Hua Jiang

James R. Roede, Eugene Y. Kim, D. Petersen, 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Long-term betaine therapy in a murine model of cystathionine beta-synthase deficient homocystinuria: decreased efficacy over time reveals a significant threshold effect between elevated homocysteine and thrombotic risk.

Hua Jiang, K. Maclean, R. Allen, 2012, Molecular genetics and metabolism.

Cystathionine beta-synthase null homocystinuric mice fail to exhibit altered hemostasis or lowering of plasma homocysteine in response to betaine treatment

J. Kraus, M. Elleder, Hua Jiang, 2010, Molecular genetics and metabolism.

Hyperhomocysteinemia is associated with hypertriglyceridemia in mice with methylenetetrahydrofolate reductase deficiency.

R. Rozen, L. Mikael, Hua Jiang, 2009, Molecular genetics and metabolism.

Biomarkers of oxidative stress, inflammation, and vascular dysfunction in inherited cystathionine β‐synthase deficient homocystinuria and the impact of taurine treatment in a phase 1/2 human clinical trial

U. Christians, K. Moreau, L. Pyle, 2019, Journal of inherited metabolic disease.

Cystathionine beta-synthase deficiency alters hepatic phospholipid and choline metabolism: Post-translational repression of phosphatidylethanolamine N-methyltransferase is a consequence rather than a cause of liver injury in homocystinuria.

D. Orlicky, R. Jacobs, Hua Jiang, 2017, Molecular genetics and metabolism.

Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease

R. Banerjee, T. Haack, D. Dimmock, 2020, Journal of inherited metabolic disease.

Characterization of Four Variant Forms of Human Propionyl-CoA Carboxylase Expressed in Escherichia coli*

V. Yee, J. Kraus, K. S. Rao, 2005, Journal of Biological Chemistry.

Altered hepatic sulfur metabolism in cystathionine β‐synthase‐deficient homocystinuria: regulatory role of taurine on competing cysteine oxidation pathways

S. Abman, Hua Jiang, K. Maclean, 2014, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Combination of machine learning-based bulk and single-cell genomics reveals necroptosis-related molecular subtypes and immunological features in autism spectrum disorder

Hua Jiang, Lichun Liu, Qingxia Fu, 2023, Frontiers in Immunology.

Increased dietary fat contributes to dysregulation of the LKB1/AMPK pathway and increased damage in a mouse model of early-stage ethanol-mediated steatosis.

D. Petersen, D. Orlicky, Hua Jiang, 2013, The Journal of nutritional biochemistry.

Hyperhomocysteinemia is associated with hypertriglyceridemia in mice with methylenetetrahydrofolate reductase deficiency.

R. Rozen, L. Mikael, Hua Jiang, 2009, Molecular genetics and metabolism.

Dysregulation of hepatic one-carbon metabolism in classical homocystinuria: Implications of redox-sensitive DHFR repression and tetrahydrofolate depletion for pathogenesis and treatment.

James R. Roede, Hua Jiang, Teodoro Bottiglieri, 2024, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.