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2022
George A, Ravi NSam, Prasad K, Panigrahi L, Koikkara S, Rajendiran V, Devaraju N, Paul J, Pai AAnand, Nakamura Y, Kurita R, Balasubramanian P, Thangavel S, Marepally S, Velayudhan SR, Srivastava A, Mohankumar KM.  2022.  Efficient and error-free correction of sickle mutation in human erythroid cells using prime editor-2.. Front Genome Ed. 4:1085111. DOI:10.3389/fgeed.2022.1085111.
Bagchi A, Devaraju N, Chambayil K, Rajendiran V, Venkatesan V, Sayed N, Pai AAnand, Nath A, David E, Nakamura Y, Balasubramanian P, Srivastava A, Thangavel S, Mohankumar KM, Velayudhan SR.  2022.  Erythroid lineage-specific lentiviral RNAi vectors suitable for molecular functional studies and therapeutic applications.. Sci Rep. 12(1):14033. DOI:10.1038/s41598-022-13783-0.
Bagchi A, Devaraju N, Chambayil K, Rajendiran V, Venkatesan V, Sayed N, Pai AAnand, Nath A, David E, Nakamura Y, Balasubramanian P, Srivastava A, Thangavel S, Mohankumar KM, Velayudhan SR.  2022.  Erythroid lineage-specific lentiviral RNAi vectors suitable for molecular functional studies and therapeutic applications.. Sci Rep. 12(1):14033. DOI:10.1038/s41598-022-13783-0.
D'Souza MNinochka, Ramakrishna S, Radhakrishna BK, Jhaveri V, Ravindran S, Yeramala L, Nair D, Palakodeti D, Muddashetty RS.  2022.  Function of FMRP Domains in Regulating Distinct Roles of Neuronal Protein Synthesis.. Mol Neurobiol. 59(12):7370-7392. DOI:10.1007/s12035-022-03049-1.
Ravi NSam, Wienert B, Wyman SK, Bell HWilliam, George A, Mahalingam G, Vu JT, Prasad K, Bandlamudi BPrasad, Devaraju N, Rajendiran V, Syedbasha N, Pai AAnand, Nakamura Y, Kurita R, Narayanasamy M, Balasubramanian P, Thangavel S, Marepally S, Velayudhan SR et al..  2022.  Identification of novel HPFH-like mutations by CRISPR base editing that elevate the expression of fetal hemoglobin.. Elife. 11 DOI:10.7554/eLife.65421.
Ravi NSam, Wienert B, Wyman SK, Bell HWilliam, George A, Mahalingam G, Vu JT, Prasad K, Bandlamudi BPrasad, Devaraju N, Rajendiran V, Syedbasha N, Pai AAnand, Nakamura Y, Kurita R, Narayanasamy M, Balasubramanian P, Thangavel S, Marepally S, Velayudhan SR et al..  2022.  Identification of novel HPFH-like mutations by CRISPR base editing that elevate the expression of fetal hemoglobin.. Elife. 11 DOI:10.7554/eLife.65421.
Saini N, Naaz A, Metur SPadma, Gahlot P, Walvekar A, Dutta A, Davathamizhan U, Sarin A, Laxman S.  2022.  Methionine uptake via the SLC43A2 transporter is essential for regulatory T-cell survival.. Life Sci Alliance. 5(12) DOI:10.26508/lsa.202201663.
Badnikar K, Jayadevi SNataraja, Pahal S, Vemula PKumar, Nayak MManjunatha, Subramanyam DNarasimhai.  2022.  Microscale engineering of hollow microneedle tips: design, manufacturing, optimization and validation.. Drug Deliv Transl Res. 12(2):350-367. DOI:10.1007/s13346-021-01062-w.
Ghosh S, Mondal S, Yadav K, Aggarwal S, Schaefer WF, Narayana C, Subramanian R.  2022.  Modulation of biliverdin dynamics and spectral properties by Sandercyanin.. RSC Adv. 12(31):20296-20304. DOI:10.1039/d2ra02880h.
Gowda NKumar Chan, Nawalpuri B, Ramakrishna S, Jhaveri V, Muddashetty RS.  2022.  NMDAR mediated dynamic changes in mA inversely correlates with neuronal translation.. Sci Rep. 12(1):11317. DOI:10.1038/s41598-022-14798-3.
