The Metabolic Origins of Mannose in Glycoproteins

Por Ichikawa, Mie, Scott, David A., Losfeld, Marie-Estelle, Freeze, Hudson H.
Publicado em 2014

Identification of Intercellular Cell Adhesion Molecule 1 (ICAM-1) as a Hypoglycosylation Marker in Congenital Disorders of Glycosylation Cells

Por He, Ping, Ng, Bobby G., Losfeld, Marie-Estelle, Zhu, Wenhong, Freeze, Hudson H.
Publicado em 2012

A sensitive green fluorescent protein biomarker of N-glycosylation site occupancy

Por Losfeld, Marie-Estelle, Soncin, Francesca, Ng, Bobby G., Singec, Ilyas, Freeze, Hudson H.
Publicado em 2012

Mutations in STT3A and STT3B cause two congenital disorders of glycosylation

Por Shrimal, Shiteshu, Ng, Bobby G., Losfeld, Marie-Estelle, Gilmore, Reid, Freeze, Hudson H.
Publicado em 2013

DDOST Mutations Identified by Whole-Exome Sequencing Are Implicated in Congenital Disorders of Glycosylation

Por Jones, Melanie A., Ng, Bobby G., Bhide, Shruti, Chin, Ephrem, Rhodenizer, Devin, He, Ping, Losfeld, Marie-Estelle, He, Miao, Raymond, Kimiyo, Berry, Gerard, Freeze, Hudson H., Hegde, Madhuri R.
Publicado em 2012

A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex

Por Losfeld, Marie Estelle, Ng, Bobby G., Kircher, Martin, Buckingham, Kati J., Turner, Emily H., Eroshkin, Alexey, Smith, Joshua D., Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., Freeze, Hudson H.
Publicado em 2014