P. Ambrugger

发表

Endocrine active compounds affect thyrotropin and thyroid hormone levels in serum as well as endpoints of thyroid hormone action in liver, heart and kidney.

A. Grüters, P. J. Hofmann, L. Schomburg, 2004, Toxicology.

MC4R oligomerizes independently of extracellular cysteine residues

A. Grüters, H. Biebermann, H. Krude, 2006, Peptides.

A Heterozygous Mutation in the Third Transmembrane Domain Causes a Dominant-Negative Effect on Signalling Capability of the MC4R

J. Hebebrand, A. Hinney, K. Widhalm, 2008, Obesity Facts.

Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism.

A. Grüters, H. Biebermann, P. Ambrugger, 2001, European journal of endocrinology.

Extended clinical phenotype, endocrine investigations and functional studies of a loss-of-function mutation A150V in the thyroid hormone specific transporter MCT8.

H. Biebermann, U. Schweizer, A. von Moers, 2005, European journal of endocrinology.

Endocrine Disruptors and the Thyroid Gland—A Combined in Vitro and in Vivo Analysis of Potential New Biomarkers

A. Grüters, J. Köhrle, B. Radovic, 2007, Environmental health perspectives.

The ultraviolet filter benzophenone 2 interferes with the thyroid hormone axis in rats and is a potent in vitro inhibitor of human recombinant thyroid peroxidase.

A. Grüters, J. Köhrle, C. Hoang‐Vu, 2007, Endocrinology.

Molecular Pathogenesis of Neonatal Hypothyroidism

A. Grüters, H. Biebermann, H. Krude, 2000, Hormone Research in Paediatrics.

Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome

K. K. Yong, N. Risch, Hua Tang, 2003, Nature Genetics.