Rani DSelvi, Kumar AVijaya, Nallari P, Sampathkumar K, Dhandapany PS, Narasimhan C, Rathinavel A, Thangaraj K.  2022.  Novel Mutations in β- Gene in Indian Patients With Dilated Cardiomyopathy.. CJC Open. 4(1):1-11. DOI:10.1016/j.cjco.2021.07.020.
Rani DSelvi, Kumar AVijaya, Nallari P, Sampathkumar K, Dhandapany PS, Narasimhan C, Rathinavel A, Thangaraj K.  2022.  Novel Mutations in β- Gene in Indian Patients With Dilated Cardiomyopathy.. CJC Open. 4(1):1-11. DOI:10.1016/j.cjco.2021.07.020.
Ghate V, Renjith A, Badnikar K, Pahal S, Jayadevi SN, Nayak MM, Vemula PK, Subramanyam DN.  2022.  Single step fabrication of hollow microneedles and an experimental package for controlled drug delivery.. Int J Pharm. 632:122546. DOI:10.1016/j.ijpharm.2022.122546.
Lesurf R, Said A, Akinrinade O, Breckpot J, Delfosse K, Liu T, Yao R, Persad G, McKenna F, Noche RR, Oliveros W, Mattioli K, Shah S, Miron A, Yang Q, Meng G, Yue MChan Seng, Sung WWL, Thiruvahindrapuram B, Lougheed J et al..  2022.  Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy.. NPJ Genom Med. 7(1):18. DOI:10.1038/s41525-022-00288-y.
2021
Mahadevan J, Pathak AKumar, Vemula A, Nadella RKumar, Viswanath B, Jain S, Purushottam M, Mondal M.  2021.  Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genes.. Sci Rep. 11(1):21088. DOI:10.1038/s41598-021-00123-x.
Ramakrishna S, Jhaveri V, Konings SC, Nawalpuri B, Chakraborty S, Holst B, Schmid B, Gouras GK, Freude KK, Muddashetty RS.  2021.  APOE4 Affects Basal and NMDAR-Mediated Protein Synthesis in Neurons by Perturbing Calcium Homeostasis.. J Neurosci. 41(42):8686-8709. DOI:10.1523/JNEUROSCI.0435-21.2021.
Chandrasekaran A, Dittlau KStoklund, Corsi GI, Haukedal H, Doncheva NT, Ramakrishna S, Ambardar S, Salcedo C, Schmidt SI, Zhang Y, Cirera S, Pihl M, Schmid B, Nielsen TTolstrup, Nielsen JE, Kolko M, Kobolák J, Dinnyés A, Hyttel P, Palakodeti D et al..  2021.  Astrocytic reactivity triggered by defective autophagy and metabolic failure causes neurotoxicity in frontotemporal dementia type 3.. Stem Cell Reports. 16(11):2736-2751. DOI:10.1016/j.stemcr.2021.09.013.
Chandrasekaran A, Dittlau KStoklund, Corsi GI, Haukedal H, Doncheva NT, Ramakrishna S, Ambardar S, Salcedo C, Schmidt SI, Zhang Y, Cirera S, Pihl M, Schmid B, Nielsen TTolstrup, Nielsen JE, Kolko M, Kobolák J, Dinnyés A, Hyttel P, Palakodeti D et al..  2021.  Astrocytic reactivity triggered by defective autophagy and metabolic failure causes neurotoxicity in frontotemporal dementia type 3.. Stem Cell Reports. 16(11):2736-2751. DOI:10.1016/j.stemcr.2021.09.013.
Lakshmanan V, N ST, Bansal D, Padubidri SV, Palakodeti D, Krishna S.  2021.  Comprehensive annotation and characterization of planarian tRNA and tRNA-derived fragments (tRFs).. RNA. DOI:10.1261/rna.077701.120.
Fernandes G, Mishra PK, Nawaz MSarfaraz, Donlin-Asp PG, Rahman MMostafizur, Hazra A, Kedia S, Kayenaat A, Songara D, Wyllie DJA, Schuman EM, Kind PC, Chattarji S.  2021.  Correction of amygdalar dysfunction in a rat model of fragile X syndrome.. Cell Rep. 37(2):109805. DOI:10.1016/j.celrep.2021.109805.
