| Year |
Citation |
Score |
| 2022 |
Rodden LN, Gilliam KM, Lam C, Rojsajjakul T, Mesaros C, Dionisi C, Pook M, Pandolfo M, Lynch DR, Blair IA, Bidichandani SI. DNA methylation in Friedreich ataxia silences expression of frataxin isoform E. Scientific Reports. 12: 5031. PMID 35322126 DOI: 10.1038/s41598-022-09002-5 |
0.306 |
|
| 2021 |
Rodden LN, Gilliam KM, Lam C, Lynch DR, Bidichandani SI. Epigenetic Heterogeneity in Friedreich Ataxia Underlies Variable Reactivation. Frontiers in Neuroscience. 15: 752921. PMID 34899161 DOI: 10.3389/fnins.2021.752921 |
0.303 |
|
| 2021 |
Rodden LN, Chutake YK, Gilliam K, Lam C, Soragni E, Hauser L, Gilliam M, Wiley G, Anderson MP, Gottesfeld JM, Lynch DR, Bidichandani SI. Methylated and unmethylated epialleles support variegated epigenetic silencing in Friedreich ataxia. Human Molecular Genetics. PMID 33432325 DOI: 10.1093/hmg/ddaa267 |
0.792 |
|
| 2016 |
Chutake YK, Lam CC, Costello WN, Anderson MP, Bidichandani SI. Reversal of epigenetic promoter silencing in Friedreich ataxia by a class I histone deacetylase inhibitor. Nucleic Acids Research. PMID 26896803 DOI: 10.1093/Nar/Gkw107 |
0.798 |
|
| 2015 |
Chutake YK, Costello WN, Lam CC, Parikh AC, Hughes TT, Michalopulos MG, Pook MA, Bidichandani SI. FXN Promoter Silencing in the Humanized Mouse Model of Friedreich Ataxia. Plos One. 10: e0138437. PMID 26393353 DOI: 10.1371/Journal.Pone.0138437 |
0.801 |
|
| 2014 |
Chutake YK, Lam C, Costello WN, Anderson M, Bidichandani SI. Epigenetic promoter silencing in Friedreich ataxia is dependent on repeat length. Annals of Neurology. 76: 522-8. PMID 25112975 DOI: 10.1002/Ana.24249 |
0.801 |
|
| 2014 |
Chutake YK, Costello WN, Lam C, Bidichandani SI. Altered nucleosome positioning at the transcription start site and deficient transcriptional initiation in Friedreich ataxia. The Journal of Biological Chemistry. 289: 15194-202. PMID 24737321 DOI: 10.1074/Jbc.M114.566414 |
0.81 |
|
| 2012 |
Bourn RL, De Biase I, Pinto RM, Sandi C, Al-Mahdawi S, Pook MA, Bidichandani SI. Pms2 suppresses large expansions of the (GAA·TTC)n sequence in neuronal tissues. Plos One. 7: e47085. PMID 23071719 DOI: 10.1371/Journal.Pone.0047085 |
0.779 |
|
| 2011 |
Rindler PM, Bidichandani SI. Role of transcript and interplay between transcription and replication in triplet-repeat instability in mammalian cells. Nucleic Acids Research. 39: 526-35. PMID 20843782 DOI: 10.1093/Nar/Gkq788 |
0.411 |
|
| 2011 |
Bidichandani S, Castro A, Chutake Y. RNA-mediated transcriptional gene silencing in Friedreich ataxia Current Opinion in Biotechnology. 22: S16. DOI: 10.1016/J.Copbio.2011.05.010 |
0.759 |
|
| 2009 |
De Biase I, Chutake YK, Rindler PM, Bidichandani SI. Epigenetic silencing in Friedreich ataxia is associated with depletion of CTCF (CCCTC-binding factor) and antisense transcription. Plos One. 4: e7914. PMID 19956589 DOI: 10.1371/Journal.Pone.0007914 |
0.806 |
|
| 2009 |
Bourn RL, Rindler PM, Pollard LM, Bidichandani SI. E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA.TTC)(n) sequence. Mutation Research. 661: 71-7. PMID 19046977 DOI: 10.1016/J.Mrfmmm.2008.11.003 |
