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2021
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.
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.
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.
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.
Mlcochova P, Kemp SA, Dhar MShanker, Papa G, Meng B, Ferreira IATM, Datir R, Collier DA, Albecka A, Singh S, Pandey R, Brown J, Zhou J, Goonawardane N, Mishra S, Whittaker C, Mellan T, Marwal R, Datta M, Sengupta S et al..  2021.  SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion.. Nature. 599(7883):114-119. DOI:10.1038/s41586-021-03944-y.
Mlcochova P, Kemp SA, Dhar MShanker, Papa G, Meng B, Ferreira IATM, Datir R, Collier DA, Albecka A, Singh S, Pandey R, Brown J, Zhou J, Goonawardane N, Mishra S, Whittaker C, Mellan T, Marwal R, Datta M, Sengupta S et al..  2021.  SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion.. Nature. 599(7883):114-119. DOI:10.1038/s41586-021-03944-y.
Emery A, Hardwick BS, Crooks AT, Milech N, Watt PM, Mithra C, Kumar V, Giridharan S, Sadasivam G, Mathivanan S, Sudhakar S, Bairy S, Bharatham K, Hurakadli MA, Prasad TK, Kamariah N, Muellner M, Coelho M, Torrance CJ, McKenzie GJ et al..  2021.  Target identification for small-molecule discovery in the FOXO3a tumor-suppressor pathway using a biodiverse peptide library.. Cell Chem Biol. DOI:10.1016/j.chembiol.2021.05.009.
2022
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.
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.
2024
Rajendiran V, Devaraju N, Haddad M, Ravi NSam, Panigrahi L, Paul J, Gopalakrishnan C, Wyman S, Ariudainambi K, Mahalingam G, Periyasami Y, Prasad K, George A, Sukumaran D, Gopinathan S, Pai AAnand, Nakamura Y, Balasubramanian P, Ramalingam R, Thangavel S et al..  2024.  Base editing of key residues in the BCL11A-XL-specific zinc finger domains derepresses fetal globin expression.. Mol Ther. 32(3):663-677. DOI:10.1016/j.ymthe.2024.01.023.
Ulschmid CM, Sun MR, Jabbarpour CR, Steward AC, Rivera-González KS, Cao J, Martin AA, Barnes M, Wicklund L, Madrid A, Papale LA, Joseph DB, Vezina CM, Alisch RS, Lipinski RJ.  2024.  Disruption of DNA methylation-mediated cranial neural crest proliferation and differentiation causes orofacial clefts in mice.. Proc Natl Acad Sci U S A. 121(3):e2317668121. DOI:10.1073/pnas.2317668121.

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