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Results: 1-25 | 26-34
Results: 1-25/34
Is the SLC7A10 gene on chromosome 19 a candidate locus for cystinuria?
Authors: Leclerc, D Wu, Q Ellis, JR Goodyer, P Rozen, R
Citation: D. Leclerc et al., Is the SLC7A10 gene on chromosome 19 a candidate locus for cystinuria?, MOL GEN MET, 73(4), 2001, pp. 333-339
Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aorticlipid deposition
Authors: Chen, ZT Karaplis, AC Ackerman, SL Pogribny, IP Melnyk, S Lussier-Cacan, S Chen, MF Pai, A John, SWM Smith, RS Bottiglieri, T Bagley, P Selhub, J Rudnicki, MA James, SJ Rozen, R
Citation: Zt. Chen et al., Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aorticlipid deposition, HUM MOL GEN, 10(5), 2001, pp. 433-443
Plasma homocysteine concentration in children with chronic renal failure
Authors: Merouani, A Lambert, M Delvin, EE Genest, J Robitaille, P Rozen, R
Citation: A. Merouani et al., Plasma homocysteine concentration in children with chronic renal failure, PED NEPHROL, 16(10), 2001, pp. 805-811
Growth rate and biofilm thickness of Streptococcus sobrinus and Streptococcus mutans on hydroxapatite
Authors: Rozen, R Bachrach, G Zachs, B Steinberg, D
Citation: R. Rozen et al., Growth rate and biofilm thickness of Streptococcus sobrinus and Streptococcus mutans on hydroxapatite, APMIS, 109(2), 2001, pp. 155-160
The role of fructans on dental biofilm formation by Streptococcus sobrinus, Streptococcus mutans, Streptococcus gordonii and Actinomyces viscosus
Authors: Rozen, R Bachrach, G Bronshteyn, M Gedalia, I Steinberg, D
Citation: R. Rozen et al., The role of fructans on dental biofilm formation by Streptococcus sobrinus, Streptococcus mutans, Streptococcus gordonii and Actinomyces viscosus, FEMS MICROB, 195(2), 2001, pp. 205-210
Socio-economic disparities in preterm birth: causal pathways and mechanisms
Authors: Kramer, MS Goulet, L Lydon, J Seguin, L McNamara, H Dassa, C Platt, RW Chen, MF Gauthier, H Genest, J Kahn, S Libman, M Rozen, R Masse, A Miner, L Asselin, G Benjamin, A Klein, J Koren, G
Citation: Ms. Kramer et al., Socio-economic disparities in preterm birth: causal pathways and mechanisms, PAED PERIN, 15, 2001, pp. 104-123
Glycine N-methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia
Authors: Mudd, SH Cerone, R Schiaffino, MC Fantasia, AR Minniti, G Caruso, U Lorini, R Watkins, D Matiaszuk, N Rosenblatt, DS Schwahn, B Rozen, R LeGros, L Kotb, M Capdevila, A Luka, Z Finkelstein, JD Tangerman, A Stabler, SP Allen, RH Wagner, C
Citation: Sh. Mudd et al., Glycine N-methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia, J INH MET D, 24(4), 2001, pp. 448-464
The 129XA -> C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine
Authors: Weisberg, IS Jacques, PF Selhub, J Bostom, AG Chen, ZT Ellison, RC Eckfeldt, JH Rozen, R
Citation: Is. Weisberg et al., The 129XA -> C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine, ATHEROSCLER, 156(2), 2001, pp. 409-415
Fenofibrate raises plasma homocysteine levels in the fasted and fed states
Authors: Bissonnette, R Treacy, E Rozen, R Boucher, B Cohn, JS Genest, J
Citation: R. Bissonnette et al., Fenofibrate raises plasma homocysteine levels in the fasted and fed states, ATHEROSCLER, 155(2), 2001, pp. 455-462
Polymorphisms of folate and cobalamin metabolism
Authors: Rozen, R
Citation: R. Rozen, Polymorphisms of folate and cobalamin metabolism, HOMOCYSTEINE IN HEALTH AND DISEASE, 2001, pp. 259-269
Improved bacterial SOS promoter:: lux fusions for genotoxicity detection
Authors: Davidov, Y Rozen, R Smulski, DR Van Dyk, TK Vollmer, AC Elsemore, DA LaRossa, RA Belkin, S
Citation: Y. Davidov et al., Improved bacterial SOS promoter:: lux fusions for genotoxicity detection, MUT RES-GTE, 466(1), 2000, pp. 97-107
Association between the methylenetetrahydrofolate reductase 677C -> T missense mutation and schizophrenia
Authors: Joober, R Benkelfat, C Lal, S Bloom, D Labelle, A Lalonde, P Turecki, G Rozen, R Rouleau, GA
Citation: R. Joober et al., Association between the methylenetetrahydrofolate reductase 677C -> T missense mutation and schizophrenia, MOL PSYCHI, 5(3), 2000, pp. 323-326
A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease
Authors: Brown, CA McKinney, KQ Kaufman, JS Gravel, RA Rozen, R
