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phosphoserine and Congenital Disorders of Glycosylation

phosphoserine has been researched along with Congenital Disorders of Glycosylation in 1 studies

Phosphoserine: The phosphoric acid ester of serine.

Congenital Disorders of Glycosylation: A genetically heterogeneous group of heritable disorders resulting from defects in protein N-glycosylation.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gibbs, BF1
Yasinska, IM1
Pchejetski, D1
Wyszynski, RW1
Sumbayev, VV1

Other Studies

1 other study available for phosphoserine and Congenital Disorders of Glycosylation

ArticleYear
Differential control of hypoxia-inducible factor 1 activity during pro-inflammatory reactions of human haematopoietic cells of myeloid lineage.
    The international journal of biochemistry & cell biology, 2012, Volume: 44, Issue:11

    Topics: Basophils; Cell Lineage; Congenital Disorders of Glycosylation; HEK293 Cells; Hematopoietic System;

2012