Sreeraj VS, Puzhakkal JC, Holla B, Nadella RKumar, Sheth S, Balachander S, Ithal D, Ali F, Viswanath B, Muralidharan K, Venkatasubramanian G, John JP, Benegal V, Murthy P, Varghese M, Reddy YJanardhan, Jain S.  2021.  Cross-diagnostic evaluation of minor physical anomalies in psychiatric disorders.. J Psychiatr Res. 142:54-62. DOI:10.1016/j.jpsychires.2021.07.028.
Nawalpuri B, Sharma A, Chattarji S, Muddashetty RS.  2021.  Distinct temporal expression of the GW182 paralog TNRC6A in neurons regulates dendritic arborization.. J Cell Sci. 134(16) DOI:10.1242/jcs.258465.
Chakravarthy A, Nandakumar A, George G, Ranganathan S, Umashankar S, Shettigar N, Palakodeti D, Gulyani A, Ramesh A.  2021.  Engineered RNA biosensors enable ultrasensitive SARS-CoV-2 detection in a simple color and luminescence assay.. Life Sci Alliance. 4(12) DOI:10.26508/lsa.202101213.
Dhar MS, Marwal R, Vs R, Ponnusamy K, Jolly B, Bhoyar RC, Sardana V, Naushin S, Rophina M, Mellan TA, Mishra S, Whittaker C, Fatihi S, Datta M, Singh P, Sharma U, Ujjainiya R, Bhatheja N, Divakar MKumar, Singh MK et al..  2021.  Genomic characterization and epidemiology of an emerging SARS-CoV-2 variant in Delhi, India.. Science. :eabj9932. DOI:10.1126/science.abj9932.
Dhar MS, Marwal R, Vs R, Ponnusamy K, Jolly B, Bhoyar RC, Sardana V, Naushin S, Rophina M, Mellan TA, Mishra S, Whittaker C, Fatihi S, Datta M, Singh P, Sharma U, Ujjainiya R, Bhatheja N, Divakar MKumar, Singh MK et al..  2021.  Genomic characterization and epidemiology of an emerging SARS-CoV-2 variant in Delhi, India.. Science. :eabj9932. DOI:10.1126/science.abj9932.
Biswas R, Banerjee A, Lembo S, Zhao Z, Lakshmanan V, Lim R, Le S, Nakasaki M, Kutyavin V, Wright G, Palakodeti D, Ross RS, Jamora C, Vasioukhin V, Jie Y, Raghavan S.  2021.  Mechanical instability of adherens junctions overrides intrinsic quiescence of hair follicle stem cells.. Dev Cell. 56(6):761-780.e7. DOI:10.1016/j.devcel.2021.02.020.
Pahal S, Badnikar K, Ghate V, Bhutani U, Nayak MManjunatha, Subramanyam DNarasimhai, Vemula PKumar.  2021.  Microneedles for Extended Transdermal Therapeutics: A Route to Advanced Healthcare.. Eur J Pharm Biopharm. 159:151-169. DOI:10.1016/j.ejpb.2020.12.020.
Wiley CD, Sharma R, Davis SS, Lopez-Dominguez JAlberto, Mitchell KP, Wiley S, Alimirah F, Kim DEun, Payne T, Rosko A, Aimontche E, Deshpande SM, Neri F, Kuehnemann C, Demaria M, Ramanathan A, Campisi J.  2021.  Oxylipin biosynthesis reinforces cellular senescence and allows detection of senolysis.. Cell Metab. DOI:10.1016/j.cmet.2021.03.008.
Sreeraj VS, Holla B, Ithal D, Nadella RKumar, Mahadevan J, Balachander S, Ali F, Sheth S, Narayanaswamy JC, Venkatasubramanian G, John JP, Varghese M, Benegal V, Jain S, Reddy YJanardhan, Viswanath B.  2021.  Psychiatric symptoms and syndromes transcending diagnostic boundaries in Indian multiplex families: The cohort of ADBS study.. Psychiatry Res. 296:113647. DOI:10.1016/j.psychres.2020.113647.
Sreeraj VS, Holla B, Ithal D, Nadella RKumar, Mahadevan J, Balachander S, Ali F, Sheth S, Narayanaswamy JC, Venkatasubramanian G, John JP, Varghese M, Benegal V, Jain S, Reddy YJanardhan, Viswanath B.  2021.  Psychiatric symptoms and syndromes transcending diagnostic boundaries in Indian multiplex families: The cohort of ADBS study.. Psychiatry Res. 296:113647. DOI:10.1016/j.psychres.2020.113647.

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