These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 33051492)

  • 61. Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan.
    Tsai PC; Liao YC; Jih KY; Soong BW; Lin KP; Lee YC
    Neurobiol Aging; 2018 Dec; 72():188.e1-188.e2. PubMed ID: 30054183
    [TBL] [Abstract][Full Text] [Related]  

  • 62. The structure of a bacterial L-amino acid oxidase from Rhodococcus opacus gives new evidence for the hydride mechanism for dehydrogenation.
    Faust A; Niefind K; Hummel W; Schomburg D
    J Mol Biol; 2007 Mar; 367(1):234-48. PubMed ID: 17234209
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Insights on the structural perturbations in human MTHFR Ala222Val mutant by protein modeling and molecular dynamics.
    Abhinand PA; Shaikh F; Bhakat S; Radadiya A; Bhaskar LV; Shah A; Ragunath PK
    J Biomol Struct Dyn; 2016; 34(4):892-905. PubMed ID: 26273990
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Computational Investigation on Electrostatic Loop Mutants Instigating Destabilization and Aggregation on Human SOD1 Protein Causing Amyotrophic Lateral Sclerosis.
    Srinivasan E; Rajasekaran R
    Protein J; 2019 Feb; 38(1):37-49. PubMed ID: 30701485
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Parsing disease-relevant protein modifications from epiphenomena: perspective on the structural basis of SOD1-mediated ALS.
    Schmitt ND; Agar JN
    J Mass Spectrom; 2017 Jul; 52(7):480-491. PubMed ID: 28558143
    [TBL] [Abstract][Full Text] [Related]  

  • 66. FIG4 variants in central European patients with amyotrophic lateral sclerosis: a whole-exome and targeted sequencing study.
    Osmanovic A; Rangnau I; Kosfeld A; Abdulla S; Janssen C; Auber B; Raab P; Preller M; Petri S; Weber RG
    Eur J Hum Genet; 2017 Feb; 25(3):324-331. PubMed ID: 28051077
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Simultaneous synthesis of l-DOPA and oxidation of d-amino acid by specific coupling of a peroxidase to d-amino acid oxidase.
    Chen Y; Chu H; Liu W; Feng W
    Enzyme Microb Technol; 2019 Feb; 121():8-16. PubMed ID: 30554648
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Discovery, SAR, and pharmacokinetics of a novel 3-hydroxyquinolin-2(1H)-one series of potent D-amino acid oxidase (DAAO) inhibitors.
    Duplantier AJ; Becker SL; Bohanon MJ; Borzilleri KA; Chrunyk BA; Downs JT; Hu LY; El-Kattan A; James LC; Liu S; Lu J; Maklad N; Mansour MN; Mente S; Piotrowski MA; Sakya SM; Sheehan S; Steyn SJ; Strick CA; Williams VA; Zhang L
    J Med Chem; 2009 Jun; 52(11):3576-85. PubMed ID: 19438227
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Contributions of spinal D-amino acid oxidase to bone cancer pain.
    Huang JL; Chen XL; Guo C; Wang YX
    Amino Acids; 2012 Nov; 43(5):1905-18. PubMed ID: 22996731
    [TBL] [Abstract][Full Text] [Related]  

  • 70. D-Amino acid oxidase: new findings.
    Pilone MS
    Cell Mol Life Sci; 2000 Nov; 57(12):1732-47. PubMed ID: 11130179
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Focus on the Role of D-serine and D-amino Acid Oxidase in Amyotrophic Lateral Sclerosis/Motor Neuron Disease (ALS).
    Kondori NR; Paul P; Robbins JP; Liu K; Hildyard JCW; Wells DJ; de Belleroche JS
    Front Mol Biosci; 2018; 5():8. PubMed ID: 29487852
    [TBL] [Abstract][Full Text] [Related]  

