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Lista de obras de Gian Marco Ghiggeri

"Cheek-to-cheek" urinary proteome profiling via combinatorial peptide ligand libraries: A novel, unexpected elution system.

artículo científico publicado en 2011

'Congenital solitary functioning kidneys: which ones warrant follow-up into adult life?'

artículo científico publicado en 2011

2D-electrophoresis and the urine proteome map: where do we stand?

scientific article published on 22 December 2009

2DE maps in the discovery of human autoimmune kidney diseases: the case of membranous glomerulonephritis

artículo científico publicado en 2015

A DNA element in the alpha1 type III collagen promoter mediates a stimulatory response by angiotensin II.

artículo científico

A Pilot Study of IL2 in Drug-Resistant Idiopathic Nephrotic Syndrome

artículo científico publicado en 2015

A mild form of rituximab-associated lung injury in two adolescents treated for nephrotic syndrome

artículo científico publicado en 2015

A modification of the 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB) method for the determination of the sulphhydryl content of human serum albumin

artículo científico publicado en 1983

A new biallelic DNA polymorphism of the human COL5A1 gene

article

A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis

artículo científico publicado en 2010

A prospective observational study of associated anomalies in Hirschsprung's disease

artículo científico publicado en 2013

A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13.

artículo científico publicado en 2009

AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis

scientific journal article

ANTI-ATP SYNTHASE β-CHAIN AUTOANTIBODIES

Activation of COL3A1 promoter activity by cyclosporine

artículo científico publicado en 1998

Activation of the intracellular glutathione system by oxydative stress during cardiopulmonary bypass and myocardial perfusion

artículo científico publicado en 1995

Active Focal Segmental Glomerulosclerosis Is Associated with Massive Oxidation of Plasma Albumin

artículo científico publicado en 2007

Adverse events linked with the use of chimeric and humanized anti-CD20 antibodies in children with idiopathic nephrotic syndrome.

artículo científico publicado en 2018

Albumin heterogeneity in low-abundance fluids. The case of urine and cerebro-spinal fluid

artículo científico

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics

article

Amoxicillin-associated interference in an HPLC–EC assay for urinary fractionated metanephrines: Potential pitfall in pheochromocytoma biochemical diagnosis

artículo científico publicado en 2014

An Update on Antibodies to Necleosome Components as Biomarkers of Sistemic Lupus Erythematosus and of Lupus Flares

artículo científico publicado en 2019

Analysis of albumin charge by direct immunofixation in ultrathin gels

artículo científico publicado en 1990

Analysis of the oxido-redox status of plasma proteins. Technology advances for clinical applications.

scientific article published on 03 December 2010

Angiotensin-converting enzyme (ACE) haplotypes and cyclosporine A (CsA) response: a model of the complex relationship between ACE quantitative trait locus and pathological phenotypes

artículo científico publicado en 2005

Annexin A1 and Autoimmunity: From Basic Science to Clinical Applications.

artículo científico publicado en 2018

Anti-CD20 Antibodies for Idiopathic Nephrotic Syndrome in Children

artículo científico publicado en 2015

Anti-alpha-enolase antibodies in membranous nephropathy: isotype matters

artículo científico publicado en 2016

Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis.

artículo científico publicado en 2003

Are the nail-patella syndrome and the autosomal Goltz-like syndrome the phenotypic expressions of different alleles at the COL5A1 locus?

artículo científico publicado en 1993

Association of the macrophage migration inhibitory factor -173*C allele with childhood nephrotic syndrome

artículo científico publicado en 2008

Atypical IgM on T cells predict relapse and steroid dependence in idiopathic nephrotic syndrome

artículo científico publicado en 2019

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

artículo científico publicado en 2019

Autoimmunity in membranous nephropathy targets aldose reductase and SOD2.

artículo científico publicado en 2010

Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus

scientific article published on 01 October 1998

Blue silver: a very sensitive colloidal Coomassie G-250 staining for proteome analysis

artículo científico publicado en 2004

Both the rituximab dose and maintenance immunosuppression in steroid-dependent/frequently-relapsing nephrotic syndrome have important effects on outcomes

artículo científico publicado en 2019

Broadening the spectrum of diseases related to podocin mutations

artículo científico publicado en 2003

CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS).

