• 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
Spo13 protects meiotic cohesin at centromeres in meiosis I
Spo13 protects meiotic cohesin at centromeres in meiosis I

... before spore formation. We followed meiotic progression in spo13⌬ diploids, assessing entry into and exit from meiosis I by the formation and disappearance of metaphase I spindles. Once recombination is complete, short spindles form (Padmore et al. 1991) and are maintained, whereas chromosomes attac ...
Massive Changes in Genome Architecture Accompany
Massive Changes in Genome Architecture Accompany

... The suppression of recombination across such a region will be selected for if it creates linkage between the sex-determining locus and other genes that are sexually antagonistic in that their functions are beneficial to only one of the sexes. The nonrecombining region can be formed from the spread of ...
x-linked female-sterile loci in drosophzla melanogaster
x-linked female-sterile loci in drosophzla melanogaster

... with rare alleles are actually essential genes (6DISCUSSION). Classification of X-linked female-sterile loci: Because of the size of these X-chromosomal mutagenesis screens, it is useful to assemble a list of all of the female steriles in the X chromosome that have been studied and to provide a brie ...
Meiosis and Sexual Reproduction
Meiosis and Sexual Reproduction

...  An adaptive trait tends to spread more quickly through a sexually reproducing population than through an asexually reproducing one ...
Meiosis - Aurora City Schools
Meiosis - Aurora City Schools

... 10 Meiosis What term is used to ...
Balanced reciprocal translocation at amniocentesis - FUNPEC-RP
Balanced reciprocal translocation at amniocentesis - FUNPEC-RP

... It is at least as good at identifying aneuploidies and unbalanced rearrangements as karyotyping. However, it is not able to identify balanced translocations or triploidies (Wapner et al., 2012). Instead, it can detect small microdeletions/microduplications (copy number variations) with unknown funct ...
Bonus, a Drosophila TIF1 homologue, is a chromatin
Bonus, a Drosophila TIF1 homologue, is a chromatin

... during the first instar larval stage for bon434 and bon241, partial loss-of-function alleles, and bon21B, a null allele (Fig. 1B) (BECKSTEAD et al. 2001). We observed that all bon434 and bon241 homozygous males died as first instar larvae, while all mutant females survived at least to the second in ...
1 Article: Investigation Evidence for Stabilizing Selection on Codon
1 Article: Investigation Evidence for Stabilizing Selection on Codon

... mutations. This gene arrangement polymorphism has been stable in natural populations for over seventy years (Figure 1A; Dobzhansky and Sturtevant 1938). Frequencies of particular chromosome arrangements form a classical cline across the species range in the American southwest despite the predicted e ...
Chapter 13
Chapter 13

... • Mutations (changes in an organism’s DNA) are the original source of genetic diversity • Mutations create different versions of genes called alleles • Reshuffling of alleles during sexual reproduction produces genetic variation ...
Genetics of Primary ciliary dyskinesia - HAL
Genetics of Primary ciliary dyskinesia - HAL

... genetic heterogeneity in PCD. Each of the several hundreds of proteins that constitute a cilia could potentially cause the disease. Such complexity makes approaches based on genetic linkage difficult to apply; except in case of large and/or consanguineous families, a situation which is exceptional. ...
meiosis and heredity
meiosis and heredity

... ____ 16. The principle of independent assortment states that a. alleles on different homologous chromosomes are randomly sorted to individual gametes. b. genes on the same chromosome are not randomly sorted to different gametes. c. two alleles for a single trait are randomly sorted to individual gam ...
continued
continued

... 10.1 What Is the Physical Basis of Inheritance?  Genes are sequences of nucleotides at specific locations on chromosomes – Inheritance is the process by which the characteristics of individuals are passed to their offspring – A gene is a unit of heredity that encodes information needed to produce ...
Expansion of the Pseudo-autosomal Region and Ongoing
Expansion of the Pseudo-autosomal Region and Ongoing

... chromosome evolution, but the genetic map, even of its sex chromosomes, remains sparse (Bergero et al. 2007) because, until recently, very few genes on these chromosomes had been identified. Those that have been mapped and sequenced from the X and Y demonstrate the existence of at least two evolution ...
File
File

... Before Harriet was born, a doctor suggested that Fiona should have the embryo ‘screened’. ...
A Common Polygenic Basis for Quinine and
A Common Polygenic Basis for Quinine and

