• Study Resource
  • Explore
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
What are chromosomes?
What are chromosomes?

... Most are rod-shaped. In body cells, chromosomes are found in Body cells are all the cells except sperm and egg cells. Each kind of organism has a specific number of chromosomes. For a example, every body cell of a fruit fly has S chromosomes (4 pairs); human has 46 (23 pairs); a garden pea has 14 (7 ...
Week 1 - Speyside High School
Week 1 - Speyside High School

... Fertilisation in when the nucleus of a male sex cell fuses with the nucleus of a female sex cell The cell that is produced after fertilisation is called a Zygote Variation occurs due to the random combination of parental gametes. ...
Chromosomal theory of inheritance
Chromosomal theory of inheritance

... Sex Chromosomes Dosage compensation ensures an equal expression of genes from the sex chromosomes even though females have 2 X chromosomes and males have only 1. In each female cell, 1 X chromosome is inactivated and is highly condensed into a Barr body. Females heterozygous for genes on the X chro ...
File
File

... inactivating the translation (1) / less translation; less PG (1) to solubilize pectin of wall; fruit takes longer to ripen; ...
Crossing-Over Introduction
Crossing-Over Introduction

... due to a process our chromosomes undergo, known as genetic recombination. Genetic recombination happens during meiosis. Inside the cells that produce sperm and eggs, homologous chromosomes become paired. Homologous chromosomes contain all same genes, but may have different versions of these genes ca ...
Crop Improvement - Northern Illinois University
Crop Improvement - Northern Illinois University

... • It is possible to graft a potato rootstock to a tomato top, so both underground potato tubers and aboveground tomato fruits are formed on the same plant. ...
Chapter 14 The Human Genome
Chapter 14 The Human Genome

... Down syndrome is correlated with the age of the mother; older mothers have an increased risk of giving birth to a child with Down syndrome ...
HONORS BIOLOGY FINAL EXAM STUDY GUIDE 2015
HONORS BIOLOGY FINAL EXAM STUDY GUIDE 2015

... Draw a diagram of the steps the parent cell would have taken to become two daughter cells. 3. Overexposure to certain chemicals and UV light causes body cells to divide uncontrollably. What type of cell division is this, and what health problem results from this uncontrolled cell division? How does ...
Bb - gpisd
Bb - gpisd

... result, gangliosides build up in the lysosomes and overload cells. Their buildup ultimately causes damage to nerve cells. ...
Meiosis
Meiosis

... Homozygotes for the dominant allele will breed true and always be scored correctly: 0.33 of F2 with dominant phenotype scored correctly For each of the ten progeny of a heteozygote: 3/4 chance it shows the dominant phenotype 1/4 chance it shows the recessive phenotype (which would reveal the genotyp ...
the title overview
the title overview

... MS-LS4-5. Gather and synthesize information about the technologies that have changed the way humans influence the inheritance of desired traits in organisms. HS-LS3-1. Ask questions to clarify relationships about the role of DNA and chromosomes in coding the instructions for characteristic traits pa ...
How is DNA packed in the nucleus?
How is DNA packed in the nucleus?

... most genes (2968), and the Y chromosome has the fewest (231). The total number of genes is estimated at 20,000 to 25, 000 Almost all (99.9%) nucleotide bases are exactly the same in all people. The functions are unknown for over 50% of discovered genes. ...
EVOLUTIONARY GENETICS (Genome 453) Practice problems for
EVOLUTIONARY GENETICS (Genome 453) Practice problems for

... “third chimpanzee” hypothesis). Previously it appeared obvious that chimps, bonobos and gorillas must be most closely related because they all walk on their knuckles, while humans do not. How could this disagreement between genetics and morphology be explained? Note that knuckle-walking is not purel ...
Preimplantation Genetic Testing
Preimplantation Genetic Testing

... changes include chromosome translocations which occur when chromosomal material from two or more chromosomes are rearranged. These can also be detected using aCGH. ...
Mutations
Mutations

... Frame shift mutations result from either addition or deletion of one or two nucleotide bases. When this occurs the "reading frame" is changed so that all the codons read after the mutation are incorrect, even though the bases themselves may be still present. ...
Introduction to Genetics using Punnett Squares
Introduction to Genetics using Punnett Squares

... chromosomes or 23 pairs of chromosomes. • Half of the chromosomes come from one parent and half come from the other parent. Here is the detailed structure of a chromosome ...
6.2 Human Genetic Disorders
6.2 Human Genetic Disorders

