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Immobilization induces anabolic resistance in human myofibrillar protein synthesis with low and high dose amino acid infusion

The Journal of physiology, 2008-12, Vol.586 (24), p.6049-6061

2008

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Chemical generation of bispecific antibodies

Proceedings of the National Academy of Sciences - PNAS, 2010-12, Vol.107 (52), p.22611-22616

2010

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Inhibiting complex IL-17A and IL-17RA interactions with a linear peptide

Scientific reports, 2016-05, Vol.6 (1), p.26071, Article 26071

2016

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Low-volume resistance exercise attenuates the decline in strength and muscle mass associated with immobilization

Muscle & nerve, 2010-10, Vol.42 (4), p.539-546

2010

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Evolution of Potent and Stable Placental-Growth-Factor-1-Targeting CovX-Bodies from Phage Display Peptide Discovery

Journal of medicinal chemistry, 2011-03, Vol.54 (5), p.1256-1265

2011

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 4: synthesis and structure–Activity relationships for 1-[ N-(Methyl)- N-(phenylsulfonyl)amino]-2-(phenyl)-4-(4-( N-(alkyl)- N-(benzyloxycarbonyl)amino)piperidin-1-yl)butanes

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (18), p.2475-2479

2001

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Glycosyltransferase Inhibitors: Synthesis of d-threo-PDMP, l-threo-PDMP, and Other Brain Glucosylceramide Synthase Inhibitors from d- or l-Serine

Journal of organic chemistry, 1998-11, Vol.63 (24), p.8837-8842

1998

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Development of novel linkers to conjugate pharmacophores to a carrier antibody

Bioorganic & medicinal chemistry letters, 2012-07, Vol.22 (13), p.4249-4253

2012

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Resistance exercise decreases eIF2Bε phosphorylation and potentiates the feeding-induced stimulation of p70 S6K1 and rpS6 in young men

American journal of physiology. Regulatory, integrative and comparative physiology, 2008-08, Vol.295 (2), p.R604-R610

2008

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Resistance exercise decreases eIF2Bepsilon phosphorylation and potentiates the feeding-induced stimulation of p70S6K1 and rpS6 in young men

American journal of physiology. Regulatory, integrative and comparative physiology, 2008-08, Vol.295 (2), p.R604-R610

2008

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Resistance exercise decreases eIF2B[epsilon] phosphorylation and potentiates the feeding-induced stimulation of p70^sup S6K1^ and rpS6 in young men

American journal of physiology. Regulatory, integrative and comparative physiology, 2008-08, Vol.295 (2), p.R604

2008

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Activation of signaling pathways regulating translation initiation in human skeletal muscle with feeding and resistance exercise

The FASEB journal, 2007, Vol.21 (6), p.A1207-A1207

2007

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Sex‐based comparisons in skeletal muscle fatigue and twitch potentiation

The FASEB journal, 2007, Vol.21 (6), p.A939-A940

2007

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Resistance exercise decreases eIF2Bε phosphorylation and potentiates the feeding-induced stimulation of p70S6K1 and rpS6 in young men

American journal of physiology. Regulatory, integrative and comparative physiology, 2008, Vol.64 (2)

2008

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Disuse atrophy delays and reduces amino acid induced activation of key translational signaling proteins in humans

The FASEB journal, 2008-03, Vol.22 (S1)

2008

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 1: Discovery and initial structure-activity relationships for 1-amino-2-phenyl-4-(piperidin-1-yl)butanes

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (2), p.259-264

2001

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Changes in muscle cross‐sectional area and strength during leg immobilization: amelioration through resistance exercise with or without whey protein supplementation

The FASEB journal, 2007, Vol.21 (6), p.A945-A945

2007

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 2: Structure-activity relationships for substituted 2-aryl-1-[N-(methyl)-N-(phenylsulfonyl)amino]-4-(piperidin-1-yl)butanes

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (2), p.265-270

2001

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1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 2: lead optimization affording selective, orally bioavailable compounds with potent Anti-HIV activity

Bioorganic & medicinal chemistry letters, 2001-10, Vol.11 (20), p.2741-2745

2001

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Discovery of human CCR5 antagonists containing hydantoins for the treatment of HIV-1 infection

Bioorganic & medicinal chemistry letters, 2001-12, Vol.11 (24), p.3099-3102

2001

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Design, synthesis, and SAR of heterocycle-containing antagonists of the human CCR5 receptor for the treatment of HIV-1 infection

