Mitosis
Spindle Apparatus
CDC2 Protein Kinase
Cell Cycle Proteins
Interphase
Cell Cycle
Anaphase
Telophase
Kinetochores
Microtubules
Cyclin B
Centrosome
Metaphase
HeLa Cells
Chromosomes
G2 Phase
Aurora Kinases
Nocodazole
Protein-Serine-Threonine Kinases
Schizosaccharomyces
Aurora Kinase B
Centromere
Nuclear Proteins
Anaphase-Promoting Complex-Cyclosome
Ubiquitin-Protein Ligase Complexes
Chromosomal Proteins, Non-Histone
Cyclin B1
Phosphorylation
Schizosaccharomyces pombe Proteins
Cell Nucleus
Prophase
Microtubule-Associated Proteins
Chromatids
Cell Division
Tubulin
cdc25 Phosphatases
Nuclear Envelope
Kinesin
Meiosis
Cdc20 Proteins
Mad2 Proteins
S Phase
M Phase Cell Cycle Checkpoints
Microscopy, Fluorescence
Molecular Sequence Data
Mutation
Saccharomyces cerevisiae Proteins
Centrioles
Amino Acid Sequence
Cdh1 Proteins
Protein Kinases
G1 Phase
Chromosomes, Human
RNA Interference
Xenopus Proteins
Chromatin
Nuclear Matrix-Associated Proteins
Drosophila Proteins
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome
Genes, cdc
Saccharomyces cerevisiae
Aurora Kinase A
Cell Nucleolus
Fluorescent Antibody Technique
Potoroidae
Recombinant Fusion Proteins
Cyclin A
Cyclins
Aspergillus nidulans
Xenopus
Histones
Tubulin Modulators
Models, Biological
Polyploidy
Lamins
Protein Binding
Green Fluorescent Proteins
Protamine Kinase
CDC28 Protein Kinase, S cerevisiae
Saccharomycetales
Phosphoprotein Phosphatases
DNA-Binding Proteins
Securin
Cyclin-Dependent Kinases
Drosophila
Embryo, Nonmammalian
Dyneins
Chromosomal Instability
Nucleolus Organizer Region
RNA, Small Interfering
Multiprotein Complexes
Cytoplasm
ran GTP-Binding Protein
Separase
DNA Damage
Protein Transport
Nuclear Pore
Maturation-Promoting Factor
Drosophila melanogaster
Lamin Type B
Microscopy, Video
Apc6 Subunit, Anaphase-Promoting Complex-Cyclosome
Dipodomys
Sequence Homology, Amino Acid
Cell Cycle Checkpoints
Colchicine
DNA
Cells, Cultured
Oocytes
Aneuploidy
Phenotype
Benomyl
Cyclin A2
Time-Lapse Imaging
Geminin
Ligases
Luminescent Proteins
Microscopy, Electron
Ubiquitin-Protein Ligases
Aphidicolin
Analysis of the effects of food and of digestive secretions on the small intestine of the rat. 1. Mucosal morphology and epithelial replacement. (1/11754)
A modified Roux-en-Y repositioning of rat small intestine was performed so that the proximal segment of bowel (A) received only bile and pancreastic secretions, the second (B) received food direct from the stomach, and these two segments drained into a third (C). Four to five weeks after operation, cell production was assessed by injection of vincristine into operated, sham-operated and unoperated rats, and counts of blocked metaphases were made on isolated microdissected crypts. Villus height, crypt depth, and the number of crypts per villus (crypt/villus ratio) were also measured. Most of segment A showed no significant differences from sham-operated intestine, although the normal proximo-distal gradient of villus height was abolished. At the distal end (near the anastomosis with segments B and C), crypt depth and cell production were increased. The villus height gradient in segment B was also abolished, although crypt depth and cell production were significantly increased, especially at the proximal end. Crypt/villus ratio was also increased. Segment C showed all the characteristics of small bowel promoted to a more proximal position: increased villus height, crypt depth and cell production. Increased crypt/villus ratio was also observed. These results are discussed in terms of the role of food and of digestive secretions in the control of mucosal morphology and epithelial replacement. (+info)Functions of cyclin A1 in the cell cycle and its interactions with transcription factor E2F-1 and the Rb family of proteins. (2/11754)
