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Molecular Genetics and Metabolism
|
June 6, 2022
Integration of metabolomics with genomics: Metabolic gene prioritization using metabolomics data and genomic variant (CADD) scores
Michiel Bongaerts, Ramon Bonte, Serwet Demirdas, et al.
Journal of Inherited Metabolic Disease
|
March 17, 2025
Cystathionine β-Synthase Deficiency in the E-HOD Registry-Part II: Dietary and Pharmacological Treatment
Andrew A M Morris, Jitka Sokolová, Markéta Pavlíková, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 18, 2014
Protein arginine hypomethylation in a mouse model of cystathionine β-synthase deficiency
Ruben Esse, Apolline Imbard, Cristina Florindo, et al.
Journal of Electrocardiology
|
February 17, 2020
Novel use of repolarization parameters in electrocardiographic imaging to uncover arrhythmogenic substrate
L J Blom, S A Groeneveld, B M Wulterkens, et al.
Journal of Inherited Metabolic Disease
|
December 9, 2020
Cystathionine β-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis
Viktor Kožich, Jitka Sokolová, Andrew A M Morris, et al.
Journal of Child and Adolescent Psychopharmacology
|
February 20, 2024
Pharmacogenetic Factors Influence Escitalopram Pharmacokinetics and Adverse Events in Youth with a Family History of Bipolar Disorder: A Preliminary Study
Duncan C Honeycutt, Thomas J Blom, Laura B Ramsey, et al.
Journal of Reproduction and Fertility
|
March 1, 1995
Development of methionine synthase, cystathionine-beta-synthase and S-adenosyl-homocysteine hydrolase during gestation in rats
L A VanAerts, C M Poirot, C A Herberts, et al.
JIMD Reports
|
March 11, 2020
Cystathionine beta synthase deficiency and brain edema associated with methionine excess under betaine supplementation: Four new cases and a review of the evidence
Bernd C Schwahn, Thomas Scheffner, Hedwig Stepman, et al.
Metabolism: Clinical and Experimental
|
December 1, 1994
Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?
R P Steegers-Theunissen, G H Boers, F J Trijbels, et al.
Arthritis and Rheumatism
|
November 17, 2001
The C677T mutation in the methylenetetrahydrofolate reductase gene: a genetic risk factor for methotrexate-related elevation of liver enzymes in rheumatoid arthritis patients
A E van Ede, R F Laan, H J Blom, et al.
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of 72
Search research articles
Search
Showing results (541-550 of 717) with videos related to
Sort By:
Page
of 72
Molecular Genetics and Metabolism
|
June 6, 2022
Integration of metabolomics with genomics: Metabolic gene prioritization using metabolomics data and genomic variant (CADD) scores
Michiel Bongaerts, Ramon Bonte, Serwet Demirdas, et al.
Journal of Inherited Metabolic Disease
|
March 17, 2025
Cystathionine β-Synthase Deficiency in the E-HOD Registry-Part II: Dietary and Pharmacological Treatment
Andrew A M Morris, Jitka Sokolová, Markéta Pavlíková, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 18, 2014
Protein arginine hypomethylation in a mouse model of cystathionine β-synthase deficiency
Ruben Esse, Apolline Imbard, Cristina Florindo, et al.
Journal of Electrocardiology
|
February 17, 2020
Novel use of repolarization parameters in electrocardiographic imaging to uncover arrhythmogenic substrate
L J Blom, S A Groeneveld, B M Wulterkens, et al.
Journal of Inherited Metabolic Disease
|
December 9, 2020
Cystathionine β-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis
Viktor Kožich, Jitka Sokolová, Andrew A M Morris, et al.
Journal of Child and Adolescent Psychopharmacology
|
February 20, 2024
Pharmacogenetic Factors Influence Escitalopram Pharmacokinetics and Adverse Events in Youth with a Family History of Bipolar Disorder: A Preliminary Study
Duncan C Honeycutt, Thomas J Blom, Laura B Ramsey, et al.
Journal of Reproduction and Fertility
|
March 1, 1995
Development of methionine synthase, cystathionine-beta-synthase and S-adenosyl-homocysteine hydrolase during gestation in rats
L A VanAerts, C M Poirot, C A Herberts, et al.
JIMD Reports
|
March 11, 2020
Cystathionine beta synthase deficiency and brain edema associated with methionine excess under betaine supplementation: Four new cases and a review of the evidence
Bernd C Schwahn, Thomas Scheffner, Hedwig Stepman, et al.
Metabolism: Clinical and Experimental
|
December 1, 1994
Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?
R P Steegers-Theunissen, G H Boers, F J Trijbels, et al.
Arthritis and Rheumatism
|
November 17, 2001
The C677T mutation in the methylenetetrahydrofolate reductase gene: a genetic risk factor for methotrexate-related elevation of liver enzymes in rheumatoid arthritis patients
A E van Ede, R F Laan, H J Blom, et al.
Page
of 72