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Target-specific requirements for RNA interference can arise through restricted RNA amplification despite the lack of specialized pathways.
Knudsen-Palmer DR, Raman P, Ettefa F, De Ravin L, Jose AM. Knudsen-Palmer DR, et al. Among authors: raman p. bioRxiv [Preprint]. 2024 Jun 3:2023.02.07.527351. doi: 10.1101/2023.02.07.527351. bioRxiv. 2024. Update in: Elife. 2024 Aug 20;13:RP97487. doi: 10.7554/eLife.97487 PMID: 36798330 Free PMC article. Updated. Preprint.
RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions.
Fratter C, Raman P, Alston CL, Blakely EL, Craig K, Smith C, Evans J, Seller A, Czermin B, Hanna MG, Poulton J, Brierley C, Staunton TG, Turnpenny PD, Schaefer AM, Chinnery PF, Horvath R, Turnbull DM, Gorman GS, Taylor RW. Fratter C, et al. Among authors: raman p. Neurology. 2011 Jun 7;76(23):2032-4. doi: 10.1212/WNL.0b013e31821e558b. Neurology. 2011. PMID: 21646632 Free PMC article. No abstract available.
Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions.
Alston CL, Schaefer AM, Raman P, Solaroli N, Krishnan KJ, Blakely EL, He L, Craig K, Roberts M, Vyas A, Nixon J, Horvath R, Turnbull DM, Karlsson A, Gorman GS, Taylor RW. Alston CL, et al. Among authors: raman p. Neurology. 2013 Dec 3;81(23):2051-3. doi: 10.1212/01.wnl.0000436931.94291.e6. Epub 2013 Nov 6. Neurology. 2013. PMID: 24198295 Free PMC article.
New 7-hydroxycoumarin acetamide derivatives as human carbonic anhydrase IX and XII inhibitors: Design, synthesis, biological evaluation and molecular docking studies.
Maddipatla S, Bakchi B, Shinde MA, Bonardi A, Raman PK, Bhalerao HA, Singampalli A, Nanduri S, Godugu C, Sonti R, Supuran CT, Yaddanapudi VM. Maddipatla S, et al. Among authors: raman pk. Arch Pharm (Weinheim). 2025 Jan;358(1):e2400482. doi: 10.1002/ardp.202400482. Arch Pharm (Weinheim). 2025. PMID: 39686882
266 results