相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Glycosylation disorders of membrane trafficking
Claire Rosnoblet et al.
GLYCOCONJUGATE JOURNAL (2013)
Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDG
Gert Matthijs et al.
GLYCOCONJUGATE JOURNAL (2013)
Understanding Human Glycosylation Disorders: Biochemistry Leads the Charge
Hudson H. Freeze
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Extreme C-terminal sites are posttranslocationally glycosylated by the STT3B isoform of the OST
Shiteshu Shrimal et al.
JOURNAL OF CELL BIOLOGY (2013)
DDOST Mutations Identified by Whole-Exome Sequencing Are Implicated in Congenital Disorders of Glycosylation
Melanie A. Jones et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Diseases of glycosylation beyond classical congenital disorders of glycosylation
Thierry Hennet
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (2012)
A sensitive green fluorescent protein biomarker of N-glycosylation site occupancy
Marie-Estelle Losfeld et al.
FASEB JOURNAL (2012)
STT3B-Dependent Posttranslational N-Glycosylation as a Surveillance System for Secretory Protein
Takashi Sato et al.
MOLECULAR CELL (2012)
Neurology of inherited glycosylation disorders
Hudson H. Freeze et al.
LANCET NEUROLOGY (2012)
Nogo-B receptor is necessary for cellular dolichol biosynthesis and protein N-glycosylation
Kenneth D. Harrison et al.
EMBO JOURNAL (2011)
The impact of mass spectrometry in the diagnosis of congenital disorders of glycosylation
Luisa Sturiale et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2011)
Cotranslational and Posttranslational N-Glycosylation of Polypeptides by Distinct Mammalian OST Isoforms
Catalina Ruiz-Canada et al.
CELL (2009)
A defect in the TUSC3 gene is associated with autosomal recessive mental retardation
Masoud Garshasbi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation
Florence Molinari et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Proteomic analysis of mammalian oligosaccharyltransferase reveals multiple subcomplexes that contain sec61, TRAP, and two potential new subunits
T Shibatani et al.
BIOCHEMISTRY (2005)
Molecular and clinical description of the first US patients with congenital disorder of glycosylation Ig
EA Eklund et al.
MOLECULAR GENETICS AND METABOLISM (2005)
Oligosaccharyltransferase isoforms that contain different catalytic STT3 subunits have distinct enzymatic properties
DJ Kelleher et al.
MOLECULAR CELL (2003)
Photocross-linking of nascent chains to the STT3 subunit of the oligosaccharyltransferase complex
I Nilsson et al.
JOURNAL OF CELL BIOLOGY (2003)
Studies on the function of oligosaccharyl transferase subunits - Stt3p is directly involved in the glycosylation process
G Yan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
N-linked glycosylation in Campylobacter jejuni and its functional transfer into E-coli
M Wacker et al.
SCIENCE (2002)