Physical mapping of D8S7 and D8S11 to the band 8p23.1 of the short arm of chromosome 8.

Por Alkan, M, Wood, S, Borer, U, Hofmann, S, Bühler, E
Publicado em 1989

15/15 translocation in Prader-Willi syndrome.

Por Fraccaro, M, Zuffardi, O, Buhler, E M, Jurik, L P
Publicado em 1977

Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.

Por Müller, H, Bühler, E M, Signer, E, Egli, F, Stalder, G R
Publicado em 1972

A high-density-lipoprotein receptor appears to mediate the transfer of essential fatty acids from high-density lipoprotein to lymphocytes.

Por Xu, Q, Bühler, E, Steinmetz, A, Schönitzer, D, Böck, G, Jürgens, G, Wick, G
Publicado em 1992

Chronic activation in presymptomatic amyotrophic lateral sclerosis (ALS) mice of a feedback loop involving Fas, Daxx, and FasL

Por Raoul, C., Buhler, E., Sadeghi, C., Jacquier, A., Aebischer, P., Pettmann, B., Henderson, C. E., Haase, G.
Publicado em 2006

Factor IXBasel: a Swiss family with severe haemophilia B having a point mutation in EGF type B domain.

Por Alkan, M, Rodriguez Ponte, M, Malik, N J, Hofmann, S, Bösch-Al Jadooa, N, Müller, H, Bühler, E M
Publicado em 1991

Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.

Por Tupler, R, Bortotto, L, Bühler, E M, Alkan, M, Malik, N J, Bösch-Al Jadooa, N, Memo, L, Maraschio, P
Publicado em 1992

Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine model

Por Lozovaya, N., Gataullina, S., Tsintsadze, T., Tsintsadze, V., Pallesi-Pocachard, E., Minlebaev, M., Goriounova, N. A., Buhler, E., Watrin, F., Shityakov, S., Becker, A. J., Bordey, A., Milh, M., Scavarda, D., Bulteau, C., Dorfmuller, G., Delalande, O., Represa, A., Cardoso, C., Dulac, O., Ben-Ari, Y., Burnashev, N.
Publicado em 2014