| Year |
Citation |
Score |
| 2020 |
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. Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of function. Human Molecular Genetics. PMID 32160274 DOI: 10.1093/Hmg/Ddaa042 |
0.34 |
|
| 2020 |
Idigo NJ, Soares DC, Abbott CM. Translation elongation factor 1A2 is encoded by one of four closely related eef1a genes and is dispensable for survival in zebrafish. Bioscience Reports. 40. PMID 31950975 DOI: 10.1042/Bsr20194191 |
0.426 |
|
| 2018 |
McLachlan F, Sires AM, Abbott CM. The role of translation elongation factor eEF1 subunits in neurodevelopmental disorders. Human Mutation. PMID 30370994 DOI: 10.1002/Humu.23677 |
0.353 |
|
| 2017 |
Davies FC, Hope JE, McLachlan F, Nunez F, Doig J, Bengani H, Smith C, Abbott CM. Biallelic mutations in the gene encoding eEF1A2 cause seizures and sudden death in F0 mice. Scientific Reports. 7: 46019. PMID 28378778 DOI: 10.1038/Srep46019 |
0.372 |
|
| 2016 |
Lam WW, Millichap JJ, Soares DC, Chin R, McLellan A, FitzPatrick DR, Elmslie F, Lees MM, Schaefer GB, Abbott CM. Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability. Molecular Genetics & Genomic Medicine. 4: 465-74. PMID 27441201 DOI: 10.1002/Mgg3.219 |
0.307 |
|
| 2014 |
Cao Y, Portela M, Janikiewicz J, Doig J, Abbott CM. Characterisation of translation elongation factor eEF1B subunit expression in mammalian cells and tissues and co-localisation with eEF1A2. Plos One. 9: e114117. PMID 25436608 DOI: 10.1371/Journal.Pone.0114117 |
0.32 |
|
| 2013 |
Doig J, Griffiths LA, Peberdy D, Dharmasaroja P, Vera M, Davies FJ, Newbery HJ, Brownstein D, Abbott CM. In vivo characterization of the role of tissue-specific translation elongation factor 1A2 in protein synthesis reveals insights into muscle atrophy. The Febs Journal. 280: 6528-40. PMID 24460877 DOI: 10.1111/Febs.12554 |
0.312 |
|
| 2012 |
Griffiths LA, Doig J, Churchhouse AM, Davies FC, Squires CE, Newbery HJ, Abbott CM. Haploinsufficiency for translation elongation factor eEF1A2 in aged mouse muscle and neurons is compatible with normal function. Plos One. 7: e41917. PMID 22848658 DOI: 10.1371/Journal.Pone.0041917 |
0.344 |
|
| 2011 |
Newbery HJ, Stancheva I, Zimmerman LB, Abbott CM. Evolutionary importance of translation elongation factor eEF1A variant switching: eEF1A1 down-regulation in muscle is conserved in Xenopus but is controlled at a post-transcriptional level. Biochemical and Biophysical Research Communications. 411: 19-24. PMID 21722626 DOI: 10.1016/J.Bbrc.2011.06.062 |
0.315 |
|
| 2010 |
Li Z, Qi CF, Shin DM, Zingone A, Newbery HJ, Kovalchuk AL, Abbott CM, Morse HC. Eef1a2 promotes cell growth, inhibits apoptosis and activates JAK/STAT and AKT signaling in mouse plasmacytomas. Plos One. 5: e10755. PMID 20505761 DOI: 10.1371/Journal.Pone.0010755 |
0.334 |
|
| 2009 |
Abbott CM, Newbery HJ, Squires CE, Brownstein D, Griffiths LA, Soares DC. eEF1A2 and neuronal degeneration. Biochemical Society Transactions. 37: 1293-7. PMID 19909265 DOI: 10.1042/Bst0371293 |
0.354 |
|
| 2007 |
Newbery HJ, Loh DH, O'Donoghue JE, Tomlinson VA, Chau YY, Boyd JA, Bergmann JH, Brownstein D, Abbott CM. Translation elongation factor eEF1A2 is essential for post-weaning survival in mice. The Journal of Biological Chemistry. 282: 28951-9. PMID 17640869 DOI: 10.1074/Jbc.M703962200 |
0.657 |
|
| 2007 |
Tomlinson VA, Newbery HJ, Bergmann JH, Boyd J, Scott D, Wray NR, Sellar GC, Gabra H, Graham A, Williams AR, Abbott CM. Expression of eEF1A2 is associated with clear cell histology in ovarian carcinomas: overexpression of the gene is not dependent on modifications at the EEF1A2 locus. British Journal of Cancer. 96: 1613-20. PMID 17437010 DOI: 10.1038/Sj.Bjc.6603748 |
