Putative binding sites for mir‐125 family miRNAs in the mouse Lfng 3′UTR affect transcript expression in the segmentation clock, but mir‐125a‐5p is dispensable for normal somitogenesis-Reference-Cited by-同舟云学术

Putative binding sites for mir‐125 family miRNAs in the mouse Lfng 3′UTR affect transcript expression in the segmentation clock, but mir‐125a‐5p is dispensable for normal somitogenesis

Published:2017-08-18 Issue:10 Volume:246 Page:740-748
ISSN:1058-8388
Container-title:Developmental Dynamics
language:en
Short-container-title:Dev. Dyn.

Author:

Wahi Kanu¹,Friesen Sophia¹,Coppola Vincenzo²,Cole Susan E.¹^ORCID

Affiliation:

1. Department of Molecular Genetics, College of Arts and SciencesThe Ohio State UniversityColumbusOhio

2. Department of Cancer Biology and Genetics, College of MedicineThe Ohio State UniversityColumbus Ohio

Funder

National Science Foundation

National Institutes of Health

Publisher

Wiley

Subject

Developmental Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/dvdy.24552

Reference60 articles.

1. Dynamic Expression oflunatic fringeSuggests a Link betweennotchSignaling and an Autonomous Cellular Oscillator Driving Somite Segmentation

2. Wnt3a Plays a Major Role in the Segmentation Clock Controlling Somitogenesis

3. A β-catenin gradient links the clock and wavefront systems in mouse embryo segmentation

4. Beyond Secondary Structure: Primary-Sequence Determinants License Pri-miRNA Hairpins for Processing

5. MicroRNAs: Target Recognition and Regulatory Functions

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