Kääb, S;Barth, AS;Margerie, D;Dugas, M;Gebauer, M;Zwermann, L;Merk, S;Pfeufer, A;Steinmeyer, K;Bleich, M;Kreuzer, E;Steinbeck, G;Näbauer, M
Global gene expression in human myocardium-oligonucleotide microarray analysis of regional diversity and transcriptional regulation in heart failure.
J Mol Med
2004
82
5
308-16

Prokisch, H;Andreoli, C;Scharfe, C;Steinmetz, L;Meitinger, T
Integrative analysis of the mitochondrial proteome
Biochim Biophys Acta
2004
1657 Suppl
19-19

Thalhammer, S;Langer, S;Speicher, MR;Heckl, WM;Geigl, JB
Generation of chromosome painting probes from single chromosomes by laser microdissection and linker-adaptor PCR.
Chromosome Res
2004
12
4
337-43

Hortnagel, K;Nardocci, N;Zorzi, G;Garavaglia, B;Botz, E;Meitinger, T;Klopstock, T
Infantile neuroaxonal dystrophy and pantothenate-kinase-associated neurodegeneration: locus heterogeneity.
Neurology
2004
63
5
922-4

Binder, EB;Salyakina, D;Lichtner, P;Wochnik, GM;Ising, M;Pütz, B;Papiol, S;Seaman, S;Lucae, S;Kohli, MA;Nickel, T;Künzel, HE;Fuchs, B;Majer, M;Pfennig, A;Kern, N;Brunner, J;Modell, S;Baghai, T;Deiml, T;Zill, P;Bondy, B;Rupprecht, R;Messer, T;Köhnlein, O;Dabitz, H;Brückl, T;Muller, N;Pfister, H;Lieb, R;Mueller, JC;Lõhmussaar, E;Strom, TM;Bettecken, T;Meitinger, T;Uhr, M;Rein, T;Holsboer, F;Müller-Myhsok, B
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment.
Nat Genet
2004
36
12
1319-25

Langer, S;Kraus, J;Jentsch, I;Speicher, MR
Multicolor chromosome painting in diagnostic and research applications.
Chromosome Res
2004
12
1
15-23

Gangnus, R;Langer, S;Breit, E;Pantel, K;Speicher, MR
Genomic profiling of viable and proliferative micrometastatic cells from early-stage breast cancer patients.
Clin Cancer Res
2004
10
10
3457-64

Codina-Pascual, M;Kraus, J;Speicher, MR;Oliver-Bonet, M;Murcia, V;Sarquella, J;Egozcue, J;Navarro, J;Benet, J
Characterization of all human male synaptonemal complexes by subtelomere multiplex-FISH.
Cytogenet Genome Res
2004
107
1-2
18-21

Zimprich, A;Biskup, S;Leitner, P;Lichtner, P;Farrer, M;Lincoln, S;Kachergus, J;Hulihan, M;Uitti, RJ;Calne, DB;Stoessl, AJ;Pfeiffer, RF;Patenge, N;Carbajal, IC;Vieregge, P;Asmus, F;Müller-Myhsok, B;Dickson, DW;Meitinger, T;Strom, TM;Wszolek, ZK;Gasser, T
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Neuron
2004
44
4
601-7

Fauth, C;O'Hare, MJ;Lederer, G;Jat, PS;Speicher, MR
Order of genetic events is critical determinant of aberrations in chromosome count and structure.
Genes Chromosomes Cancer
2004
40
4
298-306