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ProteomicsNano-LC-MS/MS proteomics in amniotic fluid from CAKUT patients
The objective of the present work was to identify new renal proteins responsible for Congenital Anomalies of the Kidney and of the Urinary Tract (CAKUT pathophysiology). We conducted a comparative LC-MS/MS-based proteomics analysis of amniotic fluids (AF) collected from non-severe CAKUT (ns-CAKUT; ...
ORGANISM(S): Homo sapiens (Human) 
2023-09-26 | PXD022926 | Pride
Chronic kidney disease Cakut Proteomics Plastin-3 Amniotic fluid 
TranscriptomicsTranscriptome profile of ureter tissue originating from CAKUT patients and healthy kidney donors
Identification and analysis of differentially expressed genes and detection of miR activity from gene expression data in human CAKUT.
ORGANISM(S): Homo sapiens 
2017-11-27 | GSE83946 | GEO
UnknownMolecular causes of congenital anomalies of the kidney and urinary tract (CAKUT).
Not available
S-EPMC7904997 | biostudies-literature
UnknownIdentification and functional interpretation of miRNAs affected by rare CNVs in CAKUT.
Not available
S-EPMC9587983 | biostudies-literature
UnknownThe term CAKUT has outlived its usefulness: the case for the defense.
Not available
S-EPMC9489570 | biostudies-literature
UnknownOcular manifestations of congenital anomalies of the kidney and urinary tract (CAKUT).
Not available
S-EPMC10728251 | biostudies-literature
UnknownOverlap of vitamin A and vitamin D target genes with CAKUT-related processes.
Not available
S-EPMC9051587 | biostudies-literature
UnknownReverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
Not available
S-EPMC8876311 | biostudies-literature
UnknownPrenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT).
Not available
S-EPMC7272185 | biostudies-literature
UnknownCOL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.
Not available
S-EPMC6745245 | biostudies-literature
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