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Sphingolipid-dependent fusion of Semliki Forest virus with cholesterol-containing liposomes requires both the 3-hydroxyl group and the double bond of the sphingolipid backbone

Journal of Virology, 1995-05, Vol.69 (5), p.3220-3223

1995

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Coupling of Cholesterol and Cone-shaped Lipids in Bilayers Augments Membrane Permeabilization by the Cholesterol-specific Toxins Streptolysin O and Vibrio cholerae Cytolysin

The Journal of biological chemistry, 2001-05, Vol.276 (18), p.14628-14633

2001

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Evidence for involvement of mitogen-activated protein kinase, rather than stress-activated protein kinase, in potentiation of 1-beta-D-arabinofuranosylcytosine-induced apoptosis by interruption of protein kinase C signaling

Molecular pharmacology, 1998-11, Vol.54 (5), p.844-856

1998

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Induction of Apoptosis and Potentiation of Ceramide-mediated Cytotoxicity by Sphingoid Bases in Human Myeloid Leukemia Cells

The Journal of biological chemistry, 1996-04, Vol.271 (14), p.8275-8284

1996

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Synthesis of ether-linked analogues of lysophosphatidate and their effect on the proliferation of human epithelial cancer cells in vitro

Anticancer research, 1996-07, Vol.16 (4A), p.1813

1996

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Elastase activated liposomal delivery to nucleated cells

Biochimica et biophysica acta, 1999-07, Vol.1419 (2), p.111-126

1999

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Sphingolipids Activate Membrane Fusion of Semliki Forest Virus in a Stereospecific Manner

Biochemistry (Easton), 1995-08, Vol.34 (33), p.10319-10324

1995

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Synthesis and Evaluation of the Antiproliferative Effects of 1-O-Hexadecyl-2-O- methyl-3-O-(2‘-acetamido-2‘-deoxy-β-d-glucopyranosyl)-sn-glycerol and 1-O-Hexadecyl-2-O-methyl-3-O-(2‘-amino-2‘-deoxy-β-d-glucopyranosyl)-sn-glycerol on Epithelial Cancer Cell Growth

Journal of medicinal chemistry, 1996-03, Vol.39 (7), p.1545-1548

1996

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Stereospecific induction of apoptosis in U937 cells by N-octanoyl-sphingosine stereoisomers and N-octyl-sphingosine. The ceramide amide group is not required for apoptosis

European journal of biochemistry, 1996-03, Vol.236 (2), p.729-737

1996

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In-situ investigation of partially deuterated fatty acid and phospholipid monolayers at the air-water interface by IR reflection-absorption spectroscopy

Thin solid films, 1996-09, Vol.284, p.428-431

1996

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Erratum to “In-situ investigation of partially deuterated fatty acid and phospholipid monolayers at the air-water interface by IR reflection-absorption spectroscopy” [thinsolid films284–285 (1996) 428–431]

Thin solid films, 1997, Vol.292 (1), p.330-332

1997

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Synthesis of Sphingomyelin and Ceramide 1-Phosphate from Ceramide without Protection of the Allylic Hydroxyl Group

Journal of organic chemistry, 1994-10, Vol.59 (21), p.6495-6498

1994

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Synthesis and evaluation of the antiproliferative effects of 1-O-hexadecyl-2-O-methyl-3-O-(2'-acetamido-2'-deoxy-beta-D- glucopyranosyl)-sn-glycerol and 1-O-hexadecyl-2-O-methyl-3-0- (2'-amino-2'-deoxy-beta-D-glucopyranosyl)-sn-glycerol on epithelial cancer cell growth

Journal of medicinal chemistry, 1996-03, Vol.39 (7), p.1545-1548

1996

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Partially deuterated phospholipids as IR structure probes of conformational order in bulk and monolayer phases

Journal of molecular structure, 1996, Vol.379 (1), p.227-239

1996

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ChemInform Abstract: A Facile Stereoselective Synthesis of Ether-Linked β-D- Maltosyland β-D-Lactosyl-Glycerolipids via Peracetylated Disaccharide α-Phosphoramidates

ChemInform, 1995-03, Vol.26 (13), p.no-no

1995

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Stereospecific and regiospecific ring opening of glycidol with primary and secondary alcohols mediated by diisobutylaluminium hydride

Journal of the Chemical Society, Perkin Transactions 1, 1995 (18), p.2199

1995

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ChemInform Abstract: Three-Step Synthesis of Platelet-Activating Factor from Chiral Glycidol via Regioselective Monophosphitylation of 1-O-Hexadecyl-sn- glycerol

ChemInform, 1996-04, Vol.27 (14), p.no-no

1996

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ChemInform Abstract: Synthesis of Sphingomyelin and Ceramide 1-Phosphate from Ceramide Without Protection of the Allylic Hydroxyl Group

