Literature DB >> 33856919

N-Acetyl Transferases: New Insights Into Human Congenital Cardiovascular Defects.

Timothy J Cashman1,2, Chinmay M Trivedi1,2,3.   

Abstract

Entities:  

Keywords:  Editorials; acetyltransferases; genotype; mutation; proteomics; stem cells

Mesh：

Substances：

Year:  2021        PMID： 33856919      PMCID： PMC8054922          DOI： 10.1161/CIRCRESAHA.121.319049

Source DB:  PubMed          Journal:  Circ Res        ISSN： 0009-7330            Impact factor:   23.213


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  14 in total

Review 1.  Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis.

Authors:  Denise van der Linde; Elisabeth E M Konings; Maarten A Slager; Maarten Witsenburg; Willem A Helbing; Johanna J M Takkenberg; Jolien W Roos-Hesselink
Journal:  J Am Coll Cardiol       Date:  2011-11-15       Impact factor: 24.094

2.  Ribosome-NatA architecture reveals that rRNA expansion segments coordinate N-terminal acetylation.

Authors:  Alexandra G Knorr; Christian Schmidt; Petr Tesina; Otto Berninghausen; Thomas Becker; Birgitta Beatrix; Roland Beckmann
Journal:  Nat Struct Mol Biol       Date:  2018-12-17       Impact factor: 15.369

3.  Recurrence of congenital heart defects in families.

Authors:  Nina Øyen; Gry Poulsen; Heather A Boyd; Jan Wohlfahrt; Peter K A Jensen; Mads Melbye
Journal:  Circulation       Date:  2009-07-13       Impact factor: 29.690

Review 4.  Spotlight on protein N-terminal acetylation.

Authors:  Rasmus Ree; Sylvia Varland; Thomas Arnesen
Journal:  Exp Mol Med       Date:  2018-07-27       Impact factor: 8.718

5.  Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies.

Authors:  Yingjuan Liu; Sen Chen; Liesl Zühlke; Graeme C Black; Mun-Kit Choy; Ningxiu Li; Bernard D Keavney
Journal:  Int J Epidemiol       Date:  2019-04-01       Impact factor: 7.196

6.  Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects.

Authors:  Line M Myklebust; Petra Van Damme; Svein I Støve; Max J Dörfel; Angèle Abboud; Thomas V Kalvik; Cedric Grauffel; Veronique Jonckheere; Yiyang Wu; Jeffrey Swensen; Hanna Kaasa; Glen Liszczak; Ronen Marmorstein; Nathalie Reuter; Gholson J Lyon; Kris Gevaert; Thomas Arnesen
Journal:  Hum Mol Genet       Date:  2014-12-08       Impact factor: 6.150

7.  Loss of RNA expression and allele-specific expression associated with congenital heart disease.

Authors:  David M McKean; Jason Homsy; Hiroko Wakimoto; Neil Patel; Joshua Gorham; Steven R DePalma; James S Ware; Samir Zaidi; Wenji Ma; Nihir Patel; Richard P Lifton; Wendy K Chung; Richard Kim; Yufeng Shen; Martina Brueckner; Elizabeth Goldmuntz; Andrew J Sharp; Christine E Seidman; Bruce D Gelb; J G Seidman
Journal:  Nat Commun       Date:  2016-09-27       Impact factor: 14.919

8.  Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.

Authors:  Sheng Chih Jin; Jason Homsy; Samir Zaidi; Qiongshi Lu; Sarah Morton; Steven R DePalma; Xue Zeng; Hongjian Qi; Weni Chang; Michael C Sierant; Wei-Chien Hung; Shozeb Haider; Junhui Zhang; James Knight; Robert D Bjornson; Christopher Castaldi; Irina R Tikhonoa; Kaya Bilguvar; Shrikant M Mane; Stephan J Sanders; Seema Mital; Mark W Russell; J William Gaynor; John Deanfield; Alessandro Giardini; George A Porter; Deepak Srivastava; Cecelia W Lo; Yufeng Shen; W Scott Watkins; Mark Yandell; H Joseph Yost; Martin Tristani-Firouzi; Jane W Newburger; Amy E Roberts; Richard Kim; Hongyu Zhao; Jonathan R Kaltman; Elizabeth Goldmuntz; Wendy K Chung; Jonathan G Seidman; Bruce D Gelb; Christine E Seidman; Richard P Lifton; Martina Brueckner
Journal:  Nat Genet       Date:  2017-10-09       Impact factor: 38.330

9.  Histone deacetylases 1 and 2 silence cryptic transcription to promote mitochondrial function during cardiogenesis.

Authors:  Zachary J Milstone; Sherin Saheera; Lauren M Bourke; Tomer Shpilka; Cole M Haynes; Chinmay M Trivedi
Journal:  Sci Adv       Date:  2020-04-10       Impact factor: 14.136

10.  De novo mutations in histone-modifying genes in congenital heart disease.

Authors:  Samir Zaidi; Murim Choi; Hiroko Wakimoto; Lijiang Ma; Jianming Jiang; John D Overton; Angela Romano-Adesman; Robert D Bjornson; Roger E Breitbart; Kerry K Brown; Nicholas J Carriero; Yee Him Cheung; John Deanfield; Steve DePalma; Khalid A Fakhro; Joseph Glessner; Hakon Hakonarson; Michael J Italia; Jonathan R Kaltman; Juan Kaski; Richard Kim; Jennie K Kline; Teresa Lee; Jeremy Leipzig; Alexander Lopez; Shrikant M Mane; Laura E Mitchell; Jane W Newburger; Michael Parfenov; Itsik Pe'er; George Porter; Amy E Roberts; Ravi Sachidanandam; Stephan J Sanders; Howard S Seiden; Mathew W State; Sailakshmi Subramanian; Irina R Tikhonova; Wei Wang; Dorothy Warburton; Peter S White; Ismee A Williams; Hongyu Zhao; Jonathan G Seidman; Martina Brueckner; Wendy K Chung; Bruce D Gelb; Elizabeth Goldmuntz; Christine E Seidman; Richard P Lifton
Journal:  Nature       Date:  2013-05-12       Impact factor: 49.962
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