T. Pape

发表

Accurate Prediction of the Functional Significance of Single Nucleotide Polymorphisms and Mutations in the ABCA1 Gene

Paul D Thomas, Anish Kejariwal, P. Thomas, 2005, PLoS genetics.

Intestinal ABCA1 directly contributes to HDL biogenesis in vivo.

Albert K Groen, Folkert Kuipers, M. Hayden, 2006, The Journal of clinical investigation.

Tissue-Specific Induction of Intestinal ABCA1 Expression With a Liver X Receptor Agonist Raises Plasma HDL Cholesterol Levels

M. Hayden, J. Parks, F. Kuipers, 2006, Circulation research.

Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

Marie-Pierre Dubé, Elizabeta Nemeth, Tomas Ganz, 2004, Nature Genetics.

Aggregation, organic matter, and iron oxide morphology in oxisols from Minas Gerais, Brazil

C. Muggler, P. Buurman, T. Pape, 1999 .

A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans.

M. Bortolini, F. Salzano, M. Hayden, 2010, Human molecular genetics.

Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates.

M. Hayden, X. Breakefield, B. Brais, 2004, American journal of human genetics.

Cross-species characterization of the ALS2 gene and analysis of its pattern of expression in development and adulthood

M. Hayden, B. Leavitt, G. Rouleau, 2005, Neurobiology of Disease.

Loss‐of‐function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations

M. Dubé, D. Bowsher, E. Boltshauser, 2007, Clinical genetics.

β-cell ABCA1 influences insulin secretion, glucose homeostasis and response to thiazolidinedione treatment

James D. Johnson, B. Marsh, M. Hayden, 2007, Nature Medicine.

Intestinal ABCA1 is a significant contributor to plasma HDL-C and apoB levels in vivo

J. Parks, B. Staels, F. Kuipers, 2005 .