artículo científico publicado en 2009

CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders

artículo científico publicado en 2007

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement

artículo científico publicado en 2007

COVID-19 in Children with Nephrotic Syndrome on Anti-CD20 Chronic Immunosuppression

artículo científico publicado en 2020

CYCLOSPORINE ENHANCES THE SYNTHESIS OF SELECTED EXTRACELLULAR MATRIX PROTEINS BY RENAL CELLS “IN CULTURE”

article

Characterisation of the phenylhydrazone derivatives of “glycated albumin” purified from diabetic sera

artículo científico

Characterization of oxidation end product of plasma albumin 'in vivo'.

artículo científico publicado en 2006

Characterization of plasma factors that alter the permeability to albumin within isolated glomeruli.

artículo científico publicado en 2002

Circulating anti-actin and anti-ATP synthase antibodies identify a sub-set of patients with idiopathic nephrotic syndrome.

artículo científico publicado en 2005

Circulating antipodocyte antibodies in membranous nephropathy: new findings

artículo científico publicado en 2013

Circulating suPAR in two cohorts of primary FSGS.

artículo científico publicado en 2012

Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases

artículo científico publicado en 2006

Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: Insights from molecular screening

article

Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations

artículo científico publicado en 2009

Clinical trials in minimal change disease.

artículo científico publicado en 2017

Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GN.

artículo científico publicado en 2017

Coexistence of different circulating anti-podocyte antibodies in membranous nephropathy.

artículo científico publicado en 2012

Collapsing glomerulopathy associated with inherited mitochondrial injury

Combinatorial Peptide Ligand Library and two dimensional electrophoresis: new frontiers in the study of peritoneal dialysis effluent in pediatric patients

artículo científico publicado en 2015

Combinatorial ligand libraries as a two-dimensional method for proteome analysis.

artículo científico publicado en 2013

Combinatorial peptide ligand libraries for urine proteome analysis: investigation of different elution systems

artículo científico publicado en 2009

Constitutional Nephrin Deficiency in Conditionally Immortalized Human Podocytes Induced Epithelial-Mesenchymal Transition, Supported by β-Catenin/NF-kappa B Activation: A Consequence of Cell Junction Impairment?

artículo científico publicado en 2013

Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney.

artículo científico publicado en 2015

Copy-number disorders are a common cause of congenital kidney malformations

artículo científico publicado en 2012

Cyclosporin and organ specific toxicity: clinical aspects, pharmacogenetics and perspectives

artículo científico publicado en 2008

Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study

artículo científico publicado en 2004

DQ molecules are the principal stimulators of de novo donor-specific antibodies in nonsensitized pediatric recipients receiving a first kidney transplant.

artículo científico publicado en 2014

De Novo Donor-Specific HLA Antibodies Developing Early or Late after Transplant Are Associated with the Same Risk of Graft Damage and Loss in Nonsensitized Kidney Recipients.

artículo científico publicado en 2017

Defective intracellular trafficking of uromodulin mutant isoforms

artículo científico publicado en 2006

Depletion of clusterin in renal diseases causing nephrotic syndrome

Determination of a glycosyl subunit of human serum albumin by concanavalin A-sepharose

artículo científico publicado en 1983

Determination of the oxido-redox status of plasma albumin in hemodialysis patients.

artículo científico publicado en 2008

Diagnostic specificity of autoantibodies to M-type phospholipase A2 receptor (PLA2R) in differentiating idiopathic membranous nephropathy (IMN) from secondary forms and other glomerular diseases

artículo científico publicado en 2017

Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens.

artículo científico publicado en 2011

Discordant evolution of nephrotic syndrome in mono- and dizygotic twins

scientific article published on 29 December 2005

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

artículo científico publicado en 2014

Endocellular polyamine availability modulates epithelial-to-mesenchymal transition and unfolded protein response in MDCK cells.

artículo científico publicado en 2010

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene

artículo científico publicado en 2001

Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease.

artículo científico publicado en 2000

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

article

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

artículo científico publicado en 2017

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

artículo científico publicado en 2017

Exosomes from human mesenchymal stem cells conduct aerobic metabolism in term and preterm newborn infants

artículo científico publicado en 2015

Expanding CEP290 mutational spectrum in ciliopathies

artículo científico publicado en 2009

Expression of Nuclear Transcription Factor PAX2 in Renal Biopsies of Juvenile Nephronophthisis

artículo científico publicado en 2002

Expression of collagen by renal fibroblasts treated with FK 506 in vitro.

