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Glycomics genetic approaches

TABLE 17.6 Examples of human genetic defects in glycan formation [Pg.667]

Enzyme affected by genetic defect Phenotype associated with enzyme deficiency Remark [Pg.667]

Blood group GTs Blood group polymorphism Polymorphism in ABO bgl (Aa3T), H Secrtor bgl (Fa2T), Lewis bgl (Fa3/4FT), P bgj (AT) [Pg.667]

F-transporter CDG-IIs and symptoms. CDG-Is are defects in enzymes involved in the synthesis of the pentasaccharide core and CDG-IIs are defects in extending the core of Al-glycans. [Pg.667]

Ab4T-7 Ehlers-Danlos syndrome Defect in glycostuninoglycan elongation characterized by connective tissue abnormalities. [Pg.667]

See other pages where Glycomics genetic approaches is mentioned: [Pg.666]    [Pg.667]    [Pg.666]    [Pg.667]    [Pg.597]    [Pg.268]    [Pg.268]    [Pg.116]    [Pg.2118]    [Pg.258]    [Pg.124]    [Pg.754]    [Pg.108]   
See also in sourсe #XX -- [ Pg.666 , Pg.667 ]



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