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G Zsurka

Showing results (1-10 of 7) with videos related to

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Genomics|June 13, 2001
The human mitochondrial Mrs2 protein functionally substitutes for its yeast homologue, a candidate magnesium transporterG Zsurka, J Gregán, R J Schweyen
Nucleic Acids Research|July 27, 2001
Role of DNA minor groove interactions in substrate recognition by the M.SinI and M.EcoRII DNA (cytosine-5) methyltransferasesA Kiss, G Pósfai, G Zsurka, et al.
Biological Psychiatry|October 2, 1998
No mitochondrial haplotype was found to increase risk for Alzheimer's diseaseG Zsurka, J Kálmán, A Császár, et al.
Molecular & General Genetics : MGG|March 20, 2001
The mitochondrial inner membrane protein Lpe10p, a homologue of Mrs2p, is essential for magnesium homeostasis and group II intron splicing in yeastJ Gregan, D M Bui, R Pillich, et al.
Human Genetics|April 1, 1997
Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritisG Zsurka, J Ormos, B Iványi, et al.
Seizure|September 12, 2008
Proof of progression over time: finally fulminant brain, muscle, and liver affection in Alpers syndrome associated with the A467T POLG1 mutationM Boes, J Bauer, H Urbach, et al.
Neurology|February 10, 2010
Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) geneG Zsurka, K G Hampel, I Nelson, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Genomics|June 13, 2001
The human mitochondrial Mrs2 protein functionally substitutes for its yeast homologue, a candidate magnesium transporterG Zsurka, J Gregán, R J Schweyen
Nucleic Acids Research|July 27, 2001
Role of DNA minor groove interactions in substrate recognition by the M.SinI and M.EcoRII DNA (cytosine-5) methyltransferasesA Kiss, G Pósfai, G Zsurka, et al.
Biological Psychiatry|October 2, 1998
No mitochondrial haplotype was found to increase risk for Alzheimer's diseaseG Zsurka, J Kálmán, A Császár, et al.
Molecular & General Genetics : MGG|March 20, 2001
The mitochondrial inner membrane protein Lpe10p, a homologue of Mrs2p, is essential for magnesium homeostasis and group II intron splicing in yeastJ Gregan, D M Bui, R Pillich, et al.
Human Genetics|April 1, 1997
Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritisG Zsurka, J Ormos, B Iványi, et al.
Seizure|September 12, 2008
Proof of progression over time: finally fulminant brain, muscle, and liver affection in Alpers syndrome associated with the A467T POLG1 mutationM Boes, J Bauer, H Urbach, et al.
Neurology|February 10, 2010
Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) geneG Zsurka, K G Hampel, I Nelson, et al.
Pageof 1