artículo científico publicado en 1998

Extracellular matrix formation by epithelial cells from human polycystic kidney cysts in culture

artículo científico publicado en 1992

FCGR2A single nucleotide polymorphism confers susceptibility to childhood-onset idiopathic nephrotic syndrome

artículo científico publicado en 2017

Failure of regulation results in an amplified oxidation burst by neutrophils in children with primary nephrotic syndrome

artículo científico publicado en 2010

Failure to remove de novo donor-specific HLA antibodies is influenced by antibody properties and identifies kidney recipients with late antibody-mediated rejection destined to graft loss - a retrospective study

scientific article published on 27 August 2018

Familial forms of nephrotic syndrome.

artículo científico publicado en 2010

Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds

artículo científico publicado en 2005

Five cases of severe vesico-ureteric reflux in a family with an X-linked compatible trait

artículo científico publicado en 2009

Fractionation of human serum albumin isoforms with chromatofocusing

artículo científico publicado en 1986

From hundreds to thousands: Widening the normal human Urinome (1).

artículo científico publicado en 2014

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

artículo científico publicado en 2017

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

artículo científico publicado en 2007

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

Genetic basis of human congenital anomalies of the kidney and urinary tract

artículo científico publicado en 2018

Genetic risk factors in typical haemolytic uraemic syndrome

artículo científico publicado en 2008

Genetic screening in adolescents with steroid-resistant nephrotic syndrome

artículo científico publicado en 2013

Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)

article

Genome-wide association study identifies susceptibility loci for IgA nephropathy

artículo científico publicado en 2011

Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens.

artículo científico publicado en 2014

Glomerular albumin permeability as anin vitromodel for characterizing the mechanism of focal glomerulosclerosis and predicting post-transplant recurrence

Glomerular autoimmune multicomponents of human lupus nephritis in vivo: α-enolase and annexin AI.

artículo científico publicado en 2014

Glomerular clusterin is associated with PKC-α/β regulation and good outcome of membranous glomerulonephritis in humans

artículo científico publicado en 2006

Glomerulocystic kidney disease in a family

artículo científico publicado en 2002

Glomerulocystic kidney disease in hypomelanosis of Ito

Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria

article

High-Content Screening Identifies Vanilloids as a Novel Class of Inhibitors of NET Formation

scientific article published on 30 April 2019

High-resolution 2-DE for resolving proteins, protein adducts and complexes in plasma

artículo científico publicado en 2008

Highly selective one-step chromatography of serum and urinary albumin on immobilized Cibacron Blue F3GA. Studies on normal and glycosyl albumin

artículo científico publicado en 1985

Hirschsprung disease and congenital anomalies of the kidney and urinary tract (CAKUT): a novel syndromic association.

artículo científico publicado en 2009

Human urinary exosome proteome unveils its aerobic respiratory ability

artículo científico

Hydrophobic interaction of alcian blue with soluble and erythrocyte membrane proteins

artículo científico publicado en 1988

Hypertension and Renal Selectivity Properties in Diabetic Microalbuminuria

scientific article published on 01 January 1990

Hyponatremic-hypertensive syndrome with extensive and reversible renal defects

artículo científico publicado en 2004

Identification of a new locus for medullary cystic disease, on chromosome 16p12.

artículo científico publicado en 1999

IgA Nephropathy: The Presence of Familial Disease Does Not Confer an Increased Risk for Progression

artículo científico publicado en 2006

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.

artículo científico publicado en 2000

Images in vascular medicine. A challenging case of renovascular hypertension

artículo científico publicado en 2013

Immature Renal Structures Associated With a Novel UMOD Sequence Variant

Immunity to Polyomavirus BK Infection: Immune Monitoring to Regulate the Balance between Risk of BKV Nephropathy and Induction of Alloimmunity

artículo científico publicado en 2013

Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders

artículo científico publicado en 2002

Immunology of membranous nephropathy: from animal models to humans.

artículo científico

In vivo characterization of renal auto-antigens involved in human auto-immune diseases: the case of membranous glomerulonephritis.

