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Conrad Wagner

Showing results (61-70 of 68) with videos related to

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Hepatology (Baltimore, Md.)|March 19, 2013
Excess S-adenosylmethionine reroutes phosphatidylethanolamine towards phosphatidylcholine and triglyceride synthesisMaite Martínez-Uña, Marta Varela-Rey, Ainara Cano, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 2004
S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolismIvo Baric, Ksenija Fumic, Byron Glenn, et al.
Gastroenterology|June 13, 2012
Hepatoma cells from mice deficient in glycine N-methyltransferase have increased RAS signaling and activation of liver kinase B1Nuria Martínez-López, Juan L García-Rodríguez, Marta Varela-Rey, et al.
Journal of Proteome Research|August 6, 2010
Liquid chromatography-mass spectrometry-based parallel metabolic profiling of human and mouse model serum reveals putative biomarkers associated with the progression of nonalcoholic fatty liver diseaseJonathan Barr, Mercedes Vázquez-Chantada, Cristina Alonso, et al.
Neuron|March 11, 2014
S-adenosylmethionine levels regulate the schwann cell DNA methylomeMarta Varela-Rey, Marta Iruarrizaga-Lejarreta, Juan José Lozano, et al.
Journal of Hepatology|December 3, 2014
S-Adenosylmethionine increases circulating very-low density lipoprotein clearance in non-alcoholic fatty liver diseaseMaite Martínez-Uña, Marta Varela-Rey, Daniela Mestre, et al.
Journal of Hepatology|September 23, 2015
Methionine and S-adenosylmethionine levels are critical regulators of PP2A activity modulating lipophagy during steatosisImanol Zubiete-Franco, Juan Luis García-Rodríguez, Maite Martínez-Uña, et al.
Orphanet Journal of Rare Diseases|August 21, 2015
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotesYin-Hsiu Chien, Jose E Abdenur, Federico Baronio, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Hepatology (Baltimore, Md.)|March 19, 2013
Excess S-adenosylmethionine reroutes phosphatidylethanolamine towards phosphatidylcholine and triglyceride synthesisMaite Martínez-Uña, Marta Varela-Rey, Ainara Cano, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 2004
S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolismIvo Baric, Ksenija Fumic, Byron Glenn, et al.
Gastroenterology|June 13, 2012
Hepatoma cells from mice deficient in glycine N-methyltransferase have increased RAS signaling and activation of liver kinase B1Nuria Martínez-López, Juan L García-Rodríguez, Marta Varela-Rey, et al.
Journal of Proteome Research|August 6, 2010
Liquid chromatography-mass spectrometry-based parallel metabolic profiling of human and mouse model serum reveals putative biomarkers associated with the progression of nonalcoholic fatty liver diseaseJonathan Barr, Mercedes Vázquez-Chantada, Cristina Alonso, et al.
Neuron|March 11, 2014
S-adenosylmethionine levels regulate the schwann cell DNA methylomeMarta Varela-Rey, Marta Iruarrizaga-Lejarreta, Juan José Lozano, et al.
Journal of Hepatology|December 3, 2014
S-Adenosylmethionine increases circulating very-low density lipoprotein clearance in non-alcoholic fatty liver diseaseMaite Martínez-Uña, Marta Varela-Rey, Daniela Mestre, et al.
Journal of Hepatology|September 23, 2015
Methionine and S-adenosylmethionine levels are critical regulators of PP2A activity modulating lipophagy during steatosisImanol Zubiete-Franco, Juan Luis García-Rodríguez, Maite Martínez-Uña, et al.
Orphanet Journal of Rare Diseases|August 21, 2015
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotesYin-Hsiu Chien, Jose E Abdenur, Federico Baronio, et al.
Pageof 7