Kristine Freude

Kristine Freude

Professor


Publication year:
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101 - 108 out of 108Page size: 50
  1. 2011

  2. Soluble amyloid precursor protein induces rapid neural differentiation of human embryonic stem cells

    Freude, Kristine, Penjwini, M., Davis, J. L., LaFerla, F. M. & Blurton-Jones, M., 2011, In: The Journal of Biological Chemistry. 286, 27, p. 24264-24274 11 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. 2010

  4. Nkx6 transcription factors and Ptf1a function as antagonistic lineage determinants in multipotent pancreatic progenitors

    Schaffer, A. E., Freude, Kristine, Nelson, S. B. & Sander, M., 2010, In: Developmental Cell. 18, 6, p. 1022-1029 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. 2009

  6. Nkx6-1 controls the identity and fate of red nucleus and oculomotor neurons in the mouse midbrain

    Prakash, N., Puelles, E., Freude, Kristine, Trümbach, D., Omodei, D., Di Salvio, M., Sussel, L., Ericson, J., Sander, M., Simeone, A. & Wurst, W., 2009, In: Development (Cambridge, England). 136, 15, p. 2545-2555 11 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  7. 2008

  8. A dosage-dependent requirement for Sox9 in pancreatic endocrine cell formation

    Seymour, Philip Allan, Freude, Kristine, Dubois, C. L., Shih, H., Patel, N. A. & Sander, M., 1 Nov 2008, In: Advances in Developmental Biology. 323, 1, p. 19-30 12 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. 2007

  10. SOX9 is required for maintenance of the pancreatic progenitor cell pool

    Seymour, Philip Allan, Freude, Kristine, Tran, M. N., Mayes, E. E., Jensen, J., Kist, R., Scherer, G. & Sander, M., 6 Feb 2007, In: Proceedings of the National Academy of Sciences of the United States of America. 104, 6, p. 1865-70 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  11. X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11

    Jensen, L. R., Lenzner, S., Moser, B., Freude, Kristine, Tzschach, A., Wei, C., Fryns, J., Chelly, J., Turner, G., Moraine, C., Hamel, B., Ropers, H. & Kuss, A. W., 2007, In: European Journal of Human Genetics. 15, 1, p. 68-75 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  12. 2004
  13. Published

    Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation

    Freude, K., Hoffmann, K., Jensen, L., Delatycki, M. B., des Portes, V., Moser, B., Hamel, B., van Bokhoven, H., Moraine, C., Fryns, J., Chelly, J., Gécz, J., Lenzner, S., Kalscheuer, V. M., Ropers, H. & Freude, Kristine, Aug 2004, In: American Journal of Human Genetics. 75, 2, p. 305-9 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  14. 2003
  15. Published

    Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation

    Kalscheuer, V. M., Freude, K., Musante, L., Jensen, L. R., Yntema, H. G., Gécz, J., Sefiani, A., Hoffmann, K., Moser, B., Haas, S., Gurok, U., Haesler, S., Aranda, B., Nshedjan, A., Tzschach, A., Hartmann, N., Roloff, T-C., Shoichet, S., Hagens, O., Tao, J. & 14 others, Van Bokhoven, H., Turner, G., Chelly, J., Moraine, C., Fryns, J., Nuber, U., Hoeltzenbein, M., Scharff, C., Scherthan, H., Lenzner, S., Hamel, B. C. J., Schweiger, S., Ropers, H. & Freude, Kristine, Dec 2003, In: Nature Genetics. 35, 4, p. 313-5 3 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

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