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Items: 3

1.

Mutational analysis of two residues in the DYRK homology box of the protein kinase DYRK1A.

Widowati EW, Bamberg-Lemper S, Becker W.

BMC Res Notes. 2018 May 15;11(1):297. doi: 10.1186/s13104-018-3416-4.

2.

Functional characterization of DYRK1A missense variants associated with a syndromic form of intellectual deficiency and autism.

Widowati EW, Ernst S, Hausmann R, Müller-Newen G, Becker W.

Biol Open. 2018 Apr 26;7(4). pii: bio032862. doi: 10.1242/bio.032862.

3.

DYRK1B mutations associated with metabolic syndrome impair the chaperone-dependent maturation of the kinase domain.

Abu Jhaisha S, Widowati EW, Kii I, Sonamoto R, Knapp S, Papadopoulos C, Becker W.

Sci Rep. 2017 Jul 25;7(1):6420. doi: 10.1038/s41598-017-06874-w.

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