mannoside
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MGAT1 — Mannosyl (alpha 1,3 ) glycoprotein beta 1,2 N acetylglucosaminyltransferase, also known as MGAT1, is a human gene.cite web | title = Entrez Gene: MGAT1 mannosyl (alpha 1,3 ) glycoprotein beta 1,2 N acetylglucosaminyltransferase| url =… … Wikipedia
Crich beta-mannosylation — The Crich β mannosylation is a synthetic strategy which is used in carbohydrate synthesis to generate a 1,2 cis glycosidic bond. This type of linkate is generally very difficult to make, and specific methods like the Crich β mannosylation are… … Wikipedia
POMGNT1 — Protein O linked mannose beta1,2 N acetylglucosaminyltransferase Identifiers Symbols POMGNT1; DKFZp761B182; FLJ20277; GNTI.2; MDDGA3; MDDGB3; MDDGC3; MEB; MGAT1.2 External IDs … Wikipedia
MGAT2 — Mannosyl (alpha 1,6 ) glycoprotein beta 1,2 N acetylglucosaminyltransferase, also known as MGAT2, is a human gene.cite web | title = Entrez Gene: MGAT2 mannosyl (alpha 1,6 ) glycoprotein beta 1,2 N acetylglucosaminyltransferase| url =… … Wikipedia
Mycobacterium — TEM micrograph of M. tuberculosis. Scientific classification Kingdom … Wikipedia
Phosphatidylmyo-inositol mannosides — (PIM) appear to be a glycolipid component of the cell wall of Mycobacterium tuberculosis . PIM is heavily involved with immune system interaction with M. tuberculosis , and mice that develop antibodies for this glycolipid are better at sustaining … Wikipedia
Mannotetraose 2-alpha-N-acetylglucosaminyltransferase — Identifiers EC number 2.4.1.138 CAS number 81032 47 5 … Wikipedia
MGAT5 — Mannosyl (alpha 1,6 ) glycoprotein beta 1,6 N acetyl glucosaminyltransferase, also known as MGAT5, is a human gene.cite web | title = Entrez Gene: MGAT5 mannosyl (alpha 1,6 ) glycoprotein beta 1,6 N acetyl glucosaminyltransferase| url =… … Wikipedia
MGAT4B — Mannosyl (alpha 1,3 ) glycoprotein beta 1,4 N acetylglucosaminyltransferase, isozyme B, also known as MGAT4B, is a human gene.cite web | title = Entrez Gene: MGAT4B mannosyl (alpha 1,3 ) glycoprotein beta 1,4 N acetylglucosaminyltransferase,… … Wikipedia
Dystrophie musculaire congénitale — Dystrophies musculaires congénitales Les dystrophies musculaires congénitales regroupent un ensemble de pathologies définies par l’association d’une faiblesse musculaire présente à la naissance ou apparaissant dans les premiers mois de la vie à… … Wikipédia en Français
