Evidence map›Paper›PMID 39359948›Full record

ArticleMolecular syndromology2024

Determination of the Frequency of BCL-2 Polymorphisms (c.-717C>A and c.*2364G>A) and LIF Polymorphism (c.*1414T>G) in Patients with Congenital Anomalies of the Kidney and Urinary Tract.

Tugce Oztepe, Feride Iffet Sahin, Aysun Caltik Yilmaz, Esra Baskin, Mehmet Haberal, Yunus Kasim Terzi

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular syndromology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Tugce OztepeDepartment of Medical Genetics, Baskent University, Ankara, Turkey.
Feride Iffet SahinDepartment of Medical Genetics, Baskent University, Ankara, Turkey.
Aysun Caltik YilmazDepartment of Pediatric Nephrology, Baskent University, Ankara, Turkey.
Esra BaskinDepartment of Pediatric Nephrology, Baskent University, Ankara, Turkey.
Mehmet HaberalDivision of Transplantation, Department of Surgery, Baskent University, Ankara, Turkey.
Yunus Kasim TerziDepartment of Medical Genetics, Baskent University, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Congenital anomalies of the kidney and urinary tract (CAKUT) are characterized by several malformations. Its prevalence is 0.3-0.6% in live births. The B-cell lymphoma ( Methods: Hundred and twenty-nine CAKUT patients and 105 controls were enrolled in this study. We used polymerase chain reaction-restriction fragment length polymorphism for rs2279115 and rs929271 and SNaPshot for rs4987856. The χ Results: The allele frequencies for the rs2279115 and rs4987856 polymorphisms of Conclusion: This study, which is the first time in the literature, showed that changes in

Indexed as

BCL-2Congenital anomalies of the kidney and urinary tractLIFrs2279115rs4987856rs929271

Identifiers

PMID39359948
PMCPMC11444711

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.