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Abstract Glucose-6-phosphate dehydrogenase (G6PD) deficiency, which involves the mutation of the G6PD gene on the X chromosome, is the most common enzyme defect in humans

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[DOI] [PMC free article] [PubMed] [Google Scholar] 99.Aksoy S., Szumlanski C.L., Weinshilboum R.M

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Recent studies have provided new insights into the molecular functions and biological significance of IGF-1R in BrCa by suggesting the role of novel transcription factors and mechanisms implicated in IGF-IR regulation

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