Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G

Por Muntau, Ania C., Mayerhofer, Peter U., Paton, Barbara C., Kammerer, Stefan, Roscher, Adelbert A.
Publicado em 2000

Pex19p, a Farnesylated Protein Essential for Peroxisome Biogenesis

Por Götte, Klaudia, Girzalsky, Wolfgang, Linkert, Michael, Baumgart, Evelyn, Kammerer, Stefan, Kunau, Wolf-Hubert, Erdmann, Ralf
Publicado em 1998

Large-Scale Validation of Single Nucleotide Polymorphisms in Gene Regions

Por Nelson, Matthew R., Marnellos, George, Kammerer, Stefan, Hoyal, Carolyn R., Shi, Michael M., Cantor, Charles R., Braun, Andreas
Publicado em 2004

Association testing by DNA pooling: An effective initial screen

Por Bansal, Aruna, van den Boom, Dirk, Kammerer, Stefan, Honisch, Christiane, Adam, Gail, Cantor, Charles R., Kleyn, Patrick, Braun, Andi
Publicado em 2002

Designing isoform-specific peptide disruptors of protein kinase A localization

Por Burns-Hamuro, Lora L., Ma, Yuliang, Kammerer, Stefan, Reineke, Ulrich, Self, Chris, Cook, Charles, Olson, Gary L., Cantor, Charles R., Braun, Andreas, Taylor, Susan S.
Publicado em 2003

Association between a variation in the phosphodiesterase 4D gene and bone mineral density

Por Reneland, Richard H, Mah, Steven, Kammerer, Stefan, Hoyal, Carolyn R, Marnellos, George, Wilson, Scott G, Sambrook, Philip N, Spector, Tim D, Nelson, Matthew R, Braun, Andreas
Publicado em 2005

Genetic polymorphisms in <it>DPF3 </it>associated with risk of breast cancer and lymph node metastases

Por Hoyal Carolyn R, Kammerer Stefan, Roth Richard B, Reneland Richard, Marnellos George, Kiechle Marion, Schwarz-Boeger Ulrike, Griffiths Lyn R, Ebner Florian, Rehbock Joachim, Nelson Matthew R, Braun Andreas
Publicado em 2005-08-01

Genetic polymorphisms in DPF3 associated with risk of breast cancer and lymph node metastases

Por Hoyal, Carolyn R, Kammerer, Stefan, Roth, Richard B, Reneland, Richard, Marnellos, George, Kiechle, Marion, Schwarz-Boeger, Ulrike, Griffiths, Lyn R, Ebner, Florian, Rehbock, Joachim, Nelson, Matthew R, Braun, Andreas
Publicado em 2005

Amino acid variant in the kinase binding domain of dual-specific A kinase-anchoring protein 2: A disease susceptibility polymorphism

Por Kammerer, Stefan, Burns-Hamuro, Lora L., Ma, Yuliang, Hamon, Sara C., Cànaves, Jaume M., Shi, Michael M., Nelson, Matthew R., Sing, Charles F., Cantor, Charles R., Taylor, Susan S., Braun, Andreas
Publicado em 2003

Association of the NuMA region on chromosome 11q13 with breast cancer susceptibility

Por Kammerer, Stefan, Roth, Richard B., Hoyal, Carolyn R., Reneland, Richard, Marnellos, George, Kiechle, Marion, Schwarz-Boeger, Ulrike, Griffiths, Lyn R., Ebner, Florian, Rehbock, Joachim, Cantor, Charles R., Nelson, Matthew R., Braun, Andreas
Publicado em 2005