0.375 |
|
| 2005 |
Newbery HJ, Gillingwater TH, Dharmasaroja P, Peters J, Wharton SB, Thomson D, Ribchester RR, Abbott CM. Progressive loss of motor neuron function in wasted mice: Effects of a spontaneous null mutation in the gene for the eEF1A2 translation factor Journal of Neuropathology and Experimental Neurology. 64: 295-303. PMID 15835265 DOI: 10.1093/Jnen/64.4.295 |
0.301 |
|
| 2004 |
Everett CA, Auchincloss CA, Kaufman MH, Abbott CM, West JD. Genetic influences on ovulation of primary oocytes in LT/Sv strain mice. Reproduction (Cambridge, England). 128: 565-71. PMID 15509702 DOI: 10.1530/Rep.00325 |
0.374 |
|
| 2003 |
Nürnberger B, Hofman S, Förg-Brey B, Praetzel G, Maclean A, Szymura JM, Abbott CM, Barton NH. A linkage map for the hybridising toads Bombina bombina and B. variegata (Anura: Discoglossidae). Heredity. 91: 136-42. PMID 12886280 DOI: 10.1038/Sj.Hdy.6800291 |
0.328 |
|
| 2002 |
Newbery HJ, Abbott CM. Of mice, men and motor neurons. Trends in Molecular Medicine. 8: 88-92. PMID 11815275 DOI: 10.1016/S1471-4914(02)02283-9 |
0.312 |
|
| 2001 |
Chambers DM, Rouleau GA, Abbott CM. Comparative genomic analysis of genes encoding translation elongation factor 1B(alpha) in human and mouse shows EEF1B1 to be a recent retrotransposition event. Genomics. 77: 145-8. PMID 11597139 DOI: 10.1006/Geno.2001.6626 |
0.462 |
|
| 2001 |
Newbery HJ, Abbott CM. Of mice, men and motor neurons. Trends in Genetics : Tig. 17: S2-6. PMID 11585669 DOI: 10.1016/S0168-9525(01)02459-3 |
0.312 |
|
| 2000 |
Pennisi DJ, Gardner J, Chambers D, Hosking B, Peters J, Muscat G, Abbott C, Koopman P. Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice. Nature Genetics. 24: 434-437. PMID 10742113 DOI: 10.1038/74301 |
0.366 |
|
| 2000 |
Schmidt KH, Abbott CM, Leach DR. Two opposing effects of mismatch repair on CTG repeat instability in Escherichia coli. Molecular Microbiology. 35: 463-71. PMID 10652107 DOI: 10.1046/J.1365-2958.2000.01727.X |
0.311 |
|
| 1999 |
Hendrich B, Abbott C, McQueen H, Chambers D, Cross S, Bird A. Genomic structure and chromosomal mapping of the murine and human Mbd1, Mbd2, Mbd3, and Mbd4 genes. Mammalian Genome. 10: 906-912. PMID 10441743 DOI: 10.1007/S003359901112 |
0.454 |
|
| 1998 |
Chambers DM, Kipling D, Abbott CM. Isolation of a microsatellite that reveals paralogy between the subtelomeric regions of mouse chromosomes 17 and 19: further evidence for telomere-telomere exchange in the mouse. Genomics. 53: 113-4. PMID 9787084 DOI: 10.1006/Geno.1998.5477 |
0.384 |
|
| 1998 |
Durkin ME, Albrechtsen R, Chambers DM, Abbott CM, Wewer UM. Evaluation of Lama5 as a candidate for the mouse ragged (Ra) mutation. Biochemical and Biophysical Research Communications. 250: 125-30. PMID 9735344 DOI: 10.1006/Bbrc.1998.9285 |
0.374 |
|
| 1998 |
Peters J, Siracusa LD, Pomp D, Zuberi AR, Church D, Koratkar R, Abbott CM. Encyclopedia of the mouse genome VII. Mouse chromosome 2. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: S27-49. PMID 9662619 DOI: 10.1007/S003359900647 |
0.383 |
|
| 1998 |
Chambers DM, Peters J, Abbott CM. 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. Proceedings of the National Academy of Sciences of the United States of America. 95: 4463-8. PMID 9539760 DOI: 10.1073/Pnas.95.8.4463 |
0.422 |
|
| 1997 |
Siracusa LD, Abbott CM, Morgan JL, Zuberi AR, Pomp D, Peters J. Mouse chromosome 2. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: S28-44. PMID 9233385 DOI: 10.1007/S003359900314 |
