Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- 45. How does p53 operate in normal cells? A. Facilitates the repair of damage within cells B. Halting the growth and division cycle of damaged cells C. Triggering apoptosis of cells that may pose as a threat D. All of the abovearrow_forwardParamecium is a single-cell eukaryotic organism that can reproduce by mitotic cell division. Prior to the M phase of the cell cycle, which of the following must occur? A. The cell must replicate its chromosomes. B. The nucleus must divide. C. The cell must first be fertilized. D. Sister chromatids must be separated. A. The cell must replicate its chromosomes.arrow_forwardE. Coli, Chinese hamster ovary (CHO) and HEK293 are all cell lines used to for protein production. a. What differentiates these cells? b. Under what conditions would you use each of these different cells?arrow_forward
- In order for a cell to begin to replicate its DNA: a. Lamin proteins must be phosphorylated b. p53 must be phosphorylated c. The Rb protein must be phosphorylated d. M-cyclin must bind to M-Cdkarrow_forward11.The critical decision point at which a cell determines its fate at the end of the G1 phase of the cell cycle is called ----. a. transition point. b. resolution point. c. commitment point. d. restriction point. 12. In the familial form of retinoblastoma, multiple foci of tumors are seen arising in both eyes, which is not seen in sporadic form of the disease. This is because -- a. familial form of the disease progresses rapidly b. mitogenic factors trigger growth in the familial form c. all retinal cells in the familial disease carry one defective copy of the Rb gene at birth d. sporadic form has other active tumor suppressors 13. What ensures that the cell cycle moves in only one direction, e.g. from G1 → S, and not go backwards? a. the cyclin from one phase is degraded as the cell moves to the next phase b. level of the appropriate cyclin of next phase rises as the cell is about to enter that phase c. a and b d. level of appropriate CDK rises and falls at each phase e. a, b and carrow_forward38.If a chromosome contains a mutation such that it cannot bind to the kinetochore complex, what would be the consequence? A. That chromosome would not be able to be replicated. B. That chromosome would not be able to condense. C. That chromosome would not be able to bind to the mitotic spindle, D. That chromosome would not be able to interact with histone proteins. 39. The stage of mitosis characterized by the physical separation of sister chromatids is called: A. Anaphase B. Metaphase C. Prometaphase D. Telophase 40.A duplicate copy of all of the hereditary information contained in the nucleus of eukaryotic cells is made during what stage of the cell cycle? A. G 1 B. S C. G2 D. Mitosis 41. Which structures indicate where crossing over has occurred? A. centromeres B. kinetochores C. chiasmata D. centrioles 42. What immediately follows meiosis 1? A. metaphase II B. prophase II C. synapsis of homologues D. crossing over of homologues 43.An allele for a particular trait that is only…arrow_forward
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- 38. What are the principal tissue stains used in histology and describe where and what color each stain? A. The hematoxylin stains cell nuclei blue, and eosin stains the extracellular matrix and cytoplasm pink. B. The hematoxylin stains cell nuclei pink, and eosin stains the extracellular matrix and cytoplasm blue. C. The hematoxylin stains the extracellular matrix and cytoplasm blue, and eosin stains the cell nuclei pink. D. The hematoxylin stains the extracellular matrix and cytoplasm pink, and eosin stains the cell nuclei blue.arrow_forward1. How did your results differ from the class data for each phase of mitosis? 2. Write a brief paragraph stating whether or not your hypothesis was supported by the class data that you collected and an explanation of why/why not.arrow_forwardWhich of the following is a characteristic of a cell undergoing cellular senescence? a.Doubling in physical size b.Production of SASPs c.Atypically low NGF1-A levels d.Abnormally high rate of proliferationarrow_forward
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