simultaneous detection of ΔF508, G542X, N1303K, G551D, and 1717-1G→A cystic fibrosis alleles by a multiplex DNA enzyme immunoassay

artículo científico publicado en 1995

Small Fragment Homologous Replacement (SFHR): sequence-specific modification of genomic DNA in eukaryotic cells by small DNA fragments

artículo científico publicado en 2014

Small fragment homologous replacement: evaluation of factors influencing modification efficiency in an eukaryotic assay system

artículo científico publicado en 2012

Specific miRNA and Gene Deregulation Characterize the Increased Angiogenic Remodeling of Thoracic Aneurysmatic Aortopathy in Marfan Syndrome

scientific article published on 19 September 2020

Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L).

artículo científico publicado en 1998

TCF7L2 gene polymorphisms and type 2 diabetes: association with diabetic retinopathy and cardiovascular autonomic neuropathy

article

Three new mutations (P183T, V150L, 528insG) and eleven sequence polymorphisms in Italian patients with galactose-1-phosphate uridyltransferase (GALT) deficiency

article

Toward the pharmacogenomics of cystic fibrosis--an update.

artículo científico publicado en 2004

Towards the pharmacogenomics of cystic fibrosis.

artículo científico publicado en 2002

Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis

artículo científico publicado en 2014

Two Different Therapeutic Approaches for SARS-CoV-2 in hiPSCs-Derived Lung Organoids

artículo científico publicado en 2022

Lista de obras de Federica Sangiuolo

108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands

3'-UTR OLR1/LOX-1 gene polymorphism and endothelial dysfunction: molecular and vascular data in never-treated hypertensive patients

A Perturbed MicroRNA Expression Pattern Characterizes Embryonic Neural Stem Cells Derived from a Severe Mouse Model of Spinal Muscular Atrophy (SMA).

A new method for direct analysis of polymerase chain reaction-amplified human papillomavirus using DNA enzyme immunoassay

A pilot beta-thalassaemia screening program in the Albanian population for a health planning program.

A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis

An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene

Analysis of 14 cystic fibrosis mutations in five South European populations

Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies

Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian population.

Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery

Application of Next Generation Sequencing for personalized medicine for sudden cardiac death

Carrier frequency of CFTR variants in the non-Caucasian populations by genome aggregation database (gnomAD)-based analysis

Cellular genetic therapy.

Cftr gene targeting in mouse embryonic stem cells mediated by Small Fragment Homologous Replacement (SFHR)

Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes

Comparative analysis between saliva and buccal swabs as source of DNA: lesson from HLA-B*57:01 testing.

Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?

Delta F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish families.

Diagnostic CFTR mutation analysis.

Effects of Simulated Microgravity on Wild Type and Marfan hiPSCs-Derived Embryoid Bodies

Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study

Exclusion of the elastin gene in the pathogenesis of Costello syndrome

Expression analysis and protein localization of the human HPC-1/syntaxin 1A, a gene deleted in Williams syndrome.

Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues

FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation.

Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms

Gene transfection efficiency of tracheal epithelial cells by DC-chol-DOPE/DNA complexes.

Generation of Human Induced Pluripotent Stem Cells from Extraembryonic Tissues of Fetuses Affected by Monogenic Diseases.

IPLEX Administration Improves Motor Neuron Survival and Ameliorates Motor Functions in a Severe Mouse Model of Spinal Muscular Atrophy ⬇️

In Vitro Restoration of Functional SMN Protein in Human Trophoblast Cells Affected by Spinal Muscular Atrophy by Small Fragment Homologous Replacement

In vitro correction of cystic fibrosis epithelial cell lines by small fragment homologous replacement (SFHR) technique.

In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.

MicroRNA genetic variations: association with type 2 diabetes

Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy

Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience

Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome

Polymorphic DNA haplotypes and ΔF508 deletion in 212 Italian CF families

Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy

Recessive congenital myotonia resulting from maternal isodisomy of chromosome 7: a case report

Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cells

Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism.

SARS-COV-2 and infectivity: Possible increase in infectivity associated to integrin motif expression

Simultaneous detection of ΔF508, G542X, N1303K, G551D, and 1717-1G→A cystic fibrosis alleles by a multiplex DNA enzyme immunoassay

Small Fragment Homologous Replacement (SFHR): sequence-specific modification of genomic DNA in eukaryotic cells by small DNA fragments

Small fragment homologous replacement: evaluation of factors influencing modification efficiency in an eukaryotic assay system

Specific miRNA and Gene Deregulation Characterize the Increased Angiogenic Remodeling of Thoracic Aneurysmatic Aortopathy in Marfan Syndrome

Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L).

TCF7L2 gene polymorphisms and type 2 diabetes: association with diabetic retinopathy and cardiovascular autonomic neuropathy

Three new mutations (P183T, V150L, 528insG) and eleven sequence polymorphisms in Italian patients with galactose-1-phosphate uridyltransferase (GALT) deficiency

Toward the pharmacogenomics of cystic fibrosis--an update.

Towards the pharmacogenomics of cystic fibrosis.

Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis

Two Different Therapeutic Approaches for SARS-CoV-2 in hiPSCs-Derived Lung Organoids