0.385 |
|
| 1997 |
Kent J, Lee M, Schedl A, Boyle S, Fantes J, Powell M, Rushmere N, Abbott C, van Heyningen V, Bickmore WA. The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse. Genomics. 42: 260-7. PMID 9192846 DOI: 10.1006/Geno.1997.4706 |
0.458 |
|
| 1997 |
Allen J, Colleaux L, Davidson D, Graham E, Lee M, Hill R, Abbott C, Gordon C. Expression and mapping of the mouse S7/Pmsc2 gene, homolog of an essential mitotic gene in yeast Mammalian Genome. 8: 352-354. PMID 9107682 DOI: 10.1007/S003359900439 |
0.41 |
|
| 1997 |
Alfred JB, Rance K, Taylor BA, Phillips SJ, Abbott CM, Jackson IJ. Mapping in the region of Danforth's short tail and the localization of tail length modifiers. Genome Research. 7: 108-17. PMID 9049629 DOI: 10.1101/Gr.7.2.108 |
0.416 |
|
| 1996 |
Peichel CL, Abbott CM, Vogt TF. Genetic and physical mapping of the mouse Ulnaless locus. Genetics. 144: 1757-67. PMID 8978061 |
0.316 |
|
| 1996 |
Chambers DM, Abbott CM. Isolation and mapping of novel mouse brain cDNA clones containing trinucleotide repeats, and demonstration of novel alleles in recombinant inbred strains. Genome Research. 6: 715-23. PMID 8858346 DOI: 10.1101/Gr.6.8.715 |
0.379 |
|
| 1996 |
Malas S, Pilz A, Lalley PA, Pate L, Stephenson DA, Abbott C. The isolation and mapping of PCR markers specific to mouse Chromosome 2 Mammalian Genome. 7: 145-148. PMID 8835533 DOI: 10.1007/S003359900036 |
0.404 |
|
| 1995 |
Williamson CM, Dutton ER, Abbott CM, Beechey CV, Ball ST, Peters J. Thirteen genes (Cebpb, E2f1, Tcf4, Cyp24, Pck1, Acra4, Edn3, Kcnb1, Mc3r, Ntsr, Cd40, Plcg1 and Rcad) that probably lie in the distal imprinting region of mouse chromosome 2 are not monoallelically expressed. Genetical Research. 65: 83-93. PMID 7781998 DOI: 10.1017/S0016672300033103 |
0.465 |
|
| 1995 |
Pilz A, Woodward K, Povey S, Abbott C. Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse Genomics. 25: 139-149. PMID 7774911 DOI: 10.1016/0888-7543(95)80119-7 |
0.425 |
|
| 1995 |
Pilz A, Glenister P, Povey S, Lyon M, Abbott C. The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the tw18 or th20 deletions. Genomics. 26: 420-421. PMID 7601476 DOI: 10.1016/0888-7543(95)80234-D |
0.451 |
|
| 1995 |
Poleev A, Wendler F, Fickenscher H, Zannini MS, Yaginuma K, Abbott C, Plachov D. Distinct Functional Properties of Three Human Paired‐Box‐Protein, PAX8, Isoforms Generated by Alternative Splicing in Thyroid, Kidney and Wilms' Tumors Febs Journal. 228: 899-911. DOI: 10.1111/J.1432-1033.1995.0899M.X |
0.337 |
|
| 1994 |
Pilz A, Prohaska R, Peters J, Abbott C. Genetic linkage analysis of the Ak1, Col5a1, Epb7.2, Fpgs, Grp78, Pbx3, and Notch1 genes in the region of mouse chromosome 2 homologous to human chromosome 9q Genomics. 21: 104-109. PMID 8088777 DOI: 10.1006/Geno.1994.1230 |
0.461 |
|
| 1994 |
Abbott C, Malas S, Pilz A, Pate L, Ali R, Peters J. Linkage mapping around the ragged (Ra) and wasted (wst) loci on distal mouse chromosome 2 Genomics. 20: 94-98. PMID 8020960 DOI: 10.1006/Geno.1994.1131 |
0.399 |
|
| 1994 |
Malas S, Peters J, Abbott C. The genes for endothelin 3, vitamin D 24-hydroxylase, and melanocortin 3 receptor map to distal mouse chromosome 2, in the region of conserved synteny with human chromosome 20. Mammalian Genome. 5: 577-579. PMID 8000144 DOI: 10.1007/Bf00354934 |
0.411 |
|
| 1994 |
Abbott C, Chambers D. Analysis of CAG trinucleotide repeats from mouse cDNA sequences Annals of Human Genetics. 58: 87-94. PMID 7979162 DOI: 10.1111/J.1469-1809.1994.Tb01878.X |
