207 related articles for article (PubMed ID: 31950975)
1. Translation elongation factor 1A2 is encoded by one of four closely related eef1a genes and is dispensable for survival in zebrafish.
Idigo NJ; Soares DC; Abbott CM
Biosci Rep; 2020 Jan; 40(1):. PubMed ID: 31950975
[TBL] [Abstract][Full Text] [Related]
2. Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death.
Cao S; Smith LL; Padilla-Lopez SR; Guida BS; Blume E; Shi J; Morton SU; Brownstein CA; Beggs AH; Kruer MC; Agrawal PB
Hum Mol Genet; 2017 Sep; 26(18):3545-3552. PubMed ID: 28911200
[TBL] [Abstract][Full Text] [Related]
3. Biallelic mutations in the gene encoding eEF1A2 cause seizures and sudden death in F0 mice.
Davies FC; Hope JE; McLachlan F; Nunez F; Doig J; Bengani H; Smith C; Abbott CM
Sci Rep; 2017 Apr; 7():46019. PubMed ID: 28378778
[TBL] [Abstract][Full Text] [Related]
4. In vivo characterization of the role of tissue-specific translation elongation factor 1A2 in protein synthesis reveals insights into muscle atrophy.
Doig J; Griffiths LA; Peberdy D; Dharmasaroja P; Vera M; Davies FJ; Newbery HJ; Brownstein D; Abbott CM
FEBS J; 2013 Dec; 280(24):6528-40. PubMed ID: 24460877
[TBL] [Abstract][Full Text] [Related]
5. Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of function.
Davies FCJ; Hope JE; McLachlan F; Marshall GF; Kaminioti-Dumont L; Qarkaxhija V; Nunez F; Dando O; Smith C; Wood E; MacDonald J; Hardt O; Abbott CM
Hum Mol Genet; 2020 Jun; 29(10):1592-1606. PubMed ID: 32160274
[TBL] [Abstract][Full Text] [Related]
6. Endogenous epitope tagging of eEF1A2 in mice reveals early embryonic expression of eEF1A2 and subcellular compartmentalisation of neuronal eEF1A1 and eEF1A2.
Davies FCJ; Marshall GF; Pegram E; Gadd D; Abbott CM
Mol Cell Neurosci; 2023 Sep; 126():103879. PubMed ID: 37429391
[TBL] [Abstract][Full Text] [Related]
7. eEF1A2 and neuronal degeneration.
Abbott CM; Newbery HJ; Squires CE; Brownstein D; Griffiths LA; Soares DC
Biochem Soc Trans; 2009 Dec; 37(Pt 6):1293-7. PubMed ID: 19909265
[TBL] [Abstract][Full Text] [Related]
8. Translation elongation factor eEF1A2 is essential for post-weaning survival in mice.
Newbery HJ; Loh DH; O'Donoghue JE; Tomlinson VAL; Chau YY; Boyd JA; Bergmann JH; Brownstein D; Abbott CM
J Biol Chem; 2007 Sep; 282(39):28951-28959. PubMed ID: 17640869
[TBL] [Abstract][Full Text] [Related]
9. The lethal mutation of the mouse wasted (wst) is a deletion that abolishes expression of a tissue-specific isoform of translation elongation factor 1alpha, encoded by the Eef1a2 gene.
Chambers DM; Peters J; Abbott CM
Proc Natl Acad Sci U S A; 1998 Apr; 95(8):4463-8. PubMed ID: 9539760
[TBL] [Abstract][Full Text] [Related]
10. The role of translation elongation factor eEF1 subunits in neurodevelopmental disorders.
McLachlan F; Sires AM; Abbott CM
Hum Mutat; 2019 Feb; 40(2):131-141. PubMed ID: 30370994
[TBL] [Abstract][Full Text] [Related]
11. Identification of Dmrt2a downstream genes during zebrafish early development using a timely controlled approach.
Pinto RA; Almeida-Santos J; Lourenço R; Saúde L
BMC Dev Biol; 2018 Jun; 18(1):14. PubMed ID: 29914374
[TBL] [Abstract][Full Text] [Related]
12. Autism- and epilepsy-associated
Mohamed MS; Klann E
Proc Natl Acad Sci U S A; 2023 Sep; 120(38):e2307704120. PubMed ID: 37695913
[TBL] [Abstract][Full Text] [Related]
13. Dilated cardiomyopathy in a patient with autosomal dominant EEF1A2-related neurodevelopmental disorder.
Kaneko M; Rosser T; Raca G
Eur J Med Genet; 2021 Jan; 64(1):104121. PubMed ID: 33307280
[TBL] [Abstract][Full Text] [Related]
14. Investigation of Islet2a function in zebrafish embryos: Mutants and morphants differ in morphologic phenotypes and gene expression.
Moreno RL; Williams K; Jones KL; Ribera AB
PLoS One; 2018; 13(6):e0199233. PubMed ID: 29927984
[TBL] [Abstract][Full Text] [Related]
15. Loss of zebrafish Smyd1a interferes with myofibrillar integrity without triggering the misfolded myosin response.
Paone C; Rudeck S; Etard C; Strähle U; Rottbauer W; Just S
Biochem Biophys Res Commun; 2018 Feb; 496(2):339-345. PubMed ID: 29331378
[TBL] [Abstract][Full Text] [Related]
16. Porcine EEF1A1 and EEF1A2 genes: genomic structure, polymorphism, mapping and expression.
Svobodová K; Horák P; Stratil A; Bartenschlager H; Van Poucke M; Chalupová P; Dvořáková V; Knorr C; Stupka R; Čítek J; Šprysl M; Palánová A; Peelman LJ; Geldermann H; Knoll A
Mol Biol Rep; 2015 Aug; 42(8):1257-64. PubMed ID: 25749814
[TBL] [Abstract][Full Text] [Related]
17. Dimethylation of eEF1A at Lysine 55 Plays a Key Role in the Regulation of eEF1A2 on Malignant Cell Functions of Acute Myeloid Leukemia.
Xiao S; Wang Y; Ma Y; Liu J; Tang C; Deng A; Fang C
Technol Cancer Res Treat; 2020; 19():1533033820914295. PubMed ID: 32347192
[TBL] [Abstract][Full Text] [Related]
18. Face-valid phenotypes in a mouse model of the most common mutation in EEF1A2-related neurodevelopmental disorder.
Marshall GF; Fasol M; Davies FCJ; Le Seelleur M; Fernandez Alvarez A; Bennett-Ness C; Gonzalez-Sulser A; Abbott CM
Dis Model Mech; 2024 Jun; 17(6):. PubMed ID: 38179821
[TBL] [Abstract][Full Text] [Related]
19. Zebrafish pitx3 is necessary for normal lens and retinal development.
Shi X; Bosenko DV; Zinkevich NS; Foley S; Hyde DR; Semina EV; Vihtelic TS
Mech Dev; 2005 Apr; 122(4):513-27. PubMed ID: 15804565
[TBL] [Abstract][Full Text] [Related]
20. Mild epileptic phenotype associates with de novo eef1a2 mutation: Case report and review.
De Rinaldis M; Giorda R; Trabacca A
Brain Dev; 2020 Jan; 42(1):77-82. PubMed ID: 31477274
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