... Inbred strains of mice (Mus musculus) differ greatly in ability to taste various bitter compounds. For some compounds, the differences result from allelic variation at a single locus. However, segregation patterns incompatible with monogenic inheritance have been found for quinine avoidance. The Soa ...
1 Modeling Endosymbiosis Name Section Overall goal – to visualize
1 Modeling Endosymbiosis Name Section Overall goal – to visualize

... index card, and tape the 3 prink chromosomes inside the blue to make the nucleus. Loosely tape the index card to one side of the black membrane. ...
The first page should show the paper title, names and addresses of
The first page should show the paper title, names and addresses of

... Galliformes could be resolved using the FISH on lampbrush chromosomes as an investigative procedure? On the other hand, why should we still use time-consuming methods like comparative FISH mapping on LBCs when next-generation sequencing approaches are opening up new opportunities for genome-wide ana ...
Ch15 ppt - WEB . WHRSD . ORG
Ch15 ppt - WEB . WHRSD . ORG

... www.kimunity.com ...
Chapter 14.
Chapter 14.

... www.kimunity.com ...
Motion
Motion

... Prophase I • As homologous chromosomes condense, they are bound together in a process called synapsis, which allows for crossing over. • Crossing over – chromosomal segments are exchanged between a pair of homologous chromosomes. • Crossing over produces exchange of genetic information. ...
The phenotypic consequences of MECP2 mutations extend beyond
The phenotypic consequences of MECP2 mutations extend beyond

... in each of the known cases of asymptomatic carriers with fortunate XCI, an affected family member with the same mutation has a random pattern [Schanen et al., 1997; Sirianni et al., 1998; Wan et al., 1999]. Similarly, there is limited evidence suggesting that early truncating mutations have deleteri ...
Chapter 4: EXTENSIONS OF MENDELIAN INHERITANCE
Chapter 4: EXTENSIONS OF MENDELIAN INHERITANCE

... that obey two laws: the law of segregation and the law of independent assortment. Until now, we have mainly considered traits that are affected by a single gene that is found in two different alleles. In these cases, one allele is dominant over the other. This type of inheritance is sometimes called ...
Genome-Wide Scan of Obesity in the Old Order Amish*
Genome-Wide Scan of Obesity in the Old Order Amish*

... 25 kg/m2 or greater (1). Obesity is a well-established risk factor for many chronic diseases, such as type 2 diabetes, hypertension, gallbladder disease, osteoarthritis, and some cancers (2). A higher BMI is also associated with higher all-cause mortality (3). The economic cost attributable to obesi ...
Linkage, Recombination, and the Mapping of Genes on Chromosomes
Linkage, Recombination, and the Mapping of Genes on Chromosomes

... • Mitotic recombination: Rarely, recombination occurs during mitosis. In multicellular organisms, mitotic recombination can produce genetic mosaicism in which different cells have different genotypes. ...


... gene dose determination by quantitative real-time PCR. The high similarity in the genome structures of the S. cerevisiae ⴛ S. kudriavzevii hybrids under study indicates that they originated from a single hybridization event. After hybridization, the hybrid genome underwent extensive chromosomal rear ...
< 1 2 3 4 5 6 7 8 9 10 ... 241 >

Skewed X-inactivation

Skewed X chromosome inactivation occurs when the inactivation of one X chromosome is favored over the other, leading to an uneven number of cells with each chromosome inactivated. It is usually defined as one allele being found on the active X chromosome in over 75% of cells, and extreme skewing is when over 90% of cells have inactivated the same X chromosome. It can be caused by primary nonrandom inactivation, either by chance due to a small cell pool or directed by genes, or caused by secondary nonrandom inactivation, which occurs by selection. Most females will have some levels of skewing. It is relatively common in adult females; around 35% of women have skewed ratio over 70:30, and 7% of women have an extreme skewed ratio of over 90:10. This is of medical significance due to the potential for the expression of disease genes present on the X chromosome that are normally not expressed due to random X inactivation. X chromosome inactivation occurs in females to provide dosage compensation between the sexes. If females kept both X chromosomes active they would have twice the number of active X genes than males, who only have one copy of the X chromosome. At approximately the time of implantation (see Implantation (human embryo), one of the two X chromosomes is randomly selected for inactivation. The cell undergoes transcriptional and epigenetic changes to ensure this inactivation is permanent. All progeny from these initial cells will maintain the inactivation of the same chromosome, resulting in a mosaic pattern of cells in females.
  • studyres.com © 2025
  • DMCA
  • Privacy
  • Terms
  • Report