Lars Hansen
Guest Researcher
Glycomics Program
Blegdamsvej 3
2200 København N.
Member of:
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- Published
A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2
Kjær, K. W., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hagen, C. B. V. D., Rosendahl, K., Tommerup, Niels & Mundlos, S., 2006, In: Journal of Medical Genetics. 43, 3, p. 225-231 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46
Hansen, Lars, Yao, W., Eiberg, Hans Rudolf Lytchoff, Funding, M., Riise, R., Kjær, K. W., Hejtmancik, J. F. & Rosenberg, T., 2006, In: Molecular Vision. 12, 116, p. 1033-1039 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene
Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Kjer, B., Hansen, T., Pedersen, O., Bille, M., Rosenberg, T. & Tranebjaerg, L., 2006, In: Journal of Medical Genetics. 43, 5, p. 435-440 5 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
Research output: Contribution to journal › Journal article › Research › peer-review
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184
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The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
Research output: Contribution to journal › Journal article › Research › peer-review
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75
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Display of the human mucinome with defined O-glycans by gene engineered cells
Research output: Contribution to journal › Journal article › Research › peer-review
Published