Evidence map›Paper›PMID 36636694›Full record

ReviewAmerican journal of clinical and experimental urology2022

Modeling development of genitourinary birth defects to understand disruption due to changes in gene dosage.

Victor A Ruthig, Dolores J Lamb

Open access · greenAbstract readReview
In one paragraph

Review in American journal of clinical and experimental urology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% of its field
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
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

2 authors at 1 institution in 2 countries.

Victor A RuthigDepartment of Urology, Weill Cornell Medicine New York, NY, USA.
Dolores J LambDepartment of Urology, Weill Cornell Medicine New York, NY, USA.
Cornell University · US

Funding

Improving the Diagnosis of Congenital Genitourinary Defects.R01DK078121 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI LAMB, DOLORES JEAN · 2007 to 2021
$4.8M
Intravital point-scanning confocal microscopeS10RR027867 · NCRR · DUKE UNIVERSITY · PI CHILKOTI, ASHUTOSH · 2010 to 2010
$500k
DND1 Mediated Posttranscriptional Regulation in Murine Prospermatogonia During G1/G0 ArrestF32GM129956 · NIGMS · DUKE UNIVERSITY · PI RUTHIG, VICTOR A. · 2018 to 2020
$140k
NCRR NIH HHS S10 RR027867NIDDK NIH HHS R01 DK078121NIGMS NIH HHS F32 GM129956
6 · The paper itself

Abstract

Genitourinary development is a delicately orchestrated process that begins in the embryo. Once complete, the genitourinary system is a collection of functionally disparate organs spread throughout the abdominal and pelvic regions. These distinct organs are interconnected through an elaborate duct system which aggregates the organs' products to a common exit point. The complicated nature of the genitourinary system makes it highly susceptible to developmental disruptions that produce anomalies. In fact, genitourinary anomalies are among the most common class of human birth defects. Aside from congenital anomalies of the kidney and urinary tract (CAKUT), for males, these birth defects can also occur in the penis (hypospadias) and testis (cryptorchism), which impact male fertility and male mental health. As genetic technology has advanced, it has become clear that a subset of cases of genitourinary birth defects are due to gene variation causing dosage changes in critical regulatory genes. Here we first review the parallels between human and mouse genitourinary development. We then demonstrate how translational research leverages mouse models of human gene variation cases to advance mechanistic understanding of causation in genitourinary birth defects. We close with a view to the future highlighting upcoming technologies that will provide a deeper understanding of gene variation affecting regulation of genitourinary development, which should ultimately advance treatment options for patients.

Indexed as

copy number variant (CNV)cryptorchidismMicrodeletion/microduplicationspenile anomalies

Identifiers

PMID36636694
PMCPMC9831917
OpenAlexW4315928666

What Socratic 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 Socratic graph.