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Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway
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Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen
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Cyclin E Ablation In the Mouse
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Geng Y, Yu Q, Sicinska E, Das M, Schneider JE, Bhattacharya S, Rideout W, Bronson RT, Gardner H, Sicinski P. 2003. Cyclin E ablation in the mouse. Cell 114: 431-443.
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Cardiac malformations and midline skeletal defects in mice lacking filamin A
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Hart AW, Morgan JE, Schneider J, West K, McKie L, Bhattacharya S, Jackson IJ, Cross SH. 2006. Cardiac malformations and midline skeletal defects in mice lacking filamin A. Hum Mol Genet 15: 2457-2467.
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Pinch1 is required for normal development of cranial and cardiac neural crest-derived structures
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Liang X, Sun Y, Schneider J, Ding JH, Cheng H, Ye M, Bhattacharya S, Rearden A, Evans S, Chen J. 2007. Pinch1 is required for normal development of cranial and cardiac neural crest-derived structures. Circ Res 100: 527-535.
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Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency
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MacDonald ST, Bamforth SD, Chen CM, Farthing CR, Franklyn A, Broadbent C, Schneider JE, Saga Y, Lewandoski M, Bhattacharya S. 2008. Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency. Cardiovasc Res 79: 448-457.
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MicroMRIHREM pipeline for high-throughput, high-resolution phenotyping of murine embryos
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Pieles G, Geyer SH, Szumska D, Schneider J, Neubauer S, Clarke K, Dorfmeister K, Franklyn A, Brown SD, Bhattacharya S, et al. 2007. MicroMRIHREM pipeline for high-throughput, high-resolution phenotyping of murine embryos. J Anat 211: 132-137.
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Schneider JE, Bamforth SD, Grieve SM, Clarke K, Bhattacharya S, Neubauer S. 2003. High-resolution, high-throughput magnetic resonance imaging of mouse embryonic anatomy using a fast gradient-echo sequence. Magma 16: 43-51.
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Identification of cardiac malformations in mice lacking Ptdsr using a novel highthroughput magnetic resonance imaging technique
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Schneider JE, Bose J, Bamforth SD, Gruber AD, Broadbent C, Clarke K, Neubauer S, Lengeling A, Bhattacharya S. 2004. Identification of cardiac malformations in mice lacking Ptdsr using a novel highthroughput magnetic resonance imaging technique. BMC Dev Biol 4: 16.
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VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5
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