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Our Animal Connection: What Sapiens Can Learn from Other Species

Second edition., 2020

Volltextzugriff (PDF)

Enantioselective Synthesis of Janus Kinase Inhibitor INCB018424 via an Organocatalytic Aza-Michael Reaction

Organic letters, 2009-05, Vol.11 (9), p.1999-2002

2009

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Numerical Response Surfaces of Volume of Ablation and Retropulsion Amplitude by Settings of Ho:YAG Laser Lithotripter

Journal of healthcare engineering, 2018-01, Vol.2018, p.8261801-11

2018

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Discovery of INCB10820/PF-4178903, a potent, selective, and orally bioavailable dual CCR2 and CCR5 antagonist

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (5), p.1442-1446

2011

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Discovery of INCB3284, a Potent, Selective, and Orally Bioavailable hCCR2 Antagonist

ACS medicinal chemistry letters, 2011-06, Vol.2 (6), p.450-454

2011

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Temporal Variations in the Hepatitis C Virus Intrahost Population during Chronic Infection

Journal of Virology, 2011-07, Vol.85 (13), p.6369-6380

2011

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The Desferrithiocin Pharmacophore

Journal of medicinal chemistry, 1994-05, Vol.37 (10), p.1411-1417

1994

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Our Animal Connection: What Sapiens Can Learn from Other Species

2, 2021

Volltextzugriff (PDF)

Discovery of INCB3344, a potent, selective and orally bioavailable antagonist of human and murine CCR2

Bioorganic & medicinal chemistry letters, 2010-12, Vol.20 (24), p.7473-7478

2010

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Total syntheses of (+)-hypusine and its (2S,9S)-diastereomer

Journal of organic chemistry, 1993-11, Vol.58 (24), p.6804-6806

1993

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Monohalogenated acetamide-induced cellular stress and genotoxicity are related to electrophilic softness and thiol/thiolate reactivity

Journal of environmental sciences (China), 2017-08, Vol.58 (8), p.224-230

2017

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Discovery of INCB8761/PF-4136309, a Potent, Selective, and Orally Bioavailable CCR2 Antagonist

ACS medicinal chemistry letters, 2011-12, Vol.2 (12), p.913-918

2011

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Synthesis of new proton-ionizable and neutral macrocyclic, macrobicyclic and macrotricyclic crown compounds containing dibenzo-16-crown-5 units

Journal of heterocyclic chemistry, 1998-11, Vol.35 (6), p.1381-1387

1998

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Discovery of ((1S,3R)-1-isopropyl-3-((3S,4S)-3-methoxy-tetrahydro-2H-pyran-4-ylamino)cyclopentyl)(4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1-yl)methanone, PF-4254196, a CCR2 antagonist with an improved cardiovascular profile

Bioorganic & medicinal chemistry letters, 2011-05, Vol.21 (9), p.2626-2630

2011

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Discovery of INCB9471, a Potent, Selective, and Orally Bioavailable CCR5 Antagonist with Potent Anti-HIV-1 Activity

ACS medicinal chemistry letters, 2010-12, Vol.1 (9), p.483-487

2010

Volltextzugriff (PDF)

Discovery of ((1S,3R)-1-isopropyl-3-((3S,4S)-3-methoxy-tetrahydro-2H-pyran-4-yl a mino)cyclopentyl)(4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1 - y l)methanone, PF-4254196, a CCR2 antagonist with an improved cardiovascular profile

Bioorganic & medicinal chemistry letters, 2011-05, Vol.21 (9), p.2626-2630

2011

Volltextzugriff (PDF)

Discovery of (1S,3R)-1-isopropyl-3-((3S,4S)-3-methoxy-tetrahydro-2H-pyran-4-ylamino)cyclopentyl4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1-ylmethanone, PF-4254196, a CCR2 antagonist with an improved cardiovascular profile

Bioorganic & medicinal chemistry letters, 2011, Vol.21 (9), p.2626-2630

2011

Volltextzugriff (PDF)

Discovery of ((1 S,3 R)-1-isopropyl-3-((3 S,4 S)-3-methoxy-tetrahydro-2 H-pyran-4-ylamino)cyclopentyl)(4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1-yl)methanone, PF-4254196, a CCR2 antagonist with an improved cardiovascular profile

Bioorganic & medicinal chemistry letters, 2011, Vol.21 (9), p.2626-2630

2011

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Shape and topology optimization for tailoring the ratio between two flexural eigenfrequencies of atomic force microscopy cantilever probe

Frontiers of Mechanical Engineering, 2014-03, Vol.9 (1), p.50-57

2014

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Evolutionary Lineages and Functional Diversification of Plant Hexokinases

Molecular plant, 2010-03, Vol.3 (2), p.334-346

2010

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T Cell Repertoire Diversity Is Decreased in Type 1 Diabetes Patients

