R. Shtofman

Mec1p associates with functionally compromised telomeres

K. Berkner, K. Runge, A. Ray, 2012, Chromosoma.

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K-dependent coagulation factor deficiency.

J. Rosa, K. Berkner, R. Shtofman, 2006, Blood.

Compound heterozygosity of novel missense mutations in the γ-carboxylase gene causes hereditary combined vitamin K-dependent coagulation factor deficiency

K. Berkner, R. Shtofman, D. Darghouth, 2006 .

Tel1p preferentially associates with short telomeres to stimulate their elongation.

K. Berkner, K. Runge, A. Ray, 2007, Molecular cell.

Brønsted analysis reveals Lys218 as the carboxylase active site base that deprotonates vitamin K hydroquinone to initiate vitamin K-dependent protein carboxylation.

K. Berkner, K. Runge, R. Shtofman, 2006, Biochemistry.

Mec1p associates with functionally compromised telomeres

K. Berkner, K. Runge, A. Ray, 2012, Chromosoma.

A network of PUF proteins and Ras signaling promote mRNA repression and oogenesis in C. elegans.

T. C. Evans, Arnaud Hubstenberger, Cristiana Cameron, 2012, Developmental biology.