Pearson eText Biology: Life on Earth with Physiology -- Instant Access (Pearson+)
Pearson eText Biology: Life on Earth with Physiology -- Instant Access (Pearson+)
12th Edition
ISBN: 9780135755785
Author: Gerald Audesirk, Teresa Audesirk
Publisher: PEARSON+
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Chapter 13.4, Problem 1CSC
Summary Introduction

To describe: The way in which functional chloride channel (CFTR protein) can produce CFTR alleles that cause cystic fibrosis.

Introduction: Cystic fibrosis is a genetic disorder that causes severe damage to the lungs, pancreas, digestive system, and other parts of the body. This genetic disorder affects the cells that produce sweat and mucus. In cystic fibrosis, a mutation in a gene changes a protein that controls the movement of salt in and out of cells, resulting in a thick, sticky mucus in the respiratory, reproductive and digestive system as well as increased salt in sweat.

Summary Introduction

To describe: The way in which a gene can affect the timing and rate of transcription and translation.

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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY