Evidence map›Paper›PMID 42465522›Full record

ArticlebioRxiv : the preprint server for biology2026

BxbI-mediated insertion of a 77kb human RET sensitive haplotype into the mouse genome to generate a humanized model of Hirschsprung disease.

Ryan D Fine, Benjamin E Low, Jarod Rollins, Jon M Laurent, Michael V Wiles, Aamir Zuberi, Jef D Boeke, Aravinda Chakravarti

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

8 authors.

Ryan D FineCenter for Human Genetics and Genomics, NYU Grossman School of Medicine, New York, NY.ORCID 0000-0002-3165-9110
Benjamin E LowTechnology Evaluation and Development, The Jackson Laboratory, Bar Harbor, ME.
Jarod RollinsTechnology Evaluation and Development, The Jackson Laboratory, Bar Harbor, ME.
Jon M LaurentInstitute for Systems Genetics and Department of Biochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY.
Michael V WilesTechnology Evaluation and Development, The Jackson Laboratory, Bar Harbor, ME.
Aamir ZuberiTechnology Evaluation and Development, The Jackson Laboratory, Bar Harbor, ME.
Jef D BoekeInstitute for Systems Genetics and Department of Biochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY.
Aravinda ChakravartiCenter for Human Genetics and Genomics, NYU Grossman School of Medicine, New York, NY.

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
Supplement for Center for Synthetic Regulatory Genomics: Building CACNA1C alleles associated with Neuropsychiatric DisordersRM1HG009491 · NHGRI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Jef D BOEKE · 2018 to 2026
$20.9M
Genetic Analysis of Hirschsprung Disease - RenewalR01HD028088 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHAKRAVARTI, ARAVINDA · 1991 to 2024
$6.2M
Genetic Analysis of Hirschsprung DiseaseR37HD028088 · NICHD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CHAKRAVARTI, ARAVINDA · 2010 to 2019
$6.2M
Site-specific Integration of Large (10-100 kb) DNA Constructs into the Mouse Genome and Human Induced Pluripotent Stem Cells Using the Cas9-Bxb1 Integrase ToolboxR01CA265978 · NCI · JACKSON LABORATORY · PI Vishnu Hosur · 2022 to 2026
$3.2M
NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA265978NHGRI NIH HHS RM1 HG009491NICHD NIH HHS R01 HD028088NICHD NIH HHS R37 HD028088
6 · The paper itself

Abstract

Hirschsprung disease (HSCR) is a complex developmental disorder of the enteric nervous system, primarily driven by regulatory variants within enhancer elements of the

Indexed as

Humanized geneMouseRETSyntheticYeast

Identifiers

PMID42465522
PMCPMC13371033

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.