Search Results - "Stiege, A"

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  1. 1

    Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2−/− mouse model by Hecht, J., Seitz, V., Urban, M., Wagner, F., Robinson, P.N., Stiege, A., Dieterich, C., Kornak, U., Wilkening, U., Brieske, N., Zwingman, C., Kidess, A., Stricker, S., Mundlos, S.

    Published in Gene Expression Patterns (01-01-2007)
    “…Runx2 is an essential factor for skeletogenesis and heterozygous loss causes cleidocranial dysplasia in humans and a corresponding phenotype in the mouse…”
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  2. 2
  3. 3

    A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution by Stricker, S., Poustka, A.J., Wiecha, U., Stiege, A., Hecht, J., Panopoulou, G., Vilcinskas, A., Mundlos, S., Seitz, V.

    Published in Developmental and comparative immunology (01-09-2003)
    “…Runt-homologous molecules are characterized by their DNA binding runt-domain which is highly conserved within bilaterians. The three mammalian runt-genes are…”
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  4. 4

    Shape and DNA packaging activity of bacteriophage SPP1 procapsid: protein components and interactions during assembly by Dröge, A, Santos, M A, Stiege, A C, Alonso, J C, Lurz, R, Trautner, T A, Tavares, P

    Published in Journal of molecular biology (11-02-2000)
    “…The procapsid of the Bacillus subtilis bacteriophage SPP1 is formed by the major capsid protein gp13, the scaffolding protein gp11, the portal protein gp6, and…”
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  5. 5

    Purification and properties of the RecR protein from Bacillus subtilis 168 by ALONSO, J. C, STIEGE, A. C, DOBRINSKI, B, LURZ, R

    Published in The Journal of biological chemistry (15-01-1993)
    “…Genetic evidence suggests that the Bacillus subtilis recR gene product is involved in DNA repair and recombination. To assign a biochemical function to the…”
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  6. 6

    Specific targeting of a DNA‐binding protein to the SPP1 procapsid by interaction with the portal oligomer by Stiege, Asita C., Isidro, Anabela, Dröge, Anja, Tavares, Paulo

    Published in Molecular microbiology (01-09-2003)
    “…Summary The icosahedral procapsid of tailed bacteriophages is composed of a large number of identical subunits and of minor proteins found in a few copies…”
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  7. 7

    The complete nucleotide sequence and functional organization of Bacillus subtilis bacteriophage SPP1 by Alonso, Juan C, Lüder, Gerhild, Stiege, Asita C, Chai, Sunghee, Weise, Frank, Trautner, Thomas A

    Published in Gene (19-12-1997)
    “…The complete nucleotide sequence of the B. subtilis bacteriophage SPP1 is described. The genome is 44 007 bp in size and has a base composition of 43.7% dG+dC…”
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  8. 8

    Genetic recombination in Bacillus subtilis 168: effect of recN, recF, recH and addAB mutations on DNA repair and recombination by Alonso, J C, Stiege, A C, Lüder, G

    Published in Molecular & general genetics (01-05-1993)
    “…A recN- (recN1) strain of Bacillus subtilis was constructed. The effects of this and recF, recH and addAB mutations on recombination proficiency were tested…”
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    RecR is a zinc metalloprotein from Bacillus subtilis 168 by Ayora, Silvia, Stiege, Asita C., Alonso, Juan C.

    Published in Molecular microbiology (01-02-1997)
    “…The Bacillus subtilis RecR protein is required for DNA repair and recombination in vivo. In its N‐terminal portion, RecR possesses potential zinc‐ligand…”
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  11. 11

    Functional analysis of the leading strand replication origin of plasmid pUB110 in Bacillus subtilis by ALONSO, J. C, LEONHARDT, H, STIEGE, C. A

    Published in Nucleic acids research (11-10-1988)
    “…Supercoiled plasmid DNA is the substrate for initiation of pUB110 replication, and - by inference - for binding of its initiator protein (RepU) to the plasmid…”
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  12. 12

    Molecular analysis of the Bacillus subtilis recF function by Alonso, J C, Stiege, A C

    Published in Molecular & general genetics (01-09-1991)
    “…recF resides between the dnaN and gyrB genes of Bacillus subtilis. The recF15 mutation results in replacement of a glutamate residue in the wild type with a…”
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  13. 13

    Bacillus subtilis 168 RecR protein-DNA complexes visualized as looped structures by Ayora, S, Stiege, A C, Lurz, R, Alonso, J C

    Published in Molecular & general genetics (18-03-1997)
    “…The Bacillus subtilis 168 RecR protein bound to duplex DNA in the presence of ATP and divalent cations (Mg2+ and Zn2+) was visualized by electron microscopy as…”
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  14. 14

    Functional analysis of the dna (Ts) mutants of Bacillus subtilis: plasmid pUB110 replication as a model system by Alonso, J C, Stiege, C A, Tailor, R H, Viret, J F

    Published in Molecular & general genetics (01-11-1988)
    “…We determined the effect of various Bacillus subtilis dna(Ts) mutations on pUB110 and chromosomal replication. Leading strand DNA synthesis of pUB110, starting…”
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  15. 15

    Structure of a viral DNA gatekeeper at 10Aa resolution by cryo-electron microscopy by Orlova, E V, Gowen, B, Droege, A, Stiege, A, Weise, F, Lurz, R, Van Heel, M, Tavares, P

    Published in The EMBO journal (01-03-2003)
    “…In tailed bacteriophages and herpes viruses, the viral DNA is packaged through the portal protein channel. Channel closure is essential to prevent DNA release…”
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  16. 16

    Sequential Headful Packaging and Fate of the Cleaved DNA Ends in Bacteriophage SPP1 by Tavares, Paulo, Lurz, Rudi, Stiege, Asita, Rückert, Beate, Trautner, Thomas A.

    Published in Journal of molecular biology (20-12-1996)
    “…The virulent Bacillus subtilisbacteriophage SPP1 packages its DNA from a precursor concatemer by a headful mechanism. Following disruption of mature virions…”
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  17. 17

    Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2 super(-/-) mouse model by Hecht, J, Seitz, V, Urban, M, Wagner, F, Robinson, P N, Stiege, A, Dieterich, C, Kornak, U, Wilkening, U, Brieske, N, Zwingman, C, Kidess, A, Stricker, S, Mundlos, S

    Published in Gene Expression Patterns (01-01-2007)
    “…Runx2 is an essential factor for skeletogenesis and heterozygous loss causes cleidocranial dysplasia in humans and a corresponding phenotype in the mouse…”
    Get full text
    Journal Article
  18. 18

    A molecular pathogenesis for transcription factor associated poly-alanine tract expansions by Albrecht, Andrea N., Kornak, Uwe, Böddrich, Annett, Süring, Kathrin, Robinson, Peter N., Stiege, Asita C., Lurz, Rudi, Stricker, Sigmar, Wanker, Erich E., Mundlos, Stefan

    Published in Human molecular genetics (15-10-2004)
    “…Poly-alanine (Ala) tract expansions in transcription factors have been shown to be associated with human birth defects such as malformations of the brain, the…”
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