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0016 Autoimmunity To Hypocretin And Molecular Mimicry To Flu In Type 1 Narcolepsy

Sleep (New York, N.Y.), 2019-04, Vol.42 (Supplement_1), p.A6-A7

2019

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0030 Involvement Of Regulatory Factor X4 In Narcolepsy

Sleep (New York, N.Y.), 2018-04, Vol.41 (suppl_1), p.A12-A13

Luo, G

2018

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TA 0201. T 0201

Drugs in R&D, 1999-07, Vol.2 (1), p.33-34

1999

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0461 Can a water.rest.shade intervention reduce the risk of chronic kidney disease among sugarcane workers?

Occupational and environmental medicine (London, England), 2017-08, Vol.74 (Suppl 1), p.A146

2017

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058 Life-threateningneurological impairment as a primary manifestation of adult onset Still'sdisease: successfully treated with anakinra

Rheumatology (Oxford, England), 2018-04, Vol.57 (suppl_3)

2018

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094 Anakinra in treatment resistant hospitalised acute polyarticular gout

Rheumatology (Oxford, England), 2018-04, Vol.57 (suppl_3)

2018

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1-(0-chlorophenyl)-1(p-chlorophenyl)2,2,2-trichloroethane induces functional progestin receptors in the rat hypothalamus and pituitary gland

Endocrinology (Philadelphia), 1984-12, Vol.115 (6), p.2052-2058

1984

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1-(1,3-Benzodioxol-5-yl-carbo-nyl) Piperidine, a Modulator of [alpha]-Amino-3-hydroxy-5-methyl-4-isoxazole Propionic Acid Receptor, Ameliorates Exercise-Induced Fatigue in Mice

Biological & pharmaceutical bulletin, 2014-01, Vol.37 (1), p.13

2014

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1-(1,3-Benzodioxol-5-yl-carbo-nyl) Piperidine, a Modulator of α-Amino-3-hydroxy-5-methyl-4-isoxazole Propionic Acid Receptor, Ameliorates Exercise-Induced Fatigue in Mice

Biological and Pharmaceutical Bulletin, 2014-01, Vol.37 (1), p.13-17

2014

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1-(1,3-Benzodioxol-5-yl-carbo-nyl) Piperidine, a Modulator of α-Amino-3-hydroxy-5-methyl-4-isoxazole Propionic Acid Receptor, Ameliorates Exercise-Induced Fatigue in Mice

Biological and Pharmaceutical Bulletin, 2014/01/01, Vol.37(1), pp.13-17

2014

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1 + 1 = 4? Balanced anaesthesia: A sum that is greater than its parts

British journal of pharmacology, 2019-12, Vol.176 (24), p.4785-4786

2019

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The 1.1 Å Crystal Structure of Human TGF-β Type II Receptor Ligand Binding Domain

Structure (London), 2002-07, Vol.10 (7), p.913-919

2002

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The 1.1 å crystal structure of the neuronal acetylcholine receptor antagonist, α-conotoxin PnIA from Conus pennaceus

Structure (London), 1996-04, Vol.4 (4), p.417-423

1996

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1,1-Bis(3′-indolyl)-1-(p-chlorophenyl)methane activates the orphan nuclear receptor Nurr1 and inhibits bladder cancer growth

Molecular cancer therapeutics, 2008-12, Vol.7 (12), p.3825-3833

2008

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1,1-Bis(3'-indolyl)-1-(p-substituted phenyl)methanes induce autophagic cell death in estrogen receptor negative breast cancer

BMC cancer, 2010-12, Vol.10 (1), p.669-669, Article 669

2010

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1,1-Bis(3'-indolyl)-1-(p-substituted phenyl)methanes inhibit ovarian cancer cell growth through peroxisome proliferator-activated receptor-dependent and independent pathways

Molecular cancer therapeutics, 2006-09, Vol.5 (9), p.2324-2336

2006

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1,1-Bis (3′-indolyl)-1-(p-substitutedphenyl)methane compounds inhibit lung cancer cell and tumor growth in a metastasis model

European journal of pharmaceutical sciences, 2013-10, Vol.50 (2), p.227-241

2013

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1,1-Bis(3'-indolyl)-1-(p-substitutedphenyl)methanes induce peroxisome proliferator-activated receptor γ-mediated growth inhibition, transactivation, and differentiation markers in colon cancer cells

Cancer research (Chicago, Ill.), 2004-09, Vol.64 (17), p.5994-6001

2004

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1,1-bis(3'-indolyl)-1-(p-substitutedphenyl)methanes inhibit growth, induce apoptosis, and decrease the androgen receptor in LNCaP prostate cancer cells through peroxisome proliferator-activated receptor gamma-independent pathways

Molecular pharmacology, 2007-02, Vol.71 (2), p.558-569

2007

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1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene (p,p'-DDE) disrupts the estrogen-androgen balance regulating the growth of hormone-dependent breast cancer cells

