W D Kruger - JoVE Visualize

Showing results (11-20 of 25) with videos related to

Pageof 3

Sort By:

Human Molecular Genetics|December 1, 1996

Cloning, mapping and RNA analysis of the human methionine synthase geneY N Li, S Gulati, P J Baker, et al.

Current Alzheimer Research|November 27, 2009

Diet-induced hyperhomocysteinemia increases amyloid-beta formation and deposition in a mouse model of Alzheimer's diseaseJ-M Zhuo, G S Portugal, W D Kruger, et al.

American Journal of Respiratory and Critical Care Medicine|February 24, 2001

The spectrum of mutations in TSC1 and TSC2 in women with tuberous sclerosis and lymphangiomyomatosisG D Strizheva, T Carsillo, W D Kruger, et al.

Developmental Biology|January 1, 1987

Sequences expressed sex-specifically in Drosophila melanogaster adultsA J DiBenedetto, D M Lakich, W D Kruger, et al.

American Journal of Medical Genetics|May 9, 2001

Disposition of homocysteine in subjects heterozygous for homocystinuria due to cystathionine beta-synthase deficiency: relationship between genotype and phenotypeA B Guttormsen, P M Ueland, W D Kruger, et al.

Amino Acids|March 8, 2003

Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: challenging the gene dosage effect hypothesis (Part II)M S Cheon, M Bajo, S H Kim, et al.

Journal of Inherited Metabolic Disease|June 24, 2017

Cysteamine revisited: repair of arginine to cysteine mutationsL Gallego-Villar, Luciana Hannibal, J Häberle, et al.

Advances in Enzyme Regulation|September 2, 1999

Homocysteine metabolism in cardiovascular cells and tissues: implications for hyperhomocysteinemia and cardiovascular diseaseP Chen, R Poddar, E V Tipa, et al.

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.

Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:

Pageof 3

Human Molecular Genetics|December 1, 1996

Cloning, mapping and RNA analysis of the human methionine synthase geneY N Li, S Gulati, P J Baker, et al.

Current Alzheimer Research|November 27, 2009

Diet-induced hyperhomocysteinemia increases amyloid-beta formation and deposition in a mouse model of Alzheimer's diseaseJ-M Zhuo, G S Portugal, W D Kruger, et al.

American Journal of Respiratory and Critical Care Medicine|February 24, 2001

The spectrum of mutations in TSC1 and TSC2 in women with tuberous sclerosis and lymphangiomyomatosisG D Strizheva, T Carsillo, W D Kruger, et al.

Developmental Biology|January 1, 1987

Sequences expressed sex-specifically in Drosophila melanogaster adultsA J DiBenedetto, D M Lakich, W D Kruger, et al.

American Journal of Medical Genetics|May 9, 2001

Disposition of homocysteine in subjects heterozygous for homocystinuria due to cystathionine beta-synthase deficiency: relationship between genotype and phenotypeA B Guttormsen, P M Ueland, W D Kruger, et al.

Amino Acids|March 8, 2003

Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: challenging the gene dosage effect hypothesis (Part II)M S Cheon, M Bajo, S H Kim, et al.

Journal of Inherited Metabolic Disease|June 24, 2017

Cysteamine revisited: repair of arginine to cysteine mutationsL Gallego-Villar, Luciana Hannibal, J Häberle, et al.

Advances in Enzyme Regulation|September 2, 1999

Homocysteine metabolism in cardiovascular cells and tissues: implications for hyperhomocysteinemia and cardiovascular diseaseP Chen, R Poddar, E V Tipa, et al.

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.

Pageof 3