Article in Development (Cambridge, England), 2025. 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
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.
Lucas D Lo VercioDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0002-5465-6801
Rebecca M GreenDepartment of Oral and Craniofacial Sciences, Center for Craniofacial and Dental Genetics, University of Pittsburgh, Pittsburgh, PA 15219, USA.ORCID 0000-0001-7319-0755
Andreas DauterDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0002-5151-6619
Elizabeth C BarrettoDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0003-1374-6429
Marta Vidal-GarcíaDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0001-7617-7329
Jay DevineDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0003-0600-1058
Marta MarchiniDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0001-5767-5875
Samuel RobertsonDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0002-7254-159X
Xiang ZhaoDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.
Anandita MahikaDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.
M Bilal ShakirDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.
Sienna GuoDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.
Julia C BoughnerDepartment of Anatomy, Physiology and Pharmacology, College of Medicine, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.ORCID 0000-0003-1147-364X
Heather Szabo-RogersDepartment of Anatomy, Physiology and Pharmacology, College of Medicine, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.ORCID 0000-0002-7921-8031
Wendy DeanDepartment of Cell Biology & Anatomy, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0001-9441-5044
Arthur D LanderDepartment of Developmental and Cell Biology, University of California, Irvine, Irvine, CA 92697, USA.ORCID 0000-0002-4380-5525
Ralph S MarcucioDepartment of Orthopaedic Surgery, University of California San Francisco, San Francisco, CA 94110, USA.ORCID 0000-0002-0537-818X
Nils D ForkertAlberta Children's Hospital Research Institute, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0003-2556-3224
Benedikt HallgrímssonAlberta Children's Hospital Research Institute, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0002-7192-9103
Funding
The role of continuous phenotypic variation in structural defects of the faceR01DE019638 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Benedikt Hallgrimsson, Ralph S Marcucio · 2010 to 2026
$7.3M
A National Short Course in Systems Biology: Tackling Spatial Dynamics in Cells anR25GM096989 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D, WAN, FREDERIC Y.M. · 2011 to 2015
$858k
Alberta Children's Hospital FoundationAlberta InnovatesCanada Foundation for Innovation 36262Canada Research Chairs RGPIN-2024-06098CIHRCompute CanadaCumming School of Medicine, University of CalgaryInstitute of Musculoskeletal Health and ArthritisNatural Sciences and Engineering Research Council of Canada 238992Natural Sciences and Engineering Research Council of Canada RGPIN-2024-06098NIDCR NIH HHS R01 DE019638NIDCR NIH HHS R01-DE019638NIGMS NIH HHS R25 GM096989University of CalgaryUniversity of PittsburghWestern Canada Research Grid
6 · The paper itself
Abstract
Morphogenesis requires highly coordinated, complex interactions between cellular processes: proliferation, migration and apoptosis, along with physical tissue interactions. How these cellular and tissue dynamics drive morphogenesis remains elusive. Three dimensional (3D) microscopic imaging holds great promise, and generates elegant images, but generating even moderate throughput for quantified images is challenging for many reasons. As a result, the association between morphogenesis and cellular processes in 3D developing tissues has not been fully explored. To address this gap, we have developed an imaging and image analysis pipeline to enable 3D quantification of cellular dynamics along with 3D morphology for the same individual embryo. Specifically, we focus on how 3D distribution of proliferation relates to morphogenesis during mouse facial development. Our method involves imaging with light-sheet microscopy, automated segmentation of cells and tissues using machine learning-based tools, and quantification of external morphology by geometric morphometrics. Applying this framework, we show that changes in proliferation are tightly correlated with changes in morphology over the course of facial morphogenesis. These analyses illustrate the potential of this pipeline to investigate mechanistic relationships between cellular dynamics and morphogenesis during embryonic development.
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.
Quantifying the relationship between cell proliferation and morphology during development of the face. · full record | OpenQuestion