Breast cancer research : BCR, 2008-01, Vol.10 (1), p.R16-R16, Article R16

2008

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1-1). Sjögren's Syndrome

Internal Medicine, 1999, Vol.38(2), pp.165-166

SUMIDA, Takayuki

1999

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1,10-bis(guanidino)decane inhibits N-methyl-D-aspartate responses in vitro and in vivo

The Journal of pharmacology and experimental therapeutics, 1991-11, Vol.259 (2), p.626

1991

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The (1-14) fragment of parathyroid hormone (PTH) activates intact and amino-terminally truncated PTH-1 receptors

Molecular endocrinology (Baltimore, Md.), 1999-05, Vol.13 (5), p.670-680

1999

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1.15 Å Crystal structure of the X. tropicalis Spred1 EVH1 domain suggests a fourth distinct peptide‐binding mechanism within the EVH1 family

FEBS letters, 2005-02, Vol.579 (5), p.1161-1166

2005

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1-[2-(2-Methoxyphenylthio) benzyl]-4-arylpiperazines derivatives: Synthesis and evaluation for dual 5-HT 1A/SSRI activities

Chinese chemical letters, 2008, Vol.19 (1), p.37-39

2008

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0016 Autoimmunity To Hypocretin And Molecular Mimicry To Flu In Type 1 Narcolepsy

0030 Involvement Of Regulatory Factor X4 In Narcolepsy

TA 0201. T 0201

0461 Can a water.rest.shade intervention reduce the risk of chronic kidney disease among sugarcane workers?

058 Life-threateningneurological impairment as a primary manifestation of adult onset Still'sdisease: successfully treated with anakinra

094 Anakinra in treatment resistant hospitalised acute polyarticular gout

1-(0-chlorophenyl)-1(p-chlorophenyl)2,2,2-trichloroethane induces functional progestin receptors in the rat hypothalamus and pituitary gland

1-(1,3-Benzodioxol-5-yl-carbo-nyl) Piperidine, a Modulator of [alpha]-Amino-3-hydroxy-5-methyl-4-isoxazole Propionic Acid Receptor, Ameliorates Exercise-Induced Fatigue in Mice

1-(1,3-Benzodioxol-5-yl-carbo-nyl) Piperidine, a Modulator of α-Amino-3-hydroxy-5-methyl-4-isoxazole Propionic Acid Receptor, Ameliorates Exercise-Induced Fatigue in Mice

1-(1,3-Benzodioxol-5-yl-carbo-nyl) Piperidine, a Modulator of α-Amino-3-hydroxy-5-methyl-4-isoxazole Propionic Acid Receptor, Ameliorates Exercise-Induced Fatigue in Mice

1 + 1 = 4? Balanced anaesthesia: A sum that is greater than its parts

The 1.1 Å Crystal Structure of Human TGF-β Type II Receptor Ligand Binding Domain

The 1.1 å crystal structure of the neuronal acetylcholine receptor antagonist, α-conotoxin PnIA from Conus pennaceus

1,1-Bis(3′-indolyl)-1-(p-chlorophenyl)methane activates the orphan nuclear receptor Nurr1 and inhibits bladder cancer growth

1,1-Bis(3'-indolyl)-1-(p-substituted phenyl)methanes induce autophagic cell death in estrogen receptor negative breast cancer

1,1-Bis(3'-indolyl)-1-(p-substituted phenyl)methanes inhibit ovarian cancer cell growth through peroxisome proliferator-activated receptor-dependent and independent pathways

1,1-Bis (3′-indolyl)-1-(p-substitutedphenyl)methane compounds inhibit lung cancer cell and tumor growth in a metastasis model

1,1-Bis(3'-indolyl)-1-(p-substitutedphenyl)methanes induce peroxisome proliferator-activated receptor γ-mediated growth inhibition, transactivation, and differentiation markers in colon cancer cells

1,1-bis(3'-indolyl)-1-(p-substitutedphenyl)methanes inhibit growth, induce apoptosis, and decrease the androgen receptor in LNCaP prostate cancer cells through peroxisome proliferator-activated receptor gamma-independent pathways

1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene (p,p'-DDE) disrupts the estrogen-androgen balance regulating the growth of hormone-dependent breast cancer cells

1-1). Sjögren's Syndrome

1,10-bis(guanidino)decane inhibits N-methyl-D-aspartate responses in vitro and in vivo

The (1-14) fragment of parathyroid hormone (PTH) activates intact and amino-terminally truncated PTH-1 receptors

1.15 Å Crystal structure of the X. tropicalis Spred1 EVH1 domain suggests a fourth distinct peptide‐binding mechanism within the EVH1 family

1-[2-(2-Methoxyphenylthio) benzyl]-4-arylpiperazines derivatives: Synthesis and evaluation for dual 5-HT 1A/SSRI activities

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