Lars Hansen
Guest Researcher
Glycomics Program
Blegdamsvej 3
2200 København N.
Member of:
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- Published
A novel mutation in IRF6 resulting in VWS-PPS spectrum disorder with renal aplasia
Medeiros, F. D., Hansen, Lars, Mawlad, E., Eiberg, Hans Rudolf Lytchoff, Asklund, C., Tommerup, Niels & Jakobsen, L. P., 2008, In: American Journal of Medical Genetics. Part A. 146A, 12, p. 1605-1608 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression.
Eiberg, Hans Rudolf Lytchoff, Troelsen, J., Boyd, M., Mikkelsen, Annemette Friis, Mengel-From, J., Kjaer, K. W. & Hansen, Lars, 2008, In: Human Genetics. 123, 2, p. 177-87 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2
Wissinger, B., Dangel, S., Jagle, H., Hansen, Lars, Baumann, B., Rudolph, G., Wolf, C., Bonin, M., Koeppen, K., Ladewig, T., Kohl, S., Zrenner, E. & Rosenberg, T., 2008, In: Investigative Ophthalmology & Visual Science. 49, 2, p. 751-757 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 544414
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Precise integration of inducible transcriptional elements (PrIITE) enables absolute control of gene expression
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184
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The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
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75
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Display of the human mucinome with defined O-glycans by gene engineered cells
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Published