BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 23973726)

  • 21. Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activity.
    Pérez Mato I; Sanchez del Pino MM; Chamberlin ME; Mudd SH; Mato JM; Corrales FJ
    J Biol Chem; 2001 Apr; 276(17):13803-9. PubMed ID: 11278456
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Normal brain myelination in a patient homozygous for a mutation that encodes a severely truncated methionine adenosyltransferase I/III.
    Hazelwood S; Bernardini I; Shotelersuk V; Tangerman A; Guo J; Mudd H; Gahl WA
    Am J Med Genet; 1998 Feb; 75(4):395-400. PubMed ID: 9482646
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Analysis of five cases of hypermethioninemia diagnosed by neonatal screening.
    Zhang Z; Wang Y; Ma D; Cheng W; Sun Y; Jiang T
    J Pediatr Endocrinol Metab; 2020 Jan; 33(1):47-52. PubMed ID: 31851615
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Methionine adenosyltransferase (MAT) I/III deficiency with concurrent hyperhomocysteinaemia: two novel cases.
    Linnebank M; Lagler F; Muntau AC; Röschinger W; Olgemöller B; Fowler B; Koch HG
    J Inherit Metab Dis; 2005; 28(6):1167-8. PubMed ID: 16435220
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic analysis of isolated persistent hypermethioninemia with dominant inheritance.
    Nagao M; Oyanagi K
    Acta Paediatr Jpn; 1997 Oct; 39(5):601-6. PubMed ID: 9363660
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene.
    Chamberlin ME; Ubagai T; Mudd SH; Levy HL; Chou JY
    Am J Hum Genet; 1997 Mar; 60(3):540-6. PubMed ID: 9042912
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hepatic methionine adenosyltransferase deficiency in a 31-year-old man.
    Gahl WA; Finkelstein JD; Mullen KD; Bernardini I; Martin JJ; Backlund P; Ishak KG; Hoofnagle JH; Mudd SH
    Am J Hum Genet; 1987 Jan; 40(1):39-49. PubMed ID: 3812486
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [A case report of pyridoxine-responsive homocystinuria].
    Milosević-Tosić M; Borota J; Katanić D; Vlaski J
    Med Pregl; 1999; 52(11-12):501-4. PubMed ID: 10748775
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Methionine Adenosyltransferase I/III Deficiency Detected by Newborn Screening.
    Hübner V; Hannibal L; Janzen N; Grünert SC; Freisinger P
    Genes (Basel); 2022 Jun; 13(7):. PubMed ID: 35885946
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Reversible white matter lesion in methionine adenosyltransferase I/III deficiency.
    Tada H; Takanashi J; Barkovich AJ; Yamamoto S; Kohno Y
    AJNR Am J Neuroradiol; 2004; 25(10):1843-5. PubMed ID: 15569761
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Methionine adenosyltransferase I/III deficiency: Long-term follow-up and treatment of 3 adult siblings.
    Bannick A; Chase S; Miner A; Seeterlin M; Conway RL
    Eur J Med Genet; 2020 Dec; 63(12):104076. PubMed ID: 32980525
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Analysis of MAT1A gene mutations in a child affected with simple hypermethioninemia].
    Sun Y; Ma D; Wang Y; Yang B; Jiang T
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):98-101. PubMed ID: 28186605
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Disorders of transsulfuration; disorders of sulfur-aminoacids metabolism].
    Hase Y
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):205-18. PubMed ID: 9590029
    [No Abstract]   [Full Text] [Related]  

  • 34. Maternal methionine adenosyltransferase I/III deficiency: reproductive outcomes in a woman with four pregnancies.
    Mudd SH; Tangerman A; Stabler SP; Allen RH; Wagner C; Zeisel SH; Levy HL
    J Inherit Metab Dis; 2003; 26(5):443-58. PubMed ID: 14518826
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Methionine Adenosyltransferase I/III Deficiency in Portugal: High Frequency of a Dominantly Inherited Form in a Small Area of Douro High Lands.
    Martins E; Marcão A; Bandeira A; Fonseca H; Nogueira C; Vilarinho L
    JIMD Rep; 2012; 6():107-12. PubMed ID: 23430947
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations.
    Nashabat M; Al-Khenaizan S; Alfadhel M
    Ther Clin Risk Manag; 2018; 14():225-229. PubMed ID: 29440907
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Newborn screening and variant analysis for methionine adenosyltransferase I/III deficiency].
    Lin C; Zheng Q; Jiang M; Lin Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May; 37(5):527-531. PubMed ID: 32335878
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Plasma homocysteine after insulin infusion in type II diabetic patients with and without methionine intolerance.
    Ventura P; Panini R; Emiliani S; Salvioli G
    Exp Clin Endocrinol Diabetes; 2004 Jan; 112(1):44-51. PubMed ID: 14758571
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.