ChemInform, 1995-04, Vol.26 (16), p.no-no

1995

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ChemInform Abstract: Antitumor Phospholipids: A One-Pot Introduction of a Phosphocholine Moiety into Lipid Hydroxy Acceptors

ChemInform, 1994-12, Vol.25 (52), p.no-no

1994

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Bio-Analytical Method Development and Validation for Estimation of Zaltoprofen in Human Plasma by Reverse Phase -HPLC Method

Current pharmaceutical analysis, 2021-01, Vol.17 (6), p.774-781

2021

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Bacterial lipopolysaccharide has structural similarity to ceramide and stimulates ceramide-activated protein kinase in myeloid cells

The Journal of biological chemistry, 1994-07, Vol.269 (26), p.17606-17610

1994

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A comparison of the lytic properties of two ether-linked lipids, one with and one without antineoplastic activity

Biochemistry and cell biology, 1994-07, Vol.72 (7-8), p.297-303

1994

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Sphingolipid-dependent fusion of Semliki Forest virus with cholesterol-containing liposomes requires both the 3-hydroxyl group and the double bond of the sphingolipid backbone

Coupling of Cholesterol and Cone-shaped Lipids in Bilayers Augments Membrane Permeabilization by the Cholesterol-specific Toxins Streptolysin O and Vibrio cholerae Cytolysin

Evidence for involvement of mitogen-activated protein kinase, rather than stress-activated protein kinase, in potentiation of 1-beta-D-arabinofuranosylcytosine-induced apoptosis by interruption of protein kinase C signaling

Induction of Apoptosis and Potentiation of Ceramide-mediated Cytotoxicity by Sphingoid Bases in Human Myeloid Leukemia Cells

Synthesis of ether-linked analogues of lysophosphatidate and their effect on the proliferation of human epithelial cancer cells in vitro

Elastase activated liposomal delivery to nucleated cells

Sphingolipids Activate Membrane Fusion of Semliki Forest Virus in a Stereospecific Manner

Synthesis and Evaluation of the Antiproliferative Effects of 1-O-Hexadecyl-2-O- methyl-3-O-(2‘-acetamido-2‘-deoxy-β-d-glucopyranosyl)-sn-glycerol and 1-O-Hexadecyl-2-O-methyl-3-O-(2‘-amino-2‘-deoxy-β-d-glucopyranosyl)-sn-glycerol on Epithelial Cancer Cell Growth

Stereospecific induction of apoptosis in U937 cells by N-octanoyl-sphingosine stereoisomers and N-octyl-sphingosine. The ceramide amide group is not required for apoptosis

In-situ investigation of partially deuterated fatty acid and phospholipid monolayers at the air-water interface by IR reflection-absorption spectroscopy

Erratum to “In-situ investigation of partially deuterated fatty acid and phospholipid monolayers at the air-water interface by IR reflection-absorption spectroscopy” [thinsolid films284–285 (1996) 428–431]

Synthesis of Sphingomyelin and Ceramide 1-Phosphate from Ceramide without Protection of the Allylic Hydroxyl Group

Synthesis and evaluation of the antiproliferative effects of 1-O-hexadecyl-2-O-methyl-3-O-(2'-acetamido-2'-deoxy-beta-D- glucopyranosyl)-sn-glycerol and 1-O-hexadecyl-2-O-methyl-3-0- (2'-amino-2'-deoxy-beta-D-glucopyranosyl)-sn-glycerol on epithelial cancer cell growth

Partially deuterated phospholipids as IR structure probes of conformational order in bulk and monolayer phases

ChemInform Abstract: A Facile Stereoselective Synthesis of Ether-Linked β-D- Maltosyland β-D-Lactosyl-Glycerolipids via Peracetylated Disaccharide α-Phosphoramidates

Stereospecific and regiospecific ring opening of glycidol with primary and secondary alcohols mediated by diisobutylaluminium hydride

ChemInform Abstract: Three-Step Synthesis of Platelet-Activating Factor from Chiral Glycidol via Regioselective Monophosphitylation of 1-O-Hexadecyl-sn- glycerol

ChemInform Abstract: Synthesis of Sphingomyelin and Ceramide 1-Phosphate from Ceramide Without Protection of the Allylic Hydroxyl Group

ChemInform Abstract: Antitumor Phospholipids: A One-Pot Introduction of a Phosphocholine Moiety into Lipid Hydroxy Acceptors

Bio-Analytical Method Development and Validation for Estimation of Zaltoprofen in Human Plasma by Reverse Phase -HPLC Method

Bacterial lipopolysaccharide has structural similarity to ceramide and stimulates ceramide-activated protein kinase in myeloid cells

A comparison of the lytic properties of two ether-linked lipids, one with and one without antineoplastic activity

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