Kristine Freude
Professor
Pathobiological Sciences
Grønnegårdsvej 7, 1870 Frederiksberg C
- 2009
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
- 2008
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
- 2007
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
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
- 2004
- 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
- 2003
- 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, , Dec 2003, In: Nature Genetics. 35, 4, p. 313-5 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 38189431
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Induced pluripotent stem cells derived from Alzheimer's disease patients: the promise, the hope and the path ahead
Research output: Contribution to journal › Review › Research › peer-review
Published -
462
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Patient iPSC-derived neurons for disease modeling of frontotemporal dementia with mutation in CHMP2B
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
334
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Generation of induced pluripotent stem cells (iPSCs) stably expressing CRISPR-based synergistic activation mediator (SAM)
Research output: Contribution to journal › Journal article › Research › peer-review
Published