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Hepatic AdipoR2 signaling plays a protective role against progression of nonalcoholic steatohepatitis in mice

Hepatology (Baltimore, Md.), 2008-08, Vol.48 (2), p.458-473

2008

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Evaluating the severity of nonalcoholic steatohepatitis with superparamagnetic iron oxide-enhanced magnetic resonance imaging

Journal of magnetic resonance imaging, 2008-12, Vol.28 (6), p.1444-1450

2008

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Utility of quantitative 99mTc-phytate scintigraphy to diagnose early-stage non-alcoholic steatohepatitis

Scandinavian journal of gastroenterology, 2009, Vol.44 (2), p.229-236

2009

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Utility of quantitative 99m Tc-phytate scintigraphy to diagnose early-stage non-alcoholic steatohepatitis

Scandinavian journal of gastroenterology, 2009-01, Vol.44 (2), p.229-236

2009

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Determination of Steroid-nonsteroid Equilibrium and Analysis of Its Factors Using Dithiolane and Dioxolane

Heterocycles, 1985, Vol.23 (1), p.216

1985

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Microbiologically Modified Chiral Synthon. III. 4,9-Dimethyl-3,5-dioxo-.DELTA.4(10)-octalin for Formal Total Syntheses of Certain Sesquiterpenoids

Chemical & pharmaceutical bulletin, 1991, Vol.39 (11), p.2973-2979

1991

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Microbiologically modified 4,9-dimethyl-.DELTA.4(10)-octal-3,7-diones as the chiral synthon for formal total syntheses of C(8) oxygenated sesquiterpenoids

Chemical & pharmaceutical bulletin, 1987, Vol.35 (1), p.429-432

1987

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Conformational Analysis of Curdione and Neocurdione

Chemical and Pharmaceutical Bulletin, 1987/09/25, Vol.35(9), pp.3866-3869

1987

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Microbiological asymmetric induction of 4,9-dimethyl-3,5-dioxo-.DELTA.4(10)-octalin

Chemical & pharmaceutical bulletin, 1989, Vol.37 (9), p.2561-2563

1989

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Microbiologically modified chiral synthon. I. 3,8-Dioxo-4-methoxycarbonyl-9-methyl-.DELTA.4(10)-octalin for formal total syntheses of certain sesquiterpenoids and diterpenoids

Chemical & pharmaceutical bulletin, 1989, Vol.37 (3), p.712-717

1989

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Microbiologically modified chiral synthon. II. 4,9-Dimethyl-3,7-dioxo-.DELTA.4(10)-octalin for formal total syntheses of certain C(8) oxygenated sesquiterpenoids

Chemical & pharmaceutical bulletin, 1989, Vol.37 (4), p.1023-1027

1989

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Isolation and structure of new pseudoguaianolides, 4-epipulchellin and 4-epineopulchellin from Gaillardia pulchella

Heterocycles, 1988, Vol.27 (1), p.83-87

1988

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Microbiological asymmetric reduction of 4-carbomethoxy-3,8-dioxo-9-methyl-.DELTA.4(10)-octalin

Chemical & pharmaceutical bulletin, 1986, Vol.34 (6), p.2660-2663

1986

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Studies on Non-sesquiterpenoid Constituents of Gaillardia pulchella. II. Less Lipophilic Substances, Methyl Caffeate as an Antitumor Catecholic

Chemical and Pharmaceutical Bulletin, 1984/03/25, Vol.32(3), pp.1135-1141

1984

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The Complete Structure of Spathulin, a Crystallographic Study of Diacetylspathulin

Chemical and Pharmaceutical Bulletin, 1977/08/25, Vol.25(8), pp.1928-1933

1977

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Ambrosic acid, a new irritant principle from Ambrosia arthemisiifolia

Chemical and Pharmaceutical Bulletin, 1974/06/25, Vol.22(6), pp.1435-1437

1974

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A Novel Pseudotwistane, Pulchellon from Gaillardia pulchella

Chemical and Pharmaceutical Bulletin, 1975/11/25, Vol.23(11), pp.2998-3007

1975

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Microbiologically Modified Chiral Synthon. III. 4, 9-Dimethyl-3, 5-dioxo-Δ4(10)-octalin for Formal Total Syntheses of Certain Sesquiterpenoids

Chemical and Pharmaceutical Bulletin, 1991/11/25, Vol.39(11), pp.2973-2979

1991

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Microbiologically Modified Chiral Synthon. III. 4, 9-Dimethyl-3, 5-dioxo-[delta]4(10)-octalin for Formal Total Syntheses of Certain Sesquiterpenoids

Chemical & pharmaceutical bulletin, 1991-11, Vol.39 (11), p.2973

1991

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Stereoisomeric Effect in Electron Impact Reaction (EI/MS) of Compounds Having Sulfer Containing Ring (Dithiolate and Dithiane)

Heterocycles, 1986, Vol.24 (1), p.262

1986

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Dithioacetal; as a Chiroptical Functional Group to Determine Absolute and Relative Configuration by CD and 1H NMR Spectra

