Anil B Mukherjee

Anil B Mukherjee

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Anil B Mukherjee

Anil B Mukherjee

Publications by authors named "Anil B Mukherjee"

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Cln3-mutations underlying juvenile neuronal ceroid lipofuscinosis cause significantly reduced levels of Palmitoyl-protein thioesterases-1 (Ppt1)-protein and Ppt1-enzyme activity in the lysosome.

J Inherit Metab Dis 2019 Sep 14;42(5):944-954. Epub 2019 May 14.

Section on Developmental Genetics, Program on Endocrinology and Molecular Genetics, Eunice Kennedy-Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/jimd.12106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739123PMC
September 2019

Emerging new roles of the lysosome and neuronal ceroid lipofuscinoses.

Mol Neurodegener 2019 01 16;14(1). Epub 2019 Jan 16.

Section on Developmental Genetics, Program on Endocrinology and Molecular Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, The National Institutes of Health, Bethesda, Maryland, 20892-1830, USA.

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https://molecularneurodegeneration.biomedcentral.com/article
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http://dx.doi.org/10.1186/s13024-018-0300-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335712PMC
January 2019

Misrouting of v-ATPase subunit V0a1 dysregulates lysosomal acidification in a neurodegenerative lysosomal storage disease model.

Nat Commun 2017 03 7;8:14612. Epub 2017 Mar 7.

Section on Developmental Genetics, PEMG, Eunice Kennedy-Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-1830, USA.

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http://dx.doi.org/10.1038/ncomms14612DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344305PMC
March 2017

Suppression of agrin-22 production and synaptic dysfunction in Cln1 (-/-) mice.

Ann Clin Transl Neurol 2015 Dec 6;2(12):1085-104. Epub 2015 Nov 6.

Section on Developmental Genetics Program on Developmental Endocrinology and Genetics Eunice Kennedy-Shriver National Institute of Child Health and Human Development NIH Bethesda Maryland 20892-1830.

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http://dx.doi.org/10.1002/acn3.261DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693586PMC
December 2015

Cln1 gene disruption in mice reveals a common pathogenic link between two of the most lethal childhood neurodegenerative lysosomal storage disorders.

Hum Mol Genet 2015 Oct 9;24(19):5416-32. Epub 2015 Jul 9.

Section on Developmental Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-1830, USA

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http://hmg.oxfordjournals.org/content/24/19/5416.full.pdf
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http://www.hmg.oxfordjournals.org/lookup/doi/10.1093/hmg/ddv
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http://dx.doi.org/10.1093/hmg/ddv266DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572073PMC
October 2015

Evaluation of disease progression in INCL by MR spectroscopy.

Ann Clin Transl Neurol 2015 Aug 1;2(8):797-809. Epub 2015 Jul 1.

Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH Bethesda, Maryland, USA, 20892.

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http://dx.doi.org/10.1002/acn3.222DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554441PMC
August 2015

Mice homozygous for c.451C>T mutation in Cln1 gene recapitulate INCL phenotype.

Ann Clin Transl Neurol 2014 Dec 18;1(12):1006-23. Epub 2014 Nov 18.

Program on Developmental Endocrinology and Genetics, Section on Developmental Genetics, Eunice Kennedy-Shriver National Institute of Child Health and Human Development Bethesda, Maryland.

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http://dx.doi.org/10.1002/acn3.144DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284126PMC
December 2014

Oral cysteamine bitartrate and N-acetylcysteine for patients with infantile neuronal ceroid lipofuscinosis: a pilot study.

Lancet Neurol 2014 Aug 2;13(8):777-87. Epub 2014 Jul 2.

Program on Developmental Endocrinology and Genetics, Eunice Kennedy-Shriver National Institute of Child Health and Human Development (NICHD), NIH, Bethesda, MD, USA. Electronic address:

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http://dx.doi.org/10.1016/S1474-4422(14)70142-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139936PMC
August 2014

Neuroprotection and lifespan extension in Ppt1(-/-) mice by NtBuHA: therapeutic implications for INCL.

Nat Neurosci 2013 Nov 22;16(11):1608-17. Epub 2013 Sep 22.

1] Section on Developmental Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA. [2].

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http://dx.doi.org/10.1038/nn.3526DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812271PMC
November 2013

Dynamic palmitoylation links cytosol-membrane shuttling of acyl-protein thioesterase-1 and acyl-protein thioesterase-2 with that of proto-oncogene H-ras product and growth-associated protein-43.

J Biol Chem 2013 Mar 8;288(13):9112-25. Epub 2013 Feb 8.

Section on Developmental Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver NICHD, National Institutes of Health, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1074/jbc.M112.421073DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610984PMC
March 2013

Evaluation of neurodegeneration in a mouse model of infantile batten disease by magnetic resonance imaging and magnetic resonance spectroscopy.

Neurodegener Dis 2012 9;9(4):159-69. Epub 2012 Feb 9.

In Vivo NMR Center-HNQ2-3, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1159/000334838DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3369263PMC
October 2012

The blood-brain barrier is disrupted in a mouse model of infantile neuronal ceroid lipofuscinosis: amelioration by resveratrol.