0.459 |
|
| 1994 |
Breen M, Deakln L, Macdonald B, Miller S, Sibson R, Tarttelln E, Avner P, Bourgade F, Guenet J, Montagutelli X, Polrier C, Simon D, Tailor D, Bishop M, Kelly M, ... ... Abbott C, et al. Towards high resolution maps of the mouse and human genomes—a facility for ordering markers to 0.1 cM resolution Human Molecular Genetics. 3: 621-627. DOI: 10.1093/Hmg/3.4.621 |
0.401 |
|
| 1993 |
Pilz AJ, Povey S, Gruss P, Abbott CM. Mapping of the human homologs of the murine paired-box-containing genes. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 78-82. PMID 8431641 DOI: 10.1007/Bf00290430 |
0.453 |
|
| 1993 |
Abbott CM, Blank R, Eppig JT, Fiedorek FT, Frankel W, Friedman JM, Huppi KE, Jackson I, Steel K, Mock BA. Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 4. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: S58-71. PMID 8268685 DOI: 10.1007/Bf00360830 |
0.377 |
|
| 1993 |
Siracusa LD, Abbott CM. Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 2. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: S31-46. PMID 8268683 DOI: 10.1007/Bf00360828 |
0.377 |
|
| 1993 |
Pilz AJ, Abbott CM. Dinucleotide repeats in the mouse Hox-4.4 and Hox-4.5 genes on chromosome 2, and their analysis in the BXD and BXH recombinant inbred strains. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 129-30. PMID 8094302 DOI: 10.1007/Bf00290440 |
0.402 |
|
| 1993 |
Pilz A, Fountain J, Peters J, Abbott C. Linkage mapping of the aldo-2, pax-5, Ambp, and D4H9S3E loci on mouse chromosome 4 in the region of homology with human chromosome 9 Genomics. 18: 705-708. PMID 7508415 DOI: 10.1016/S0888-7543(05)80379-9 |
0.39 |
|
| 1992 |
Abbott C. Characterization of mouse-hamster somatic cell hybrids by PCR: a panel of mouse-specific primers for each chromosome. Mammalian Genome. 2: 106-109. PMID 1543905 DOI: 10.1007/Bf00353858 |
0.466 |
|
| 1992 |
Darling SM, Abbott CM. Mouse models of human single gene disorders. I: Nontransgenic mice. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 14: 359-66. PMID 1503552 DOI: 10.1002/Bies.950140602 |
0.404 |
|
| 1992 |
Pilz AJ, Willer E, Povey S, Abbott CM. The genes coding for phosphoenolpyruvate carboxykinase-1 (PCK1) and neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) map to human chromosome 20, extending the known region of homology with mouse chromosome 2. Annals of Human Genetics. 56: 289-93. PMID 1492743 DOI: 10.1111/J.1469-1809.1992.Tb01155.X |
0.42 |
|
| 1992 |
Pilz A, Tissier PL, Moseley H, Peters J, Abbott C. Mapping of the structural gene for S-adenosyl homocysteine hydrolase to mouse Chromosome 2, and related sequences to Chromosomes 8 and X Mammalian Genome. 3: 633-636. PMID 1450513 DOI: 10.1007/Bf00352480 |
0.449 |
|
| 1992 |
Povey S, Smith M, Haines J, Kwiatkowski D, Fountain J, Bale A, Abbott C, Jackson I, Lawrie M, Hultén M. Report and abstracts of the First International Workshop on Chromosome 9. Held at Girton College Cambridge, UK, 22-24 March, 1992. Annals of Human Genetics. 56: 167-82. PMID 1449236 DOI: 10.1111/J.1469-1809.1992.Tb01145.X |
0.359 |
|
| 1992 |
Pilz A, Moseley H, Peters J, Abbott C. Comparative mapping of mouse chromosome 4 and human chromosome 9: Lv, Orm, and Hxb are closely linked on mouse chromosome 4. Mammalian Genome. 3: 247-249. PMID 1379092 DOI: 10.1007/Bf00292151 |
0.45 |
|
| 1992 |
Douglas AJ, Fox MF, Abbott CM, Hinks LJ, Sharpe G, Povey S, Thompson RJ. Structure and chromosomal localization of the human 2',3'-cyclic nucleotide 3'-phosphodiesterase gene. Annals of Human Genetics. 56: 243-54. PMID 1360194 DOI: 10.1111/J.1469-1809.1992.Tb01149.X |
