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Central Vein Stenosis

American journal of kidney diseases, 2013-06, Vol.61 (6), p.1001-1015

Agarwal, Anil K., MD

2013

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Laparoscopic Surgery for Gallbladder Cancer: An Expert Consensus Statement

Digestive surgery, 2019-01, Vol.36 (1), p.1-6

2019

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PSMB8 Encoding the β5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome

American journal of human genetics, 2010-12, Vol.87 (6), p.866-872

2010

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Insights into lipid accumulation in skeletal muscle in dysferlin-deficient mice

Journal of lipid research, 2019-12, Vol.60 (12), p.2057-2073

2019

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Autosomal recessive progeroid syndrome due to homozygosity for a TOMM7 variant

The Journal of clinical investigation, 2022-12, Vol.132 (23), p.1-6

2022

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Characterization of the Mouse and Human Monoacylglycerol O-Acyltransferase 1 (Mogat1) Promoter in Human Kidney Proximal Tubule and Rat Liver Cells

PloS one, 2016-09, Vol.11 (9), p.e0162504

2016

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lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology

Proceedings of the National Academy of Sciences - PNAS, 2007-12, Vol.104 (52), p.20890-20895

2007

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Complications of Vascular Access: Superior Vena Cava Syndrome

American journal of kidney diseases, 2017-02, Vol.69 (2), p.309-313

2017

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Endovascular interventions for central vein stenosis

Kidney Research and Clinical Practice, 2015, 34(4), , pp.228-232

Agarwal, Anil K

2015

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Metabolic, Reproductive, and Neurologic Abnormalities in Agpat1-Null Mice

Endocrinology (Philadelphia), 2017-11, Vol.158 (11), p.3954-3973

2017

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Reverse Digital Artery Island Flap for Finger-Tip Defects

Indian journal of plastic surgery, 2023-09, Vol.28 (2), p.73-76

2023

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Enzymatic activities of the human AGPAT isoform 3 and isoform 5: localization of AGPAT5 to mitochondria[S]

Journal of lipid research, 2011-03, Vol.52 (3), p.451-462

2011

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Genetic disorders of adipose tissue development, differentiation, and death

Annual review of genomics and human genetics, 2006-01, Vol.7 (1), p.175-199

2006

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Central Vein Stenosis: A Nephrologist's Perspective

Seminars in dialysis, 2007-01, Vol.20 (1), p.53-62

2007

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

iScience, 2024-04, Vol.27 (4), p.109517-109517, Article 109517

2024

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Enzymatic activity of the human 1-acylglycerol-3-phosphate-O-acyltransferase isoform 11: upregulated in breast and cervical cancers[S]

Journal of lipid research, 2010-08, Vol.51 (8), p.2143-2152

2010

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Genetic basis of lipodystrophies and management of metabolic complications

Annual review of medicine, 2006-01, Vol.57 (1), p.297-311

2006

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Molecular Mechanisms of Hepatic Steatosis and Insulin Resistance in the AGPAT2-Deficient Mouse Model of Congenital Generalized Lipodystrophy

Cell metabolism, 2009-02, Vol.9 (2), p.165-176

2009

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Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations

The journal of clinical endocrinology and metabolism, 2009-12, Vol.94 (12), p.4971-4983

2009

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Mogat1 deletion does not ameliorate hepatic steatosis in lipodystrophic (Agpat2−/−) or obese (ob/ob) mice

Journal of lipid research, 2016-04, Vol.57 (4), p.616-630

2016

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Leptin ameliorates insulin resistance and hepatic steatosis in Agpat2−/− lipodystrophic mice independent of hepatocyte leptin receptors[S]

Journal of lipid research, 2014-02, Vol.55 (2), p.276-288

2014

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Squamous variant of gallbladder cancer: is it different from adenocarcinoma?

The American journal of surgery, 2013-09, Vol.206 (3), p.380-385

2013

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

Nature reviews. Endocrinology, 2024-03, Vol.20 (3), p.128-129

2024

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Caveolin-1: A New Locus for Human Lipodystrophy

The journal of clinical endocrinology and metabolism, 2008-04, Vol.93 (4), p.1183-1185

2008

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Central Vein Stenosis

Seipin is required for converting nascent to mature lipid droplets

Laparoscopic Surgery for Gallbladder Cancer: An Expert Consensus Statement

PSMB8 Encoding the β5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome

Insights into lipid accumulation in skeletal muscle in dysferlin-deficient mice

Autosomal recessive progeroid syndrome due to homozygosity for a TOMM7 variant

Characterization of the Mouse and Human Monoacylglycerol O-Acyltransferase 1 (Mogat1) Promoter in Human Kidney Proximal Tubule and Rat Liver Cells

lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology

Complications of Vascular Access: Superior Vena Cava Syndrome

Endovascular interventions for central vein stenosis

Metabolic, Reproductive, and Neurologic Abnormalities in Agpat1-Null Mice

Reverse Digital Artery Island Flap for Finger-Tip Defects

Enzymatic activities of the human AGPAT isoform 3 and isoform 5: localization of AGPAT5 to mitochondria[S]

Genetic disorders of adipose tissue development, differentiation, and death

Central Vein Stenosis: A Nephrologist's Perspective

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

Enzymatic activity of the human 1-acylglycerol-3-phosphate-O-acyltransferase isoform 11: upregulated in breast and cervical cancers[S]

Genetic basis of lipodystrophies and management of metabolic complications

Molecular Mechanisms of Hepatic Steatosis and Insulin Resistance in the AGPAT2-Deficient Mouse Model of Congenital Generalized Lipodystrophy

Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations

Mogat1 deletion does not ameliorate hepatic steatosis in lipodystrophic (Agpat2−/−) or obese (ob/ob) mice

Leptin ameliorates insulin resistance and hepatic steatosis in Agpat2−/− lipodystrophic mice independent of hepatocyte leptin receptors[S]

Squamous variant of gallbladder cancer: is it different from adenocarcinoma?

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

Caveolin-1: A New Locus for Human Lipodystrophy

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