Literature DB >> 22194264

High-throughput analysis of mouse embryos by magnetic resonance imaging.

Simon D Bamforth, Jürgen E Schneider, Shoumo Bhattacharya.   

Abstract

Genetic studies in the mouse are crucial for uncovering new genes and signaling pathways associated with development. The identification of murine models with developmental malformations in high-throughput mutagenesis screens is made difficult because, after mid-embryogenesis, the embryo is opaque. Traditional phenotyping methods such as histological sectioning are labor intensive and destructive. We have developed and optimized a novel method for high-throughput multiembryo magnetic resonance imaging (MRI). Here we present our method for processing 32 mouse embryos for analysis by MRI. We describe the MR system, imaging software, and the reconstruction of two-dimensional (2D) and three-dimensional (3D) images. We also discuss the applications of this technique, highlight its advantages, and point out some disadvantages. Using this approach, we can identify developmental malformations in mutant embryos at high spatial resolution (voxel size 25.4 × 25.4 × 24.4 µm). This technique can be easily used for mouse mutagenesis screens and thus provides an important tool for identifying new mouse models for human diseases.

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Mesh:

Year:  2012        PMID: 22194264      PMCID: PMC4856208          DOI: 10.1101/pdb.prot067538

Source DB:  PubMed          Journal:  Cold Spring Harb Protoc        ISSN: 1559-6095


  12 in total

1.  A mouse for all reasons.

Authors:  Francis S Collins; Janet Rossant; Wolfgang Wurst
Journal:  Cell       Date:  2007-01-12       Impact factor: 41.582

2.  Pinch1 is required for normal development of cranial and cardiac neural crest-derived structures.

Authors:  Xingqun Liang; Yunfu Sun; Jurgen Schneider; Jian-Hua Ding; Hongqiang Cheng; Maoqing Ye; Shoumo Bhattacharya; Ann Rearden; Sylvia Evans; Ju Chen
Journal:  Circ Res       Date:  2007-02-01       Impact factor: 17.367

3.  A new partner for the international knockout mouse consortium.

Authors:  Francis S Collins; Richard H Finnell; Janet Rossant; Wolfgang Wurst
Journal:  Cell       Date:  2007-04-20       Impact factor: 41.582

4.  Cyclin E ablation in the mouse.

Authors:  Yan Geng; Qunyan Yu; Ewa Sicinska; Manjusri Das; Jürgen E Schneider; Shoumo Bhattacharya; William M Rideout; Roderick T Bronson; Humphrey Gardner; Piotr Sicinski
Journal:  Cell       Date:  2003-08-22       Impact factor: 41.582

5.  Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.

Authors:  Debora Bogani; Catherine Willoughby; Jennifer Davies; Kulvinder Kaur; Ghazala Mirza; Anju Paudyal; Heather Haines; Richard McKeone; Matthew Cadman; Guido Pieles; Jürgen E Schneider; Shoumo Bhattacharya; Andrea Hardy; Patrick M Nolan; Nikos Tripodis; Michael J Depew; Ramya Chandrasekara; Gimara Duncan; Paul T Sharpe; Andy Greenfield; Paul Denny; Steve D M Brown; Jiannis Ragoussis; Ruth M Arkell
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-18       Impact factor: 11.205

6.  VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5.

Authors:  Dorota Szumska; Guido Pieles; Rachid Essalmani; Michal Bilski; Daniel Mesnard; Kulvinder Kaur; Angela Franklyn; Kamel El Omari; Joanna Jefferis; Jamie Bentham; Jennifer M Taylor; Jurgen E Schneider; Sebastian J Arnold; Paul Johnson; Zuzanna Tymowska-Lalanne; Dave Stammers; Kieran Clarke; Stefan Neubauer; Andrew Morris; Steve D Brown; Charles Shaw-Smith; Armando Cama; Valeria Capra; Jiannis Ragoussis; Daniel Constam; Nabil G Seidah; Annik Prat; Shoumo Bhattacharya
Journal:  Genes Dev       Date:  2008-06-01       Impact factor: 11.361

7.  Cardiac malformations and midline skeletal defects in mice lacking filamin A.

Authors:  Alan W Hart; Joanne E Morgan; Jürgen Schneider; Katrine West; Lisa McKie; Shoumo Bhattacharya; Ian J Jackson; Sally H Cross
Journal:  Hum Mol Genet       Date:  2006-07-06       Impact factor: 6.150

8.  Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique.

