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Tbx5 Buffers Inherent Left/Right Asymmetry Ensuring Symmetric Forelimb Formation
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نویسنده
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sulaiman f.a. ,nishimoto s. ,murphy g.r.f. ,kucharska a. ,butterfield n.c. ,newbury-ecob r. ,logan m.p.o.
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منبع
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plos genetics - 2016 - دوره : 12 - شماره : 12
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چکیده
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The forelimbs and hindlimbs of vertebrates are bilaterally symmetric. the mechanisms that ensure symmetric limb formation are unknown but they can be disrupted in disease. in holt-oram syndrome (hos),caused by mutations in tbx5,affected individuals have left-biased upper/forelimb defects. we demonstrate a role for the transcription factor tbx5 in ensuring the symmetric formation of the left and right forelimb. in our mouse model,bilateral hypomorphic levels of tbx5 produces asymmetric forelimb defects that are consistently more severe in the left limb than the right,phenocopying the left-biased limb defects seen in hos patients. in tbx hypomorphic mutants maintained on an inv mutant background,with situs inversus,the laterality of defects is reversed. our data demonstrate an early,inherent asymmetry in the left and right limb-forming regions and that threshold levels of tbx5 are required to overcome this asymmetry to ensure symmetric forelimb formation. © 2016 sulaiman et al.
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آدرس
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division of developmental biology,mrc-national institute for medical research,mill hill,london, United Kingdom, division of developmental biology,mrc-national institute for medical research,mill hill,london,united kingdom,randall division of cell and molecular biophysics,king’s college london,guy’s campus,london, United Kingdom, randall division of cell and molecular biophysics,king’s college london,guy’s campus,london,united kingdom,dept of plastic & reconstructive surgery,great ormond st hospital for children nhs foundation trust,london, United Kingdom, division of developmental biology,mrc-national institute for medical research,mill hill,london, United Kingdom, division of developmental biology,mrc-national institute for medical research,mill hill,london, United Kingdom, department of clinical genetics,university hospitals bristol nhs foundation trust,st. michaels’s hospital,bristol, United Kingdom, division of developmental biology,mrc-national institute for medical research,mill hill,london,united kingdom,randall division of cell and molecular biophysics,king’s college london,guy’s campus,london, United Kingdom
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Authors
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