| Year |
Citation |
Score |
| 2020 |
Kulkarni CA, Nadtochiy SM, Kennedy L, Zhang J, Chhim S, Alwaseem H, Murphy E, Fu D, Brookes PS. ALKBH7 mediates necrosis via rewiring of glyoxal metabolism. Elife. 9. PMID 32795389 DOI: 10.7554/Elife.58573 |
0.304 |
|
| 2020 |
Ramos J, Proven M, Halvardson J, Hagelskamp F, Kuchinskaya E, Phelan B, Bell R, Kellner S, Feuk L, Thuresson AC, Fu D. Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorder. Rna (New York, N.Y.). PMID 32763916 DOI: 10.1261/Rna.076380.120 |
0.392 |
|
| 2020 |
Lentini JM, Alsaif HS, Faqeih E, Alkuraya FS, Fu D. DALRD3 encodes a protein mutated in epileptic encephalopathy that targets arginine tRNAs for 3-methylcytosine modification. Nature Communications. 11: 2510. PMID 32427860 DOI: 10.1038/S41467-020-16321-6 |
0.385 |
|
| 2020 |
Zhang K, Lentini JM, Prevost CT, Hashem MO, Alkuraya FS, Fu D. An intellectual disability-associated missense variant in TRMT1 impairs tRNA modification and reconstitution of enzymatic activity. Human Mutation. PMID 31898845 DOI: 10.1002/Humu.23976 |
0.351 |
|
| 2019 |
Shaheen R, Mark P, Prevost CT, AlKindi A, Alhag A, Estwani F, Al-Sheddi T, Alobeid E, Alenazi MM, Ewida N, Ibrahim N, Hashem M, Abdulwahab F, Bryant EM, Spinelli E, ... ... Fu D, et al. Biallelic Variants in CTU2 Cause DREAM-PL Syndrome and Impair Thiolation of tRNA Wobble U34. Human Mutation. PMID 31301155 DOI: 10.1002/Humu.23870 |
0.34 |
|
| 2019 |
Ramos J, Han L, Li Y, Hagelskamp F, Kellner SM, Alkuraya FS, Phizicky EM, Fu D. Formation of tRNA wobble inosine in humans is disrupted by a millennia-old mutation causing intellectual disability. Molecular and Cellular Biology. PMID 31263000 DOI: 10.1128/Mcb.00203-19 |
0.359 |
|
| 2018 |
Ramos J, Fu D. The emerging impact of tRNA modifications in the brain and nervous system. Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms. PMID 30529455 DOI: 10.1016/J.Bbagrm.2018.11.007 |
0.312 |
|
| 2018 |
Lentini JM, Ramos J, Fu D. Monitoring the 5-methoxycarbonylmethyl-2-thiouridine (mcm5s2U) modification in eukaryotic tRNAs via the gamma-toxin endonuclease. Rna (New York, N.Y.). PMID 29440318 DOI: 10.1261/Rna.065581.118 |
0.33 |
|
| 2018 |
Padgett LR, Lentini JM, Holmes MJ, Stilger KL, Fu D, Sullivan WJ. Elp3 and RlmN: A tale of two mitochondrial tail-anchored radical SAM enzymes in Toxoplasma gondii. Plos One. 13: e0189688. PMID 29293520 DOI: 10.1371/Journal.Pone.0189688 |
0.362 |
|
| 2017 |
Dewe JM, Fuller BL, Lentini JM, Kellner SM, Fu D. TRMT1-catalyzed tRNA modifications are required for redox homeostasis to ensure proper cellular proliferation and oxidative stress survival. Molecular and Cellular Biology. PMID 28784718 DOI: 10.1128/Mcb.00214-17 |
0.377 |
|
| 2017 |
Jordan JJ, Chhim S, Margulies CM, Allocca M, Bronson RT, Klungland A, Samson LD, Fu D. ALKBH7 drives a tissue and sex-specific necrotic cell death response following alkylation-induced damage. Cell Death & Disease. 8: e2947. PMID 28726787 DOI: 10.1038/Cddis.2017.343 |
0.569 |
|
| 2015 |
