Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice
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Naming CRISPR alleles: endonuclease-mediated mutation nomenclature across speciesIn vivo and in vitro disease modeling with CRISPR/Cas9.Neurogenesis: Regulation by Alternative Splicing and Related Posttranscriptional Processes.GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome.Structure of a SMG8-SMG9 complex identifies a G-domain heterodimer in the NMD effector proteins.MEF2C loss-of-function mutation contributes to congenital heart defects.Upf proteins: highly conserved factors involved in nonsense mRNA mediated decay.Nonsense-mediated mRNA decay: a 'nonsense' pathway makes sense in stem cell biology.HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.Genetic Regulatory Mechanisms of Smooth Muscle Cells Map to Coronary Artery Disease Risk LociLost in Translation: Ribosome-Associated mRNA and Protein Quality Controls
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P2860
Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice
description
2016 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2016
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im April 2016 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 2016/04/07)
@sk
vědecký článek publikovaný v roce 2016
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wetenschappelijk artikel (gepubliceerd op 2016/04/07)
@nl
наукова стаття, опублікована у квітні 2016
@uk
مقالة علمية (نشرت في 7-4-2016)
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name
Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
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Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
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Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
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type
label
Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
@ast
Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
@en
Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
@nl
prefLabel
Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
@ast
Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
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Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
@nl
P2093
P2860
P1476
Mutations in SMG9, Encoding an ...... ly Syndrome in Humans and Mice
@en
P2093
Dilek Colak
Kristina Palmer
L. Brianna Caddle
Leslie Goodwin
Mais Hashem
Mohamed Abouelhoda
Mohammed Zain Seidahmed
Ranad Shaheen
Salma M. Wakil
P2860
P304
P356
10.1016/J.AJHG.2016.02.010
P407
P577
2016-04-07T00:00:00Z