Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia

Por Dai, D, Li, L, Huebner, A, Zeng, H, Guevara, E, Claypool, D J, Liu, A, Chen, J
Publicado em 2013

High-Resolution Transcript Map of the Region Spanning D12S1629 and D12S312 at Chromosome 12q13: Triple A Syndrome-Linked Region

Por Lee, Hyoungnam, Choi, Eunkyung, Seomun, Young, Montgomery, K., Huebner, A., Lee, Eunice, Lau, Stephanie, Joo, Choun-Ki, Kucherlapati, R., Yoon, Sung-Joo Kim
Publicado em 2000

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Por Kaindl, A, Ruschendorf, F, Krause, S, Goebel, H, Koehler, K, Becker, C, Pongratz, D, Muller-Hocker, J, Nurnberg, P, Stoltenburg-Didin..., G, Lochmuller, H, Huebner, A
Publicado em 2004

FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients

Por Walter, M, Petersen, J, Stucka, R, Fischer, D, Schroder, R, Vorgerd, M, Schroers, A, Schreiber, H, Hanemann, C, Knirsch, U, Rosenbohm, A, Huebner, A, Barisic, N, Horvath, R, Komoly, S, Reilich, P, Muller-Felber, W, Pongratz, D, Muller, J, Auerswald, E, Lochmuller, H
Publicado em 2004

Distinct muscle imaging patterns in myofibrillar myopathies

Por Fischer, D., Kley, R. A., Strach, K., Meyer, C., Sommer, T., Eger, K., Rolfs, A., Meyer, W., Pou, A., Pradas, J., Heyer, C. M., Grossmann, A., Huebner, A., Kress, W., Reimann, J., Schröder, R., Eymard, B., Fardeau, M., Udd, B., Goldfarb, L., Vorgerd, M., Olivé, M.
Publicado em 2008