Search Results - "Kottwitz, D."

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  1. 1

    Evaluation of a novel multiplex RT-qPCR assay for the quantification of leukemia-associated BCR-ABL1 translocation by Kottwitz, D., EL Hadi, H., El Amrani, M., Cabezas, S., Dehbi, H., Nadifi, S., Quessar, A., Colomer, D., Moumen, Abdeladim, Sefrioui, EL Hassan

    Published in International journal of hematology (01-09-2015)
    “…Although monitoring of BCR-ABL1 translocation has become an established practice in the management of chronic myeloid leukemia (CML), the detection limit of…”
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    Journal Article
  2. 2

    Specific BRCA1 gene variations amongst young Moroccan breast cancer patients by Tazzite, A, Nadiffi, S, Kottwitz, D, El Amrani, M, Jouhadi, H, Benider, A, Moumen, A, Sefrioui, H

    Published in Genetics and molecular research (31-01-2014)
    “…Germline mutations in the BRCA1 gene are known predictive markers for the development of hereditary breast cancer. Nevertheless, no comprehensive study has…”
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    Journal Article
  3. 3

    Intracellular domain of nicotinic acetylcholine receptor: the importance of being unfolded by Kukhtina, V., Kottwitz, D., Strauss, H., Heise, B., Chebotareva, N., Tsetlin, V., Hucho, F.

    Published in Journal of neurochemistry (01-04-2006)
    “…Bioinformatics methods with subsequent verification by experimental data were applied to the structural investigation of the intracellular loop of the…”
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    Journal Article
  4. 4

    Quantitative real-time polymerase chain reaction as an efficient molecular tool for detecting minimal residual disease in Moroccan chronic myeloid leukemia patients by Moumen, A, Dehbi, H, Kottwitz, D, El Amrani, M, Bouchoutrouch, N, El Hadi, H, Quessar, A, Benchekroun, S, Nadifi, S, Sefrioui, H

    Published in Genetics and molecular research (06-02-2015)
    “…Chronic myeloid leukemia (CML) is characterized by BCR-ABL translocation and an increased number and migration of immature myeloid cells into the peripheral…”
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    Journal Article
  5. 5

    Pharmacological interference with the glucocorticoid system influences symptoms and lifespan in a mouse model of Rett syndrome by BRAUN, Sebastian, KOTTWITZ, Denise, NUBER, Ulrike A

    Published in Human molecular genetics (15-04-2012)
    “…Rett syndrome (RTT) is caused by loss-of-function mutations in the X-linked gene MECP2 coding for methyl CpG-binding protein 2 (MeCP2). This protein can act as…”
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  6. 6

    SPECIAL ISSUE: Intracellular domain of nicotinic acetylcholine receptor: the importance of being unfolded by Kukhtina, V, Kottwitz, D, Strauss, H, Heise, B, Chebotareva, N, Tsetlin, V, Hucho, F

    Published in Journal of neurochemistry (01-04-2006)
    “…Bioinformatics methods with subsequent verification by experimental data were applied to the structural investigation of the intracellular loop of the…”
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    Journal Article
  7. 7

    Intracellular domains of the δ-subunits of Torpedo and rat acetylcholine receptors—expression, purification, and characterization by Kottwitz, Denise, Kukhtina, Viktoria, Dergousova, Natalia, Alexeev, Timophey, Utkin, Yuri, Tsetlin, Victor, Hucho, Ferdinand

    Published in Protein expression and purification (01-12-2004)
    “…There are quite detailed structural data on the extracellular ligand-binding domain and the intramembrane channel-forming domain of the nicotinic acetylcholine…”
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    Journal Article
  8. 8
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