ArticleCurrent genomics2016
Genetic Basis of Ureterocele.
Article in Current genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
10 citing papers in PubMed, 26 citations in OpenAlex.
- Summary of final data from the 9-valent human papillomavirus vaccine pregnancy registry (2014-2021).Human vaccines & immunotherapeutics · 2025Article
- Bilateral complete duplex system with non-functioning upper moieties and gross hydronephrosis with bilateral intravesical ureteroceles.Annals of medicine and surgery (2012) · 2025Article
- Pathophysiology of Congenital Anomalies of the Kidney and Urinary Tract: A Comprehensive Review.Cells · 2024Review
- Ureterocele mimicking uterine polyp in a young woman presenting with a vulvar mass: A case report.Urology case reports · 2022Article
- Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformations.Kidney international · 2022Review
- Ureterocele as a cause of chronic intractable abdominal pain.BMJ case reports · 2021Article
- Review
- An adult ureterocele complicated by a large stone: A case report.International journal of surgery case reports · 2018Article
- Transurethral incision of ureteroceles in paediatric age group.Turkish journal of urology · 2017Article
- The duplicated collecting system of the urinary tract: embryology, imaging appearances and clinical considerations.Pediatric radiology · 2017Review
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Congenital anomalies of the kidney and urinary tract (CAKUT) form a group of heterogeneous disorders that affect the kidneys, ureters and bladder, with frequent asynchronous presentations and multiple CAKUT associations in the same individual. Urinary tract formation is a complex process, dependent of the interaction of multiple genes and their sub-product. The same genic alterations can lead to different molecular expressions and different morphological anomalies. The ureterocele is a cystic dilation of the distal intramural ureter, resulting in obstruction of urine flow, dilation of the ureter and renal pelvis and loss of renal function. Two key steps in the urinary tract ontogenesis may be related to ureterocele development: formation and migration of the ureteric bud and its incorporation in the bladder. This review aims to describe the morphological, cellular and biochemical steps, as well as the genes involved in the occurrence of this anomaly.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.