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Robbins & Cotran Pathologic Basis of Disease, 10th Edition Test Bank: 700+ MCQs with Verified Answers & Rationales

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Robbins & Cotran Pathologic Basis of Disease, 10th Edition Test Bank: 700+ MCQs with Verified Answers & Rationales Description Master the principles of pathology with this complete test bank for Robbins & Cotran Pathologic Basis of Disease, 10th Edition. Designed for medical, nursing, and health science students, this resource provides comprehensive coverage of all textbook chapters, transforming your study sessions into an efficient and effective path to success. This extensive collection features 20 original multiple-choice questions per chapter, totaling over 700 questions. Each item comes with a verified correct answer and a detailed, step-by-step rationale that explains the underlying pathological concepts. This goes beyond simple memorization, helping you build a deep conceptual understanding of cellular injury, inflammation, neoplasia, and system-specific diseases. The questions are crafted to align with the core curriculum and the style of board examinations, making it an ideal preparation tool for USMLE, NCLEX, and other certification exams. Stop wasting time with incomplete or unreliable study aids. This test bank is your all-in-one solution to reinforce textbook material, identify knowledge gaps, and study with confidence. You will save countless hours by having a pre-built, high-quality question bank at your fingertips, allowing you to focus on understanding the "why" behind each answer. Achieve mastery of pathology and walk into your exams fully prepared. Key Features: Full Chapter Coverage: Questions for all chapters, from "The Cell as a Unit of Health and Disease" to "The Nervous System." Verified Accuracy: Every answer includes a clear, concise rationale based directly on the textbook content. Exam-Ready Preparation: Builds critical thinking skills essential for passing high-stakes exams. Instant Digital Download: Get immediate access and start studying right away. Keywords Robbins and Cotran test bank, pathology test bank, Kumar Abbas Aster, medical exam prep, nursing pathophysiology questions, USMLE Step 1 pathology, NCLEX-RN review, disease pathology MCQ, Robbins 10th edition, pathophysiology study guide Hashtags #PathologyTestBank #RobbinsAndCotran #MedicalExamPrep #NursingSchool #USMLEStep1 #Pathophysiology #NCLEXReview #MedStudent #TestBank #MedicalEducation

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Robbins & Cotran 10th Ed. Pathology Test Bank | Chapter-
by-Chapter Questions & Verified Solutions




Robbins & Cotran Pathologic Basis of Disease
10th Edition
• Author(s)Vinay Kumar; Abul K. Abbas; Jon C. Aster

Chapter 1: The Cell as a Unit of Health and Disease
1. Chapter Section: The Genome
Question: A research study investigates a mechanism of
gene regulation that does not alter the DNA sequence
itself but involves chemical modifications to histone
proteins, making certain genes more or less accessible for
transcription. This process is best described as:
A) Genetic polymorphism
B) Autophagy
C) Epigenetic modification
D) Signal transduction
Correct Answer: C
Rationale: Epigenetic modification refers to heritable

,changes in gene expression that are not caused by
alterations in the DNA sequence. Histone acetylation and
methylation are primary epigenetic mechanisms that
regulate DNA accessibility . This is distinct from changes in
the DNA sequence itself (A), a cellular degradation process
(B), or the process of responding to extracellular signals
(D).
Teaching Point: Epigenetics controls gene expression
through modifications to DNA and histones, without
changing the genetic code.
Citation: Robbins & Cotran Pathologic Basis of Disease,
10th Ed., Chapter 1: The Genome.




2. Chapter Section: The Genome
Question: A patient is found to have a disease caused by a
mutation in a gene encoding a specific microRNA
(miRNA). Which of the following fundamental regulatory
functions is most likely impaired?
A) Synthesis of ribosomal RNA
B) Post-transcriptional gene silencing
C) Energy production in the mitochondria
D) Integrity of the nuclear membrane
Correct Answer: B
Rationale: MicroRNAs (miRNAs) are non-coding RNAs

,that primarily function in post-transcriptional gene
silencing by binding to target mRNAs and inhibiting their
translation or promoting their degradation . They are not
directly involved in ribosomal RNA synthesis (A),
mitochondrial energy production (C), or maintaining
nuclear membrane integrity (D).
Teaching Point: miRNAs are key epigenetic regulators
that silence genes by targeting mRNA after transcription.
Citation: Robbins & Cotran Pathologic Basis of Disease,
10th Ed., Chapter 1: The Genome.




3. Chapter Section: Cellular Housekeeping
Question: A 45-year-old patient with a rare
neurodegenerative disorder has a defect in an organelle
responsible for degrading worn-out proteins tagged with
ubiquitin. The dysfunctional organelle most central to this
disease process is the:
A) Golgi apparatus
B) Proteasome
C) Lysosome
D) Rough endoplasmic reticulum
Correct Answer: B
Rationale: The proteasome is a multi-subunit proteolytic
complex that degrades cytosolic proteins that have been

, tagged for destruction by ubiquitin. It is crucial for
removing misfolded or damaged proteins . The Golgi
apparatus (A) modifies and packages proteins, the
lysosome (C) degrades extracellular material and
organelles via autophagy, and the rough endoplasmic
reticulum (D) is involved in protein synthesis.
Teaching Point: Proteasomes are essential for degrading
ubiquitin-tagged intracellular proteins, and their
dysfunction can lead to protein aggregation diseases.
Citation: Robbins & Cotran Pathologic Basis of Disease,
10th Ed., Chapter 1: Cellular Housekeeping.




4. Chapter Section: Cellular Housekeeping
Question: During a lecture on cellular injury, the professor
describes a process where a cell digestes its own damaged
organelles by engulfing them in a double-membrane
vesicle that fuses with a lysosome. This vital "self-eating"
process is termed:
A) Heterophagy
B) Apoptosis
C) Autophagy
D) Necrosis
Correct Answer: C
Rationale: Autophagy is the process by which cells
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