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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Angela Huebner

Children's Hospital

Technical University

Dresden

Germany

[email]@*.tu-dresden.de

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Affiliation

Children's Hospital, Technical University, Dresden, Germany. 2000 - 2006

References

Mice lacking the nuclear pore complex protein ALADIN show female infertility but fail to develop a phenotype resembling human triple A syndrome. Huebner, A., Mann, P., Rohde, E., Kaindl, A.M., Witt, M., Verkade, P., Jakubiczka, S., Menschikowski, M., Stoltenburg-Didinger, G., Koehler, K. Mol. Cell. Biol. (2006) [Pubmed]
The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex. Huebner, A., Kaindl, A.M., Knobeloch, K.P., Petzold, H., Mann, P., Koehler, K. Endocr. Res. (2004) [Pubmed]
New insights into the molecular basis of the triple A syndrome. Huebner, A., Kaindl, A.M., Braun, R., Handschug, K. Endocr. Res. (2002) [Pubmed]
Triple A syndrome--clinical aspects and molecular genetics. Huebner, A., Yoon, S.J., Ozkinay, F., Hilscher, C., Lee, H., Clark, A.J., Handschug, K. Endocr. Res. (2000) [Pubmed]