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Determination of GPI structure of human CD59 in various KO CHO cells
To determine GPI structure of human CD59 in PGAP4-KO, PGAP3-KO, PGAP5-KO, and PGAP2-KO CHO cells.
ORGANISM(S):
Homo sapiens (Human)
2018-01-30
|
PXD008230
|
Pride
Lc-msms
Cd59
Pgap5
Pgap4
Cho cells
Pgap3
Gpi
Pgap2
Cite
PGAP2: A comprehensive toolkit for prokaryotic pan-genome analysis based on fine-grained feature networks.
Not available
S-EPMC12603064
|
biostudies-literature
Cite
Excluding Digenic Inheritance of
PGAP2
and
PGAP3
Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with
PGAP2
Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3).
Not available
S-EPMC9957281
|
biostudies-literature
Cite
PGAP2 is essential for correct processing and stable expression of GPI-anchored proteins.
Not available
S-EPMC1382328
|
biostudies-literature
Cite
A Treatable Cause of Seizures and Hyperphosphatasia: Patients with PGAP2 and PGAP3 Mutations.
Not available
S-EPMC12503530
|
biostudies-literature
Cite
PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome.
Not available
S-EPMC3617374
|
biostudies-literature
Cite
Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.
Not available
S-EPMC3617372
|
biostudies-literature
Cite
miR-483-5p offsets functional and behavioural effects of stress in male mice through synapse-targeted repression of Pgap2 in the basolateral amygdala.
Not available
S-EPMC10130081
|
biostudies-literature
Cite
A Rare Variant in
PGAP2
Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers.
Not available
S-EPMC5651094
|
biostudies-literature
Cite
Genome-Wide Identification of the AP2/ERF Gene Family and Functional Analysis of <i>PgAP2/ERF187</i> Under Cold Stress in <i>Panax ginseng</i> C. A. Meyer.
Not available
S-EPMC12473287
|
biostudies-literature
Cite
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