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Rohini Desetty
Rohini Desetty
Research Scientist I, Geisinger medical center
Verified email at geisinger.edu
Title
Cited by
Cited by
Year
Mutations of the SLX4 gene in Fanconi anemia
Y Kim, FP Lach, R Desetty, H Hanenberg, AD Auerbach, ...
Nature genetics 43 (2), 142-146, 2011
3902011
A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair
A Smogorzewska, R Desetty, TT Saito, M Schlabach, FP Lach, ME Sowa, ...
Molecular cell 39 (1), 36-47, 2010
3832010
Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegia
A Schaller, R Desetty, D Hahn, CB Jackson, JM Nuoffer, S Gallati, ...
Mitochondrion 11 (3), 488-496, 2011
242011
Dilated cardiomyopathy mutation in the converter domain of human cardiac myosin alters motor activity and response to omecamtiv mecarbil
W Tang, WC Unrath, R Desetty, CM Yengo
Journal of Biological Chemistry 294 (46), 17314-17325, 2019
202019
Isolation and heterologous expression of PHA synthesising genes from Bacillus thuringiensis R1
RD Desetty, VS Mahajan, BM Khan, SK Rawal
World Journal of Microbiology and Biotechnology 24, 1769-1774, 2008
162008
Cardiomyopathy mutations impact the actin-activated power stroke of human cardiac myosin
W Tang, J Ge, WC Unrath, R Desetty, CM Yengo
Biophysical journal 120 (11), 2222-2236, 2021
142021
Dilated cardiomyopathy mutation E525K in human beta-cardiac myosin stabilizes the interacting heads motif and super-relaxed state of myosin
DV Rasicci, P Tiwari, R Desetty, F Sadler, S Sivaramakrishnan, RW Craig, ...
Biophysical Journal 121 (3), 260a, 2022
122022
Effect of changes in the flexible arm on tRNase Z processing kinetics
L Levinger, A Hopkinson, R Desetty, C Wilson
Journal of biological chemistry 284 (23), 15685-15691, 2009
102009
Colaiá covo, MP, and Elledge, SJ (2010). A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair
A Smogorzewska, R Desetty, TT Saito, M Schlabach, FP Lach, ME Sowa, ...
Mol. Cell 39, 36-47, 0
7
Deafness mutation in the MYO3A motor domain impairs actin protrusion elongation mechanism
LK Gunther, JA Cirilo Jr, R Desetty, CM Yengo
Molecular biology of the cell 33 (1), ar5, 2022
22022
Dilated cardiomyopathy mutation in beta-cardiac myosin enhances actin activation of the power stroke and phosphate release
SML Bodt, J Ge, W Ma, DV Rasicci, R Desetty, JA McCammon, CM Yengo
bioRxiv, 2023
12023
Dilated cardiomyopathy mutation (E525K) in human beta-cardiac myosin enhances actin-activated phosphate release but stabilizes the auto-inhibited super-relaxed state
SML Bodt, DV Rasicci, R Desetty, CM Yengo
Biophysical journal 122 (3), 259a, 2023
2023
Switch I and Switch II Mutants Differentially Impact the Recovery Stroke in Myosin V
LK Gunther, R Desetty, CM Yengo
Biophysical Journal 120 (3), 344a, 2021
2021
Cardiomyopathy Mutations Impact the Power Stroke of Human Cardiac Myosin
W Tang, J Ge, WC Unrath, R Desetty, CM Yengo
bioRxiv, 2020.12. 08.416511, 2020
2020
Impact of Regulatory Light Chain Mutation (K104E) on the Atpase and Motor Properties of Human Cardiac Myosin
D Rasicci, O Kirkland, W Tang, R Desetty, CM Yengo
Biophysical Journal 118 (3), 425a, 2020
2020
Impact of Human Beta-Cardiac Myosin Mutation Implicated in Both Hypertrophic and Dilated Cardiomyopathy
W Tang, LK Gunther, J Cooper, R Desetty, CM Yengo
Biophysical Journal 116 (3), 263a-264a, 2019
2019
Impact of Dilated Cardiomyopathy Mutation and Small Molecule Regulator on Human Beta-Cardiac Myosin
W Tang, WC Unrath, R Desetty, CM Yengo
Biophysical Journal 114 (3), 496a, 2018
2018
Impairment of mitochondrial tRNAᴵˡᵉ processing by a novel mutation associated with chronic progressive external ophthalmoplegia
A Schaller, R Desetty, D Hahn, CB Jackson, JM Nuoffer, S Gallati, ...
Mitochondrion 11 (3), 2011
2011
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