Genomics, proteomics & bioinformatics, 2016-12, Vol.14 (6), p.338-348

2016

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Responses of Plant Community and Soil Properties to Inter-Annual Precipitation Variability and Grazing Durations in a Desert Steppe in Inner Mongolia

Journal of Integrative Agriculture, 2014-06, Vol.13 (6), p.1171-1182

WANG Zhen, YUN Xiang-jun, WEI Zhi-jun, Michael P Schellenberg, WANG Yun-feng, YANGXia , HOU Xiang-yang (Member of JIA Editorial Board Key Laboratory of Grassland Resources and Ecology,)

2014

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The Salt Overly Sensitive （SOS） Pathway： Established and Emerging Roles

分子植物：英文版, 2013 (2), p.275-286

Hongtao Ji José M. Pardo Giorgia Batelli Michael J. Van Oosten Ray A. Bressan Xia Li

2013

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Phylogenetic study of the tribe Potentilleae （Rosaceae）, with further insight into the disintegration of Sibbaldia

植物分类学报：英文版, 2017, Vol.55 (3), p.177-191

Tao Feng Michael J. Moore Min-Hui Yan Yan-Xia Sun Hua-Jie Zhang Ai-Ping Meng Xiao-Dong Li Shu-Guang Jian Jian-Qiang Li Heng-Chang Wang

2017

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T Cell Repertoire Diversity Is Decreased in Type 1 Diabetes Patients

基因组蛋白质组与生物信息学报：英文版, 2016, Vol.14 (6)

Yin Tong Zhoufang Li Hua Zhang Ligang Xia Meng Zhang Ying Xu Zhanhui Wang Michael W Deem Xiaojuan Sun Jiankui He

2016

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Our Animal Connection: What Sapiens Can Learn from Other Species

Enantioselective Synthesis of Janus Kinase Inhibitor INCB018424 via an Organocatalytic Aza-Michael Reaction

Numerical Response Surfaces of Volume of Ablation and Retropulsion Amplitude by Settings of Ho:YAG Laser Lithotripter

Discovery of INCB10820/PF-4178903, a potent, selective, and orally bioavailable dual CCR2 and CCR5 antagonist

Discovery of INCB3284, a Potent, Selective, and Orally Bioavailable hCCR2 Antagonist

Temporal Variations in the Hepatitis C Virus Intrahost Population during Chronic Infection

The Desferrithiocin Pharmacophore

Our Animal Connection: What Sapiens Can Learn from Other Species

Discovery of INCB3344, a potent, selective and orally bioavailable antagonist of human and murine CCR2

Total syntheses of (+)-hypusine and its (2S,9S)-diastereomer

Monohalogenated acetamide-induced cellular stress and genotoxicity are related to electrophilic softness and thiol/thiolate reactivity

Discovery of INCB8761/PF-4136309, a Potent, Selective, and Orally Bioavailable CCR2 Antagonist

Synthesis of new proton-ionizable and neutral macrocyclic, macrobicyclic and macrotricyclic crown compounds containing dibenzo-16-crown-5 units

Discovery of ((1S,3R)-1-isopropyl-3-((3S,4S)-3-methoxy-tetrahydro-2H-pyran-4-ylamino)cyclopentyl)(4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1-yl)methanone, PF-4254196, a CCR2 antagonist with an improved cardiovascular profile

Discovery of INCB9471, a Potent, Selective, and Orally Bioavailable CCR5 Antagonist with Potent Anti-HIV-1 Activity

Discovery of ((1S,3R)-1-isopropyl-3-((3S,4S)-3-methoxy-tetrahydro-2H-pyran-4-yl a mino)cyclopentyl)(4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1 - y l)methanone, PF-4254196, a CCR2 antagonist with an improved cardiovascular profile

Discovery of (1S,3R)-1-isopropyl-3-((3S,4S)-3-methoxy-tetrahydro-2H-pyran-4-ylamino)cyclopentyl4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1-ylmethanone, PF-4254196, a CCR2 antagonist with an improved cardiovascular profile

Discovery of ((1 S,3 R)-1-isopropyl-3-((3 S,4 S)-3-methoxy-tetrahydro-2 H-pyran-4-ylamino)cyclopentyl)(4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1-yl)methanone, PF-4254196, a CCR2 antagonist with an improved cardiovascular profile

Shape and topology optimization for tailoring the ratio between two flexural eigenfrequencies of atomic force microscopy cantilever probe

Evolutionary Lineages and Functional Diversification of Plant Hexokinases

T Cell Repertoire Diversity Is Decreased in Type 1 Diabetes Patients

Responses of Plant Community and Soil Properties to Inter-Annual Precipitation Variability and Grazing Durations in a Desert Steppe in Inner Mongolia

The Salt Overly Sensitive （SOS） Pathway： Established and Emerging Roles

Phylogenetic study of the tribe Potentilleae （Rosaceae）, with further insight into the disintegration of Sibbaldia

T Cell Repertoire Diversity Is Decreased in Type 1 Diabetes Patients

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