Authors:  Jürgen E Schneider; Jens Böse; Simon D Bamforth; Achim D Gruber; Carol Broadbent; Kieran Clarke; Stefan Neubauer; Andreas Lengeling; Shoumo Bhattacharya
Journal:  BMC Dev Biol       Date:  2004-12-22       Impact factor: 1.978

9.  High-resolution, high-throughput magnetic paragraph sign resonance imaging of mouse embryonic paragraph sign anatomy using a fast gradient-echo sequence.

Authors:  Jürgen E Schneider; Simon D Bamforth; Stuart M Grieve; Kieran Clarke; Shoumo Bhattacharya; Stefan Neubauer
Journal:  MAGMA       Date:  2003-02       Impact factor: 2.310

10.  Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway.

Authors:  Simon D Bamforth; José Bragança; Cassandra R Farthing; Jürgen E Schneider; Carol Broadbent; Anna C Michell; Kieran Clarke; Stefan Neubauer; Dominic Norris; Nigel A Brown; Robert H Anderson; Shoumo Bhattacharya
Journal:  Nat Genet       Date:  2004-10-10       Impact factor: 38.330

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  7 in total

1.  Morphogenesis of the Mammalian Aortic Arch Arteries.

Authors:  Robert H Anderson; Simon D Bamforth
Journal:  Front Cell Dev Biol       Date:  2022-05-10

2.  In amnio MRI of mouse embryos.

Authors:  Thomas A Roberts; Francesca C Norris; Helen Carnaghan; Dawn Savery; Jack A Wells; Bernard Siow; Peter J Scambler; Agostino Pierro; Paolo De Coppi; Simon Eaton; Mark F Lythgoe
Journal:  PLoS One       Date:  2014-10-15       Impact factor: 3.240

3.  Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy.

Authors:  Wolfgang J Weninger; Stefan H Geyer; Alexandrine Martineau; Antonella Galli; David J Adams; Robert Wilson; Timothy J Mohun
Journal:  Dis Model Mech       Date:  2014-10       Impact factor: 5.758

4.  Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis.

Authors:  Helen M Phillips; Catherine A Stothard; Wasay M Shaikh Qureshi; Anastasia I Kousa; J Alberto Briones-Leon; Ramada R Khasawneh; Chloe O'Loughlin; Rachel Sanders; Silvia Mazzotta; Rebecca Dodds; Kerstin Seidel; Timothy Bates; Mitsushiro Nakatomi; Simon J Cockell; Jürgen E Schneider; Timothy J Mohun; René Maehr; Ralf Kist; Heiko Peters; Simon D Bamforth
Journal:  Development       Date:  2019-09-23       Impact factor: 6.868

5.  Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype.

Authors:  Ramada R Khasawneh; Ralf Kist; Rachel Queen; Rafiqul Hussain; Jonathan Coxhead; Jürgen E Schneider; Timothy J Mohun; Stéphane Zaffran; Heiko Peters; Helen M Phillips; Simon D Bamforth
Journal:  BMC Dev Biol       Date:  2021-10-06       Impact factor: 1.978

6.  Early Embryonic Expression of AP-2α Is Critical for Cardiovascular Development.

Authors:  Amy-Leigh Johnson; Jürgen E Schneider; Timothy J Mohun; Trevor Williams; Shoumo Bhattacharya; Deborah J Henderson; Helen M Phillips; Simon D Bamforth
Journal:  J Cardiovasc Dev Dis       Date:  2020-07-23

7.  Pax9 and Gbx2 Interact in the Pharyngeal Endoderm to Control Cardiovascular Development.

Authors:  Catherine A Stothard; Silvia Mazzotta; Arjun Vyas; Jurgen E Schneider; Timothy J Mohun; Deborah J Henderson; Helen M Phillips; Simon D Bamforth
Journal:  J Cardiovasc Dev Dis       Date:  2020-05-25
  7 in total

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