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A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice

Disease Models & Mechanisms(2020)10.1242/dmm.045344Source: DataRank Database

A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice is a research paper published in Disease Models & Mechanisms (2020). On theSindex it has a DataRank of 0. It has been cited 17 times.

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Open Access17 citations

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Enrichment:Funding (5 grants)OA: goldTopics (73)IDs (PubMed, PMC)Annotations (3)SDGs (1)

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Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (5)

Marshall Lukacs,Sandra Cindrić ORCID,Heymut Omran ORCID,Rolf W. Stottmann ORCID,Zakia Abdelhamed

Live enrichment

PubMed:32988999 PMC:PMC7648611

National Institutes of Health

Grant: R01NS085023

NIGMS NIH HHS

Grant: R35 GM131875

NIGMS NIH HHS

Grant: T32 GM063483

Wellcome Trust

Grant: unidentified

unidentified

National Institutes of Health

Grant: 5R01NS085023-04

Forward Genetic Analysis of Congenital Defects in Cortical Circuits and Structure

goldLicense: CC BY

publisherhttps://syndication.highwire.org/content/doi/10.1242/dmm.045344

publisherhttps://journals.biologists.com/dmm/article-pdf/doi/10.1242/dmm.045344/3484298/dmm045344.pdf

publisherhttp://journals.biologists.com/dmm/article-pdf/doi/10.1242/dmm.045344/2065994/dmm_045344v1.pdf

Europe_PMChttps://europepmc.org/articles/PMC7648611

Europe_PMChttps://europepmc.org/articles/PMC7648611?pdf=render

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciences

MeSH Terms

CiliaEpithelial CellsAnimalsMice, Inbred C57BLAnimals, NewbornMiceCiliary Motility DisordersHydrocephalusMicrotubule ProteinsMicroscopy, VideoRheologyMicrospheresOrgan SpecificityBase SequenceOrganogenesisBone DevelopmentPhenotypeMutationAlleles

Keywords

LungCiliaInfertilityHydrocephalusPrimary Ciliary DyskinesiaSpag17OrganogenesisGeneMicePathologyRB1-214Aqueductal stenosisPontocerebellar HypoplasiaInternal medicineAlleleMicroscopy, VideoRLife SciencesMicrospheresBronchiectasisPhenotypeCerebrospinal fluidOrgan SpecificityMicrotubule ProteinsMedicineRheologyRadiologyResearch ArticleCiliary Motility DisordersCell biologyCiliumEpigenetic Modifications and Their Functional ImplicationsBiochemistry, Genetics and Molecular BiologyHealth SciencesCiliopathies: Genetic Disorders Involving Primary CiliaGeneticsMotile ciliumAnimalsMolecular BiologyBiologyAllelesBone DevelopmentBase SequenceEpithelial CellsMice, Inbred C57BLAnimals, NewbornFOS: Biological sciencesMutationPediatrics, Perinatology and Child HealthDevelopment and Disorders of Fetal BrainNeuroscience

Sustainable Development Goals

SDG 3: 3. Good health

A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice

FAIR Checklist

Authors (5)

Funding (5 grants)

Open Access

Topics

Annotations (Europe PMC)