Publications by authors named "B Murali Krishnan"

Objective: To investigate whether local lesions created by stereo-electroencephalography (SEEG)-guided radiofrequency thermocoagulation (RFTC) affect distant brain connectivity and excitability in patients with focal, drug-resistant epilepsy (DRE).

Methods: Ten patients with focal DRE underwent SEEG implantation and subsequently 1 Hz bipolar repetitive electrical stimulation (RES) for 30 s before and after RFTC. Root mean square (RMS) of cortico-cortical evoked potentials (CCEPs) was calculated for 15 ms to 300 ms post-stimulation with baseline correction.

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Mice can generate a cognitive map of an environment based on self-motion signals when there is a fixed association between their starting point and the location of their goal.

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Several reports have indicated that impaired mitochondrial function contributes to the development and progression of Huntington's disease (HD). Mitochondrial genome damage, particularly DNA strand breaks (SBs), is a potential cause for its compromised functionality. We have recently demonstrated that the activity of polynucleotide kinase 3'-phosphatase (PNKP), a critical DNA end-processing enzyme, is significantly reduced in the nuclear extract of HD patients due to lower level of a metabolite fructose-2,6 bisphosphate (F2,6BP), a biosynthetic product of 6-phosphofructo-2-kinase fructose-2,6-bisphosphatase 3 (PFKFB3), leading to persistent DNA SBs with 3'-phosphate termini, refractory to subsequent steps for repair completion.

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Article Synopsis
  • The matrix metalloproteinases (MMPs) are zinc proteases that help break down components of the extracellular matrix (ECM) and are involved in processes like inflammation and cell growth.
  • A study of Drosophila MMPs Mmp1 and Mmp2 shows that while they are important for tissue remodeling, they are not necessary for embryonic development, and their localization (either membrane-anchored or released) is key in distinguishing their roles.
  • MMPs are categorized into secretory and membrane types based on their structure and function, and while humans have many MMPs, Drosophila only has two, highlighting the potential complexity of MMP regulation in disease progression.
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