Heterocycles, 1986, Vol.24 (4), p.897

1986

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A Series of Sesquiterpenes with a 7[alpha]-Isopropyl Side Chain and Related Compounds Isolated from Curcuma wenyujin

Chemical & pharmaceutical bulletin, 1991-04, Vol.39 (4), p.843

1991

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A Series of Sesquiterpenes with a 7α-Isopropyl Side Chain and Related Compounds Isolated from Curcuma wenyujin

Chemical and Pharmaceutical Bulletin, 1991/04/25, Vol.39(4), pp.843-853

1991

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MICROBIOLOGICAL ASYMMETRIC INDUCTION OF 4, 9-DIMETHYL-3, 5-DIOXO-Δ4(10)-OCTALIN

Chemical and Pharmaceutical Bulletin, 1989/09/25, Vol.37(9), pp.2561-2563

1989

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Microbiologically Modified Chiral Synthon. II. : 4, 9-Dimethyl-3, 7-dioxo-Δ4(10)-octalin for Formal Total Syntheses of Certain C(8) Oxygenated Sesquiterpenoids

Chemical and Pharmaceutical Bulletin, 1989/04/25, Vol.37(4), pp.1023-1027

1989

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Hepatic AdipoR2 signaling plays a protective role against progression of nonalcoholic steatohepatitis in mice

Evaluating the severity of nonalcoholic steatohepatitis with superparamagnetic iron oxide-enhanced magnetic resonance imaging

Utility of quantitative 99mTc-phytate scintigraphy to diagnose early-stage non-alcoholic steatohepatitis

Utility of quantitative 99m Tc-phytate scintigraphy to diagnose early-stage non-alcoholic steatohepatitis

Determination of Steroid-nonsteroid Equilibrium and Analysis of Its Factors Using Dithiolane and Dioxolane

Microbiologically Modified Chiral Synthon. III. 4,9-Dimethyl-3,5-dioxo-.DELTA.4(10)-octalin for Formal Total Syntheses of Certain Sesquiterpenoids

Microbiologically modified 4,9-dimethyl-.DELTA.4(10)-octal-3,7-diones as the chiral synthon for formal total syntheses of C(8) oxygenated sesquiterpenoids

Conformational Analysis of Curdione and Neocurdione

Microbiological asymmetric induction of 4,9-dimethyl-3,5-dioxo-.DELTA.4(10)-octalin

Microbiologically modified chiral synthon. I. 3,8-Dioxo-4-methoxycarbonyl-9-methyl-.DELTA.4(10)-octalin for formal total syntheses of certain sesquiterpenoids and diterpenoids

Microbiologically modified chiral synthon. II. 4,9-Dimethyl-3,7-dioxo-.DELTA.4(10)-octalin for formal total syntheses of certain C(8) oxygenated sesquiterpenoids

Isolation and structure of new pseudoguaianolides, 4-epipulchellin and 4-epineopulchellin from Gaillardia pulchella

Microbiological asymmetric reduction of 4-carbomethoxy-3,8-dioxo-9-methyl-.DELTA.4(10)-octalin

Studies on Non-sesquiterpenoid Constituents of Gaillardia pulchella. II. Less Lipophilic Substances, Methyl Caffeate as an Antitumor Catecholic

The Complete Structure of Spathulin, a Crystallographic Study of Diacetylspathulin

Ambrosic acid, a new irritant principle from Ambrosia arthemisiifolia

A Novel Pseudotwistane, Pulchellon from Gaillardia pulchella

Microbiologically Modified Chiral Synthon. III. 4, 9-Dimethyl-3, 5-dioxo-Δ4(10)-octalin for Formal Total Syntheses of Certain Sesquiterpenoids

Microbiologically Modified Chiral Synthon. III. 4, 9-Dimethyl-3, 5-dioxo-[delta]4(10)-octalin for Formal Total Syntheses of Certain Sesquiterpenoids

Stereoisomeric Effect in Electron Impact Reaction (EI/MS) of Compounds Having Sulfer Containing Ring (Dithiolate and Dithiane)

Dithioacetal; as a Chiroptical Functional Group to Determine Absolute and Relative Configuration by CD and 1H NMR Spectra

A Series of Sesquiterpenes with a 7[alpha]-Isopropyl Side Chain and Related Compounds Isolated from Curcuma wenyujin

A Series of Sesquiterpenes with a 7α-Isopropyl Side Chain and Related Compounds Isolated from Curcuma wenyujin

MICROBIOLOGICAL ASYMMETRIC INDUCTION OF 4, 9-DIMETHYL-3, 5-DIOXO-Δ4(10)-OCTALIN

Microbiologically Modified Chiral Synthon. II. : 4, 9-Dimethyl-3, 7-dioxo-Δ4(10)-octalin for Formal Total Syntheses of Certain C(8) Oxygenated Sesquiterpenoids

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