Evidence map›Paper›PMID 31541646›Full record

ArticleThe American journal of pathology2019

Spatiotemporal Gradient of Cortical Neuron Death Contributes to Microcephaly in Knock-In Mouse Model of Ligase 4 Syndrome.

Melody P Lun, Morgan L Shannon, Sevgi Keles, Ismail Reisli, Nicole Luche, Douglas Ryan, Kelly Capuder, Luigi D Notarangelo, Maria K Lehtinen

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 91% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. DNA damage and repair: underlying mechanisms leading to microcephaly.Frontiers in cell and developmental biology · 2023
    Review
  3. Article
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

9 authors at 3 institutions in 2 countries.

Melody P LunDepartment of Pathology, Boston Children's Hospital, Boston, Massachusetts; Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, Massachusetts.
Morgan L ShannonDepartment of Pathology, Boston Children's Hospital, Boston, Massachusetts.
Sevgi KelesDepartment of Pediatric Allergy and Immunology, Meram Medical Faculty, Necmettin Erbakan University, Konya, Turkey.
Ismail ReisliDepartment of Pediatric Allergy and Immunology, Meram Medical Faculty, Necmettin Erbakan University, Konya, Turkey.
Nicole LucheDivision of Immunology, Boston Children's Hospital, Boston, Massachusetts.
Douglas RyanDivision of Immunology, Boston Children's Hospital, Boston, Massachusetts.
Kelly CapuderDivision of Immunology, Boston Children's Hospital, Boston, Massachusetts.
Luigi D NotarangeloImmune Deficiency Genetics Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland.
Maria K LehtinenDepartment of Pathology, Boston Children's Hospital, Boston, Massachusetts. Electronic address: maria.lehtinen@childrens.harvard.edu.
Boston Children's Hospital · USNecmettin Erbakan University · TRNational Institute of Allergy and Infectious Diseases · US

Funding

Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

Cells of the developing central nervous system are particularly susceptible to formation of double-stranded DNA breaks (DSBs) arising from physiological and/or environmental insults. Therefore, efficient repair of DSBs is especially vital for maintaining cellular health and proper functioning in the developing brain. Here, increased expression of DSB initiating and nonhomologous end joining repair machinery in newborn neurons in the developing brains of both mouse and human are demonstrated. In parallel, the first characterization is provided of the brain phenotype in the Lig4

Indexed as

ApoptosisDisease Models, AnimalAnimalsCerebral CortexCraniofacial AbnormalitiesDNA Breaks, Double-StrandedDNA Ligase ATPFemaleGene Knock-In TechniquesGrowth DisordersImmunologic Deficiency SyndromesMaleMiceMicrocephalyMutationNeuronsDNA Ligase ATPLig4 protein, mouse

Identifiers

PMID31541646
PMCPMC6897336
OpenAlexW2973941139

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.