Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
Annemarie Poustka

Veröffentlichungen von Annemarie Poustka zu Poustka, Annemarie ->
weitere Veröffentlichungen von Annemarie Poustka:
Completion of the physical map of Xq28: the location of the gene for L1CAM on the human X Chromosome (1992)
Distribution and early development of microarray technology in Europe (1999)
The human rab GDI β gene with long retroposon-rich introns maps to 10p15 and its pseudogene to 7p11-p13 (1998)
A Compendium to Ensure Computational Reproducibility in High-Dimensional Classification Tasks (2004)
Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients (1997)
Construction and use of human chromosome jumping libraries from NotI-digested DNA (1987)
Homozygous deletion in Wilms tumours of a zinc-finger gene identifiedby chromosome jumping (1990)
Cloning of the T gene required in mesoderm formation in the mouse (1990)
Enhanced Fmr–1 expression in testis (1993)
Highly homologous loci on the X and Y chromosomes are hot–spots for ectopic recombinations leading to XX maleness (1994)
Parameter estimation for the calibration and variance stabilization of microarray data (2003)
DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3–26.1 is deleted in malignant brain tumours (1997)
X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markers (1996)
Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions (2000)
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters (1993)
Veröffentlichungen zu Poustka, Annemarie
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
1
Dietrich, Alexander, Korn, Bernhard, ... Completion of the physical map of Xq28: the location of the gene for L1CAM on the human X Chromosome
in: Mammalian genome , ISSN 1432-1777, Vol. 3 (3. 1992), p. 168-172
Zugang: zum Volltext
ähnliche Vorschläge
1992
zeige Details
2
Vente, Andreas, Korn, Bernd, ... Distribution and early development of microarray technology in Europe
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 22, No. 1 (1999), p. 22-22
Zugang: zum Volltext
ähnliche Vorschläge
1999
zeige Details
3
Sedlacek, Zdenek, Munstermann, Ewald, ... The human rab GDI β gene with long retroposon-rich introns maps to 10p15 and its pseudogene to 7p11-p13
in: Mammalian genome , ISSN 1432-1777, Vol. 9 (1. 1998), p. 78-80
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
4
Ruschhaupt, Markus., Huber, Wolfgang., ... A Compendium to Ensure Computational Reproducibility in High-Dimensional Classification Tasks
In: Statistical applications in genetics and molecular biology. - Berkeley, Calif. : Bepress, ISSN 1544-6115, Vol. 3, No. 1 (2004), p. 37
Zugang: zum Volltext
ähnliche Vorschläge
2004
zeige Details
5
Klauck, S. M., Münstermann, Ewald, ... Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients
in: Human genetics , ISSN 1432-1203, Vol. 100 (2. 1997), p. 224-229
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
6
Poustka, Annemarie, Pohl, Thomas M., ... Construction and use of human chromosome jumping libraries from NotI-digested DNA
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 325, No. 6102 (1987), p. 353-355
Zugang: zum Volltext
ähnliche Vorschläge
1987
zeige Details
7
Gessler, Manfred, Poustka, Annemarie, ... Homozygous deletion in Wilms tumours of a zinc-finger gene identifiedby chromosome jumping
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 343, No. 6260 (1990), p. 774-778
Zugang: zum Volltext
ähnliche Vorschläge
1990
zeige Details
8
Herrmann, Bernhard G., Labeit, Siegfried, ... Cloning of the T gene required in mesoderm formation in the mouse
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 343, No. 6259 (1990), p. 617-622
Zugang: zum Volltext
ähnliche Vorschläge
1990
zeige Details
9
Bächner, Dietmar, Steinbach, Peter, ... Enhanced Fmr–1 expression in testis
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 4, No. 2 (1993), p. 115-116
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
10
Weil, Dominique, Wang, Irène, ... Highly homologous loci on the X and Y chromosomes are hot–spots for ectopic recombinations leading to XX maleness
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 7, No. 3 (1994), p. 414-419
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
11
Huber, Wolfgang., von Heydebreck, Anja., ... Parameter estimation for the calibration and variance stabilization of microarray data
In: Statistical applications in genetics and molecular biology. - Berkeley, Calif. : Bepress, ISSN 1544-6115, Vol. 2, No. 1 (2003), p. 3
Zugang: zum Volltext
ähnliche Vorschläge
2003
zeige Details
12
Mollenhauer, Jan, Wiemann, Stefan, ... DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3–26.1 is deleted in malignant brain tumours
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 17, No. 1 (1997), p. 32-39
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
13
Hu, Ling-Jia, Laporte, Jocelyn, ... X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markers
in: Human genetics , ISSN 1432-1203, Vol. 98 (2. 1996), p. 178-181
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
14
Reichwald, Kathrin, Thiesen, Jens, ... Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions
in: Mammalian genome , ISSN 1432-1777, Vol. 11 (3. 2000), p. 182-190
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
15
Mosser, Jean, Douar, Anne-Marie, ... Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 361, No. 6414 (1993), p. 726-730
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
16
Dittrich, Bärbel, Buiting, Karin, ... Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 14, No. 2 (1996), p. 163-170
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
17
Laporte, Jocelyn, Hu, Ling Jia, ... A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 13, No. 2 (1996), p. 175-182
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
18
Heiss, Nina S., Knight, Stuart W., ... X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 19, No. 1 (1998), p. 32-38
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
19
Vits, Lieve, Van Camp, Guy, ... MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 7, No. 3 (1994), p. 408-413
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
20
Szatmari, Peter, Paterson, Andrew D, ... Mapping autism risk loci using genetic linkage and chromosomal rearrangements
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 3 (2007), p. 319-328
Zugang: zum Volltext
ähnliche Vorschläge
2007