Sanjay Bidichandani - Publications

Affiliations: 
University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States 
Area:
Molecular Biology, Genetics

35 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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  0.585
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  0.601
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  0.667
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  0.558
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  0.554
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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