Cargando…

Markers of disease and steroid responsiveness in paediatric idiopathic nephrotic syndrome: Whole-transcriptome sequencing of peripheral blood mononuclear cells

OBJECTIVE: To identify markers of disease and steroid responsiveness in paediatric idiopathic nephrotic syndrome. METHODS: Whole-transcriptome sequencing was performed of peripheral blood mononuclear cells (PBMCs) from patients with NS. Differentially expressed genes (DEGs) were identified in patien...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kang, Hee Gyung, Seo, Heewon, Lim, Jae Hyun, Kim, Jong Il, Han, Kyoung Hee, Park, Hye Won, Koo, Ja Wook, Kim, Kee Hyuck, Kim, Ju Han, Cheong, Hae Il, Ha, Il-Soo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2017
Materias:	Research Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536413/ https://www.ncbi.nlm.nih.gov/pubmed/28639503 http://dx.doi.org/10.1177/0300060516652762

Ejemplares similares

Long-term repeated rituximab treatment for childhood steroid-dependent nephrotic syndrome
por: Kim, Ji Hyun, et al.
Publicado: (2017)

Nephrotic syndrome: what's new, what's hot?
por: Kang, Hee Gyung, et al.
Publicado: (2015)

Genetic tests in children with steroid-resistant nephrotic syndrome
por: Cheong, Hae Il
Publicado: (2020)

Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis
por: Park, Eujin, et al.
Publicado: (2020)

Acute kidney injury in childhood-onset nephrotic syndrome: Incidence and risk factors in hospitalized patients
por: Kim, Mi Young, et al.
Publicado: (2018)

Correction: Park et al. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis. J. Clin. Med. 2020, 9, 2013
por: Park, Eujin, et al.
Publicado: (2022)

A nonsense PAX6 mutation in a family with congenital aniridia
por: Han, Kyoung Hee, et al.
Publicado: (2016)

Treatment of steroid-resistant pediatric nephrotic syndrome
por: Kang, Hee Gyung
Publicado: (2011)

Efficacy and safety of rituximab in childhood-onset, difficult-to-treat nephrotic syndrome: A multicenter open-label trial in Korea
por: Ahn, Yo Han, et al.
Publicado: (2018)

Development of Korean Rare Disease Knowledge Base
por: Seo, Heewon, et al.
Publicado: (2012)

Bilateral iliac and popliteal arterial thrombosis in a child with focal segmental glomerulosclerosis
por: Han, Kyoung Hee, et al.
Publicado: (2016)

Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndrome
por: Kang, Hee Gyung, et al.
Publicado: (2017)

Intravenous fluid prescription practices among pediatric residents in Korea
por: Lee, Jiwon M., et al.
Publicado: (2013)

Initial steroid regimen in idiopathic nephrotic syndrome can be shortened based on duration to first remission
por: Baek, Hee Sun, et al.
Publicado: (2015)

Genotype and Phenotype Analyses in Pediatric Patients with HNF1B Mutations
por: Lim, Seon Hee, et al.
Publicado: (2020)

Two Korean Infants with Genetically Confirmed Congenital Nephrotic Syndrome of Finnish Type
por: Lee, Beom Hee, et al.
Publicado: (2009)

Mechanism of Chronic Kidney Disease Progression and Novel Biomarkers: A Metabolomic Analysis of Experimental Glomerulonephritis
por: Han, Kyoung Hee, et al.
Publicado: (2020)

Outcomes of chronic dialysis in Korean children with respect to survival rates and causes of death
por: Chang, Hye Jin, et al.
Publicado: (2014)

Case report: Genetic defects in laminin α5 cause infantile steroid-resistant nephrotic syndrome
por: Sunwoo, Yoon, et al.
Publicado: (2023)

Recurrence and Treatment after Renal Transplantation in Children with FSGS
por: Kang, Hee Gyung, et al.
Publicado: (2016)

A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene
por: Lee, Se Eun, et al.
Publicado: (2011)

Renal Syndromic Hearing Loss Is Common in Childhood-onset Chronic Kidney Disease
por: Kim, Ji Hyun, et al.
Publicado: (2020)

Pathogenesis of minimal change nephrotic syndrome: an immunological concept
por: Kim, Seong Heon, et al.
Publicado: (2016)

Current understandings in treating children with steroid-resistant nephrotic syndrome
por: Lee, Jiwon M., et al.
Publicado: (2020)

Renal transplantation in a patient with Bartter syndrome and glomerulosclerosis
por: Lee, Se Eun, et al.
Publicado: (2011)

Acute kidney injury associated with Yersinia pseudotuberculosis infection: Forgotten but not gone
por: Kim, Ye Kyung, et al.
Publicado: (2019)

A familial case of Blau syndrome caused by a novel NOD2 genetic mutation
por: Kim, Woojoong, et al.
Publicado: (2016)

Association between Serum Matrix Metalloproteinase- (MMP-) 3 Levels and Systemic Lupus Erythematosus: A Meta-analysis
por: Lee, Jiwon M., et al.
Publicado: (2019)

Corrigendum to “Association between Serum Matrix Metalloproteinase- (MMP-) 3 Levels and Systemic Lupus Erythematosus: A Meta-Analysis”
por: Lee, Jiwon M., et al.
Publicado: (2020)

A case of Bartter syndrome type I with atypical presentations
por: Lee, Eun Hye, et al.
Publicado: (2010)

Reninoma: a rare cause of curable hypertension
por: Kim, Ji Hye, et al.
Publicado: (2019)

Clinicopathologic Characteristics of IgA Nephropathy with Steroid-responsive Nephrotic Syndrome
por: Kim, Sun Moon, et al.
Publicado: (2009)

Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation
por: Kim, Sejin, et al.
Publicado: (2017)

Left-ventricular diastolic dysfunction in Korean children with chronic kidney disease: data from the KNOW-Ped CKD study
por: Kim, Jeong Yeon, et al.
Publicado: (2020)

Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract
por: Ahn, Yo Han, et al.
Publicado: (2020)

Treatment of Steroid and Cyclosporine-Resistant Idiopathic Nephrotic Syndrome in Children
por: Nikibakhsh, A. A., et al.
Publicado: (2011)

An Estimation of Steroid Responsiveness of Idiopathic Nephrotic Syndrome in Iranian Children
por: Madani, Abbas, et al.
Publicado: (2010)

Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations
por: Kim, Hunmin, et al.
Publicado: (2011)

Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria
por: Kim, Ji Hyun, et al.
Publicado: (2017)

Disseminated adenovirus infection in a 10-year-old renal allograft recipient
por: Lee, Bora, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_4in5jku0ejhg4vcg57mlnsm46u