Molecular Genetics — Flashcards

Molecular Genetics — Flashcards

Molecular Genetics — Flashcards

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829 flashcards— Page 22 of 83
#211

Primary hemochromatosis is due to mutations in the _____ gene on chromosome 6, leading to increased expression of DMT1 and decreased synthesis of Hepcidin

#212

DNA replication errors lead to _____ mutations

#213

What is the mode of inheritance of G6PD deficiency? _____

#214

Once a steroid hormone has bound its receptor in the cytoplasm or nucleus, the hormone-receptor complex then _____

#215

What chromosome is cyclin D1 located on? _____

#216

What point mutations in the HFE gene are typically seen with primary hemochromatosis? _____ (more common) and H63D

#217

_____ is the normal differential expression of an allele depending on parental origin (e.g. only one allele is active)

#218

Telomerase is a rare example where _____ activity occurs endogenously in humans

Hint: enzyme

#219

What is the function of the H1 class of histones? _____

#220

A(n) Southern blot is used to analyze _____

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