scientific article published on 17 January 2011

Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin

artículo científico publicado en 2004

Inhibition of renal permeability towards albumin: a new function of apolipoproteins with possible pathogenetic relevance in focal glomerulosclerosis

artículo científico publicado en 2001

Interaction between cationic dyes and erythrocyte membranes in minimal change nephropathy: an electrophoretic approach

artículo científico publicado en 1991

Intraureteral Injection of NASHA/Dx Gel Under Direct Ureteroscopic Visualization for the Treatment of Primary High-Grade Vesicoureteral Reflux

artículo científico publicado en 2012

Isoelectric focusing in low-denaturing media: Visualization in renal disease of variation of the isoelectric point of albumin not related to a remarkable conformational variation

artículo científico publicado en 1986

Jean Jaures, la France, l'Allemagne et la Deuxieme Internationale a la veille de la Premiere Guerre mondiale

article

LPS nephropathy in mice is ameliorated by IL-2 independently of regulatory T cells activity

artículo científico publicado en 2014

Lack of cardiac anomalies in children with NPHS2 mutations

artículo científico publicado en 2007

Late onset of pANCA renal and pulmonary vasculitis in a girl affected by undifferentiated connective tissue disease

artículo científico publicado en 2010

Local TNF causes NFATc1-dependent cholesterol-mediated podocyte injury

artículo científico publicado en 2016

Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13.

artículo científico publicado en 2000

Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33

artículo científico publicado en 2007

Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations

artículo científico publicado en 2009

Low-dose ofatumumab for multidrug-resistant nephrotic syndrome in children: a randomized placebo-controlled trial

artículo científico publicado en 2020

Low-dose ofatumumab for rituximab-resistant nephrotic syndrome.

artículo científico publicado en 2015

Lupus nephritis in children and adolescents: results of the Italian Collaborative Study

artículo científico publicado en 2013

Lysyl Oxidase Activates the Transcription Activity of Human Collagene III Promoter

artículo científico publicado en 2000

MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness

artículo científico publicado en 2003

Magnetic resonance urography and laparoscopy in paediatric urology: a case series

artículo científico publicado en 2013

Mapping of the human COL5A1 gene to chromosome 9q34.3

article

Micro-injection of recombinant lysyl oxidase blocks oncogenic p21-Ha-Ras and progesterone effects on Xenopus laevis oocyte maturation

artículo científico publicado en 1997

Microvesicles as promising biological tools for diagnosis and therapy

artículo científico publicado en 2018

Multi-Autoantibody Signature and Clinical Outcome in Membranous Nephropathy

artículo científico publicado en 2020

Multi-antibody composition in lupus nephritis: isotype and antigen specificity make the difference

artículo científico publicado en 2015

Multiple mechanisms for doxorubicin cytotoxicity on glomerular epithelial cells ‘in vitro’

scientific article published on 01 September 1992

Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype

scientific journal article

Mutational Spectrum of CYP24A1 Gene in a Cohort of Italian Patients with Idiopathic Infantile Hypercalcemia.

artículo científico publicado en 2016

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium

artículo científico publicado en 2000

Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract

artículo científico publicado en 2010

N-(4-hydroxyphenyl) retinamide inhibits cystogenesis by polycystic epithelial cell lines in vitro

artículo científico publicado en 1999

Negative Staining of Proteins in Polyacrylamide Gels with Methyl Trichloroacetate

artículo científico publicado en 1996

Nephrectomy for multicystic dysplastic kidney and renal hypodysplasia in children: where do we stand?

artículo científico publicado en 2010

Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the association

artículo científico publicado en 2006

Nephrotic urine prevents increased rat glomerular albumin permeability induced by serum from the same patient with idiopathic nephrotic syndrome.

artículo científico publicado en 2003

Neutrophil Extracellular Traps protein composition is specific for patients with Lupus nephritis and includes methyl-oxidized αenolase (methionine sulfoxide 93).

artículo científico publicado en 2019

Neutrophil extracellular traps (NET) induced by different stimuli: A comparative proteomic analysis

artículo científico publicado en 2019

New insights into membranous glomerulonephritis: from bench to bedside

scientific article published on 01 August 2011

New insights into the pathogenesis and the therapy of recurrent focal glomerulosclerosis.

