BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 669702)

  • 21. Triose phosphate isomerase deficiency.
    Skala H; Dreyfus JC; Vives-Corrons JL; Matsumoto F; Beutler E
    Biochem Med; 1977 Oct; 18(2):226-34. PubMed ID: 907660
    [No Abstract]   [Full Text] [Related]  

  • 22. [Triosephosphate isomerase deficiency. Apropos of a new case].
    González Rodríguez MP; García Velázquez J; Reig del Moral C; Herrera Martín M; Hernández Martín H; Sánchez Martín S; Cuadrado Bello P
    An Esp Pediatr; 1988 Sep; 29(3):251-3. PubMed ID: 2461674
    [No Abstract]   [Full Text] [Related]  

  • 23. Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity.
    Eber SW; Pekrun A; Bardosi A; Gahr M; Krietsch WK; Krüger J; Matthei R; Schröter W
    Eur J Pediatr; 1991 Sep; 150(11):761-6. PubMed ID: 1959537
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Neurological findings in triosephosphate isomerase deficiency.
    Poll-The BT; Aicardi J; Girot R; Rosa R
    Ann Neurol; 1985 May; 17(5):439-43. PubMed ID: 4004168
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Triosephosphate isomerase deficiency: predictions and facts.
    Orosz F; Vértessy BG; Hollán S; Horányi M; Ovádi J
    J Theor Biol; 1996 Oct; 182(3):437-47. PubMed ID: 8944178
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Deficiency of triosephosphate isomerase. Apropos of 2 new cases].
    Delso Martínez MC; Uriel Miñana P; Pérez Lugmus G; Giménez Mas JA; Baldellou Vázquez A
    An Esp Pediatr; 1983 Aug; 19(2):123-7. PubMed ID: 6660640
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Triosephosphate isomerase deficiency. A case report with neuropathological findings.
    Clay SA; Shore NA; Landing BH
    Am J Dis Child; 1982 Sep; 136(9):800-2. PubMed ID: 7114003
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Triose phosphate isomerase deficiency associated with two novel mutations in TPI gene.
    Fermo E; Bianchi P; Vercellati C; Rees DC; Marcello AP; Barcellini W; Zanella A
    Eur J Haematol; 2010 Aug; 85(2):170-3. PubMed ID: 20374271
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics.
    Roland BP; Zeccola AM; Larsen SB; Amrich CG; Talsma AD; Stuchul KA; Heroux A; Levitan ES; VanDemark AP; Palladino MJ
    PLoS Genet; 2016 Mar; 12(3):e1005941. PubMed ID: 27031109
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Triosephosphate isomerase deficiency: consequences of an inherited mutation at mRNA, protein and metabolic levels.
    Oláh J; Orosz F; Puskás LG; Hackler L; Horányi M; Polgár L; Hollán S; Ovádi J
    Biochem J; 2005 Dec; 392(Pt 3):675-83. PubMed ID: 16086671
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Triose phosphate isomerase deficiency: a rare erythrocyte enzymopathy with a poor prognosis].
    Julien M; Todosi C; Fouyssac F; Lesesve JF; Gérard D; Perrin J
    Ann Biol Clin (Paris); 2023 Mar; 81(2):. PubMed ID: 36866814
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of two new electrophoretic variants of human triosephosphate isomerase: stability, kinetic, and immunological properties.
    Asakawa J; Mohrenweiser HW
    Biochem Genet; 1982 Feb; 20(1-2):59-76. PubMed ID: 7092803
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Electrophoretic variants of blood proteins in Japanese. III. Triosephosphate isomerase.
    Asakawa J; Satoh C; Takahashi N; Fujita M; Kaneko J; Goriki K; Hazama R; Kageoka T
    Hum Genet; 1984; 68(2):185-8. PubMed ID: 6500570
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The feasibility of replacement therapy for inherited disorder of glycolysis: triosephosphate isomerase deficiency (review).
    Ationu A; Humphries A
    Int J Mol Med; 1998 Dec; 2(6):701-4. PubMed ID: 9850739
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency.
    Segal J; Mülleder M; Krüger A; Adler T; Scholze-Wittler M; Becker L; Calzada-Wack J; Garrett L; Hölter SM; Rathkolb B; Rozman J; Racz I; Fischer R; Busch DH; Neff F; Klingenspor M; Klopstock T; Grüning NM; Michel S; Lukaszewska-McGreal B; Voigt I; Hartmann L; Timmermann B; Lehrach H; Wolf E; Wurst W; Gailus-Durner V; Fuchs H; H de Angelis M; Schrewe H; Yuneva M; Ralser M
    J Inherit Metab Dis; 2019 Sep; 42(5):839-849. PubMed ID: 31111503
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosis.
    Pekrun A; Neubauer BA; Eber SW; Lakomek M; Seidel H; Schröter W
    Clin Genet; 1995 Apr; 47(4):175-9. PubMed ID: 7628118
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Origin of human triosephosphate isomerase isozymes: further evidence for the single structural locus hypothesis with Japanese variants.
    Asakawa J; Iida S
    Hum Genet; 1985; 71(1):22-6. PubMed ID: 3861565
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Characterization of triosephosphate isomerase mutants with reduced enzyme activity in Mus musculus.
    Merkle S; Pretsch W
    Genetics; 1989 Dec; 123(4):837-44. PubMed ID: 2693209
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Human triosephosphate isomerase deficiency resulting from mutation of Phe-240.
    Chang ML; Artymiuk PJ; Wu X; Hollán S; Lammi A; Maquat LE
    Am J Hum Genet; 1993 Jun; 52(6):1260-9. PubMed ID: 8503454
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal diagnosis of a red-cell enzymopathy: triose phosphate isomerase deficiency.
    Bellingham AJ; Lestas AN; Williams LH; Nicolaides KH
    Lancet; 1989 Aug; 2(8660):419-21. PubMed ID: 2569601
    [TBL] [Abstract][Full Text] [Related]  

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