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Molecular basis of CD36 deficiency. Evidence that a 478C-->T substitution (proline90-->serine) in CD36 cDNA accounts for CD36 deficiency.

Data up to Jan 2025

Published1995
Citations105
References37

Total Citations Per Year

Abstract

References (37)

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Identification of molecular defects in a subject with type I CD36 deficiency

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A Novel Polymorphism in Glycoprotein IV (Replacement of Proline-90 by Serine) Predominates in Subjects with Platelet GPIV Deficiency

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Identification of a human CD36 isoform produced by exon skipping. Conservation of exon organization and pre-mRNA splicing patterns with a CD36 gene family member, CLA-1.

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Characterization of two alternatively spliced 5′-untranslated exons of the human CD36 gene in different cell types

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Platelet glycoprotein IV (CD36) deficiency is associated with the absence (type I) or the presence (type II) of glycoprotein IV on monocytes

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A monoclonal antibody against an erythrocyte ontogenic antigen identifies fetal and adult erythroid progenitors

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Identification of molecular defects in a subject with type I CD36 deficiency

1994 • 7 citations

Presence of the entire coding region of GP IV mRNA in Nak(a)-negative platelets.

1993 • 6 citations

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