Horányi M - Search Results

1

Distinct behavior of mutant triosephosphate isomerase in hemolysate and in isolated form: molecular basis of enzyme deficiency.

Orosz F, Oláh J, Alvarez M, Keseru GM, Szabó B, Wágner G, Kovári Z, Horányi M, Baróti K, Martial JA, Hollán S, Ovádi J. Orosz F, et al. Among authors: horanyi m. Blood. 2001 Nov 15;98(10):3106-12. doi: 10.1182/blood.v98.10.3106. Blood. 2001. PMID: 11698297 Free article.

2

Triosephosphate isomerase deficiency: consequences of an inherited mutation at mRNA, protein and metabolic levels.

Oláh J, Orosz F, Puskás LG, Hackler L Jr, Horányi M, Polgár L, Hollán S, Ovádi J. Oláh J, et al. Among authors: horanyi m. Biochem J. 2005 Dec 15;392(Pt 3):675-83. doi: 10.1042/BJ20050993. Biochem J. 2005. PMID: 16086671 Free PMC article.

3

Triosephosphate isomerase deficiency: predictions and facts.

Orosz F, Vértessy BG, Hollán S, Horányi M, Ovádi J. Orosz F, et al. Among authors: horanyi m. J Theor Biol. 1996 Oct 7;182(3):437-47. doi: 10.1006/jtbi.1996.0184. J Theor Biol. 1996. PMID: 8944178

4

Enhanced association of mutant triosephosphate isomerase to red cell membranes and to brain microtubules.

Orosz F, Wágner G, Liliom K, Kovács J, Baróti K, Horányi M, Farkas T, Hollán S, Ovádi J. Orosz F, et al. Among authors: horanyi m. Proc Natl Acad Sci U S A. 2000 Feb 1;97(3):1026-31. doi: 10.1073/pnas.97.3.1026. Proc Natl Acad Sci U S A. 2000. PMID: 10655478 Free PMC article.

5

Increased formation of methylglyoxal and protein glycation, oxidation and nitrosation in triosephosphate isomerase deficiency.

Ahmed N, Battah S, Karachalias N, Babaei-Jadidi R, Horányi M, Baróti K, Hollan S, Thornalley PJ. Ahmed N, et al. Among authors: horanyi m. Biochim Biophys Acta. 2003 Oct 15;1639(2):121-32. doi: 10.1016/j.bbadis.2003.08.002. Biochim Biophys Acta. 2003. PMID: 14559119 Free article.

6

Erythrocyte lipids in triose-phosphate isomerase deficiency.

Hollán S, Dey I, Szollár L, Horányi M, Magócsi M, Harsányi V, Farkas T. Hollán S, et al. Among authors: horanyi m. Proc Natl Acad Sci U S A. 1995 Jan 3;92(1):268-71. doi: 10.1073/pnas.92.1.268. Proc Natl Acad Sci U S A. 1995. PMID: 7816830 Free PMC article.

7

Search for the pathogenesis of the differing phenotype in two compound heterozygote Hungarian brothers with the same genotypic triosephosphate isomerase deficiency.

Hollán S, Magócsi M, Fodor E, Horányi M, Harsányi V, Farkas T. Hollán S, et al. Among authors: horanyi m. Proc Natl Acad Sci U S A. 1997 Sep 16;94(19):10362-6. doi: 10.1073/pnas.94.19.10362. Proc Natl Acad Sci U S A. 1997. PMID: 9294216 Free PMC article.

8

Diminished blood levels of reduced glutathione and alpha-tocopherol in two triosephosphate isomerase-deficient brothers.

Karg E, Németh I, Horányi M, Pintér S, Vécsei L, Hollán S. Karg E, et al. Among authors: horanyi m. Blood Cells Mol Dis. 2000 Feb;26(1):91-100. doi: 10.1006/bcmd.2000.0280. Blood Cells Mol Dis. 2000. PMID: 10772880

9

[Glycolytic enzyme defects and neurodegeneration].

Hollán S, Vécsei L, Karg E, Németh I, Horanyi M, Inselt-Kovács M, Farkas T. Hollán S, et al. Among authors: horanyi m. C R Seances Soc Biol Fil. 1998;192(5):929-45. C R Seances Soc Biol Fil. 1998. PMID: 9871806 French.

10

Identical germ-line mutations in the triosephosphate isomerase alleles of two brothers are associated with distinct clinical phenotypes.

Valentin C, Cohen-Solal M, Maquat L, Horányi M, Inselt-Kovács M, Hollán S. Valentin C, et al. Among authors: horanyi m. C R Acad Sci III. 2000 Mar;323(3):245-50. doi: 10.1016/s0764-4469(00)00128-1. C R Acad Sci III. 2000. PMID: 10782327

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