Pages that link to "Q28264202"
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The following pages link to Genetic analysis of the subunit organization and function of the conserved oligomeric golgi (COG) complex: studies of COG5- and COG7-deficient mammalian cells (Q28264202):
Displaying 50 items.
- COG complex-mediated recycling of Golgi glycosyltransferases is essential for normal protein glycosylation (Q24301433) (← links)
- COG-7-deficient Human Fibroblasts Exhibit Altered Recycling of Golgi Proteins (Q24306195) (← links)
- GOLPH3 bridges phosphatidylinositol-4- phosphate and actomyosin to stretch and shape the Golgi to promote budding (Q24336708) (← links)
- Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation (Q24337849) (← links)
- Direct interaction between the COG complex and the SM protein, Sly1, is required for Golgi SNARE pairing (Q24338692) (← links)
- Bridging the Gap between Glycosylation and Vesicle Traffic (Q26750822) (← links)
- Moonlighting functions of the NRZ (mammalian Dsl1) complex (Q26825961) (← links)
- Regulating the large Sec7 ARF guanine nucleotide exchange factors: the when, where and how of activation (Q26827528) (← links)
- Structural analysis of conserved oligomeric Golgi complex subunit 2 (Q27645684) (← links)
- Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene (Q27656862) (← links)
- Purification of active HOPS complex reveals its affinities for phosphoinositides and the SNARE Vam7p (Q27935373) (← links)
- IntraGolgi distribution of the Conserved Oligomeric Golgi (COG) complex (Q28253094) (← links)
- Subunit architecture of the conserved oligomeric Golgi complex (Q28261773) (← links)
- COG lobe B sub-complex engages v-SNARE GS15 and functions via regulated interaction with lobe A sub-complex. (Q30379553) (← links)
- Selection and evaluation of new reference genes for RT-qPCR analysis in Epinephelus akaara based on transcriptome data (Q31160716) (← links)
- A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation (Q33269052) (← links)
- Regulators of cellular levels of histone acetylation in Saccharomyces cerevisiae (Q33336341) (← links)
- Comparative analyses of the Conserved Oligomeric Golgi (COG) complex in vertebrates (Q33633423) (← links)
- Deficiency of the Cog8 subunit in normal and CDG-derived cells impairs the assembly of the COG and Golgi SNARE complexes (Q33854507) (← links)
- Cog2 Null Mutant CHO Cells Show Defective Sphingomyelin Synthesis (Q34438787) (← links)
- Cog5-Cog7 crystal structure reveals interactions essential for the function of a multisubunit tethering complex (Q34480754) (← links)
- Genetic defects in the human glycome (Q34534962) (← links)
- Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II. (Q34574535) (← links)
- Identification of the first COG-CDG patient of Indian origin. (Q34682283) (← links)
- Role of the conserved oligomeric Golgi (COG) complex in protein glycosylation (Q34763238) (← links)
- The COG complex interacts directly with Syntaxin 6 and positively regulates endosome-to-TGN retrograde transport (Q35156980) (← links)
- Target silencing of components of the conserved oligomeric Golgi complex impairs HIV-1 replication (Q35659568) (← links)
- Molecular and clinical characterization of a Moroccan Cog7 deficient patient (Q35928332) (← links)
- Interaction of the conserved oligomeric Golgi complex with t-SNARE Syntaxin5a/Sed5 enhances intra-Golgi SNARE complex stability (Q36274550) (← links)
- Zebrafish fat-free is required for intestinal lipid absorption and Golgi apparatus structure (Q36468243) (← links)
- Molecular insights into vesicle tethering at the Golgi by the conserved oligomeric Golgi (COG) complex and the golgin TATA element modulatory factor (TMF) (Q36596289) (← links)
- COG Complex Complexities: Detailed Characterization of a Complete Set of HEK293T Cells Lacking Individual COG Subunits (Q36744232) (← links)
- COG5-CDG: expanding the clinical spectrum (Q36972265) (← links)
- A new role for RINT-1 in SNARE complex assembly at the trans-Golgi network in coordination with the COG complex (Q37167924) (← links)
- Golgi function and dysfunction in the first COG4-deficient CDG type II patient (Q37295069) (← links)
- Role of vesicle tethering factors in the ER-Golgi membrane traffic. (Q37626903) (← links)
- The Acidic Environment of the Golgi Is Critical for Glycosylation and Transport (Q37785147) (← links)
- Structure of Golgi transport proteins (Q37911065) (← links)
- Re'COG'nition at the Golgi. (Q37980873) (← links)
- The conserved oligomeric Golgi complex is required for fucosylation of N-glycans in Caenorhabditis elegans (Q41854051) (← links)
- Dissecting functions of the conserved oligomeric Golgi tethering complex using a cell-free assay (Q41873044) (← links)
- A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia. (Q41918755) (← links)
- Mutations in Cog7 affect Golgi structure, meiotic cytokinesis and sperm development during Drosophila spermatogenesis (Q43439533) (← links)
- More than just sugars: Conserved oligomeric Golgi complex deficiency causes glycosylation-independent cellular defects. (Q52343676) (← links)
- COG8 deficiency causes new congenital disorder of glycosylation type IIh. (Q52577405) (← links)
- The Arl3 and Arl1 GTPases co-operate with Cog8 to regulate selective autophagy via Atg9 trafficking. (Q52601986) (← links)
- Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation. (Q53377114) (← links)
- Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques (Q57822680) (← links)
- Detailed Analysis of the Interaction of Yeast COG Complex (Q58480397) (← links)
- Novel compound heterozygous COG5 mutations in a Chinese male patient with severe clinical symptoms and type IIi congenital disorder of glycosylation: A case report (Q90402210) (← links)