0.783 |
|
| 2008 |
Pollard LM, Bourn RL, Bidichandani SI. Repair of DNA double-strand breaks within the (GAA*TTC)n sequence results in frequent deletion of the triplet-repeat sequence. Nucleic Acids Research. 36: 489-500. PMID 18045804 DOI: 10.1093/Nar/Gkm1066 |
0.767 |
|
| 2007 |
Pollard LM, Chutake YK, Rindler PM, Bidichandani SI. Deficiency of RecA-dependent RecFOR and RecBCD pathways causes increased instability of the (GAA*TTC)n sequence when GAA is the lagging strand template. Nucleic Acids Research. 35: 6884-94. PMID 17932052 DOI: 10.1093/Nar/Gkm810 |
0.758 |
|
| 2007 |
De Biase I, Rasmussen A, Monticelli A, Al-Mahdawi S, Pook M, Cocozza S, Bidichandani SI. Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life. Genomics. 90: 1-5. PMID 17498922 DOI: 10.1016/j.ygeno.2007.04.001 |
0.312 |
|
| 2007 |
De Biase I, Rasmussen A, Endres D, Al-Mahdawi S, Monticelli A, Cocozza S, Pook M, Bidichandani SI. Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients. Annals of Neurology. 61: 55-60. PMID 17262846 DOI: 10.1002/ana.21052 |
0.309 |
|
| 2007 |
Clark RM, De Biase I, Malykhina AP, Al-Mahdawi S, Pook M, Bidichandani SI. The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model. Human Genetics. 120: 633-40. PMID 17024371 DOI: 10.1007/s00439-006-0249-3 |
0.339 |
|
| 2006 |
M Rindler P, Clark RM, Pollard LM, De Biase I, Bidichandani SI. Replication in mammalian cells recapitulates the locus-specific differences in somatic instability of genomic GAA triplet-repeats. Nucleic Acids Research. 34: 6352-61. PMID 17142224 DOI: 10.1093/Nar/Gkl846 |
0.77 |
|
| 2006 |
Clark RM, Bhaskar SS, Miyahara M, Dalgliesh GL, Bidichandani SI. Expansion of GAA trinucleotide repeats in mammals. Genomics. 87: 57-67. PMID 16316739 DOI: 10.1016/j.ygeno.2005.09.006 |
0.306 |
|
| 2004 |
Pollard LM, Sharma R, Gómez M, Shah S, Delatycki MB, Pianese L, Monticelli A, Keats BJ, Bidichandani SI. Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia. Nucleic Acids Research. 32: 5962-71. PMID 15534367 DOI: 10.1093/Nar/Gkh933 |
0.766 |
|
| 2004 |
Potaman VN, Oussatcheva EA, Lyubchenko YL, Shlyakhtenko LS, Bidichandani SI, Ashizawa T, Sinden RR. Length-dependent structure formation in Friedreich ataxia (GAA)n*(TTC)n repeats at neutral pH. Nucleic Acids Research. 32: 1224-31. PMID 14978261 DOI: 10.1093/Nar/Gkh274 |
0.33 |
|
| 2004 |
Clark RM, Dalgliesh GL, Endres D, Gomez M, Taylor J, Bidichandani SI. Expansion of GAA triplet repeats in the human genome: unique origin of the FRDA mutation at the center of an Alu. Genomics. 83: 373-83. PMID 14962663 DOI: 10.1016/j.ygeno.2003.09.001 |
0.363 |
|
| 2002 |
Sharma R, Bhatti S, Gomez M, Clark RM, Murray C, Ashizawa T, Bidichandani SI. The GAA triplet-repeat sequence in Friedreich ataxia shows a high level of somatic instability in vivo, with a significant predilection for large contractions. Human Molecular Genetics. 11: 2175-87. PMID 12189170 DOI: 10.1093/Hmg/11.18.2175 |
