C
Cholsoon Jang
Researcher at University of California, Irvine
Publications - 88
Citations - 6775
Cholsoon Jang is an academic researcher from University of California, Irvine. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 32, co-authored 56 publications receiving 4236 citations. Previous affiliations of Cholsoon Jang include KAIST & Harvard University.
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Journal ArticleDOI
Glucose feeds the TCA cycle via circulating lactate.
Sheng Hui,Jonathan M. Ghergurovich,Raphael J. Morscher,Cholsoon Jang,Xin Teng,Wenyun Lu,Lourdes A Esparza,Tannishtha Reya,Le Zhan,Jessie Yanxiang Guo,Eileen White,Joshua D. Rabinowitz,Joshua D. Rabinowitz +12 more
TL;DR: It is found that lactate can be a primary source of carbon for the TCA cycle and thus of energy, and during the fasted state, the contribution of glucose to tissue TCA metabolism is primarily indirect (via circulating lactate) in all tissues except the brain.
Journal ArticleDOI
Metabolomics and Isotope Tracing
TL;DR: The basics of metabolite measurement by MS are described, including sample preparation, metabolomic analysis, and data interpretation, and the ways in which metabolomics and isotope tracing can illuminate biology are highlighted.
Journal ArticleDOI
Cardiac angiogenic imbalance leads to peripartum cardiomyopathy
Ian S. Patten,Sarosh Rana,Sajid Shahul,Glenn C. Rowe,Cholsoon Jang,Laura Liu,Michele R. Hacker,Julie S. Rhee,John D. Mitchell,Feroze Mahmood,Philip E. Hess,Caitlin Farrell,Nicole Koulisis,Eliyahu V. Khankin,Suzanne D. Burke,Suzanne D. Burke,I. Tudorache,Johann Bauersachs,Federica del Monte,Denise Hilfiker-Kleiner,S. Ananth Karumanchi,S. Ananth Karumanchi,Zoltan Arany +22 more
TL;DR: The data indicate that PPCM is mainly a vascular disease, caused by excess anti-angiogenic signalling in the peripartum period, and explain how late pregnancy poses a threat to cardiac homeostasis, and why pre-eclampsia and multiple gestation are important risk factors for the development of P PCM.
Journal ArticleDOI
The Small Intestine Converts Dietary Fructose into Glucose and Organic Acids
Cholsoon Jang,Sheng Hui,Wenyun Lu,Alexis J. Cowan,Raphael J. Morscher,Gina Lee,Wei Liu,Gregory J. Tesz,Morris J. Birnbaum,Joshua D. Rabinowitz +9 more
TL;DR: It is proposed that the small intestine shields the liver from otherwise toxic fructose exposure, finding that dietary fructose is cleared by theSmall intestine, both by prior exposure to fructose and by feeding.
Journal ArticleDOI
A branched-chain amino acid metabolite drives vascular fatty acid transport and causes insulin resistance
Cholsoon Jang,Sungwhan F. Oh,Shogo Wada,Glenn C. Rowe,Laura Liu,Mun Chun Chan,James Rhee,James Rhee,Atsushi Hoshino,Boa Kim,Ayon Ibrahim,Luisa G Baca,Esl Kim,Chandra C. Ghosh,Samir M. Parikh,Aihua Jiang,Qingwei Chu,Daniel E. Forman,Stewart H. Lecker,Saikumari Y. Krishnaiah,Joshua D. Rabinowitz,Aalim M. Weljie,Joseph A. Baur,Dennis L. Kasper,Zoltan Arany +24 more
TL;DR: PPARGC1a is leveraged, a transcriptional coactivator that regulates broad programs of fatty acid consumption, to identify 3-hydroxyisobutyrate (3-HIB), a catabolic intermediate of the BCAA valine, as a new paracrine regulator of trans-endothelial fatty acid transport, providing a mechanistic explanation for how increased BCAA catabolic flux can cause diabetes.