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POMK gene

Known as: SgK196, PROTEIN-O-MANNOSE KINASE, FLJ23356 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Pathogenic homozygous variant in POMK gene is the cause of prenatally detected severe ventriculomegaly in two Lithuanian families
Biallelic pathogenic variants in POMK gene are associated with two types of dystroglycanopathies: limb‐girdle muscular dystrophy… 
2018
2018
P 307. Walker–Warburg’s Syndrome Due to Homozygous POMK Mutation in Preterm Twins: Case Report
2015
2015
SGK196 controls stem cell fates by promoting the degradation of TGFβ family receptors
2014
2014
POMK mutation in a family with congenital muscular dystrophy with merosin deficiency, hypomyelination, mild hearing deficit and intellectual disability
Background Congenital muscular dystrophies (CMD) with hypoglycosylation of α-dystroglycan are clinically and genetically… 
2014
2014
CONTROLS STEM CELL FATES BY PROMOTING THE DEGRADATION OF TGFΒ FAMILY RECEPTOR S BY
Much remains to be understood regarding the molecular mechanisms controlling stem cell fate. Through studies in human pluripotent… 
2013
2013
Dystroglycan Function -Mannose Kinase Required for O SGK196 Is a Glycosylation-Specific
Review
2005
Review
2005
[The role of leptin and its peptide mediators in neurophysiology].
  • I. A. Pankov
  • Vestnik Rossiiskoi akademii meditsinskikh nauk
  • 2005
  • Corpus ID: 37623576
The adipocyte hormone leptin binds to its receptors in hypothalamic neurons and decreases appetite and food consumption. Its… 
1996
1996
[Does expression of the proopiomelanocortin (POMK) gene occur in magnocellular (nonapeptidergic) nuclei of the rat hypothalamus?].
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