Evidence map›Paper›PMID 22887593›Full record

ArticleGenesis (New York, N.Y. : 2000)2012

Craniofacial abnormalities result from knock down of nonsyndromic clefting gene, crispld2, in zebrafish.

Qiuping Yuan, Brett T Chiquet, Laura Devault, Matthew L Warman, Yukio Nakamura, Eric C Swindell, Jacqueline T Hecht

Open access · bronzeAbstract read
In one paragraph

Article in Genesis (New York, N.Y. : 2000), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Disruption ofFrontiers in cell and developmental biology · 2023
    Article
  5. Article
  6. Orofacial Cleft and Mandibular Prognathism-Human Genetics and Animal Models.International journal of molecular sciences · 2022
    Review
  7. Review
  8. Article
  9. Article
  10. Zebrafish models of orofacial clefts.Developmental dynamics : an official publication of the American Association of Anatomists · 2017
    Review
  11. Article
  12. Article
  13. Zebrafish Craniofacial Development: A Window into Early Patterning.Current topics in developmental biology · 2015
    Review
  14. Article
  15. 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

7 authors at 3 institutions in 2 countries.

Qiuping YuanDepartment of Pediatrics, University of Texas Medical School at Houston, Houston, Texas, USA.
Brett T Chiquet
Laura Devault
Matthew L Warman
Yukio Nakamura
Eric C Swindell
Jacqueline T Hecht
Boston Children's Hospital · USShowa Inan General Hospital · JPThe University of Texas Health Science Center at Houston · US

Funding

COBRE for Skeletal Health and RepairP20GM104937 · NIGMS · RHODE ISLAND HOSPITAL · PI CHEN, QIAN · 2012 to 2016
$10.8M
MOLECULAR STUDIES IN NONSYNDROMIC CLEFT LIP AND PALATER01DE011931 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BLANTON, SUSAN HALLORAN, HECHT, JACQUELINE T · 1999 to 2017
$7.6M
Characterization of NSCLP gene CRISPLD2F30DE019343 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHIQUET, BRETT THOMAS · 2008 to 2010
$109k
NIDCR NIH HHS F30 DE019343NIDCR NIH HHS F30-DE019343NIDCR NIH HHS R01 DE011931NIDCR NIH HHS R01-DE011931NIGMS NIH HHS P20 GM104937
6 · The paper itself

Abstract

Nonsyndromic cleft lip and palate (NSCLP), a common birth defect, affects 4,000 newborns in the US each year. Previously, we described an association between CRISPLD2 and NSCLP and showed Crispld2 expression in the murine palate. These results suggested that a perturbation in CRISPLD2 activity affects craniofacial development. Here, we describe crispld2 expression and the phenotypic consequence of its loss of function in zebrafish. crispld2 was expressed at all stages of zebrafish morphogenesis examined and localized to the rostral end by 1-day postfertilization. Morpholino knockdown of crispld2 resulted in significant jaw and palatal abnormalities in a dose-dependent manner. Loss of crispld2 caused aberrant patterning of neural crest cells (NCC) suggesting that crispld2 is necessary for normal NCC formation. Altogether, we show that crispld2 plays a significant role in the development of the zebrafish craniofacies and alteration of normal protein levels disturbs palate and jaw formation. These data provide support for a role of CRISPLD2 in NSCLP.

Indexed as

Amino Acid SequenceAnimalsBrainCell Adhesion MoleculesCleft LipCleft PalateCraniofacial AbnormalitiesGene Knockdown TechniquesGlycoproteinsJawJaw AbnormalitiesMolecular Sequence DataMorpholinosNeural CrestPalateZebrafishCell Adhesion MoleculesCRISPLD2 protein, zebrafishGlycoproteinsMorpholinosZebrafish Proteins

Identifiers

PMID22887593
PMCPMC3535582
OpenAlexW2082090606

What OpenQuestion holds

Textmetadata
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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.