Bioorganic & medicinal chemistry letters, 2001-12, Vol.11 (24), p.3103-3106

2001

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 3: A proposed pharmacophore model for 1-[ N-(methyl)- N-(phenylsulfonyl)amino]-2-(phenyl)-4-[4-(substituted)piperidin-1-yl]butanes

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (18), p.2469-2473

2001

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Syntheses and biological evaluation of 5-(piperidin-1-yl)-3-phenyl-pentylsulfones as CCR5 antagonists

Bioorganic & medicinal chemistry letters, 2004-07, Vol.14 (13), p.3589-3593

2004

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Syntheses and biological evaluation of 5-(piperidin-1-yl)-3-phenyl-dentylsulfones as CCR5 antagonists

Bioorganic & medicinal chemistry letters, 2004, Vol.14 (13), p.3589-3593

2004

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Resistance exercise decreases eIF2B{varepsilon} phosphorylation and potentiates the feeding-induced stimulation of p70S6K1 and rpS6 in young men

American journal of physiology. Regulatory, integrative and comparative physiology, 2008-08, Vol.295 (2), p.R604

2008

Volltextzugriff (PDF)

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Immobilization induces anabolic resistance in human myofibrillar protein synthesis with low and high dose amino acid infusion

Chemical generation of bispecific antibodies

Inhibiting complex IL-17A and IL-17RA interactions with a linear peptide

Low-volume resistance exercise attenuates the decline in strength and muscle mass associated with immobilization

Evolution of Potent and Stable Placental-Growth-Factor-1-Targeting CovX-Bodies from Phage Display Peptide Discovery

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 4: synthesis and structure–Activity relationships for 1-[ N-(Methyl)- N-(phenylsulfonyl)amino]-2-(phenyl)-4-(4-( N-(alkyl)- N-(benzyloxycarbonyl)amino)piperidin-1-yl)butanes

Glycosyltransferase Inhibitors: Synthesis of d-threo-PDMP, l-threo-PDMP, and Other Brain Glucosylceramide Synthase Inhibitors from d- or l-Serine

Development of novel linkers to conjugate pharmacophores to a carrier antibody

Resistance exercise decreases eIF2Bε phosphorylation and potentiates the feeding-induced stimulation of p70 S6K1 and rpS6 in young men

Resistance exercise decreases eIF2Bepsilon phosphorylation and potentiates the feeding-induced stimulation of p70S6K1 and rpS6 in young men

Resistance exercise decreases eIF2B[epsilon] phosphorylation and potentiates the feeding-induced stimulation of p70^sup S6K1^ and rpS6 in young men

Activation of signaling pathways regulating translation initiation in human skeletal muscle with feeding and resistance exercise

Sex‐based comparisons in skeletal muscle fatigue and twitch potentiation

Resistance exercise decreases eIF2Bε phosphorylation and potentiates the feeding-induced stimulation of p70S6K1 and rpS6 in young men

Disuse atrophy delays and reduces amino acid induced activation of key translational signaling proteins in humans

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 1: Discovery and initial structure-activity relationships for 1-amino-2-phenyl-4-(piperidin-1-yl)butanes

Changes in muscle cross‐sectional area and strength during leg immobilization: amelioration through resistance exercise with or without whey protein supplementation

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 2: Structure-activity relationships for substituted 2-aryl-1-[N-(methyl)-N-(phenylsulfonyl)amino]-4-(piperidin-1-yl)butanes

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 2: lead optimization affording selective, orally bioavailable compounds with potent Anti-HIV activity

Discovery of human CCR5 antagonists containing hydantoins for the treatment of HIV-1 infection

Design, synthesis, and SAR of heterocycle-containing antagonists of the human CCR5 receptor for the treatment of HIV-1 infection

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 3: A proposed pharmacophore model for 1-[ N-(methyl)- N-(phenylsulfonyl)amino]-2-(phenyl)-4-[4-(substituted)piperidin-1-yl]butanes

Syntheses and biological evaluation of 5-(piperidin-1-yl)-3-phenyl-pentylsulfones as CCR5 antagonists

Syntheses and biological evaluation of 5-(piperidin-1-yl)-3-phenyl-dentylsulfones as CCR5 antagonists

Resistance exercise decreases eIF2B{varepsilon} phosphorylation and potentiates the feeding-induced stimulation of p70S6K1 and rpS6 in young men

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