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disorder of sulfur-bearing amino acid metabolism相关文献:
Sulfur amino acid metabolism and related metabotypes of autism spectrum disorder: A review of biochemical evidence for a hypothesis.
Indika NR, Deutz NEP, Engelen MPKJ, Peiris H, Wijetunge S, Perera R.
Biochimie. 2021 May;184:143-157. doi: 10.1016/j.biochi.2021.02.018. Epub 2021 Mar 4.
PMID:33675854
The Multifaceted Therapeutic Role of N-Acetylcysteine (NAC) in Disorders Characterized by Oxidative Stress.
Raghu G, Berk M, Campochiaro PA, Jaeschke H, Marenzi G, Richeldi L, Wen FQ, Nicoletti F, Calverley PMA.
Curr Neuropharmacol. 2021;19(8):1202-1224. doi: 10.2174/1570159X19666201230144109.
PMID:33380301
Amino acids and immune function.
Li P, Yin YL, Li D, Kim SW, Wu G.
Br J Nutr. 2007 Aug;98(2):237-52. doi: 10.1017/S000711450769936X. Epub 2007 Apr 3.
PMID:17403271
The role of methionine on metabolism, oxidative stress, and diseases.
Martínez Y, Li X, Liu G, Bin P, Yan W, Más D, Valdivié M, Hu CA, Ren W, Yin Y.
Amino Acids. 2017 Dec;49(12):2091-2098. doi: 10.1007/s00726-017-2494-2. Epub 2017 Sep 19.
PMID:28929442
Homocysteine: Biochemistry, Molecular Biology and Role in Disease.
Hermann A, Sitdikova G.
Biomolecules. 2021 May 15;11(5):737. doi: 10.3390/biom11050737.
PMID:34063494
One-Carbon Metabolism: Linking Nutritional Biochemistry to Epigenetic Programming of Long-Term Development.
Clare CE, Brassington AH, Kwong WY, Sinclair KD.
Annu Rev Anim Biosci. 2019 Feb 15;7:263-287. doi: 10.1146/annurev-animal-020518-115206. Epub 2018 Nov 9.
PMID:30412672
Homocysteine and Mitochondria in Cardiovascular and Cerebrovascular Systems.
Kaplan P, Tatarkova Z, Sivonova MK, Racay P, Lehotsky J.
Int J Mol Sci. 2020 Oct 18;21(20):7698. doi: 10.3390/ijms21207698.
PMID:33080955
Amino Acid Restriction Triggers Angiogenesis via GCN2/ATF4 Regulation of VEGF and H(2)S Production.
Longchamp A, Mirabella T, Arduini A, MacArthur MR, Das A, Treviño-Villarreal JH, Hine C, Ben-Sahra I, Knudsen NH, Brace LE, Reynolds J, Mejia P, Tao M, Sharma G, Wang R, Corpataux JM, Haefliger JA, Ahn KH, Lee CH, Manning BD, Sinclair DA, Chen CS, Ozaki CK, Mitchell JR.
Cell. 2018 Mar 22;173(1):117-129.e14. doi: 10.1016/j.cell.2018.03.001.
PMID:29570992
Inherited disorders of sulfur amino acid metabolism: recent advances in therapy.
Kožich V, Majtan T.
Curr Opin Clin Nutr Metab Care. 2021 Jan;24(1):62-70. doi: 10.1097/MCO.0000000000000705.
PMID:33060459
Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency.
Huemer M, Diodato D, Schwahn B, Schiff M, Bandeira A, Benoist JF, Burlina A, Cerone R, Couce ML, Garcia-Cazorla A, la Marca G, Pasquini E, Vilarinho L, Weisfeld-Adams JD, Kožich V, Blom H, Baumgartner MR, Dionisi-Vici C.
J Inherit Metab Dis. 2017 Jan;40(1):21-48. doi: 10.1007/s10545-016-9991-4. Epub 2016 Nov 30.
PMID:27905001
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