W. Wooderchak

Repository of SMAD4 Mutations: Reference for Genotype/ Phenotype Correlation

D. Crockett, P. Bayrak-Toydemir, J. McDonald, 2010 .

Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis

P. Bayrak-Toydemir, J. McDonald, W. Wooderchak, 2011, Clinical genetics.

Assays for S‐Adenosylmethionine (AdoMet/SAM)‐Dependent Methyltransferases

J. Hevel, Z. Zhou, W. Wooderchak, 2008, Current protocols in toxicology.

Investigation of the Molecular Origins of Protein-arginine Methyltransferase I (PRMT1) Product Specificity Reveals a Role for Two Conserved Methionine Residues*

Sean J. Johnson, Joan M Hevel, J. Hevel, 2011, The Journal of Biological Chemistry.

An enzyme-coupled continuous spectrophotometric assay for S-adenosylmethionine-dependent methyltransferases.

J. Hevel, Z. Zhou, Yinqiu Cui, 2006, Analytical biochemistry.

Characterization of the Substrate Specificity and Mechanism of Protein Arginine Methyltransferase 1

W. Wooderchak, 2009 .

Hereditary hemorrhagic telangiectasia: two distinct ENG deletions in one family

P. Bayrak-Toydemir, M. McDonald, W. Wooderchak, 2010, Clinical genetics.

Substrate profiling of PRMT1 reveals amino acid sequences that extend beyond the "RGG" paradigm.

Joan M Hevel, J. Hevel, Z. Zhou, 2008, Biochemistry.