The molecular basis of paroxysmal nocturnal hemoglobinuria.

Rosse, W F

The molecular basis of paroxysmal nocturnal hemoglobinuria. [electronic resource] - Blood Nov 1995 - 3277-86 p. digital

Publication Type: Journal Article; Review

0006-4971


Acetylglucosamine--metabolism
Animals
CD55 Antigens--metabolism
Carbohydrate Sequence
Complement Activation
Endoplasmic Reticulum--metabolism
Glycosylphosphatidylinositols--deficiency
Hematopoiesis
Hemoglobinuria, Paroxysmal--genetics
Humans
Lymphocytes--metabolism
Membrane Proteins--deficiency
Mice
Mice, Mutant Strains
Models, Biological
Molecular Sequence Data
Mutation
Phosphatidylinositol Diacylglycerol-Lyase
Phosphatidylinositols--metabolism
Phosphoric Diester Hydrolases--metabolism
Protein Processing, Post-Translational
RNA Splicing
RNA, Messenger--genetics
X Chromosome