Fu D, Samson LD, Hübscher U, van Loon B. The interaction between ALKBH2 DNA repair enzyme and PCNA is direct, mediated by the hydrophobic pocket of PCNA and perturbed in naturally-occurring ALKBH2 variants. Dna Repair. 35: 13-18. PMID 26408825 DOI: 10.1016/J.Dnarep.2015.09.008 |
0.542 |
|
| 2013 |
Fu D, Jordan JJ, Samson LD. Human ALKBH7 is required for alkylation and oxidation-induced programmed necrosis. Genes & Development. 27: 1089-100. PMID 23666923 DOI: 10.1101/Gad.215533.113 |
0.592 |
|
| 2012 |
Fu D, Calvo JA, Samson LD. Balancing repair and tolerance of DNA damage caused by alkylating agents. Nature Reviews. Cancer. 12: 104-20. PMID 22237395 DOI: 10.1038/Nrc3185 |
0.626 |
|
| 2012 |
Fu D, Samson LD. Direct repair of 3,N(4)-ethenocytosine by the human ALKBH2 dioxygenase is blocked by the AAG/MPG glycosylase. Dna Repair. 11: 46-52. PMID 22079122 DOI: 10.1016/J.Dnarep.2011.10.004 |
0.64 |
|
| 2010 |
Fu D, Brophy JA, Chan CT, Atmore KA, Begley U, Paules RS, Dedon PC, Begley TJ, Samson LD. Human AlkB homolog ABH8 Is a tRNA methyltransferase required for wobble uridine modification and DNA damage survival. Molecular and Cellular Biology. 30: 2449-59. PMID 20308323 DOI: 10.1128/Mcb.01604-09 |
0.693 |
|
| 2008 |
Errington TM, Fu D, Wong JM, Collins K. Disease-associated human telomerase RNA variants show loss of function for telomere synthesis without dominant-negative interference. Molecular and Cellular Biology. 28: 6510-20. PMID 18710936 DOI: 10.1128/Mcb.00777-08 |
0.597 |
|
| 2007 |
Fu D, Collins K. Purification of human telomerase complexes identifies factors involved in telomerase biogenesis and telomere length regulation. Molecular Cell. 28: 773-85. PMID 18082603 DOI: 10.1016/J.Molcel.2007.09.023 |
0.556 |
|
| 2006 |
Fu D, Collins K. Human telomerase and Cajal body ribonucleoproteins share a unique specificity of Sm protein association. Genes & Development. 20: 531-6. PMID 16481465 DOI: 10.1101/Gad.1390306 |
0.495 |
|
| 2003 |
Fu D, Collins K. Distinct biogenesis pathways for human telomerase RNA and H/ACA small nucleolar RNAs. Molecular Cell. 11: 1361-72. PMID 12769858 DOI: 10.1016/S1097-2765(03)00196-5 |
0.498 |
|
| 2001 |
Xiao H, Sandaltzopoulos R, Wang HM, Hamiche A, Ranallo R, Lee KM, Fu D, Wu C. Dual functions of largest NURF subunit NURF301 in nucleosome sliding and transcription factor interactions Molecular Cell. 8: 531-543. PMID 11583616 DOI: 10.1016/S1097-2765(01)00345-8 |
0.543 |
|
| 2000 |
Payne WE, Kaiser CA, Bevis BJ, Soderholm J, Fu D, Sears IB, Glick BS. Identification of YPDI, a gene of Candida albicans which encodes a two-component phosphohistidine intermediate protein Yeast. 16: 1053-1059. PMID 10923027 DOI: 10.1002/1097-0061(200008)16:11<1053::Aid-Yea598>3.0.Co;2-H |
0.472 |
|
| 2000 |
Payne WE, Kaiser CA, Bevis BJ, Soderholm J, Fu D, Sears IB, Glick BS. Isolation of Pichia pastoris genes involved in ER-to-Golgi transport. Yeast (Chichester, England). 16: 979-93. PMID 10923020 DOI: 10.1002/1097-0061(200008)16:11<979::Aid-Yea594>3.0.Co;2-C |
0.5 |
|
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