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Jun Gu

Researcher at Peking University

Publications -  24
Citations -  23637

Jun Gu is an academic researcher from Peking University. The author has contributed to research in topics: Longevity & Genome-wide association study. The author has an hindex of 13, co-authored 21 publications receiving 22240 citations. Previous affiliations of Jun Gu include Sun Yat-sen University & Zhejiang University.

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Journal ArticleDOI

Initial sequencing and analysis of the human genome.

Eric S. Lander, +248 more
- 15 Feb 2001 - 
TL;DR: The results of an international collaboration to produce and make freely available a draft sequence of the human genome are reported and an initial analysis is presented, describing some of the insights that can be gleaned from the sequence.
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Characterization of the structure and function of the fourth member of p38 group mitogen-activated protein kinases, p38delta.

TL;DR: Cloned and characterized a new member of the p38 group of mitogen-activated protein kinases here termed p38δ, which contains the TGY dual phosphorylation site and is activated by a group of extracellular stimuli including cytokines and environmental stresses that also activate the other three known p38 isoforms.
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Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921))

Eric S. Lander, +258 more
- 02 Aug 2001 - 
Journal ArticleDOI

Novel loci and pathways significantly associated with longevity

TL;DR: A genome-wide association study of Han Chinese with a sample size 2.7 times the largest previously published GWAS on centenarians suggests protective mechanisms including immunity and nutrient metabolism and their interactions with environmental stress play key roles in human longevity.
Journal ArticleDOI

Regulation of TNF Expression by Multiple Mitogen-Activated Protein Kinase Pathways

TL;DR: In this article, four mitogen-activated protein (MAP) kinase pathways are activated in LPS-stimulated macrophages: the extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase/stressactivated protein kinase, p38, and Big MAP kinase(BMK)/ERK5 pathways.