0.436 |
|
| 1992 |
Abbott C, Pilz A, Moseley H, Peter J. The gene for proliferating cell nuclear antigen (Pcna) maps to mouse chromosome 2. Mammalian Genome. 3: 286-289. PMID 1353383 DOI: 10.1007/Bf00292157 |
0.385 |
|
| 1992 |
Pilz A, Moseley H, Peters J, Abbott C. Comparative mapping of mouse chromosome 2 and human chromosome 9q : the genes for gelsolin and dopamine β-hydroxylase map to mouse chromosome 2 Genomics. 12: 715-719. PMID 1315305 DOI: 10.1016/0888-7543(92)90300-H |
0.424 |
|
| 1991 |
Abbott C, Povey S. Development of human chromosome-specific PCR primers for characterization of somatic cell hybrids. Genomics. 9: 73-77. PMID 2004769 DOI: 10.1016/0888-7543(91)90222-Z |
0.416 |
|
| 1991 |
Abbott CM, Evans EP, Burtenshaw M, Ball ST, Skidmore CJ, Jones J, Peters J. Adenosine deaminase, Ada, is in mouse chromosome 2H3, and is not allelic with wasted, wst. Biochemical Genetics. 29: 537-44. PMID 1820019 DOI: 10.1007/Bf02426869 |
0.317 |
|
| 1991 |
Abbott C, Jackson IJ, Carritt B, Povey S. The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4. Genomics. 11: 471-473. PMID 1769662 DOI: 10.1016/0888-7543(91)90160-G |
0.466 |
|
| 1991 |
Florian F, Hornigold N, Griffin DK, Delhanty JD, Sefton L, Abbott C, Jones C, Goodfellow PN, Wolfe J. The use of irradiation and fusion gene transfer (IFGT) hybrids to isolate DNA clones from human chromosome region 9q33-q34 Somatic Cell and Molecular Genetics. 17: 445-453. PMID 1763385 DOI: 10.1007/Bf01233168 |
0.383 |
|
| 1991 |
Tripodi M, Abbott C, Vivian N, Cortese R, Lovell-Badge R. Disruption of the LF-A1 and LF-B1 binding sites in the human alpha-1-antitrypsin gene has a differential effect during development in transgenic mice. The Embo Journal. 10: 3177-82. PMID 1717262 DOI: 10.1002/J.1460-2075.1991.Tb04879.X |
0.364 |
|
| 1990 |
Jeremiah SJ, Abbott CM, Murad Z, Povey S, Thomas HJ, Solomon E, DiScipio RG, Fey GH. The assignment of the genes coding for human complement components C6 and C7 to chromosome 5. Annals of Human Genetics. 54: 141-7. PMID 2382968 DOI: 10.1111/J.1469-1809.1990.Tb00370.X |
0.321 |
|
| 1990 |
Tripodi M, Perfumo S, Ali R, Amicone L, Abbott C, Cortese R. Generation of small mutation in large genomic fragments by homologous recombination: description of the technique and examples of its use. Nucleic Acids Research. 18: 6247-51. PMID 2243773 DOI: 10.1093/Nar/18.21.6247 |
0.312 |
|
| 1990 |
Abbott C, Piaggio G, Ammendola R, Solomon E, Povey S, Gounari F, Simone VD, Cortese R. Mapping of the gene TCF2 coding for the transcription factor LFB3 to human chromosome 17 by polymerase chain reaction. Genomics. 8: 165-167. PMID 2081590 DOI: 10.1016/0888-7543(90)90239-Q |
0.442 |
|
| 1989 |
Abbott C, West L, Povey S, Jeremiah S, Murad Z, DiScipio R, Fey G. The gene for human complement component C9 mapped to chromosome 5 by polymerase chain reaction. Genomics. 4: 606-609. PMID 2744767 DOI: 10.1016/0888-7543(89)90286-3 |
0.432 |
|
| 1989 |
Whitehouse DB, Abbott CM, Lovegrove JU, McIntosh I, McMahon CJ, Mieli-Vergani G, Mowat AP, Hopkinson DA. Genetic studies on a new deficiency gene (PI*Ztun) at the PI locus. Journal of Medical Genetics. 26: 744-9. PMID 2575668 DOI: 10.1136/Jmg.26.12.744 |
0.329 |
|
| 1986 |
Abbott CM, Skidmore CJ, Searle AG, Peters J. Deficiency of adenosine deaminase in the wasted mouse. Proceedings of the National Academy of Sciences of the United States of America. 83: 693-5. PMID 3456164 DOI: 10.1073/Pnas.83.3.693 |
0.358 |
|
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