File:Embryos with mutation in Mks1krc, a cause of Meckel syndrome.png

Embryos_with_mutation_in_Mks1krc,_a_cause_of_Meckel_syndrome.png(512 × 491 pixels, file size: 520 KB, MIME type: image/png)

Summary

Description
English: Embryos with mutation in Mks1krc, a cause of Meckel syndrome.

pone.0173399.g001: Loss of Bbs4 enhances Hh signaling phenotypes in Mks1krc mutant embryos.(A-D) Double heterozygous (A), Bbs4-/- (B), Mks1krc/krc (C), or Mks1krc/krc;Bbs4-/- double mutant (D) embryos at E13.5. Note that double mutant embryos exhibit microopthalmia, polydactyly, and general edema. (E-H) Higher magnification images of the hindlimbs of the embryos indicated above. Each digit is denoted by *. Approximately 25% of Mks1krc/krc exhibit polydactyly on at least one limb as in (G). Double mutant embryos exhibit fully penetrant polydactyly on all four limbs (H). (I-L) Transverse sections through the neural tube of embryos of the indicated genotype at E10.5. Sections were taken at the level of the forelimbs and immunostained with antibodies against OLIG2 (red) and NKX2.2 (green). Scale bar, 100μm.
Date
Source https://openi.nlm.nih.gov/detailedresult?img=PMC5349470_pone.0173399.g001&query=Meckel%20syndrome&it=xg&lic=by&req=4&npos=1
Author Goetz SC1,2, Bangs F1, Barrington CL2, Katsanis N3, Anderson KV1.

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Embryos with mutation in Mks1krc, a cause of Meckel syndrome.

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14 March 2017

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current14:25, 2 January 2020Thumbnail for version as of 14:25, 2 January 2020512 × 491 (520 KB)Steve MUser created page with UploadWizard
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