Schneider JE - Search Results

1

Maternal high-fat diet interacts with embryonic Cited2 genotype to reduce Pitx2c expression and enhance penetrance of left-right patterning defects.

Bentham J, Michell AC, Lockstone H, Andrew D, Schneider JE, Brown NA, Bhattacharya S. Bentham J, et al. Among authors: schneider je. Hum Mol Genet. 2010 Sep 1;19(17):3394-401. doi: 10.1093/hmg/ddq251. Epub 2010 Jun 21. Hum Mol Genet. 2010. PMID: 20566713 Free PMC article.

2

Rapid identification and 3D reconstruction of complex cardiac malformations in transgenic mouse embryos using fast gradient echo sequence magnetic resonance imaging.

Schneider JE, Bamforth SD, Farthing CR, Clarke K, Neubauer S, Bhattacharya S. Schneider JE, et al. J Mol Cell Cardiol. 2003 Feb;35(2):217-22. doi: 10.1016/s0022-2828(02)00291-2. J Mol Cell Cardiol. 2003. PMID: 12606262

3

High-resolution imaging of normal anatomy, and neural and adrenal malformations in mouse embryos using magnetic resonance microscopy.

Schneider JE, Bamforth SD, Farthing CR, Clarke K, Neubauer S, Bhattacharya S. Schneider JE, et al. J Anat. 2003 Feb;202(2):239-47. doi: 10.1046/j.1469-7580.2003.00157.x. J Anat. 2003. PMID: 12647873 Free PMC article.

4

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

Schneider JE, Bamforth SD, Grieve SM, Clarke K, Bhattacharya S, Neubauer S. Schneider JE, et al. MAGMA. 2003 Feb;16(1):43-51. doi: 10.1007/s10334-003-0002-z. MAGMA. 2003. PMID: 12695885

5

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

Bamforth SD, Bragança J, Farthing CR, Schneider JE, Broadbent C, Michell AC, Clarke K, Neubauer S, Norris D, Brown NA, Anderson RH, Bhattacharya S. Bamforth SD, et al. Among authors: schneider je. Nat Genet. 2004 Nov;36(11):1189-96. doi: 10.1038/ng1446. Epub 2004 Oct 10. Nat Genet. 2004. PMID: 15475956

6

Making the mouse embryo transparent: identifying developmental malformations using magnetic resonance imaging.

Schneider JE, Bhattacharya S. Schneider JE, et al. Birth Defects Res C Embryo Today. 2004 Sep;72(3):241-9. doi: 10.1002/bdrc.20017. Birth Defects Res C Embryo Today. 2004. PMID: 15495185 Review.

7

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

Schneider JE, Böse J, Bamforth SD, Gruber AD, Broadbent C, Clarke K, Neubauer S, Lengeling A, Bhattacharya S. Schneider JE, et al. BMC Dev Biol. 2004 Dec 22;4:16. doi: 10.1186/1471-213X-4-16. BMC Dev Biol. 2004. PMID: 15615595 Free PMC article.

8

Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency.

MacDonald ST, Bamforth SD, Chen CM, Farthing CR, Franklyn A, Broadbent C, Schneider JE, Saga Y, Lewandoski M, Bhattacharya S. MacDonald ST, et al. Among authors: schneider je. Cardiovasc Res. 2008 Aug 1;79(3):448-57. doi: 10.1093/cvr/cvn101. Epub 2008 Apr 25. Cardiovasc Res. 2008. PMID: 18440989 Free PMC article.

9

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

Szumska D, Pieles G, Essalmani R, Bilski M, Mesnard D, Kaur K, Franklyn A, El Omari K, Jefferis J, Bentham J, Taylor JM, Schneider JE, Arnold SJ, Johnson P, Tymowska-Lalanne Z, Stammers D, Clarke K, Neubauer S, Morris A, Brown SD, Shaw-Smith C, Cama A, Capra V, Ragoussis J, Constam D, Seidah NG, Prat A, Bhattacharya S. Szumska D, et al. Among authors: schneider je. Genes Dev. 2008 Jun 1;22(11):1465-77. doi: 10.1101/gad.479408. Genes Dev. 2008. PMID: 18519639 Free PMC article.

10

Comparative SNR for high-throughput mouse embryo MR microscopy.

Zhang X, Schneider JE, Portnoy S, Bhattacharya S, Henkelman RM. Zhang X, et al. Among authors: schneider je. Magn Reson Med. 2010 Jun;63(6):1703-7. doi: 10.1002/mrm.22352. Magn Reson Med. 2010. PMID: 20512875 Free article.

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