artículo científico publicado en 2005

New iodo-acetamido cyanines for labeling cysteine thiol residues. A strategy for evaluating plasma proteins and their oxido-redox status

artículo científico publicado en 2009

Normal levels of urinary brush border antigens and other tubular markers in children

artículo científico publicado en 1993

Novel ELISA for thrombospondin type 1 domain-containing 7A autoantibodies in membranous nephropathy

scientific article published on 01 March 2019

Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy

article

Ofatumumab in two pediatric nephrotic syndrome patients allergic to rituximab.

artículo científico publicado en 2016

Ofatumumab-associated acute pneumonitis: Not new but still the first case

artículo científico publicado en 2016

Ofatumumab-associated acute respiratory manifestations: clinical characteristics and treatment

artículo científico publicado en 2016

Oxidative stress and galactose-deficient IgA1 as markers of progression in IgA nephropathy

artículo científico publicado en 2011

Oxidized albumin. The long way of a protein of uncertain function

artículo científico publicado en 2013

PRE-TRANSPLANT PERMEABILITY ACTIVITY TO ALBUMIN IS ASSOCIATED WITH GRAFT LOSS IN CHILDREN WITH FOCAL GLOMERULAR SCLEROSIS (FGS)

Permeability plasma factors in nephrotic syndrome: more than one factor, more than one inhibitor

scientific article published on 01 May 2001

Peroxidative damage of the erythrocyte membrane in children with nephrotic syndrome

artículo científico publicado en 1989

Phenotypic and genetic heterogeneity in Dent's disease—the results of an Italian collaborative study

article

Phenotypic expansion of DGKE-associated diseases

artículo científico publicado en 2014

Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood

Podocin-related mechanisms in posttransplant [corrected] recurrence of focal segmental glomerulosclerosis [corrected]

artículo científico publicado en 2006

Post-translational modified proteins are biomarkers of autoimmune-processes: NETosis and the inflammatory-autoimmunity connection

artículo científico publicado en 2016

Post-transplant proteinuria associated with everolimus: Definition of main features with proteomics

artículo científico publicado en 2008

Posttransplant Recurrence of Proteinuria in a Case of Focal Segmental Glomerulosclerosis Associated with WT1 Mutation

scientific article published on 19 June 2006

Posttransplant Soluble B-Cell Activating Factor Kinetics in Pediatric Recipients of First Kidney Allograft

artículo científico publicado en 2015

Posttransplant de novo donor-specific hla antibodies identify pediatric kidney recipients at risk for late antibody-mediated rejection.

artículo científico publicado en 2012

Posttransplant proteinuria associated with everolimus.

artículo científico publicado en 2009

Prediction and treatment of recurrent focal segmental glomerulosclerosis after renal transplantation in children

scientific article published on 01 December 1999

Preparative High Performance Chromatography of a Major Browning Compound Derived from Lysine and Glucose

scientific article published on 01 January 1989

Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study

artículo científico publicado en 2006

Progression of Chronic Adriamycin Nephropathy in Leukopenic Rats

artículo científico publicado en 1993

Proteins and protein fragments in nephrotic syndrome: Clusters, specificity and mechanisms

artículo científico publicado en 2008

Protein–protein interaction heterogeneity of plasma apolipoprotein A1 in nephrotic syndrome

artículo científico publicado en 2011

Proteomic Analysis of Urinary Extracellular Vesicles Reveals a Role for the Complement System in Medullary Sponge Kidney Disease ⬇️

artículo científico

Proteomic Analysis of Urinary Microvesicles and Exosomes in Medullary Sponge Kidney Disease and Autosomal Dominant Polycystic Kidney Disease

scientific article published on 24 April 2019

Proteomics of plasma and urine in primary nephrotic syndrome in children

artículo científico publicado en 2008

Protracted high-dose interferon gamma therapy for chronic experimental nephropathy

artículo científico publicado en 1994

Protracted remission of proteinuria after combined therapy with plasmapheresis and anti-CD20 antibodies/cyclophosphamide in a child with oligoclonal IgM and glomerulosclerosis

artículo científico publicado en 2007

Publisher Correction: Biological surface properties in extracellular vesicles and their effect on cargo proteins

scientific article published on 05 December 2019

Purification and partial characterization of a new 85 KDa amyloidosis-related protein in chronic hemodialysis

artículo científico publicado en 1991

Purification of Proteinase-Free Collagenase from Commercial Batches of the Enzyme

artículo científico publicado en 1990

Purification of alpha-1-antitrypsin monomer by preparative electrophoresis

artículo científico publicado en 1994

Purification of intact concanavalin A in tetramers by isoelectric focusing

artículo científico publicado en 1987

Puromycin aminonucleoside metabolism by glomeruli and glomerular epithelial cells in vitro

artículo científico publicado en 1991

Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.

