133 related articles for article (PubMed ID: 27207470)
1. Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?
Barić I; Erdol S; Saglam H; Lovrić M; Belužić R; Vugrek O; Blom HJ; Fumić K
JIMD Rep; 2017; 31():101-106. PubMed ID: 27207470
[TBL] [Abstract][Full Text] [Related]
2. Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders.
Barić I; Staufner C; Augoustides-Savvopoulou P; Chien YH; Dobbelaere D; Grünert SC; Opladen T; Petković Ramadža D; Rakić B; Wedell A; Blom HJ
J Inherit Metab Dis; 2017 Jan; 40(1):5-20. PubMed ID: 27671891
[TBL] [Abstract][Full Text] [Related]
3. Hypermethioninemias of genetic and non-genetic origin: A review.
Mudd SH
Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):3-32. PubMed ID: 21308989
[TBL] [Abstract][Full Text] [Related]
4. Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemia.
Mudd SH; Cerone R; Schiaffino MC; Fantasia AR; Minniti G; Caruso U; Lorini R; Watkins D; Matiaszuk N; Rosenblatt DS; Schwahn B; Rozen R; LeGros L; Kotb M; Capdevila A; Luka Z; Finkelstein JD; Tangerman A; Stabler SP; Allen RH; Wagner C
J Inherit Metab Dis; 2001 Aug; 24(4):448-64. PubMed ID: 11596649
[TBL] [Abstract][Full Text] [Related]
5. Adenosine kinase deficiency with neurodevelopemental delay and recurrent hepatic dysfunction: A case report.
Shakiba M; Mahjoub F; Fazilaty H; Rezagholizadeh F; Shakiba A; Ziadlou M; Gahl WA; Behnam B
Adv Rare Dis; 2016; 3():. PubMed ID: 27500280
[TBL] [Abstract][Full Text] [Related]
6. Mechanistic basis of hypermethioninemia.
Schweinberger BM; Wyse AT
Amino Acids; 2016 Nov; 48(11):2479-2489. PubMed ID: 27465642
[TBL] [Abstract][Full Text] [Related]
7. Alterations of methionine metabolism in hepatocarcinogenesis: the emergent role of glycine N-methyltransferase in liver injury.
Simile MM; Latte G; Feo CF; Feo F; Calvisi DF; Pascale RM
Ann Gastroenterol; 2018; 31(5):552-560. PubMed ID: 30174391
[TBL] [Abstract][Full Text] [Related]
8. Effects of methyl-group acceptors on the regulation of plasma cholesterol level in rats fed high cholesterol diets.
Sugiyama K; Ohishi A; Siyu H; Takeuchi H
J Nutr Sci Vitaminol (Tokyo); 1989 Dec; 35(6):613-26. PubMed ID: 2534519
[TBL] [Abstract][Full Text] [Related]
9. Methionine adenosyltransferase deficiency: new enzymatic defect associated with hypermethioninemia.
Gaull GE; Tallan HH
Science; 1974 Oct; 186(4158):59-60. PubMed ID: 4421454
[TBL] [Abstract][Full Text] [Related]
10. Glycine N-methyltransferase-/- mice develop chronic hepatitis and glycogen storage disease in the liver.
Liu SP; Li YS; Chen YJ; Chiang EP; Li AF; Lee YH; Tsai TF; Hsiao M; Huang SF; Chen YM
Hepatology; 2007 Nov; 46(5):1413-25. PubMed ID: 17937387
[TBL] [Abstract][Full Text] [Related]
11. Neonatal methionine adenosyltransferase I/III deficiency with abnormal signal intensity in the central tegmental tract.
Kido J; Sawada T; Momosaki K; Suzuki Y; Uetani H; Kitajima M; Mitsubuchi H; Nakamura K; Matsumoto S
Brain Dev; 2019 Apr; 41(4):382-388. PubMed ID: 30389272
[TBL] [Abstract][Full Text] [Related]
12. HYPERMETHIONINEMIA: A METABOLIC DISORDER ASSOCIATED WITH CIRRHOSIS, ISLET CELL HYPERPLASIA, AND RENAL TUBULAR DEGENERATION.
PERRY TL; HARDWICK DF; DIXON GH; DOLMAN CL; HANSEN S
Pediatrics; 1965 Aug; 36():236-50. PubMed ID: 14320034
[No Abstract] [Full Text] [Related]
13. Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
Augoustides-Savvopoulou P; Luka Z; Karyda S; Stabler SP; Allen RH; Patsiaoura K; Wagner C; Mudd SH
J Inherit Metab Dis; 2003; 26(8):745-59. PubMed ID: 14739680
[TBL] [Abstract][Full Text] [Related]
14. Hypermethioninemia associated with methionine adenosyltransferase deficiency: clinical, morphologic, and biochemical observations on four patients.
Gaull GE; Tallan HH; Lonsdale D; Przyrembel H; Schaffner F; von Bassewitz DB
J Pediatr; 1981 May; 98(5):734-41. PubMed ID: 7229751
[TBL] [Abstract][Full Text] [Related]
15. The neuroprotective role of melatonin in a gestational hypermethioninemia model.
Figueiró PW; Moreira DS; Dos Santos TM; Prezzi CA; Rohden F; Faccioni-Heuser MC; Manfredini V; Netto CA; Wyse ATS
Int J Dev Neurosci; 2019 Nov; 78():198-209. PubMed ID: 31476364
[TBL] [Abstract][Full Text] [Related]
16. A glycine N-methyltransferase knockout mouse model for humans with deficiency of this enzyme.
Luka Z; Capdevila A; Mato JM; Wagner C
Transgenic Res; 2006 Jun; 15(3):393-7. PubMed ID: 16779654
[TBL] [Abstract][Full Text] [Related]
17. Confirmation that
Muriello MJ; Viall S; Bottiglieri T; Cusmano-Ozog K; Ferreira CR
Mol Genet Metab Rep; 2017 Dec; 13():9-12. PubMed ID: 28748147
[TBL] [Abstract][Full Text] [Related]
18. Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap.
Harvey Mudd S; Braverman N; Pomper M; Tezcan K; Kronick J; Jayakar P; Garganta C; Ampola MG; Levy HL; McCandless SE; Wiltse H; Stabler SP; Allen RH; Wagner C; Borschel MW
Mol Genet Metab; 2003 May; 79(1):6-16. PubMed ID: 12765841
[TBL] [Abstract][Full Text] [Related]
19. Tumor suppressor gene glycine N-methyltransferase and its potential in liver disorders and hepatocellular carcinoma.
Chen M; Yang MH; Chang MM; Tyan YC; Chen YA
Toxicol Appl Pharmacol; 2019 Sep; 378():114607. PubMed ID: 31170416
[TBL] [Abstract][Full Text] [Related]
20. Maternal Hypermethioninemia Affects Neurons Number, Neurotrophins Levels, Energy Metabolism, and Na
Schweinberger BM; Rodrigues AF; Turcatel E; Pierozan P; Pettenuzzo LF; Grings M; Scaini G; Parisi MM; Leipnitz G; Streck EL; Barbé-Tuana FM; Wyse ATS
Mol Neurobiol; 2018 Feb; 55(2):980-988. PubMed ID: 28084592
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
