Tales from the front lines: the creative essay as a tool for teaching genetics.

Por Koehler, K E, Hawley, R S
Publicado em 1999

TP53 mutational status is predictive of pazopanib response in advanced sarcomas

Por Koehler, K., Liebner, D., Chen, J. L.
Publicado no Ann Oncol (2016)

Genetic analysis of familial non-syndromic primary failure of eruption

Por Frazier-Bowers, S., Simmons, D, Koehler, K, Zhou, J
Publicado em 2009

Structure and function of the zeta-globin upstream regulatory element.

Por Sabath, D E, Koehler, K M, Yang, W Q
Publicado em 1996

The effects of calcium ions and pH on bovine prothrombin fragment 1. Intrinsic fluroescence studies.

Por Scott, M E, Koehler, K A, Hiskey, R G
Publicado em 1979

Kinetic and equilibrium metal-ion-binding behaviour reflected in a metal-ion-dependent antigenic determinant in bovine prothrombin. Comparison with bovine prothrombin fragment 1.

Por Madar, D A, Hall, T J, Hiskey, R G, Koehler, K A
Publicado em 1981

The nature of the slow metal ion-dependent conformational transition in bovine prothrombin.

Por Marsh, H C, Scott, M E, Hiskey, R G, Koehler, K A
Publicado em 1979

The prosome: an ubiquitous morphologically distinct RNP particle associated with repressed mRNPs and containing specific ScRNA and a characteristic set of proteins.

Por Schmid, H P, Akhayat, O, Martins De Sa, C, Puvion, F, Koehler, K, Scherrer, K
Publicado em 1984

Evaluating population folate exposure through a complete frequency distribution.

Por Koehler, K M, Pareo-Tubbeh, S L, Baumgartner, R N, Romero, L J, Garry, P J
Publicado em 1996

Analysis of the phorbol ester pharmacophore on protein kinase C as a guide to the rational design of new classes of analogs.

Por Wender, P A, Koehler, K F, Sharkey, N A, Dell'Aquila, M L, Blumberg, P M
Publicado em 1986

Modeling of the bryostatins to the phorbol ester pharmacophore on protein kinase C.

Por Wender, P A, Cribbs, C M, Koehler, K F, Sharkey, N A, Herald, C L, Kamano, Y, Pettit, G R, Blumberg, P M
Publicado em 1988

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