Arking, DE;Pfeufer, A;Post, W;Kao, WH;Newton-Cheh, C;Ikeda, M;West, K;Kashuk, C;Akyol, M;Perz, S;Jalilzadeh, S;Illig, T;Gieger, C;Guo, CY;Larson, MG;Wichmann, HE;Marbán, E;O'Donnell, CJ;Hirschhorn, JN;Kääb, S;Spooner, PM;Meitinger, T;Chakravarti, A
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
Nat Genet
2006
38
6
644-51

Antonini, A;Goldwurm, S;Benti, R;Prokisch, H;Ebhardt, M;Cilia, R;Zini, M;Righini, A;Cossu, G;Pezzoli, G
Genetic, clinical, and imaging characterization of one patient with late-onset, slowly progressive, pantothenate kinase-associated neurodegeneration.
Mov Disord
2006
21
3
417-8

Islinger, M;Lüers, GH;Zischka, H;Ueffing, M;Völkl, A
Insights into the membrane proteome of rat liver peroxisomes: microsomal glutathione-S-transferase is shared by both subcellular compartments.
Proteomics
2006
6
3
804-16

Horvath, R;Abicht, A;Holinski-Feder, E;Laner, A;Gempel, K;Prokisch, H;Lochmüller, H;Klopstock, T;Jaksch, M
Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA).
J Neurol Neurosurg Psychiatry
2006
77
1
74-6

Fauth, C;Gribble, SM;Porter, KM;Codina-Pascual, M;Ng, BL;Kraus, J;Uhrig, S;Leifheit, J;Haaf, T;Fiegler, H;Carter, NP;Speicher, MR
Micro-array analyses decipher exceptional complex familial chromosomal rearrangement.
Hum Genet
2006
119
1-2
145-53

Codina-Pascual, M;Navarro, J;Oliver-Bonet, M;Kraus, J;Speicher, MR;Arango, O;Egozcue, J;Benet, J
Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes.
Hum Reprod
2006
21
6
1490-7

Codina-Pascual, M;Campillo, M;Kraus, J;Speicher, MR;Egozcue, J;Navarro, J;Benet, J
Crossover frequency and synaptonemal complex length: their variability and effects on human male meiosis.
Mol Hum Reprod
2006
12
2
123-33

Zischka, H;Braun, RJ;Marantidis, EP;Büringer, D;Bornhövd, C;Hauck, SM;Demmer, O;Gloeckner, CJ;Reichert, AS;Madeo, F;Ueffing, M
Differential analysis of Saccharomyces cerevisiae mitochondria by free flow electrophoresis.
Mol Cell Proteomics
2006
5
11
2185-200

Langer, S;Geigl, JB;Wagenstaller, J;Lederer, G;Hempel, M;Daumer-Haas, C;Leifheit, HJ;Speicher, MR
Delineation of a 2q deletion in a girl with dysmorphic features and epilepsy.
Am J Med Genet A
2006
140
7
764-8

Perocchi, F;Jensen, LJ;Gagneur, J;Ahting, U;von Mering, C;Bork, P;Prokisch, H;Steinmetz, LM
Assessing systems properties of yeast mitochondria through an interaction map of the organelle.
PLoS Genet
2006
2
10
e170