0.372 |
|
| 2002 |
Hai M, Bidichandani SI, Hogan ME, Patel PI. Competitive binding of triplex-forming oligonucleotides in the two alternate promoters of the PMP22 gene. Antisense & Nucleic Acid Drug Development. 11: 233-46. PMID 11572600 DOI: 10.1089/108729001317022232 |
0.75 |
|
| 2001 |
Hai M, Bidichandani SI, Patel PI. Identification of a positive regulatory element in the myelin-specific promoter of the PMP22 gene. Journal of Neuroscience Research. 65: 508-19. PMID 11550219 DOI: 10.1002/Jnr.1181 |
0.759 |
|
| 2000 |
Désarnaud F, Bidichandani S, Patel PI, Baulieu EE, Schumacher M. Glucocorticosteroids stimulate the activity of the promoters of peripheral myelin protein-22 and protein zero genes in Schwann cells. Brain Research. 865: 12-6. PMID 10814728 DOI: 10.1016/S0006-8993(00)02130-2 |
0.584 |
|
| 2000 |
Bidichandani SI, Garcia CA, Patel PI, Dimachkie MM. Very late-onset Friedreich ataxia despite large GAA triplet repeat expansions. Archives of Neurology. 57: 246-51. PMID 10681084 DOI: 10.1001/Archneur.57.2.246 |
0.6 |
|
| 2000 |
Bidichandani SI, Purandare SM, Taylor EE, Gumin G, Machkhas H, Harati Y, Gibbs RA, Ashizawa T, Patel PI. Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence. Human Molecular Genetics. 8: 2425-36. PMID 10556290 DOI: 10.1093/Hmg/8.13.2425 |
0.666 |
|
| 1998 |
Machkhas H, Bidichandani SI, Patel PI, Harati Y. A mild case of Friedreich ataxia: lymphocyte and sural nerve analysis for GAA repeat length reveals somatic mosaicism. Muscle & Nerve. 21: 390-3. PMID 9486868 DOI: 10.1002/(Sici)1097-4598(199803)21:3<390::Aid-Mus13>3.0.Co;2-3 |
0.557 |
|
| 1998 |
Bidichandani SI, Ashizawa T, Patel PI. The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure. American Journal of Human Genetics. 62: 111-21. PMID 9443873 DOI: 10.1086/301680 |
0.64 |
|
| 1998 |
Bidichandani SI, Baldini A, Patel PI. Reply to Callen The American Journal of Human Genetics. 63: 270. DOI: 10.1086/301938 |
0.538 |
|
| 1996 |
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, et al. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science (New York, N.Y.). 271: 1423-7. PMID 8596916 DOI: 10.1126/Science.271.5254.1423 |
0.553 |
|
| 1995 |
Bidichandani SI, Lanyon WG, Shiach CR, Lowe GD, Connor JM. Detection of mutations in ectopic factor VIII transcripts from nine haemophilia A patients and the correlation with phenotype. Human Genetics. 95: 531-8. PMID 7759074 DOI: 10.1007/BF00223865 |
0.377 |
|
| 1994 |
Tuddenham EG, Schwaab R, Seehafer J, Millar DS, Gitschier J, Higuchi M, Bidichandani S, Connor JM, Hoyer LW, Yoshioka A. Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. Nucleic Acids Research. 22: 3511-33. PMID 7937051 DOI: 10.1093/Nar/22.17.3511 |
0.385 |
|
| 1994 |
Bidichandani SI, Lanyon WG, Connor JM. Characterisation of a 5-bp deletion in exon 4 of the factor VIII gene: concordance with slipped-mispairing at DNA replication. Human Genetics. 94: 447-9. PMID 7927348 DOI: 10.1007/BF00201612 |
0.38 |
|
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