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    Results: 1 to 20 of 29

    1.

    Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations.

    Garg A, Subramanyam L, Agarwal AK, Simha V, Levine B, D'Apice MR, Novelli G, Crow Y.

    J Clin Endocrinol Metab. 2009 Oct 29. [Epub ahead of print]PMID: 19875478 [PubMed - as supplied by publisher]Related articles

    2.

    Functional characterization of the human 1-acylglycerol-3-phosphate-O-acyltransferase isoform 10/glycerol-3-phosphate acyltransferase isoform 3.

    Sukumaran S, Barnes RI, Garg A, Agarwal AK.

    J Mol Endocrinol. 2009 Jun;42(6):469-78. Epub 2009 Mar 24.PMID: 19318427 [PubMed - indexed for MEDLINE]Related articles

    3.

    Molecular mechanisms of hepatic steatosis and insulin resistance in the AGPAT2-deficient mouse model of congenital generalized lipodystrophy.

    Cortés VA, Curtis DE, Sukumaran S, Shao X, Parameswara V, Rashid S, Smith AR, Ren J, Esser V, Hammer RE, Agarwal AK, Horton JD, Garg A.

    Cell Metab. 2009 Feb;9(2):165-76.PMID: 19187773 [PubMed - indexed for MEDLINE]Related articles

    4.

    Lipodystrophies: disorders of adipose tissue biology.

    Garg A, Agarwal AK.

    Biochim Biophys Acta. 2009 Jun;1791(6):507-13. Epub 2009 Jan 7. Review.PMID: 19162222 [PubMed - indexed for MEDLINE]Related articles

    5.

    Severe mandibuloacral dysplasia-associated lipodystrophy and progeria in a young girl with a novel homozygous Arg527Cys LMNA mutation.

    Agarwal AK, Kazachkova I, Ten S, Garg A.

    J Clin Endocrinol Metab. 2008 Dec;93(12):4617-23. Epub 2008 Sep 16.PMID: 18796515 [PubMed - indexed for MEDLINE]Related articles

    6.

    Novel subtype of congenital generalized lipodystrophy associated with muscular weakness and cervical spine instability.

    Simha V, Agarwal AK, Aronin PA, Iannaccone ST, Garg A.

    Am J Med Genet A. 2008 Sep 15;146A(18):2318-26.PMID: 18698612 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

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

    Szymanski KM, Binns D, Bartz R, Grishin NV, Li WP, Agarwal AK, Garg A, Anderson RG, Goodman JM.

    Proc Natl Acad Sci U S A. 2007 Dec 26;104(52):20890-5. Epub 2007 Dec 18.PMID: 18093937 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Functional characterization of human 1-acylglycerol-3-phosphate-O-acyltransferase isoform 9: cloning, tissue distribution, gene structure, and enzymatic activity.

    Agarwal AK, Sukumaran S, Bartz R, Barnes RI, Garg A.

    J Endocrinol. 2007 Jun;193(3):445-57.PMID: 17535882 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Mislocalization of prelamin A Tyr646Phe mutant to the nuclear pore complex in human embryonic kidney 293 cells.

    Pan Y, Garg A, Agarwal AK.

    Biochem Biophys Res Commun. 2007 Mar 30;355(1):78-84. Epub 2007 Jan 31.PMID: 17291448 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Cofactors, redox state, and directional preferences of hydroxysteroid dehydrogenases.

    Sherbet DP, Papari-Zareei M, Khan N, Sharma KK, Brandmaier A, Rambally S, Chattopadhyay A, Andersson S, Agarwal AK, Auchus RJ.

    Mol Cell Endocrinol. 2007 Feb;265-266:83-8. Epub 2007 Jan 12. Review.PMID: 17222963 [PubMed - indexed for MEDLINE]Related articles

    11.

    Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiency.

    Agarwal AK, Zhou XJ, Hall RK, Nicholls K, Bankier A, Van Esch H, Fryns JP, Garg A.

    J Investig Med. 2006 May;54(4):208-13.PMID: 17152860 [PubMed - indexed for MEDLINE]Related articles

    12.

    Genetic disorders of adipose tissue development, differentiation, and death.

    Agarwal AK, Garg A.

    Annu Rev Genomics Hum Genet. 2006;7:175-99. Review.PMID: 16722806 [PubMed - indexed for MEDLINE]Related articles

    13.

    Functional characterization of human 1-acylglycerol-3-phosphate acyltransferase isoform 8: cloning, tissue distribution, gene structure, and enzymatic activity.

    Agarwal AK, Barnes RI, Garg A.

    Arch Biochem Biophys. 2006 May 15;449(1-2):64-76. Epub 2006 Mar 29.PMID: 16620771 [PubMed - indexed for MEDLINE]Related articles

    14.

    Genetic basis of lipodystrophies and management of metabolic complications.

    Agarwal AK, Garg A.

    Annu Rev Med. 2006;57:297-311. Review.PMID: 16409151 [PubMed - indexed for MEDLINE]Related articles

    15.

    A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features.

    Van Esch H, Agarwal AK, Debeer P, Fryns JP, Garg A.

    J Clin Endocrinol Metab. 2006 Feb;91(2):517-21. Epub 2005 Nov 8.PMID: 16278265 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Phenotypic heterogeneity in body fat distribution in patients with atypical Werner's syndrome due to heterozygous Arg133Leu lamin A/C mutation.

    Jacob KN, Baptista F, dos Santos HG, Oshima J, Agarwal AK, Garg A.

    J Clin Endocrinol Metab. 2005 Dec;90(12):6699-706. Epub 2005 Sep 20.PMID: 16174718 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia.

    Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK.

    J Clin Endocrinol Metab. 2005 Sep;90(9):5259-64. Epub 2005 Jul 5. Review.PMID: 15998779 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Minireview: cellular redox state regulates hydroxysteroid dehydrogenase activity and intracellular hormone potency.

    Agarwal AK, Auchus RJ.

    Endocrinology. 2005 Jun;146(6):2531-8. Epub 2005 Mar 17. Review.PMID: 15774561 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Enzymatic activity of naturally occurring 1-acylglycerol-3-phosphate-O-acyltransferase 2 mutants associated with congenital generalized lipodystrophy.

    Haque W, Garg A, Agarwal AK.

    Biochem Biophys Res Commun. 2005 Feb 11;327(2):446-53.PMID: 15629135 [PubMed - indexed for MEDLINE]Related articles

    20.

    Seipin: a mysterious protein.

    Agarwal AK, Garg A.

    Trends Mol Med. 2004 Sep;10(9):440-4. Review. No abstract available. PMID: 15350896 [PubMed - indexed for MEDLINE]Related articles

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