Author details

Full Name

Jin Xue

Affiliation

ORCID

Career Start Year

2003

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34184915	Intermittent Hypoxia and Hypercapnia Alter Diurnal Rhythms of Luminal Gut Microbiome and Metabolome.	mSystems	2021
33897472	Influence of Intermittent Hypoxia/Hypercapnia on Atherosclerosis, Gut Microbiome, and Metabolome.	Front Physiol	2021
33576765	Genetic interactions regulate hypoxia tolerance conferred by activating Notch in excitatory amino acid transporter 1-positive glial cells in Drosophila melanogaster.	G3 (Bethesda)	2021
34248668	Microbiota Modulates Cardiac Transcriptional Responses to Intermittent Hypoxia and Hypercapnia.	Front Physiol	2021
31058230	Intermittent Hypoxia and Hypercapnia Reproducibly Change the Gut Microbiome and Metabolome across Rodent Model Systems.	mSystems	2019
31618063	Intermittent hypoxia and hypercapnia induces inhibitor of nuclear factor-ÎºB kinase subunit Î²-dependent atherosclerosis in pulmonary arteries.	Am J Physiol Regul Integr Comp Physiol	2019
29896566	Intermittent Hypoxia and Hypercapnia, a Hallmark of Obstructive Sleep Apnea, Alters the Gut Microbiome and Metabolome.	mSystems	2018
30029588	Exploring miRNA-mRNA regulatory network in cardiac pathology in Na<sup>+</sup>/H<sup>+</sup> exchanger isoform 1 transgenic mice.	Physiol Genomics	2018
28678519	Intermittent Hypoxia and Hypercapnia Accelerate Atherosclerosis, Partially via Trimethylamine-Oxide.	Am J Respir Cell Mol Biol	2017
24555826	Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes.	Genome Biol	2014
24069262	Quantitative evaluation of the mitochondrial proteomes of Drosophila melanogaster adapted to extreme oxygen conditions.	PLoS One	2013
23954164	Whole-genome sequencing uncovers the genetic basis of chronic mountain sickness in Andean highlanders.	Am J Hum Genet	2013
23028948	Ultrastructural modifications in the mitochondria of hypoxia-adapted Drosophila melanogaster.	PLoS One	2012
21677276	Identification of a neuronal gene expression signature: role of cell cycle arrest in murine neuronal differentiation in vitro.	Am J Physiol Regul Integr Comp Physiol	2011
24348887	Severe Hypoxia: Consequences to Neural Stem Cells and Neurons.	J Neurol Res	2011
21262834	Experimental selection of hypoxia-tolerant Drosophila melanogaster.	Proc Natl Acad Sci U S A	2011
20460605	Elevated myocardial Na+/H+ exchanger isoform 1 activity elicits gene expression that leads to cardiac hypertrophy.	Physiol Genomics	2010
18927626	Mechanisms underlying hypoxia tolerance in Drosophila melanogaster: hairy as a metabolic switch.	PLoS Genet	2008
17977915	Role of transporters and ion channels in neuronal injury under hypoxia.	Am J Physiol Regul Integr Comp Physiol	2008
18056785	Gene expression in mouse brain following chronic hypoxia: role of sarcospan in glial cell death.	Physiol Genomics	2008
17481584	Hypoxia increases BK channel activity in the inner mitochondrial membrane.	Biochem Biophys Res Commun	2007
17534440	Experimental selection for Drosophila survival in extremely low O(2) environment.	PLoS One	2007
17289818	Novel functional interaction between Na+/H+ exchanger 1 and tyrosine phosphatase SHP-2.	Am J Physiol Regul Integr Comp Physiol	2007
16888043	Effect of carbon dioxide on neonatal mouse lung: a genomic approach.	J Appl Physiol (1985)	2006
15927756	Intermittent hypoxia modulates Na+ channel expression in developing mouse brain.	Int J Dev Neurosci	2005
15115704	Effect of chronically elevated CO2 on CA1 neuronal excitability.	Am J Physiol Cell Physiol	2004
15306696	Na+/H+ exchanger 1 deficiency alters gene expression in mouse brain.	Physiol Genomics	2004
12665539	Chronic intermittent hypoxia decreases the expression of Na/H exchangers and HCO3-dependent transporters in mouse CNS.	J Appl Physiol (1985)	2003
14596847	Expression of Na+/H+ and HCO3- -dependent transporters in Na+/H+ exchanger isoform 1 null mutant mouse brain.	Neuroscience	2003
12522174	Na+ channel expression and neuronal function in the Na+/H+ exchanger 1 null mutant mouse.	J Neurophysiol	2003