artículo científico publicado en 2006

Rat model of perchloroethylene-induced renal dysfunctions

article

Reaction of 2-amino-2-deoxy-D-glucose and lysine: isolation and characterization of 2,5-bis(tetrahydroxybutyl)pyrazine.

artículo científico publicado en 1988

Reaction of human serum albumin with aldoses

Reaction of lysine with aldoses

Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin

artículo científico publicado en 2003

Recurrent Nephrotic Syndrome in Homozygous Truncating NPHS2 Mutation Is Not Due to Anti-Podocin Antibodies

artículo científico publicado en 2006

Recurrent autosomal-dominant focal segmental glomerulosclerosis

artículo científico publicado en 2006

Recurrent focal glomerulosclerosis in the era of genetics of podocyte proteins: theory and therapy

artículo científico publicado en 2004

Recurrent lymphomatoid papulosis associated with nephrotic syndrome. An occurrence of uncertain origin

artículo científico publicado en 2007

Regarding Maas's editorial letter on serum suPAR levels

artículo científico publicado en 2012

Regulation of innate immunity by the nucleotide pathway in children with idiopathic nephrotic syndrome

artículo científico publicado en 2011

Regulatory T cells and minimal change nephropathy: in the midst of a complex network

artículo científico

Renal denervation for severe hypertension in a small child with Turner syndrome: miniaturisation of the procedure and results

artículo científico publicado en 2015

Renal fibrosis and proteomics: current knowledge and still key open questions for proteomic investigation

artículo científico publicado en 2011

Renal outcome in patients with congenital anomalies of the kidney and urinary tract.

artículo científico publicado en 2009

Renal-retinal syndromes: association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus

artículo científico publicado en 1998

Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndrome.

artículo científico publicado en 2006

Resolution of fibronectin and other uncharacterized proteins by two-dimensional polyacrylamide electrophoresis with thiourea

artículo científico publicado en 1998

Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial

artículo científico publicado en 2015

Rituximab in children with resistant idiopathic nephrotic syndrome

artículo científico publicado en 2012

Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome

scientific article published on 05 June 2013

SIX2 and BMP4 mutations associate with anomalous kidney development

artículo científico publicado en 2008

Selective enhancement by cyclosporin A of collagen expression by mesangial cells 'in culture'.

artículo científico publicado en 1994

Separation of the 9-anthryldiazomethane derivatives of fatty acids by high-performance liquid chromatography on a Fatty Acid Analysis Column®

Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome

artículo científico publicado en 2002

Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial

artículo científico publicado en 2011

Silver stain of proteins in ultra-thin gels containing carrier ampholytes — detection of glycosyl albumin with anionic and cationic charge in serums of diabetic patients

scientific article published on 01 May 1984

Soft immobilized pH gradient gels in proteome analysis: A follow-up

article

Spectrophotometric determination of advanced products of non-enzymatic glycosylation of lysine by means of their reaction with diazonium salts

Spectrophotometric determination of browning products of glycation of protein amino groups based on their reactivity with nitro blue tetrazolium salts

artículo científico publicado en 1988

Stable incorporation of α-smooth muscle actin into stress fibers is dependent on specific tropomyosin isoforms

artículo científico publicado en 2015

Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy

article

TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.

artículo científico publicado en 2011

Teaching molecular genetics: chapter 4-positional cloning of genetic disorders

artículo científico publicado en 2007

The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemia

artículo científico publicado en 2014

The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait.

artículo científico publicado en 2005

The Latest Advancements in Proteomic Two-dimensional Gel Electrophoresis Analysis Applied to Biological Samples

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Urinary secretion and extracellular aggregation of mutant uromodulin isoforms.

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