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The New England Journal of Medicine|April 16, 1998
Reduction of plasma homocyst(e)ine levels by breakfast cereal fortified with folic acid in patients with coronary heart diseaseM R Malinow, P B Duell, D L Hess, et al.
Human Molecular Genetics|March 21, 1998
Functional modeling of vitamin responsiveness in yeast: a common pyridoxine-responsive cystathionine beta-synthase mutation in homocystinuriaC E Kim, P M Gallagher, A B Guttormsen, et al.
The American Journal of Cardiology|April 6, 1999
Reduction of homocysteine levels in coronary artery disease by low-dose folic acid combined with vitamins B6 and B12A Lobo, A Naso, K Arheart, et al.
Journal of Inherited Metabolic Disease|June 27, 2019
Analysis of the Qatari R336C cystathionine β-synthase protein in miceSapna Gupta, Lorena Gallego-Villar, Liqun Wang, et al.
Molecular Genetics and Metabolism|June 2, 2000
Polymorphisms in the CBS gene associated with decreased risk of coronary artery disease and increased responsiveness to total homocysteine lowering by folic acidW D Kruger, A A Evans, L Wang, et al.
Diabetes|July 11, 2014
Hyperhomocysteinemia potentiates hyperglycemia-induced inflammatory monocyte differentiation and atherosclerosisPu Fang, Daqing Zhang, Zhongjian Cheng, et al.
Iscience|February 24, 2022
Aberrant cyclin C nuclear release induces mitochondrial fragmentation and dysfunction in <i>MED13L</i> syndrome fibroblastsKai-Ti Chang, Jan Jezek, Alicia N Campbell, et al.
Cancer Research|July 2, 2009
Mice heterozygous for germ-line mutations in methylthioadenosine phosphorylase (MTAP) die prematurely of T-cell lymphomaYuwaraj Kadariya, Bu Yin, Baiqing Tang, et al.
Redox Biology|June 6, 2024
Deciphering pathophysiological mechanisms underlying cystathionine beta-synthase-deficient homocystinuria using targeted metabolomics, liver proteomics, sphingolipidomics and analysis of mitochondrial functionTomas Majtan, Thomas Olsen, Jitka Sokolova, et al.
Human Mutation|November 9, 2018
In silico and in vivo models for Qatari-specific classical homocystinuria as basis for development of novel therapiesHesham M Ismail, Navaneethakrishnan Krishnamoorthy, Nader Al-Dewik, et al.
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