Serum betaine, N,N-dimethylglycine and N-methylglycine levels in patients with cobalamin and folate deficiency and related inborn errors of metabolism.
about
Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiencySex and menopausal status influence human dietary requirements for the nutrient cholineEffectiveness of N,N-dimethylglycine in autism and pervasive developmental disorderSerum methionine metabolites are risk factors for metastatic prostate cancer progressionConstitutive induction of pro-inflammatory and chemotactic cytokines in cystathionine beta-synthase deficient homocystinuria.Cystathionine beta-synthase null homocystinuric mice fail to exhibit altered hemostasis or lowering of plasma homocysteine in response to betaine treatment.MTHFR C677T genotype influences the isotopic enrichment of one-carbon metabolites in folate-compromised men consuming d9-choline.Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine beta-synthase (CBS) deficiency.High homocysteine and thrombosis without connective tissue disorders are associated with a novel class of cystathionine beta-synthase (CBS) mutations.An indirect response model of homocysteine suppression by betaine: optimising the dosage regimen of betaine in homocystinuria.Pharmacokinetics of oral betaine in healthy subjects and patients with homocystinuria.S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolismMaternal diet supplemented with methyl-donors protects against atherosclerosis in F1 ApoE(-/-) mice.Metabolomic anatomy of an animal model revealing homeostatic imbalances in dyslipidaemia.Proteomic analysis of 4-hydroxynonenal (4-HNE) modified proteins in liver mitochondria from chronic ethanol-fed rats.Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expressionHomocysteine metabolism in renal disease.Nuclear localization of de novo thymidylate biosynthesis pathway is required to prevent uracil accumulation in DNATwo patients with hepatic mtDNA depletion syndromes and marked elevations of S-adenosylmethionine and methionineElevated serum S-adenosylhomocysteine in cobalamin-deficient megaloblastic anemiaHigh homocysteine induces betaine depletion.Supplementation of Antipsychotic Treatment with the Amino Acid Sarcosine Influences Proton Magnetic Resonance Spectroscopy Parameters in Left Frontal White Matter in Patients with Schizophrenia.Betaine: a key modulator of one-carbon metabolism and homocysteine status.Hydroxocobalamin dose escalation improves metabolic control in cblC.Sex-specific association of sequence variants in CBS and MTRR with risk for promoter hypermethylation in the lung epithelium of smokers.S-adenosylhomocysteine hydrolase deficiency in a 26-year-old man.S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapyCytoplasmic serine hydroxymethyltransferase regulates the metabolic partitioning of methylenetetrahydrofolate but is not essential in miceMthfd1 is an essential gene in mice and alters biomarkers of impaired one-carbon metabolism.Metabolic profiling of total homocysteine and related compounds in hyperhomocysteinemia: utility and limitations in diagnosing the cause of puzzling thrombophilia in a familyThe metabolic burden of methyl donor deficiency with focus on the betaine homocysteine methyltransferase pathwayNuclear magnetic resonance-based serum metabolic profiling of dairy cows with footrot.Maternal Folate Status and the BHMT c.716G>A Polymorphism Affect the Betaine Dimethylglycine Pathway during Pregnancy.Alpha-lipoic acid induces elevated S-adenosylhomocysteine and depletes S-adenosylmethionine.Choline and betaine in health and disease.Regulation of vascular endothelial growth factor by metabolic context of the cell.Potential Misdiagnosis of Hyperhomocysteinemia due to Cystathionine Beta-Synthase Deficiency During Pregnancy.Enzyme replacement with PEGylated cystathionine β-synthase ameliorates homocystinuria in murine model.In silico experimentation with a model of hepatic mitochondrial folate metabolism.Cystathionine protects against endoplasmic reticulum stress-induced lipid accumulation, tissue injury, and apoptotic cell death.
P2860
Q24290887-6C786D90-C90B-4EA9-86EB-DA438CA49A53Q24651451-BC2BA133-2EFE-435C-9260-6B05CED325F6Q28212767-254DF497-70E9-4B7E-BC58-97F0F43C4FC4Q28476490-9C8A9265-8245-4AB0-8CBE-8C791E1F6AA6Q34077617-050DDD62-9BAF-40D5-8D55-D9C417009CACQ34195828-B599FC26-9240-46BA-B37F-1908E5A37706Q34492987-A61A796D-C9F8-42AD-BFF2-C76835C428D7Q34521242-A46EF790-DF25-4BE6-9FB0-71E5FD006B05Q34523117-17C05FB7-55FA-4545-A64A-C217638F73B4Q34526733-2AB146B5-61BC-46F3-8981-38DDF00B8F1AQ34530590-9B35F5BA-DDBC-44AF-A5F6-517C15866DEDQ34546376-486036DD-8745-4B00-8FA7-D4EF698A6F38Q34598501-F7C14E41-006E-4E5F-985C-9729E02FE181Q34626549-DC056A58-7AE3-4F94-8B85-24D98E19F9FDQ34980950-0B214654-403D-45E7-8F90-BD3252061477Q35341241-663F7391-9A6C-497B-8296-34E3AB590FB5Q35600420-3958712E-AF6D-439E-8CBD-758C5ECAF1E4Q35626099-34C3E41D-855A-47B6-91B2-768C7CBD469DQ35690872-BC1804EA-4C82-4A17-ADDB-FF722F7DFAAEQ35987712-ABD8666B-92F4-41E3-BCB2-B0FACF8ACF35Q36185101-80F05498-1FDD-45B8-944C-69F8A09200F1Q36246819-65469DD6-E00A-4845-9D3A-CEDBDA11F5C3Q36273334-95DAD949-119C-4610-B0EC-9CBC8EB83ED3Q36341671-9C8F61C2-B0F3-434D-A796-4C662DCE2090Q36401994-80532653-801A-4C0A-8007-79FF6BAB89A6Q36726616-226C8D11-9392-417D-95B8-7937265EAA65Q36740605-B3B9C772-21FE-450C-B746-9D3361C9CA18Q36871683-F7548A58-3F0E-4DF5-B6EC-5AB0AC758685Q37041614-A501CE60-E37E-400A-B34E-4D4C229A308DQ37127627-DD46238E-B138-4BBA-BB32-53E9CA841264Q37235361-BFDED039-E3FB-45C7-8311-BE5661933E09Q37329586-B7ED1471-C06C-4670-A4C9-2BEB9B4D3429Q37373892-A2320840-DBA3-4F8E-A7DC-8E1B23739C4FQ37436541-D6236A41-E6DD-4E21-9567-7D8B4E713CF5Q37743322-560E8AE7-D874-4EB8-A10C-3F0FF791C5A7Q38248551-E9FC3FA5-94AE-425C-81F0-64E3A8F10805Q38919234-95F5E573-FFE5-4838-BFA7-3ABC9B79C695Q39763307-8048B255-7CC6-45C3-89E1-2F7E30E734C4Q41763852-01254E31-0171-445A-BF97-5C3372E97F9FQ41832603-29CD1C96-AB3F-49D4-89BF-E572284C24F0
P2860
Serum betaine, N,N-dimethylglycine and N-methylglycine levels in patients with cobalamin and folate deficiency and related inborn errors of metabolism.
description
1993 nî lūn-bûn
@nan
1993 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@ast
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@en
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@nl
type
label
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@ast
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@en
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@nl
prefLabel
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@ast
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@en
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@nl
P2093
P1433
P1476
Serum betaine, N,N-dimethylgly ...... d inborn errors of metabolism.
@en
P2093
Lindenbaum J
Stabler SP
P304
P356
10.1016/0026-0495(93)90198-W
P577
1993-11-01T00:00:00Z