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GenomicsDifferential gene expression in NPHS2-Cre +/+ mouse glomeruli versus wild-type control
Differential gene expression in NPHS2-Cre +/+ mouse glomeruli versus wild-type control
PRJNA481767 | ENA
TranscriptomicsThe effect of cortex/medulla proportions on molecular diagnoses in kidney transplant biopsies: rejection and injury can be assessed in medulla
Histologic assessment of kidney transplant biopsies relies on cortex rather than medulla, but for microarray studies, the proportion cortex in a biopsy is typically unknown and could affect the molecular readings. The present study aimed to develop a molecular estimate of proportion cortex in biopsi...
ORGANISM(S): Homo sapiens 
2017-04-27 | E-GEOD-95611 | biostudies-arrayexpress
TranscriptomicsDifferential gene expression in NPHS2-Cre +/+ mouse glomeruli versus wild-type control
To investigate differential gene expression that might account for the differing glomerular phenotype of NPHS2-Cre +/+ mice when compared with wild-type control, including altered GBM thickness, loss of normal foot process morphology, and decrease in podocyte number, RNA sequencing analysis was perf...
ORGANISM(S): Mus musculus 
2019-02-11 | GSE117331 | GEO
UnknownNPHS2 variation in sporadic focal segmental glomerulosclerosis.
Not available
S-EPMC4096868 | biostudies-literature
UnknownNPHS2 mutations account for only 15% of nephrotic syndrome cases.
Not available
S-EPMC4589073 | biostudies-literature
UnknownNPHS2 Mutations: A Closer Look to Latin American Countries.
Not available
S-EPMC5529630 | biostudies-literature
UnknownAnalysis of NPHS2 Gene Mutations in Egyptian Children with Nephrotic Syndrome.
Not available
S-EPMC6953933 | biostudies-literature
UnknownNPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele.
Not available
S-EPMC151634 | biostudies-literature
UnknownLow prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
Not available
S-EPMC5495478 | biostudies-literature
UnknownA novel mutation in NPHS2 causing nephrotic syndrome in a Saudi Arabian family.
Not available
S-EPMC4421432 | biostudies-literature
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