Hum Mol Genet 2012 May 13;21(10):2233-44. Epub 2012 Feb 13.

Section on Developmental Genetics, Program on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1093/hmg/dds038DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335311PMC
May 2012

Stop codon read-through with PTC124 induces palmitoyl-protein thioesterase-1 activity, reduces thioester load and suppresses apoptosis in cultured cells from INCL patients.

Mol Genet Metab 2011 Nov 13;104(3):338-45. Epub 2011 Jun 13.

Section on Developmental Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892–1830, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S109671921100192
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http://dx.doi.org/10.1016/j.ymgme.2011.05.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220191PMC
November 2011

Allergic asthma: influence of genetic and environmental factors.

J Biol Chem 2011 Sep 28;286(38):32883-9. Epub 2011 Jul 28.

Section on Developmental Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver NICHD, National Institutes of Health, Bethesda, Maryland 20892-1830, USA.

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http://dx.doi.org/10.1074/jbc.R110.197046DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190897PMC
September 2011

Disruption of adaptive energy metabolism and elevated ribosomal p-S6K1 levels contribute to INCL pathogenesis: partial rescue by resveratrol.

Hum Mol Genet 2011 Mar 28;20(6):1111-21. Epub 2010 Dec 28.

Section on Developmental Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-1830, USA.

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https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
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http://dx.doi.org/10.1093/hmg/ddq555DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043662PMC
March 2011

Omega-3 and omega-6 fatty acids suppress ER- and oxidative stress in cultured neurons and neuronal progenitor cells from mice lacking PPT1.

Neurosci Lett 2010 Aug 4;479(3):292-6. Epub 2010 Jun 4.

Section on Developmental Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892-1830, United States.

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http://dx.doi.org/10.1016/j.neulet.2010.05.083DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2904481PMC
August 2010

Lack of an endogenous anti-inflammatory protein in mice enhances colonization of B16F10 melanoma cells in the lungs.

J Biol Chem 2010 Apr 29;285(14):10822-31. Epub 2010 Jan 29.

Section on Developmental Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver NICHD, National Institutes of Health, Bethesda, Maryland 20892-1830, USA.

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http://www.jbc.org/lookup/doi/10.1074/jbc.M109.083550
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http://dx.doi.org/10.1074/jbc.M109.083550DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856288PMC
April 2010

Children with infantile neuronal ceroid lipofuscinosis have an increased risk of hypothermia and bradycardia during anesthesia.

Anesth Analg 2009 Aug;109(2):372-8

Department of Anesthesia and Surgical Services, National Institutes of Health Clinical Center, National Institutes of Health, Bethesda, Maryland 20892-1512, USA.

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http://dx.doi.org/10.1213/ane.0b013e3181aa6e95DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743022PMC
August 2009

RAGE signaling contributes to neuroinflammation in infantile neuronal ceroid lipofuscinosis.

FEBS Lett 2008 Nov 21;582(27):3823-31. Epub 2008 Oct 21.

Section on Developmental Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-1830, United States.

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http://dx.doi.org/10.1016/j.febslet.2008.10.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2597448PMC
November 2008

Palmitoyl protein thioesterase-1 deficiency impairs synaptic vesicle recycling at nerve terminals, contributing to neuropathology in humans and mice.

J Clin Invest 2008 Sep;118(9):3075-86

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, NIH, Bethesda, Maryland 20892-1830, USA.

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http://dx.doi.org/10.1172/JCI33482DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2515381PMC
September 2008

Uteroglobin interacts with the heparin-binding site of fibronectin and prevents fibronectin-IgA complex formation found in IgA-nephropathy.

FEBS Lett 2008 Mar 1;582(5):611-5. Epub 2008 Feb 1.

Section on Developmental Genetics, Heritable Disorders Branch, NICHD, NIH, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1016/j.febslet.2008.01.025DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323101PMC
March 2008

ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperones.

Hum Mol Genet 2008 Feb 7;17(4):469-77. Epub 2007 Nov 7.

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1093/hmg/ddm324DOI Listing
February 2008

Uteroglobin: a steroid-inducible immunomodulatory protein that founded the Secretoglobin superfamily.

Endocr Rev 2007 Dec 4;28(7):707-25. Epub 2007 Oct 4.

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, National Institute of Health, Building 10, Bethesda, Maryland 20892-1830, USA.

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http://dx.doi.org/10.1210/er.2007-0018DOI Listing
December 2007

Production of lysophosphatidylcholine by cPLA2 in the brain of mice lacking PPT1 is a signal for phagocyte infiltration.

Hum Mol Genet 2007 Apr 6;16(7):837-47. Epub 2007 Mar 6.

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Developement, The National Institutes of Health, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1093/hmg/ddm029DOI Listing
April 2007

Uteroglobin suppresses allergen-induced TH2 differentiation by down-regulating the expression of serum amyloid A and SOCS-3 genes.

