Discover Biology (Sixth Core Edition)
6th Edition
ISBN: 9780393936735
Author: Anu Singh-Cundy, Gary Shin
Publisher: W. W. Norton & Company
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Chapter 10, Problem 7SGP
Summary Introduction
To determine: On the basis of given pedigree, whether phenylketonuria is a dominant or a recessive trait, disorder allele is located on autosome or X chromosome, and determine the genotypes of individuals 1 and 2 in generation I.
Introduction: Phenylketonuria is an inherited disorder that leads to increased amounts of phenylalanine in blood. It is caused due to mutations in PAH gene that encodes phenylalanine hydroxylase enzyme.
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DNK dagi nukleotidlar va undan sintezlangan oqsildagi peptid boglar farqi 901 taga teng bo'lib undagi A jami H boglardan 6,5 marta kam bo'lsa DNK dagi jami H bog‘lar sonini toping
One of the ways for a cell to generate ATP is through the oxidative phosphorylation. In oxidative phosphorylation 3 ATP are produced from every one NADH molecule. In respiration, every glucose molecule produces 10 NADH molecules. If a cell is growing on 5 glucose molecules, how much ATP can be produced using oxidative phosphorylation/aerobic respiration?
If a cell is growing on 5 glucose molecules, how much ATP can be produced using oxidative phosphorylation/aerobic respiration?
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