Publications by authors named "G Rajiv Gandhi"

Spinal muscular atrophy (SMA) is a neuromuscular disorder caused by mutations or deletions in the survival motoneuron 1 () gene, resulting in deficiency of the SMN protein that is essential for motoneuron function. Smn depletion in mice disturbs axonal RNA transport and translation, thereby contributing to axon growth impairment, muscle denervation, and motoneuron degeneration. However, the mechanisms whereby Smn loss causes axonal defects remain unclear.

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AMCP convened a panel of clinical and managed care experts to identify insights regarding the prevalence, clinical manifestations, and management approaches for immunoglobulin E-mediated food allergies. This article aims to summarize expert perspectives on health care system challenges and areas of agreement concerning the management of food allergies, and to advance payers' understanding of their role in supporting health care for patients with food allergies. Food allergy management requires dietary modification and is associated with significant patient and caregiver burdens.

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Introduction  Mechanical low back pain frequently originates from the lumbar facet joint (LFJ). Axial low back discomfort can result from osteoarthritis in the LFJ. Depending on the severity of LFJ degeneration, the effect of intra-articular (IA) LFJ corticosteroid injection may vary.

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Article Synopsis
  • Spinal muscular atrophy (SMA) is a genetic disorder caused by issues with the SMN1 gene, leading to insufficient production of the necessary SMN protein, with no current cure available.
  • The study investigated the role of microRNA (miRNA) in SMA, specifically looking for dysregulated miRNAs in patient-derived iPSCs through miRNA microarray analysis and validation.
  • Findings revealed that hsa-miR-663a is differentially expressed in SMA patients and targets specific genes involved in the PI3K-AKT pathway, indicating its potential as a therapeutic target for treating SMA.
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