Results 1 to 10 of about 55,919 (216)

Ueber Adenin und Hypoxanthin [PDF]

Berichte der deutschen chemischen Gesellschaft, 1890
n ...
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Associations between muscle quality and whole-body vibration exercise-induced changes in plasma hypoxanthine following an oral glucose load in healthy male subjects

Endocrine Journal
Blood levels of hypoxanthine (HX) have been suggested as potential biomarkers associated with intramuscular metabolic dynamics in response to exercise.
Tomoyuki Hara, Yuya Fujishima, Hitoshi Nishizawa, Yusuke Kawachi, Takashi Nakamura, Seigo Akari, Yoshiyuki Ono, Hirotaka Watanabe, Taka-aki Sakaue, Yoshinari Obata, Hirofumi Nagao, Shiro Fukuda, Takashi Kanamoto, Mitsuyoshi Takahara, Naoto Katakami, Ken Nakata, Iichiro Shimomura   +16 more
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Hypoxanthine in stored blood [PDF]

Transfusion, 1991
R. Paroni, E. Bolzacchini, M. Samaja
openaire   +2 more sources

Brain network and energy imbalance in Parkinson’s disease: linking ATP reduction and α-synuclein pathology

Frontiers in Molecular Neuroscience
Parkinson’s disease (PD) involves the disruption of brain energy homeostasis. This encompasses broad-impact factors such as mitochondrial dysfunction, impaired glycolysis, and other metabolic disturbances, like disruptions in the pentose phosphate ...
Hirohisa Watanabe, Sayuri Shima, Kazuya Kawabata, Yasuaki Mizutani, Akihiro Ueda, Akihiro Ueda, Mizuki Ito, Mizuki Ito   +7 more
doaj   +1 more source

Simultaneous Electrochemical Determination of Uric Acid, Xanthine, and Hypoxanthine Using AgNPs/MIL-101(Cr) Modified Electrode

ECS Sensors Plus
This paper presents silver nanoparticles supported by the Matérial Institute Lavoisier-101 (AgNPs/MIL-101(Cr)) for electrochemical determination of uric acid (URA), xanthine (XAT), and hypoxanthine (HPX).
Nguyen Quang Man, Nguyen Ngoc Nghia, Vo Thi Khanh Ly, Nguyen Duc Vu Quyen, Le Thi Hoa, Ho Van Minh Hai, Le Van Thanh Son, Le Thi Hong Phong, Nguyen Dinh Luyen, Nguyen Chi Bao, Dinh Quang Khieu   +10 more
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E. coli genetically modified for purine nucleobase release promotes butyrate generation and colonic wound healing during DSS insult

Gut Microbes
The gut microbiota transforms energy stored as undigestible carbohydrates into a remarkable number of metabolites that fuel intestinal bacterial communities and the host tissue.
J. Scott Lee, Daniel J. Kao, Corey S. Worledge, Zachary F. Villamaria, Ruth X. Wang, Nichole M. Welch, Rachael E. Kostelecky, Sean P. Colgan   +7 more
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Can Non-Conventional Blood Biomarkers Improve Running Performance Prediction? A Proof of Concept

Life
Conventional measures such as maximal oxygen uptake (V˙O2max), although widely regarded as the gold standard, do not fully capture endurance performance.
Matija Dvorski, Marija Rakovac, Tomislav Kelava, Nataša Kovačić, Darja Flegar, Sara Aničić, Ivo Krešić, Ljiljana Ćulibrk, Filip Koražija, Damjan Dimnjaković, Alan Šućur   +10 more
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Hypoxanthine Promotes Pulmonary Vascular Remodeling and Adenosine Deaminase Is a Therapeutic Target for Pulmonary Hypertension

JACC: Basic to Translational Science
Summary: Uric acid metabolism is implicated in the pathogenesis of pulmonary arterial hypertension, wherein the key metabolite hypoxanthine exhibits elevated levels, thereby promoting pulmonary vascular remodeling through facilitation of cell ...
Jun-Zhuo Shi, MS, Yong-Jian Zhu, MD, Meng-Jie Zhang, BS, Yi Yan, PhD, Lu-Ling Zhao, MS, Hong-Da Zhang, MD, Yan Liu, MD, Wen-Hui Wu, PhD, Zhe Cheng, MD, Chun-Guang Qiu, MD, Jie-Jian Kou, MS, Yun-Feng Zhou, PhD, Xiao-Bin Pang, PhD, Ji-Wang Chen, MD, Xin-Mei Xie, MS, Yang-Yang He, PhD, Zhi-Cheng Jing, MD   +16 more
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Establishment and optimization of a novel mouse model of hyperuricemic nephropathy

Renal Failure
Hyperuricemia is a metabolic disorder characterized by elevated serum uric acid levels. Soluble urate can activate immune responses, and the excessive accumulation of urate in the kidneys results in hyperuricemic nephropathy (HN). However, the lack of an
Jiamin Wang, Rong Chen, Kaireng Wu, Juxian Mo, Minghui Li, Zhe Chen, Guixiang Wang, Ping Zhou, Tian Lan   +8 more
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First case of hereditary xanthinuria in a Moroccan family

PAMJ Clinical Medicine, 2019
The xanthinuria is a rare hereditary autosomal recessive disease. It is related to xanthine oxidase deficiency also known as xanthine dehydrogenase, an enzyme involved in the metabolism of purine bases.
Aicha Ezoubeiri, Asma Labaali, Naima Fdil, Jean-François Benoist, Laila Chabaa   +4 more
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