Items where Salford Author is "Mukhopadhyay, A"
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Number of items: 14.
Article
Lal, M  ORCID: https://orcid.org/0000-0002-9235-7255, Ansari, AH ORCID: https://orcid.org/0000-0002-1172-9521, Agrawal, A and Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179
2021,
'Diagnostic and prognostic potential of MiR-379/656 MicroRNA cluster in molecular subtypes of breast cancer'
, Journal of Clinical Medicine, 10 (18)
, e4071.
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Paul, D, Ansari, AH, Lal, M and Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179
2020,
'Human brain shows recurrent non-canonical microRNA editing events enriched for seed sequence with possible functional consequence'
, Non-Coding RNA, 6 (2)
, e21.
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Tran, KT, Le, VS, Bui, HTP, Do, DH, Ly, HTT, Nguyen, HT, Dao, LTM, Nguyen, HT, Vu, DM, Ha, LT, Le, HTT, Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179 and Nguyen, LT
2020,
'Genetic landscape of autism spectrum disorder in Vietnamese children'
, Scientific Reports, 10 (1)
, p. 5034.
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Mehani, B, Narta, K, Paul, D, Raj, A, Kumar, D, Sharma, A, Kaurani, L, Nayak, S, Dash, D, Suri, A, Sarkar, C and Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179
2020,
'Fusion transcripts in normal human cortex increase with age and show distinct genomic features for single cells and tissues'
, Scientific Reports, 10 (1)
, p. 1368.
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Kumar, A, Nayak, S, Pathak, P, Purkait, S, Malgulawar, PB, Sharma, MC, Suri, V, Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179, Suri, A and Sarkar, C
2018,
'Identification of miR-379/miR-656 (C14MC) cluster downregulation and associated epigenetic and transcription regulatory mechanism in oligodendrogliomas'
, Journal of Neuro-Oncology, 139 (1)
, pp. 23-31.
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Nayak, S, Aich, M, Kumar, A, Sengupta, S, Bajad, P, Dhapola, P, Paul, D, Narta, K, Purkrait, S, Mehani, B, Suri, A, Chakraborty, D, Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179 and Sarkar, C
2018,
'Novel internal regulators and candidate miRNAs within miR-379/miR-656 miRNA cluster can alter cellular phenotype of human glioblastoma'
, Scientific Reports, 8 (2018)
, #7673.
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Paul, D, Sinha, AN, Ray, A, Lal, M, Nayak, S, Sharma, A, Mehani, B, Mukherjee, D, Laddha, SV, Suri, A, Sarkar, C and Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179
2017,
'A-to-I editing in human miRNAs is enriched in seed sequence, influenced by sequence contexts and significantly hypoedited in glioblastoma multiforme'
, Scientific Reports, 7 (2466)
.
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Sharma, A, Ansan, AH, Kumari, R, Pandey, R, Rehman, R, Mehani, B, Varma, B, Desiraju, BK, Mabalirajan, U, Agrawal, A and Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179
2017,
'Human brain harbors single nucleotide somatic variations in functionally relevant genes possibly mediated by oxidative stress'
, F1000Research, 5
, p. 2520.
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Kaurani, L, Vishal, M, Ray, J, Sen, A, Ray, K and Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179
2016,
'TBK1 duplication is found in normal tension and not in high tension glaucoma patients of Indian origin'
, Journal of Genetics, 95 (2)
, pp. 459-461.
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Vishal, M, Sharma, A, Kaurani, L, Alfano, G, Mookerjee, S, Narta, K, Agrawal, J, Bhattacharya, I, Roychoudhury, S, Ray, J, Waseem, NH, Bhattacharya, SS, Basu, A, Sen, A, Ray, K and Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179
2016,
'Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma'
, BMC Medical Genomics, 9 (15)
.
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Negi, V, Paul, D, Das, S, Bajpai, P, Singh, S, Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179, Agrawal, A and Ghosh, B
2015,
'Altered expression and editing of miRNA-100 regulates iTreg differentiation'
, Nucleic Acids Research, 43 (16)
, pp. 8057-8065.
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Vishal, M, Sharma, A, Kaurani, L, Chakraborty, S, Ray, J, Sen, A, Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179 and Ray, K
2014,
'Evaluation of genetic association of the INK4 locus with primary open
angle glaucoma in East Indian population'
, Scientific Reports, 4
, p. 5115.
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Kaurani, L, Vishal, M, Kumar, D, Sharma, A, Mehani, B, Sharma, C, Chakraborty, S, Jha, P, Ray, J, Sen, A, Dash, D, Ray, K and Mukhopadhyay, A ORCID: https://orcid.org/0000-0002-1089-7179
2014,
'Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian origins'
, Investigative Ophthalmology and Visual Sciences, 55 (5)
, pp. 3258-3264.
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Thesis
| Bui, H 2021, Investigation of de-novo copy number variants in patients with Autism Spectrum Disorder in Vietnam , PhD thesis, University of Salford. |
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