Követés
Nihar Bhattacharyya
Nihar Bhattacharyya
Post-doctoral fellow, University College London
E-mail megerősítve itt: mail.utoronto.ca
Cím
Hivatkozott rá
Hivatkozott rá
Év
Evolutionary transformation of rod photoreceptors in the all-cone retina of a diurnal garter snake
RK Schott, J Müller, CGY Yang, N Bhattacharyya, N Chan, M Xu, ...
Proceedings of the National Academy of Sciences 113 (2), 356-361, 2016
832016
Molecular adaptations for sensing and securing prey and insight into amniote genome diversity from the garter snake genome
BW Perry, DC Card, JW McGlothlin, GIM Pasquesi, RH Adams, ...
Genome Biology and Evolution 10 (8), 2110-2129, 2018
792018
TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease
MP Fautsch, ED Wieben, KH Baratz, N Bhattacharyya, AN Sadan, ...
Progress in retinal and eye research 81, 100883, 2021
522021
Cone-like rhodopsin expressed in the all-cone retina of the colubrid pine snake as a potential adaptation to diurnality
N Bhattacharyya, B Darren, RK Schott, V Tropepe, BSW Chang
Journal of Experimental Biology 220 (13), 2418-2425, 2017
392017
Evolution of nonspectral rhodopsin function at high altitudes
GM Castiglione, FE Hauser, BS Liao, NK Lujan, A Van Nynatten, ...
Proceedings of the National Academy of Sciences 114 (28), 7385-7390, 2017
352017
Modulation of thermal noise and spectral sensitivity in Lake Baikal cottoid fish rhodopsins
HL Luk, N Bhattacharyya, F Montisci, JM Morrow, F Melaccio, A Wada, ...
Scientific Reports 6 (1), 38425, 2016
352016
Evolutionary signatures of photoreceptor transmutation in geckos reveal potential adaptation and convergence with snakes
RK Schott, N Bhattacharyya, BSW Chang
Evolution 73 (9), 1958-1971, 2019
262019
An experimental comparison of human and bovine rhodopsin provides insight into the molecular basis of retinal disease
JM Morrow, GM Castiglione, SZ Dungan, PL Tang, N Bhattacharyya, ...
FEBS letters 591 (12), 1720-1731, 2017
212017
Coupling of human rhodopsin to a yeast signaling pathway enables characterization of mutations associated with retinal disease
BM Scott, SK Chen, N Bhattacharyya, AY Moalim, SV Plotnikov, E Heon, ...
Genetics 211 (2), 597-615, 2019
172019
Sortilin and prosaposin localize to detergent-resistant membrane microdomains
M Canuel, N Bhattacharyya, A Balbis, L Yuan, CR Morales
Experimental cell research 315 (2), 240-247, 2009
172009
Simultaneous expression of UV and violet SWS1 opsins expands the visual palette in a group of freshwater snakes
E Hauzman, MER Pierotti, N Bhattacharyya, JH Tashiro, CAM Yovanovich, ...
Molecular Biology and Evolution 38 (12), 5225-5240, 2021
32021
Convergent evolution of dim light vision in owls and deep-diving whales
GM Castiglione, YLI Chiu, EA Gutierrez, A Van Nynatten, FE Hauser, ...
Current Biology 33 (21), 4733-4740. e4, 2023
22023
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease
N Bhattacharyya, N Chai, NJ Hafford-Tear, AN Sadan, A Szabo, ...
bioRxiv, 2023.03. 29.534731, 2023
12023
Tissue-Specific Dynamics of TCF4 Triplet Repeat Instability Revealed by Optical Genome Mapping
C Zarouchlioti, S Efthymiou, S Fracchini, N Dominik, N Bhattacharyya, ...
bioRxiv, 2024.03. 27.587034, 2024
2024
Genetically refined and unsolved inherited corneal disease cohort offers opportunities for novel genomic discovery
MA Costa, A Szabo, N Bhattacharyya, C Zarouchlioti, N Hafford-Tear, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 373-374, 2024
2024
Deciphering novel TCF4-driven molecular origins and mechanisms underlying a common triplet repeat expansion-mediated disease
N Bhattacharyya, N Hafford-Tear, A Sadan, A Szabo, N Chai, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 375-375, 2024
2024
Utilising a CTG18. 1 expansion-negative Fuchs endothelial corneal dystrophy cohort to identify novel genetic risk loci
A Szabo, C Zarouchlioti, N Bhattacharyya, A Sadan, N Hafford-Tear, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 791-791, 2024
2024
CTG18. 1-mediated Fuchs endothelial corneal dystrophy: characterizing biomarkers of pathogenicity in patients with rare intermediate triplet repeat expansions
N Bhattacharyya, A Sadan, C Zarouchlioti, NJ Hafford-Tear, K Muthusamy, ...
Investigative Ophthalmology & Visual Science 63 (7), 1588–A0377-1588–A0377, 2022
2022
A refined amplification-free long-read sequencing method to interrogate TCF4 triplet repeats associated with Fuchs endothelial corneal dystrophy
C Zarouchlioti, NJ Hafford-Tear, YC Tsai, A Szabo, N Bhattacharyya, ...
Investigative Ophthalmology & Visual Science 63 (7), 2-2, 2022
2022
CTG18. 1-mediated Fuchs Endothelial Corneal Dystrophy: defining signatures of transcriptomic dysregulation in a common repeat-mediated disease
N Bhattacharyya, NJ Hafford-Tear, AN Sadan, C Zarouchlioti, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 44-44, 2022
2022
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