FEBS Lett 2006 Oct 5;580(25):6022-6. Epub 2006 Oct 5.

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, The National Institutes of Health, Building 10, Rm 9D42, 10, Center Drive, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1016/j.febslet.2006.09.059DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1859844PMC
October 2006

Mice lacking uteroglobin are highly susceptible to developing pulmonary fibrosis.

FEBS Lett 2006 Aug 20;580(18):4515-20. Epub 2006 Jul 20.

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, The National Institutes of Health, Building 10, Rm 9D42, 10, Center Drive, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1016/j.febslet.2006.07.031DOI Listing
August 2006

Endoplasmic reticulum stress-induced caspase-4 activation mediates apoptosis and neurodegeneration in INCL.

Hum Mol Genet 2006 Jun 27;15(11):1826-34. Epub 2006 Apr 27.

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development/NIH, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1093/hmg/ddl105DOI Listing
June 2006

Palmitoyl-protein thioesterase-1 deficiency leads to the activation of caspase-9 and contributes to rapid neurodegeneration in INCL.

Hum Mol Genet 2006 May 28;15(10):1580-6. Epub 2006 Mar 28.

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-1830, USA.

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http://dx.doi.org/10.1093/hmg/ddl078DOI Listing
May 2006

Interaction of uteroglobin with lipocalin-1 receptor suppresses cancer cell motility and invasion.

Gene 2006 Mar 19;369:66-71. Epub 2006 Jan 19.

Section on Developmental Genetics, Heritable Disorders Branch, NICHD, NIH, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1016/j.gene.2005.10.027DOI Listing
March 2006

Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in INCL.

Hum Mol Genet 2006 Jan 20;15(2):337-46. Epub 2005 Dec 20.

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, The National Institutes of Health, Bethesda, MD 20892-1830, USA.

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http://academic.oup.com/hmg/article/15/2/337/597034/Palmitoy
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http://dx.doi.org/10.1093/hmg/ddi451DOI Listing
January 2006

Yin-yang: balancing act of prostaglandins with opposing functions to regulate inflammation.

J Immunol 2005 Nov;175(10):6271-3

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.4049/jimmunol.175.10.6271DOI Listing
November 2005

Uteroglobin inhibits prostaglandin F2alpha receptor-mediated expression of genes critical for the production of pro-inflammatory lipid mediators.

J Biol Chem 2005 Sep 1;280(38):32897-904. Epub 2005 Aug 1.

Section on Developmental Genetics, Heritable Disorders Branch, NICHD, The National Institutes of Health, Bethesda, Maryland 20892-1830, USA.

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http://dx.doi.org/10.1074/jbc.M502375200DOI Listing
September 2005

Uteroglobin suppresses SCCA gene expression associated with allergic asthma.

J Biol Chem 2005 Mar 27;280(11):9761-4. Epub 2005 Jan 27.

Section on Developmental Genetics, Heritable Disorders Branch, NICHD, National Institutes of Health, Bethesda, Maryland 20892-1830, USA.

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http://dx.doi.org/10.1074/jbc.C400581200DOI Listing
March 2005

Increased susceptibility of mice lacking Clara cell 10-kDa protein to lung tumorigenesis by 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, a potent carcinogen in cigarette smoke.

J Biol Chem 2004 Jul 17;279(28):29336-40. Epub 2004 May 17.

Cell and Cancer Biology Branch, Center for Cancer Research, NCI, National Institutes of Health, Rockville, Maryland 20850, USA.

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http://dx.doi.org/10.1074/jbc.C400162200DOI Listing
July 2004

IFN-gamma stimulates the expression of a novel secretoglobin that regulates chemotactic cell migration and invasion.

J Immunol 2004 Apr;172(7):4245-52

Section on Developmental Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.4049/jimmunol.172.7.4245DOI Listing
April 2004

Neutral ceramidase gene: role in regulating ceramide-induced apoptosis.

Gene 2003 Oct;315:113-22

Section on Developmental Genetics, Heritable Disorders Branch, The National Institute of Child Health and Human Development, The National Institutes of Health, Room 9S241, Building 10, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1016/s0378-1119(03)00721-2DOI Listing
October 2003

Induction of cyclooxygenase-2 by staurosporine through the activation of nuclear factor for IL-6 (NF-IL6) and activator protein 2 (AP2) in an osteoblast-like cell line.

Biochem Pharmacol 2002 Jul;64(2):177-84

Department of Biological Science and Technology, National Chiao Tung University, 75 Po-Ai Street, Hsinchu 30050, Taiwan, ROC.

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http://dx.doi.org/10.1016/s0006-2952(02)01106-1DOI Listing
July 2002

Lys 43 and Asp 46 in alpha-helix 3 of uteroglobin are essential for its phospholipase A2 inhibitory activity.

Biochem Biophys Res Commun 2002 Jul;295(4):877-83

Section on Developmental Genetics, Heritable Disorders Branch, NICHD, Bethesda, MD 20892-1830, USA.

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http://dx.doi.org/10.1016/s0006-291x(02)00767-2DOI Listing
July 2002