  • 72. A conserved aspartate is essential for FAD binding and catalysis in the D-amino acid oxidase from Trigonopsis variabilis.
    Ju SS; Lin LL; Wang WC; Hsu WH
    FEBS Lett; 1998 Sep; 436(1):119-22. PubMed ID: 9771905
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.
    Chumakov I; Blumenfeld M; Guerassimenko O; Cavarec L; Palicio M; Abderrahim H; Bougueleret L; Barry C; Tanaka H; La Rosa P; Puech A; Tahri N; Cohen-Akenine A; Delabrosse S; Lissarrague S; Picard FP; Maurice K; Essioux L; Millasseau P; Grel P; Debailleul V; Simon AM; Caterina D; Dufaure I; Malekzadeh K; Belova M; Luan JJ; Bouillot M; Sambucy JL; Primas G; Saumier M; Boubkiri N; Martin-Saumier S; Nasroune M; Peixoto H; Delaye A; Pinchot V; Bastucci M; Guillou S; Chevillon M; Sainz-Fuertes R; Meguenni S; Aurich-Costa J; Cherif D; Gimalac A; Van Duijn C; Gauvreau D; Ouellette G; Fortier I; Raelson J; Sherbatich T; Riazanskaia N; Rogaev E; Raeymaekers P; Aerssens J; Konings F; Luyten W; Macciardi F; Sham PC; Straub RE; Weinberger DR; Cohen N; Cohen D
    Proc Natl Acad Sci U S A; 2002 Oct; 99(21):13675-80. PubMed ID: 12364586
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort.
    Verheijen J; van der Zee J; Gijselinck I; Van den Bossche T; Dillen L; Heeman B; Gómez-Tortosa E; Lladó A; Sanchez-Valle R; Graff C; Pastor P; Pastor MA; Benussi L; Ghidoni R; Binetti G; Clarimon J; de Mendonça A; Gelpi E; Tsolaki M; Diehl-Schmid J; Nacmias B; Almeida MR; Borroni B; Matej R; Ruiz A; Engelborghs S; Vandenberghe R; De Deyn PP; Cruts M; Van Broeckhoven C; Sleegers K; ;
    Neurobiol Aging; 2018 Feb; 62():245.e1-245.e7. PubMed ID: 29146049
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Comprehensive analysis of the mutation spectrum in 301 German ALS families.
    Müller K; Brenner D; Weydt P; Meyer T; Grehl T; Petri S; Grosskreutz J; Schuster J; Volk AE; Borck G; Kubisch C; Klopstock T; Zeller D; Jablonka S; Sendtner M; Klebe S; Knehr A; Günther K; Weis J; Claeys KG; Schrank B; Sperfeld AD; Hübers A; Otto M; Dorst J; Meitinger T; Strom TM; Andersen PM; Ludolph AC; Weishaupt JH;
    J Neurol Neurosurg Psychiatry; 2018 Aug; 89(8):817-827. PubMed ID: 29650794
    [TBL] [Abstract][Full Text] [Related]  

  • 76. On the reaction of D-amino acid oxidase with dioxygen: O2 diffusion pathways and enhancement of reactivity.
    Rosini E; Molla G; Ghisla S; Pollegioni L
    FEBS J; 2011 Feb; 278(3):482-92. PubMed ID: 21182588
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Delineating the relationship between amyotrophic lateral sclerosis and frontotemporal dementia: Sequence and structure-based predictions.
    Kumar V; Islam A; Hassan MI; Ahmad F
    Biochim Biophys Acta; 2016 Sep; 1862(9):1742-54. PubMed ID: 27318084
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Amyotrophic Lateral Sclerosis Type 20 - In Silico Analysis and Molecular Dynamics Simulation of hnRNPA1.
    Krebs BB; De Mesquita JF
    PLoS One; 2016; 11(7):e0158939. PubMed ID: 27414033
    [TBL] [Abstract][Full Text] [Related]  

  • 79. D-Amino acids in the brain and mutant rodents lacking D-amino-acid oxidase activity.
    Yamanaka M; Miyoshi Y; Ohide H; Hamase K; Konno R
    Amino Acids; 2012 Nov; 43(5):1811-21. PubMed ID: 22892863
    [TBL] [Abstract][Full Text] [Related]  

  • 80. TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts.
    Le Ber I; De Septenville A; Millecamps S; Camuzat A; Caroppo P; Couratier P; Blanc F; Lacomblez L; Sellal F; Fleury MC; Meininger V; Cazeneuve C; Clot F; Flabeau O; LeGuern E; Brice A;
    Neurobiol Aging; 2015 Nov; 36(11):3116.e5-3116.e8. PubMed ID: 26476236
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.