... 7.2.d Students know plant and animal cells contain many thousands of different genes and typically have two copies of every gene. The two copies (or alleles) of the gene may or may not be identical, and one may be dominant in determining the phenotype while the other is recessive. ...
Mendelian genetics complete
Mendelian genetics complete

...  _Diploid____ or _2n___ meaning they contain a _double___ set of chromosomes, half ( _23__ ) from _Dad___ and half from _Mom____.  “Matching” chromosomes are known as _homologous pairs____. A homologous pair is made up of a copy of a chromosome from each parent, with the same _genes____. ...
Daily Warm Ups, Q3
Daily Warm Ups, Q3

... When looking at a Pedigree Chart: • How can you determine if a disorder is autosomal or x-linked? • How can you determine if a disorder is Dominant or Recessive? ...
Medical Genetics 2013
Medical Genetics 2013

... D. One or more close relatives are affected by the same rare tumor E. Two or more independent primary tumors in a single individual 3. Why is familial retinoblastoma known to be inherited as an autosomal dominant trait when the responsible gene is recessive? A. This recessive gene needs only one cop ...
BIO 1 ESSAY QUESTIONS – EXAM 1
BIO 1 ESSAY QUESTIONS – EXAM 1

... C) State when oogonia are produced in large numbers in females and whether or not adult females have reproductive stem cells like males. D) Explain when meiosis I starts and ends and when meiosis II starts and ends in females. 5. A) Describe the three reasons that we discussed explaining why meiosis ...
Exam 3 Essay Questions pdf
Exam 3 Essay Questions pdf

... C) State when oogonia are produced in large numbers in females and whether or not adult females have reproductive stem cells like males. D) Explain when meiosis I starts and ends and when meiosis II starts and ends in females. 5. A) Describe the three reasons that we discussed explaining why meiosis ...
Genetic Disease
Genetic Disease

... each in the unduplicated state (most often, one from a male parent and its partner from a female parent) ...
biol b242 chromosomal evolution
biol b242 chromosomal evolution

... Because the genes are arranged on long strings, and because chromosomes themselves act as genetic elements:There may be holistic selective effects that act on 100s to 1000s of genes at a time. Evolutionary oddities about chromosomes Although we understand some of the processes involved in chromosoma ...
Entry Test Sample for MS in Bioinformatics Program Weightage Distribution:
Entry Test Sample for MS in Bioinformatics Program Weightage Distribution:

... A. n chromosomes and are genetically identical. B. n chromosomes and are genetically different. C. 2n chromosomes and are genetically identical. D. 2n chromosomes and are genetically different. 21. Both chloroplasts and mitochondria: A. are found within the nucleus C. carry extranuclear DNA ...
< 1 ... 199 200 201 202 203 204 205 206 207 ... 336 >

Ploidy



Ploidy is the number of sets of chromosomes in a cell. Usually a gamete (sperm or egg, which fuse into a single cell during the fertilization phase of sexual reproduction) carries a full set of chromosomes that includes a single copy of each chromosome, as aneuploidy generally leads to severe genetic disease in the offspring. The gametic or haploid number (n) is the number of chromosomes in a gamete. Two gametes form a diploid zygote with twice this number (2n, the zygotic or diploid number) i.e. two copies of autosomal chromosomes. For humans, a diploid species, n = 23. A typical human somatic cell contains 46 chromosomes: 2 complete haploid sets, which make up 23 homologous chromosome pairs.Because chromosome number is generally reduced only by the specialized process of meiosis, the somatic cells of the body inherit and maintain the chromosome number of the zygote. However, in many situations somatic cells double their copy number by means of endoreduplication as an aspect of cellular differentiation. For example, the hearts of two-year-old children contain 85% diploid and 15% tetraploid nuclei, but by 12 years of age the proportions become approximately equal, and adults examined contained 27% diploid, 71% tetraploid and 2% octaploid nuclei.Cells are described according to the number of sets present (the ploidy level): monoploid (1 set), diploid (2 sets), triploid (3 sets), tetraploid (4 sets), pentaploid (5 sets), hexaploid (6 sets), heptaploid or septaploid (7 sets), etc. The generic term polyploid is frequently used to describe cells with three or more sets of chromosomes (triploid or higher ploidy).
  • studyres.com © 2025
  • DMCA
  • Privacy
  • Terms
  • Report