Citation: Ca. Brown et al., A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease, J CARD RISK, 7(3), 2000, pp. 197-200
Methylenetetrahydrofolate reductase 677 C -> T polymorphism, plasma folate, vitamin B-12 concentrations, and risk of preeclampsia among black Africanwomen from Zimbabwe
Authors: Rajkovic, A Mahomed, K Rozen, R Malinow, MR King, IB Williams, MA
Citation: A. Rajkovic et al., Methylenetetrahydrofolate reductase 677 C -> T polymorphism, plasma folate, vitamin B-12 concentrations, and risk of preeclampsia among black Africanwomen from Zimbabwe, MOL GEN MET, 69(1), 2000, pp. 33-39
The thermolabile variant 677C -> T can further reduce activity when expressed in CIS with severe mutations for human methylenetetrahydrofolate reductase
Authors: Goyette, P Rozen, R
Citation: P. Goyette et R. Rozen, The thermolabile variant 677C -> T can further reduce activity when expressed in CIS with severe mutations for human methylenetetrahydrofolate reductase, HUM MUTAT, 16(2), 2000, pp. 132-138
Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria
Authors: Sibani, S Christensen, B O'Ferrall, E Saadi, I Hiou-Tim, F Rosenblatt, DS Rozen, R
Citation: S. Sibani et al., Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria, HUM MUTAT, 15(3), 2000, pp. 280-287
The molecular basis of cystinuria: An update
Authors: Goodyer, P Boutros, M Rozen, R
Citation: P. Goodyer et al., The molecular basis of cystinuria: An update, EXP NEPHROL, 8(3), 2000, pp. 123-127
Genetic modulation of homocysteinemia
Authors: Rozen, R
Citation: R. Rozen, Genetic modulation of homocysteinemia, SEM THROMB, 26(3), 2000, pp. 255-261
Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome
Authors: Hobbs, CA Sherman, SL Yi, P Hopkins, SE Torfs, CP Hine, RJ Pogribna, M Rozen, R James, SJ
Citation: Ca. Hobbs et al., Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome, AM J HU GEN, 67(3), 2000, pp. 623-630
Influence of methylenetetrahydrofolate reductase genotype, age, vitamin B-12, and folate status on plasma homocysteine in children
Authors: Delvin, EE Rozen, R Merouani, A Genest, J Lambert, M
Citation: Ee. Delvin et al., Influence of methylenetetrahydrofolate reductase genotype, age, vitamin B-12, and folate status on plasma homocysteine in children, AM J CLIN N, 72(6), 2000, pp. 1469-1473
Molecular biology of methylenetetrahydrofolate reductase (MTHFR): Interrelationships with folic acid, homocysteine and vascular disease
Authors: Rozen, R
Citation: R. Rozen, Molecular biology of methylenetetrahydrofolate reductase (MTHFR): Interrelationships with folic acid, homocysteine and vascular disease, DEV CARD M, 230, 2000, pp. 271-289
The silent T1317C mutation of methylenetetrahydrofolate reductase should not interfere with Mboll restriction isotyping of the reported A1298C mutation - Reply
Authors: Sibani, S Leclere, D Weisberg, I Rozen, R
Citation: S. Sibani et al., The silent T1317C mutation of methylenetetrahydrofolate reductase should not interfere with Mboll restriction isotyping of the reported A1298C mutation - Reply, MOL GEN MET, 68(4), 1999, pp. 512-512
A common variant in methionine synthase reductase combined with low cobalamin (vitamin B-12) increases risk for spina bifida
Authors: Wilson, A Platt, R Wu, Q Leclerc, D Christensen, B Yang, H Gravel, RA Rozen, R
Citation: A. Wilson et al., A common variant in methionine synthase reductase combined with low cobalamin (vitamin B-12) increases risk for spina bifida, MOL GEN MET, 67(4), 1999, pp. 317-323
The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia
Authors: Guenther, BD Sheppard, CA Tran, P Rozen, R Matthews, RG Ludwig, ML
Citation: Bd. Guenther et al., The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia, NAT ST BIOL, 6(4), 1999, pp. 359-365
A polymorphism of the methionine synthase gene: Association with plasma folate, vitamin B-12, homocyst(e)ine, and colorectal cancer risk
Authors: Ma, J Stampfer, MJ Christensen, B Giovannucci, E Hunter, DJ Chen, J Willett, WC Selhub, J Hennekens, CH Gravel, R Rozen, R
Citation: J. Ma et al., A polymorphism of the methionine synthase gene: Association with plasma folate, vitamin B-12, homocyst(e)ine, and colorectal cancer risk, CANC EPID B, 8(9), 1999, pp. 825-829
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