Lattice_grid_med
Powered by LatticeGrid

Search Enter term and hit return. Use '*' for as a wildcard.

Publication Listing for the MeSH term homocystinuria. Found 9 abstracts

Lee HO, Gallego-Villar L, Grisch-Chan HM, Häberle J, Thöny B, Kruger WD. Treatment of Cystathionine β-Synthase Deficiency in Mice Using a Minicircle-Based Naked DNA Vector. Human gene therapy. 2019 Sep;30(9):1093-100.   PMCID: PMC6761586
Lee HO, Gallego-Villar L, Grisch-Chan HM, Haeberle J, Thony B, Kruger WD. Treatment of CBS deficiency in mice using a minicircle-based naked DNA vector. Human gene therapy. 2019 Sep;30(9):1093-100.   PMCID: PMC6761586
Dayal S, Chauhan AK, Jensen M, Leo L, Lynch CM, Faraci FM, Kruger WD, Lentz SR. Paradoxical absence of a prothrombotic phenotype in a mouse model of severe hyperhomocysteinemia. Blood. 2012 Mar;119(13):3176-83.   PMCID: pmc3321876
Strakova J, Gupta S, Kruger WD, Dilger RN, Tryon K, Li L, Garrow TA, Stro C P. Inhibition of betaine-homocysteine S-methyltransferase in rats causes hyperhomocysteinemia and reduces liver cystathionine beta-synthase activity and methylation capacity. Nutrition Research. 2011 Jul;31(7):563-71.   PMCID: PMC3156413
Tang BQ, Mustafa A, Gupta S, Melnyk S, James SJ, Kruger WD. Methionine-deficient diet induces post-transcriptional downregulation of cystathionine beta-synthase. Nutrition. 2010 Nov;26(11-12):1170-5.   PMCID: PMC2956870
Park ES, Oh HJ, Kruger WD, Jung SC, Lee JS. Recombinant adeno-associated virus mediated gene transfer in a mouse model for homocystinuria. Experimental and Molecular Medicine. 2006 Dec;38(6):652-61.
Jhee KH, Kruger WD. The role of cystathionine beta-synthase in homocysteine metabolism. Antioxidants & redox signaling. 2005 May;7(5-6):813-22.
Singh RH, Kruger WD, Wang LQ, Pasquali M, Elsas LJ. Cystathionine beta-synthase deficiency: Effects of betaine supplementation after methionine restriction in B6-nonresponsive homocystinuria. Genetics in Medicine. 2004 Mar;6(2):90-5.
Kruger WD, Wang L, Jhee KH, Singh RH, Elsas LJ. Cystathionine beta-synthase deficiency in Georgia (USA): Correlation of clinical and biochemical phenotype with genotype. Human Mutation. 2003 Dec;22(6):434-41.
The above publications are sorted by year, faculty last name, and first author. Click on any highlighted author listed to find all publications attributed to that individual. Click on the publication title to see the abstract. First authors who are faculty are highlighted like this. Last authors who are faculty are highlighted like this. Other authors who are faculty are highlighted like this.

MeSH cloud from publications including the MeSH term homocystinuria

Last updated on Wednesday, February 05, 2020