Anil K. Agarwal

Erratum. Gain of Function NOTCH3 Variants Cause Familial Partial Lipodystrophy Due to Activation of Senescence Pathways. Diabetes 2025;74:427–438

Abhimanyu Garg, Chao Xing, Anil K. Agarwal, Aundrea K. Westfall et autres

TTP3.05 Nourish to Flourish – Improving Post-Operative Nutrition as Part of Enhanced Recovery Programme at a District General Hospital

Sharmaine Yen Ling Quake, Abdelrahman Abdelrahman, Chloe McMurrary, EJ McDonald et autres

Abstract Aim To audit our compliance with nutritional recommendations in the post-operative phase of enhanced recovery (ERAS) pathway based on the 2018 ERAS Society recommendations Method First cycle of the audit included patients who underwent elective colorectal resections between January – March …

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TTP3.04 Revisiting Enhanced Recovery (ERAS) in the Post-Operative Phase – A Quality Improvement Project at A District General Hospital

Sharmaine Yen Ling Quake, Abdelrahman Abdelrahman, Chloe McMurray, Barbara Dolaszynska et autres

Abstract Aim To re-assess our current practice of enhanced recovery (ERAS) pathway based on the 2018 ERAS Society recommendations Method First cycle of the audit included patients who underwent elective colorectal resections between January – March 2024. Post-operative elements of the ERAS …

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Gain of function NOTCH3 variants cause familial partial lipodystrophy due to activation of senescence pathways

Abhimanyu Garg, Chao Xing, Anil K. Agarwal, Aundrea K. Westfall et autres

Despite elucidation of the molecular genetic basis of several lipodystrophy syndromes, molecular defects in some ultra-rare subtypes of familial lipodystrophies remain unidentified. We analyzed whole exome sequencing (WES) data of four affected and two unaffected females from an undiagnosed autosomal dominant familial …

Gain of function NOTCH3 variants cause familial partial lipodystrophy due to activation of senescence pathways

Abhimanyu Garg, Chao Xing, Anil K. Agarwal, Aundrea K. Westfall et autres

Despite elucidation of the molecular genetic basis of several lipodystrophy syndromes, molecular defects in some ultra-rare subtypes of familial lipodystrophies remain unidentified. We analyzed whole exome sequencing (WES) data of four affected and two unaffected females from an undiagnosed autosomal dominant familial …

Gain of Function NOTCH3 Variants Cause Familial Partial Lipodystrophy Due to Activation of Senescence Pathways

Abhimanyu Garg, Chao Xing, Anil K. Agarwal, Aundrea K. Westfall et autres

Despite elucidation of the molecular genetic basis of several lipodystrophy syndromes, molecular defects in some ultra-rare subtypes of familial lipodystrophies remain unidentified. We analyzed whole-exome sequencing (WES) data of four affected and two unaffected females from an undiagnosed autosomal dominant familial partial …

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Material properties of YSt 310 steel tubular columns under extreme loading conditions

Prithvi Sangani, Devender Kumar, Isha Paliwal, M. Ramji et autres

Steel tubular columns have emerged as one of the most sought-after solutions for infrastructure development due to their exceptional mechanical properties. The properties include resistance against bi-axial bending, axial compression and also better aesthetic appearance. YSt 310 cold-formed tubular sections are widely …

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Septic Shock and Myocardial Dysfunction

Hossam Algallie, Siddhartha Banerjee, Ashish Kumar, Um I. Rubab et autres

Cardiac dysfunction in sepsis is strongly linked to increased mortality. The pathophysiology of sepsis-induced Myocardial dysfunction is multifaceted, involving impaired myocardial circulation, direct myocardial depression, and mitochondrial dysfunction. Recent studies have emphasized that mitochondrial dysfunction plays a crucial role in sepsis-induced Myocardial …

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Regulated regeneration of adipose tissue in lipodystrophic Agpat2-null mice partially ameliorates hepatic steatosis

Anil K. Agarwal, Katie Tunison, Jay D. Horton, Abhimanyu Garg

Publisher of over 50 scientific journals across the life, physical, earth, and health sciences, both independently and in partnership with scientific societies including Cell, Neuron, Immunity, Current Biology, AJHG, and the Trends Journals.

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Phospholipid biosynthetic pathways and lipodystrophies: a novel syndrome due to PLAAT3 deficiency

Anil K. Agarwal, Abhimanyu Garg

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Adipose-specific overexpression of human AGPAT2 in mice causes increased adiposity and mild hepatic dysfunction

Anil K. Agarwal, Katie Tunison, Gonçalo Vale, Jeffrey G. McDonald et autres

AGPAT2, a critical enzyme involved in the biosynthesis of phospholipids and triacylglycerol (TAG), is highly expressed in adipose tissue (AT). Whether overexpression of AGPAT2 in AT will result in increased TAG synthesis (obesity) and its metabolic complications remains unknown. We overexpressed human …

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Early‐onset diabetes mellitus as a presenting feature of Werner's syndrome in an Indian family

Fieke W. Hoff, Chao Xing, Vinaya Simha, Anil K. Agarwal et autres

BACKGROUND: Diabetes mellitus (DM) in children and adolescents is typically caused by type 1 DM, followed by type 2 DM and maturity-onset diabetes of the young (MODY). We report an unusual Asian Indian family in which three members presented with DM at …

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