Hollán S - Search Results

1

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. 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.

2

Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological symptoms.

Hollán S, Fujii H, Hirono A, Hirono K, Karro H, Miwa S, Harsányi V, Gyódi E, Inselt-Kovács M. Hollán S, et al. Hum Genet. 1993 Nov;92(5):486-90. doi: 10.1007/BF00216456. Hum Genet. 1993. PMID: 8244340

3

Triosephosphate isomerase deficiency: predictions and facts.

Orosz F, Vértessy BG, Hollán S, Horányi M, Ovádi J. Orosz F, et al. Among authors: hollan s. 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: hollan s. 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

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. 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.

6

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: hollan s. Biochem J. 2005 Dec 15;392(Pt 3):675-83. doi: 10.1042/BJ20050993. Biochem J. 2005. PMID: 16086671 Free PMC article.

7

[Glycolytic enzyme defects and neurodegeneration].

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

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: hollan s. Blood Cells Mol Dis. 2000 Feb;26(1):91-100. doi: 10.1006/bcmd.2000.0280. Blood Cells Mol Dis. 2000. PMID: 10772880

9

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: hollan s. Blood. 2001 Nov 15;98(10):3106-12. doi: 10.1182/blood.v98.10.3106. Blood. 2001. PMID: 11698297 Free article.

10

Induction of erythroid differentiation and modulation of gene expression by tiazofurin in K-562 leukemia cells.

Olah E, Natsumeda Y, Ikegami T, Kote Z, Horanyi M, Szelenyi J, Paulik E, Kremmer T, Hollan SR, Sugar J, et al. Olah E, et al. Among authors: hollan sr. Proc Natl Acad Sci U S A. 1988 Sep;85(17):6533-7. doi: 10.1073/pnas.85.17.6533. Proc Natl Acad Sci U S A. 1988. PMID: 2901100 Free PMC article.

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