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Fetal Bovine Serum impacts the observed N-glycosylation defects in TMEM165 KO HEK cells
TMEM165 is involved in a rare genetic human disease named TMEM165-CDG (Congenital Disorders of Glycosylation). It is Golgi localized, highly conserved through evolution and belongs to the uncharacterized protein family 0016 (UPF0016). The use of isogenic TMEM165 KO HEK cells was crucial in decipheri...
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| Publicado en: | J Inherit Metab Dis |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7021577/ https://ncbi.nlm.nih.gov/pubmed/31415112 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jimd.12161 |
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