choline has been researched along with CBS Deficiency in 9 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "These results suggest that reduced fat mass is common in patients with classical homocystinuria, and that alterations in homocysteine and choline pathways affect body mass and lipid metabolism." | 9.19 | Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism. ( Bandeira, IC; Blom, HJ; Castro, K; D'Almeida, V; de Souza, CF; Imbard, A; Leistner-Segal, S; Nalin, T; Poloni, S; Schwartz, IV; Spritzer, PM; Tonon, T, 2014) |
| "Patients with homocystinuria due to remethylation defects have an isolated brain choline deficiency, probably secondary to depletion of labile methyl groups produced by the transmethylation pathway." | 7.74 | Reduced brain choline in homocystinuria due to remethylation defects. ( Blom, HJ; Boulanger, Y; Debray, FG; Decarie, JC; Jakobs, C; Khiat, A; Lambert, M; Levy, E; Lortie, A; Mitchell, GA; Orquin, J; Ramos, F; Roy, MS; Struys, E; Verhoeven, NM, 2008) |
| "These results suggest that reduced fat mass is common in patients with classical homocystinuria, and that alterations in homocysteine and choline pathways affect body mass and lipid metabolism." | 5.19 | Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism. ( Bandeira, IC; Blom, HJ; Castro, K; D'Almeida, V; de Souza, CF; Imbard, A; Leistner-Segal, S; Nalin, T; Poloni, S; Schwartz, IV; Spritzer, PM; Tonon, T, 2014) |
| "Patients with homocystinuria due to remethylation defects have an isolated brain choline deficiency, probably secondary to depletion of labile methyl groups produced by the transmethylation pathway." | 3.74 | Reduced brain choline in homocystinuria due to remethylation defects. ( Blom, HJ; Boulanger, Y; Debray, FG; Decarie, JC; Jakobs, C; Khiat, A; Lambert, M; Levy, E; Lortie, A; Mitchell, GA; Orquin, J; Ramos, F; Roy, MS; Struys, E; Verhoeven, NM, 2008) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (22.22) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 6 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bahous, RH | 2 |
| Cosín-Tomás, M | 1 |
| Deng, L | 3 |
| Leclerc, D | 2 |
| Malysheva, O | 3 |
| Ho, MK | 1 |
| Pallàs, M | 1 |
| Kaliman, P | 1 |
| Bedell, BJ | 3 |
| Caudill, MA | 3 |
| Rozen, R | 4 |
| Jadavji, NM | 2 |
| Grand'maison, M | 1 |
| Poloni, S | 1 |
| Leistner-Segal, S | 1 |
| Bandeira, IC | 1 |
| D'Almeida, V | 1 |
| de Souza, CF | 1 |
| Spritzer, PM | 1 |
| Castro, K | 1 |
| Tonon, T | 1 |
| Nalin, T | 1 |
| Imbard, A | 1 |
| Blom, HJ | 2 |
| Schwartz, IV | 1 |
| Jacobs, RL | 1 |
| Jiang, H | 1 |
| Kennelly, JP | 1 |
| Orlicky, DJ | 1 |
| Allen, RH | 1 |
| Stabler, SP | 1 |
| Maclean, KN | 1 |
| Debray, FG | 1 |
| Boulanger, Y | 1 |
| Khiat, A | 1 |
| Decarie, JC | 1 |
| Orquin, J | 1 |
| Roy, MS | 1 |
| Lortie, A | 1 |
| Ramos, F | 1 |
| Verhoeven, NM | 1 |
| Struys, E | 1 |
| Jakobs, C | 1 |
| Levy, E | 1 |
| Mitchell, GA | 1 |
| Lambert, M | 1 |
| Mikael, LG | 1 |
| Pancer, J | 1 |
| Jiang, X | 1 |
| Wu, Q | 1 |
| Caudill, M | 1 |
| Benevenga, NJ | 1 |
| Perry, TL | 1 |
| Hansen, S | 1 |
| Love, DL | 1 |
| Crawford, LE | 1 |
| Tischler, B | 1 |
1 review available for choline and CBS Deficiency
| Article | Year |
|---|---|
Evidence for alternative pathways of methionine catabolism.
Topics: Animals; Betaine; Carbon Dioxide; Choline; Decarboxylation; Diet; Homocystinuria; Humans; Liver; Met | 1984 |
1 trial available for choline and CBS Deficiency
| Article | Year |
|---|---|
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism.
Topics: Adiposity; Adolescent; Adult; Amino Acids; Bone Density; Cholesterol, HDL; Choline; Ethanolamine; Fe | 2014 |
7 other studies available for choline and CBS Deficiency
| Article | Year |
|---|---|
Early Manifestations of Brain Aging in Mice Due to Low Dietary Folate and Mild MTHFR Deficiency.
Topics: Aging; Amyloid beta-Peptides; Animals; Anxiety; Brain; Cell Survival; Cerebral Cortex; Choline; CpG | 2019 |
Mouse model for deficiency of methionine synthase reductase exhibits short-term memory impairment and disturbances in brain choline metabolism.
Topics: Acetylcholinesterase; Animals; Apoptosis; Betaine; Cerebellum; Choline; Choline O-Acetyltransferase; | 2014 |
Cystathionine beta-synthase deficiency alters hepatic phospholipid and choline metabolism: Post-translational repression of phosphatidylethanolamine N-methyltransferase is a consequence rather than a cause of liver injury in homocystinuria.
Topics: Animals; Choline; Disease Models, Animal; Homocystinuria; Humans; Liver; Metabolomics; Mice; Mice, K | 2017 |
Reduced brain choline in homocystinuria due to remethylation defects.
Topics: Adolescent; Adult; Aspartic Acid; Brain; Brain Chemistry; Child; Child, Preschool; Choline; Choline | 2008 |
Severe methylenetetrahydrofolate reductase deficiency in mice results in behavioral anomalies with morphological and biochemical changes in hippocampus.
Topics: Animals; Apoptosis; Behavior, Animal; Brain; Cerebellum; Choline; Choline O-Acetyltransferase; DNA M | 2012 |
Low dietary folate and methylenetetrahydrofolate reductase deficiency may lead to pregnancy complications through modulation of ApoAI and IFN-γ in spleen and placenta, and through reduction of methylation potential.
Topics: Animals; Apolipoprotein A-I; Betaine; Choline; Diet; Female; Folic Acid; Folic Acid Deficiency; Homo | 2013 |
Treatment of homocystinuria with a low-methionine diet, supplemental cystine, and a methyl donor.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Choline; Cys | 1968 |