Lista de obras - Claudia Ricci - Dominio Público Uruguay

A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS.

artículo científico publicado en 2010

Antimicrobial activity of novel dendrimeric peptides obtained by phage display selection and rational modification

artículo científico publicado en 2005

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

artículo científico publicado en 2021

Biochemical filtering of a protein-protein docking simulation identifies the structure of a complex between a recombinant antibody fragment and alpha-bungarotoxin

artículo científico publicado en 2003

C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease

artículo científico publicado en 2016

Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene

artículo científico publicado en 2020

Corrigendum to “Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort” [GENE 568/2 (2015) 186–189]

article

D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings

artículo científico publicado en 2010

Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia

artículo científico publicado en 2014

G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype

artículo científico publicado en 2010

Genetic Variations Within KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation

article

Genotype-phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation

scientific article published on 07 June 2019

Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC) ⬇️

artículo científico publicado el 1 de julio de 2013

Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients

artículo científico publicado en 2016

Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients

artículo científico publicado en 2017

Lack of association of PON polymorphisms with sporadic ALS in an Italian population

artículo científico publicado en 2010

Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort

article

Macrophage Migration Inhibitory Factor in the Human Endometrium: Expression and Localization During the Menstrual Cycle and Early Pregnancy1

artículo científico publicado en 2001

MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis

Mitigation of UV-B Radiation Stress in Tobacco Pollen by Expression of the Tardigrade Damage Suppressor Protein (Dsup)

artículo científico publicado en 2024

No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population

article

Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells.

artículo científico publicado en 2000

Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family

artículo científico publicado en 2011

Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene

artículo científico publicado en 2010

Stable peptide inhibitors prevent binding of lethal and oedema factors to protective antigen and neutralize anthrax toxin in vivo

artículo científico publicado en 2006

Strategies for the construction and use of peptide and antibody libraries displayed on phages

artículo científico publicado en 2004

Variants in MCT10 protein do not affect FT3 levels in athyreotic patients

scientific article published on 06 July 2019

Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population

artículo científico publicado en 2007

Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene

article

miRNA Targets: From Prediction Tools to Experimental Validation

artículo científico publicado en 2020

Lista de obras de Claudia Ricci

A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS.

Antimicrobial activity of novel dendrimeric peptides obtained by phage display selection and rational modification

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

Biochemical filtering of a protein-protein docking simulation identifies the structure of a complex between a recombinant antibody fragment and alpha-bungarotoxin

C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease

Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene

Corrigendum to “Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort” [GENE 568/2 (2015) 186–189]

D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings

Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia

G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype

Genetic Variations Within KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation

Genotype-phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation

Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC) ⬇️

Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients

Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients

Lack of association of PON polymorphisms with sporadic ALS in an Italian population

Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort

Macrophage Migration Inhibitory Factor in the Human Endometrium: Expression and Localization During the Menstrual Cycle and Early Pregnancy1

MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis

Mitigation of UV-B Radiation Stress in Tobacco Pollen by Expression of the Tardigrade Damage Suppressor Protein (Dsup)

No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population

Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells.

Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family

Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene

Stable peptide inhibitors prevent binding of lethal and oedema factors to protective antigen and neutralize anthrax toxin in vivo

Strategies for the construction and use of peptide and antibody libraries displayed on phages

Variants in MCT10 protein do not affect FT3 levels in athyreotic patients

Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population

Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene

miRNA Targets: From Prediction Tools to Experimental Validation