Melegh B - Search Results

1

Inhibition of cell death by a novel 16.2 kD heat shock protein predominantly via Hsp90 mediated lipid rafts stabilization and Akt activation pathway.

Bellyei S, Szigeti A, Boronkai A, Pozsgai E, Gomori E, Melegh B, Janaky T, Bognar Z, Hocsak E, Sumegi B, Gallyas F Jr. Bellyei S, et al. Among authors: melegh b. Apoptosis. 2007 Jan;12(1):97-112. doi: 10.1007/s10495-006-0486-x. Apoptosis. 2007. PMID: 17136496

2

Phenotypic manifestations of the OCTN2 V295X mutation: sudden infant death and carnitine-responsive cardiomyopathy in Roma families.

Melegh B, Bene J, Mogyorósy G, Havasi V, Komlósi K, Pajor L, Oláh E, Kispál G, Sumegi B, Méhes K. Melegh B, et al. Am J Med Genet A. 2004 Dec 1;131(2):121-6. doi: 10.1002/ajmg.a.30207. Am J Med Genet A. 2004. PMID: 15487009

3

Identification of the novel lapine rotavirus genotype P[22] from an outbreak of enteritis in a Hungarian rabbitry.

Bányai K, Forgách P, Erdélyi K, Martella V, Bogdán A, Hocsák E, Havasi V, Melegh B, Szucs G. Bányai K, et al. Among authors: melegh b. Virus Res. 2005 Nov;113(2):73-80. doi: 10.1016/j.virusres.2005.03.029. Virus Res. 2005. PMID: 15936106

4

Mitochondrial DNA 11777C>A mutation associated Leigh syndrome: case report with a review of the previously described pedigrees.

Hadzsiev K, Maasz A, Kisfali P, Kalman E, Gomori E, Pal E, Berenyi E, Komlosi K, Melegh B. Hadzsiev K, et al. Among authors: melegh b. Neuromolecular Med. 2010 Sep;12(3):277-84. doi: 10.1007/s12017-010-8115-9. Epub 2010 May 26. Neuromolecular Med. 2010. PMID: 20502985

5

[Mitochondrial DNA and its mutations: new advances in a new field].

Sáfrány E, Csöngei V, Járomi L, Maász A, Magyari L, Sipeky C, Melegh B. Sáfrány E, et al. Among authors: melegh b. Orv Hetil. 2007 May 27;148(21):971-8. doi: 10.1556/OH.2007.28014. Orv Hetil. 2007. PMID: 17513250 Review. Hungarian.

6

Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation.

Maász A, Komlósi K, Hadzsiev K, Szabó Z, Willems PJ, Gerlinger I, Kosztolányi G, Méhes K, Melegh B. Maász A, et al. Among authors: melegh b. Curr Med Chem. 2008;15(13):1257-62. doi: 10.2174/092986708784534910. Curr Med Chem. 2008. PMID: 18537605 Review.

7

Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion.

Bene J, Nádasi E, Kosztolányi G, Méhes K, Melegh B. Bene J, et al. Among authors: melegh b. Eur J Hum Genet. 2003 May;11(5):375-9. doi: 10.1038/sj.ejhg.5200975. Eur J Hum Genet. 2003. PMID: 12734542

8

Protein tyrosine phosphatase gene C1858T allele confers risk for rheumatoid arthritis in Hungarian subjects.

Farago B, Talian GC, Komlosi K, Nagy G, Berki T, Gyetvai A, Szekanecz Z, Nyarady Z, Kiss CG, Nemeth P, Czirjak L, Melegh B. Farago B, et al. Among authors: melegh b. Rheumatol Int. 2009 May;29(7):793-6. doi: 10.1007/s00296-008-0771-9. Epub 2008 Nov 26. Rheumatol Int. 2009. PMID: 19034456

9

Sequencing and phylogenetic analysis of human genotype P[6] rotavirus strains detected in Hungary provides evidence for genetic heterogeneity within the P[6] VP4 gene.

Bányai K, Martella V, Jakab F, Melegh B, Szücs G. Bányai K, et al. Among authors: melegh b. J Clin Microbiol. 2004 Sep;42(9):4338-43. doi: 10.1128/JCM.42.9.4338-4343.2004. J Clin Microbiol. 2004. PMID: 15365040 Free PMC article.

10

Genetic diversity and zoonotic potential of human rotavirus strains, 2003-2006, Hungary.

Bányai K, Bogdán A, Domonkos G, Kisfali P, Molnár P, Tóth A, Melegh B, Martella V, Gentsch JR, Szucs G. Bányai K, et al. Among authors: melegh b. J Med Virol. 2009 Feb;81(2):362-70. doi: 10.1002/jmv.21375. J Med Virol. 2009. PMID: 19107981

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