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Results: 1-14 |
Results: 14
An mtDNA mutation, 14453G -> A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome
Authors: Ravn, K Wibrand, F Hansen, FJ Horn, N Rosenberg, T Schwartz, M
Citation: K. Ravn et al., An mtDNA mutation, 14453G -> A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome, EUR J HUM G, 9(10), 2001, pp. 805-809
Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene
Authors: Wibrand, F Ravn, K Schwartz, M Rosenberg, T Horn, N Vissing, J
Citation: F. Wibrand et al., Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene, ANN NEUROL, 50(4), 2001, pp. 540-543
Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy
Authors: Jaksch, M Horvath, R Horn, N Auer, DP Macmillan, C Peters, J Gerbitz, KD Kraegeloh-Mann, I Muntau, A Karcagi, V Kalmanchey, R Lochmuller, H Shoubridge, EA Freisinger, P
Citation: M. Jaksch et al., Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy, NEUROLOGY, 57(8), 2001, pp. 1440-1446
Characterization of the hCTR1 gene: Genomic organization, functional expression, and identification of a highly homologous processed gene
Authors: Moller, LB Petersen, C Lund, C Horn, N
Citation: Lb. Moller et al., Characterization of the hCTR1 gene: Genomic organization, functional expression, and identification of a highly homologous processed gene, GENE, 257(1), 2000, pp. 13-22
Similar splice-site mutations of the ATP7A gene lead to different phenotypes: Classical Menkes disease or occipital horn syndrome
Authors: Moller, LB Tumer, Z Lund, C Petersen, C Cole, T Hanusch, R Seidel, J Jensen, LR Horn, N
Citation: Lb. Moller et al., Similar splice-site mutations of the ATP7A gene lead to different phenotypes: Classical Menkes disease or occipital horn syndrome, AM J HU GEN, 66(4), 2000, pp. 1211-1220
Molecular genetics of intracellular copper transport
Authors: Horn, N Tumer, Z
Citation: N. Horn et Z. Tumer, Molecular genetics of intracellular copper transport, J TR EL EXP, 12(4), 1999, pp. 297-313
Accumulated experience with prenatal diagnosis of Menkes disease by neutron activation analysis of chorionic villi specimens
Authors: Heydorn, K Damsgaard, E Horn, N
Citation: K. Heydorn et al., Accumulated experience with prenatal diagnosis of Menkes disease by neutron activation analysis of chorionic villi specimens, BIOL TR EL, 71-2, 1999, pp. 551-561
Enhanced production of pediocin PA-1 and coproduction of nisin and pediocin PA-1 by Lactococcus lactis
Authors: Horn, N Martinez, MI Martinez, JM Hernandez, PE Gasson, MJ Rodriguez, JM Dodd, HM
Citation: N. Horn et al., Enhanced production of pediocin PA-1 and coproduction of nisin and pediocin PA-1 by Lactococcus lactis, APPL ENVIR, 65(10), 1999, pp. 4443-4450
Expression, purification and copper-binding studies of the first metal-binding domain of Menkes protein
Authors: Jensen, PY Bonander, N Horn, N Tumer, Z Farver, O
Citation: Py. Jensen et al., Expression, purification and copper-binding studies of the first metal-binding domain of Menkes protein, EUR J BIOCH, 264(3), 1999, pp. 890-896
Post-translational modification of nisin - The involvement of NisB in the dehydration process
Authors: Sen, AK Narbad, A Horn, N Dodd, HM Parr, AJ Colquhoun, I Gasson, MJ
Citation: Ak. Sen et al., Post-translational modification of nisin - The involvement of NisB in the dehydration process, EUR J BIOCH, 261(2), 1999, pp. 524-532
Prescribing donepezil in clinical practice
Authors: Watts-Tobin, MA Horn, N
Citation: Ma. Watts-tobin et N. Horn, Prescribing donepezil in clinical practice, BR J PSYCHI, 175, 1999, pp. 393-393
Extracorporeal liver assist devices in acute liver failure
Authors: Horn, N Unger, J Rossaint, R
Citation: N. Horn et al., Extracorporeal liver assist devices in acute liver failure, ANAESTHESIS, 48(6), 1999, pp. 387-394
Characterisation of genetically modified nisin molecules by Fourier transform ion cyclotron resonance mass spectrometry
Authors: Lavanant, H Heck, A Derrick, PJ Mellon, FA Parr, A Dodd, HM Giffard, CJ Horn, N Gasson, MJ
Citation: H. Lavanant et al., Characterisation of genetically modified nisin molecules by Fourier transform ion cyclotron resonance mass spectrometry, EUR MASS SP, 4(5), 1998, pp. 405-416
Lethal neonatal Menkes' disease with severe vasculopathy and fractures
Authors: Jankov, RP Boerkoel, CF Hellmann, J Sirkin, WL Tumer, Z Horn, N Feigenbaum, A
Citation: Rp. Jankov et al., Lethal neonatal Menkes' disease with severe vasculopathy and fractures, ACT PAEDIAT, 87(12), 1998, pp. 1297-1300
Risultati: 1-14 |