Datoteka:Embryos with mutation in Mks1krc, a cause of Meckel syndrome.png
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Sažetak
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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. |
| Datum | |
| Izvor | https://openi.nlm.nih.gov/detailedresult?img=PMC5349470_pone.0173399.g001&query=Meckel%20syndrome&it=xg&lic=by&req=4&npos=1 |
| Autor | Goetz SC1,2, Bangs F1, Barrington CL2, Katsanis N3, Anderson KV1. |
Licenciranje
This file is licensed under the Creative Commons Attribution 4.0 International license.
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| Datum/vrijeme | Smanjeni pregled | Dimenzije | Korisnik | Komentar | |
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| trenutno | 16:25, 2 januar 2020 | | 512 × 491 (520 KB) | Steve M | User created page with UploadWizard |
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