Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Publikationen

Suchbegriffe: DNA, MITOCHONDRIAL - GENETICS , . Treffer: 15

2016

Tatlisumak, T; Putaala, J; Innilä, M; Enzinger, C; Metso, TM; Curtze, S; von Sarnowski, B; Amaral-Silva, A; Jungehulsing, GJ; Tanislav, C; Thijs, V; Rolfs, A; Norrving, B; Fazekas, F; Suomalainen, A; Kolodny, EH Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient population.
J Neurol. 2016; 263(2):257-262 [OPEN ACCESS]
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2015

Ebner, S; Mangge, H; Langhof, H; Halle, M; Siegrist, M; Aigner, E; Paulmichl, K; Paulweber, B; Datz, C; Sperl, W; Kofler, B; Weghuber, D Mitochondrial Haplogroup T Is Associated with Obesity in Austrian Juveniles and Adults.
PLoS One. 2015; 10(8):e0135622-e0135622 [OPEN ACCESS]
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2014

Burgstaller, JP; Johnston, IG; Jones, NS; Albrechtová, J; Kolbe, T; Vogl, C; Futschik, A; Mayrhofer, C; Klein, D; Sabitzer, S; Blattner, M; Gülly, C; Poulton, J; Rülicke, T; Piálek, J; Steinborn, R; Brem, G MtDNA segregation in heteroplasmic tissues is common in vivo and modulated by haplotype differences and developmental stage.
Cell Rep. 2014; 7(6):2031-2041 [OPEN ACCESS]
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2013

Fischer, C; Koblmüller, S; Gülly, C; Schlötterer, C; Sturmbauer, C; Thallinger, GG Complete mitochondrial DNA sequences of the threadfin cichlid (Petrochromis trewavasae) and the blunthead cichlid (Tropheus moorii) and patterns of mitochondrial genome evolution in cichlid fishes.
PLoS One. 2013; 8(6):e67048-e67048 [OPEN ACCESS]
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Nevado, B; Mautner, S; Sturmbauer, C; Verheyen, E Water-level fluctuations and metapopulation dynamics as drivers of genetic diversity in populations of three Tanganyikan cichlid fish species.
Mol Ecol. 2013; 22(15): 3933-3948. [OPEN ACCESS]
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2011

Haemmerle, G; Moustafa, T; Woelkart, G; Büttner, S; Schmidt, A; van de Weijer, T; Hesselink, M; Jaeger, D; Kienesberger, PC; Zierler, K; Schreiber, R; Eichmann, T; Kolb, D; Kotzbeck, P; Schweiger, M; Kumari, M; Eder, S; Schoiswohl, G; Wongsiriroj, N; Pollak, NM; Radner, FP; Preiss-Landl, K; Kolbe, T; Rülicke, T; Pieske, B; Trauner, M; Lass, A; Zimmermann, R; Hoefler, G; Cinti, S; Kershaw, EE; Schrauwen, P; Madeo, F; Mayer, B; Zechner, R ATGL-mediated fat catabolism regulates cardiac mitochondrial function via PPAR-α and PGC-1.
Nat Med. 2011; 17(9):1076-1085 [OPEN ACCESS]
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Mueller, EE; Eder, W; Ebner, S; Schwaiger, E; Santic, D; Kreindl, T; Stanger, O; Paulweber, B; Iglseder, B; Oberkofler, H; Maier, R; Mayr, JA; Krempler, F; Weitgasser, R; Patsch, W; Sperl, W; Kofler, B The Mitochondrial T16189C Polymorphism Is Associated with Coronary Artery Disease in Middle European Populations
PLOS ONE. 2011; 6(1): [OPEN ACCESS]
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Schwark, T; Heinrich, A; Preusse-Prange, A; von Wurmb-Schwark, N Reliable genetic identification of burnt human remains.
Forensic Sci Int Genet. 2011; 5(5): 393-399.
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Zimmermann, FA; Mayr, JA; Feichtinger, R; Neureiter, D; Lechner, R; Koegler, C; Ratschek, M; Rusmir, H; Sargsyan, K; Sperl, W; Kofler, B Respiratory chain complex I is a mitochondrial tumor suppressor of oncocytic tumors.
Front Biosci (Elite Ed). 2011; 3:315-325
PubMed

 

2010

von Wurmb-Schwark, N; Schwark, T; Caliebe, A; Drenske, C; Nikolaus, S; Schreiber, S; Nebel, A Low level of the mtDNA(4977) deletion in blood of exceptionally old individuals.
Mech Ageing Dev. 2010; 131(3): 179-184.
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2009

von Wurmb-Schwark, N; Preusse-Prange, A; Heinrich, A; Simeoni, E; Bosch, T; Schwark, T A new multiplex-PCR comprising autosomal and y-specific STRs and mitochondrial DNA to analyze highly degraded material.
Forensic Sci Int Genet. 2009; 3(2): 96-103.
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2008

Mayr, JA; Meierhofer, D; Zimmermann, F; Feichtinger, R; Kogler, C; Ratschek, M; Schmeller, N; Sperl, W; Kofler, B Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma.
Clin Cancer Res. 2008; 14(8):2270-2275 [OPEN ACCESS]
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2007

Dhandapany, PS; Sadayappan, S; Vanniarajan, A; Karthikeyan, B; Nagaraj, C; Gowrishankar, K; Selvam, GS; Singh, L; Thangaraj, K Novel mitochondrial DNA mutations implicated in Noonan syndrome.
Int J Cardiol. 2007; 120(2): 284-285. (- Case Report)
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2003

von Wurmb-Schwark, N; Schwark, T; Meissner, C; Oehmichen, M Mitochondrial mutagenesis in the brain in forensic and pathological research.
Leg Med (Tokyo). 2003; 5(1):1-6
PubMed

 

1998

Widschwendter, M; Schröcksnadel, H; Mörtl, MG Pre-eclampsia: a disorder of placental mitochondria?
Mol Med Today. 1998; 4(7):286-291
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