A. Klink

发表

ACTH-receptor expression, regulation and role in adrenocortial tumor formation.

M Reincke, F. Beuschlein, M. Fassnacht, 2001, European journal of endocrinology.

The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability.

G. Rappold, B. Horsthemke, G. Scherer, 1995, Human molecular genetics.

High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1).

J. Weissenbach, D. Le Paslier, A. Ballabio, 1995, Genomics.

A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval

A. Meindl, H. Hellebrand, G. Rappold, 1994, Human Genetics.

New mechanisms of adrenostatic compounds in a human adrenocortical cancer cell line

F. Beuschlein, M. Fassnacht, S. Hahner, 2000, European journal of clinical investigation.

Characterization of an adrenocorticotropin (ACTH) receptor promoter polymorphism leading to decreased adrenal responsiveness to ACTH.

F. Beuschlein, M. Slawik, C. Maser-Gluth, 2004, The Journal of clinical endocrinology and metabolism.

A mammalian germ cell-specific RNA-binding protein interacts with ubiquitously expressed proteins involved in splice site selection.

D. Elliott, H. Cooke, J. Stévenin, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Double crossover in the human Xp/Yp pseudoautosomal region and its bearing on interference.

C. Fischer, G. Rappold, B. Weiss, 1994, Human molecular genetics.

Refinement of the locus for X-linked recessive chondrodysplasia punctata

Y. Fukushima, G. Rappold, T. Ogata, 1995, Human Genetics.

Pulsed-Field Gel Electrophoresis: Protocols

G. Rappold, E. Rao, B. Weiss, 1999 .

Protein Kinase X: A Novel Human Protein Kinase closely related to the Catalytic Subunit of cAMP-dependent Protein Kinase

G. Rappold, B. Zimmermann, F. Herberg, 1997 .