Human cyclin A1, a newly discovered cyclin, is expressed in testis and is thought to function in the meiotic cell cycle. Here, we show that the expression of human cyclin A1 and cyclin A1-associated kinase activities was regulated during the mitotic cell cycle. In the osteosarcoma cell line MG63, cyclin A1 mRNA and protein were present at very low levels in cells at the G0 phase. They increased during the progression of the cell cycle and reached the highest levels in the S and G2/M phases. Furthermore, the cyclin A1-associated histone H1 kinase activity peaked at the G2/M phase. We report that cyclin A1 could bind to important cell cycle regulators: the Rb family of proteins, the transcription factor E2F-1, and the p21 family of proteins. The in vitro interaction of cyclin A1 with E2F-1 was greatly enhanced when cyclin A1 was complexed with CDK2. Associations of cyclin A1 with Rb and E2F-1 were observed in vivo in several cell lines. When cyclin A1 was coexpressed with CDK2 in sf9 insect cells, the CDK2-cyclin A1 complex had kinase activities for histone H1, E2F-1, and the Rb family of proteins. Our results suggest that the Rb family of proteins and E2F-1 may be important targets for phosphorylation by the cyclin A1-associated kinase. Cyclin A1 may function in the mitotic cell cycle in certain cells. (+info)Thyroid hormone effects on Krox-24 transcription in the post-natal mouse brain are developmentally regulated but are not correlated with mitosis. (3/11754)
Krox-24 (NGFI-A, Egr-1) is an immediate-early gene encoding a zinc finger transcription factor. As Krox-24 is expressed in brain areas showing post-natal neurogenesis during a thyroid hormone (T3)-sensitive period, we followed T3 effects on Krox-24 expression in newborn mice. We analysed whether regulation was associated with changes in mitotic activity in the subventricular zone and the cerebellum. In vivo T3-dependent Krox-24 transcription was studied by polyethylenimine-based gene transfer. T3 increased transcription from the Krox-24 promoter in both areas studied at post-natal day 2, but was without effect at day 6. An intact thyroid hormone response element (TRE) in the Krox-24 promoter was necessary for these inductions. These stage-dependent effects were also seen in endogenous Krox-24 mRNA levels: activation at day 2 and no effect at day 6. Moreover, similar results were obtained by examining beta-galactosidase expression in heterozygous mice in which one allele of the Krox-24 gene was disrupted with an inframe Lac-Z insertion. However, bromodeoxyuridine incorporation showed mitosis to continue through to day 6. We conclude first, that T3 activates Krox-24 transcription during early post-natal mitosis but that this effect is extinguished as development proceeds and second, loss of T3-dependent Krox-24 expression is not correlated with loss of mitotic activity. (+info)Diverse developing mouse lineages exhibit high-level c-Myb expression in immature cells and loss of expression upon differentiation. (4/11754)
The c-myb gene encodes a sequence specific transactivator that is required for fetal hematopoiesis, but its potential role in other tissues is less clear because of the early fetal demise of mice with targeted deletions of the c-myb gene and incomplete of knowledge about c-myb's expression pattern. In the hematopoietic system, c-Myb protein acts on target genes whose expression is restricted to individual lineages, despite Myb's presence and role in multiple immature lineages. This suggests that c-Myb actions within different cell type-specific contexts are strongly affected by combinatorial interactions. To consider the possibility of similar c-Myb actions could extend into non-hematopoietic systems in other cell and tissue compartments, we characterized c-myb expression in developing and adult mice using in situ hybridization and correlated this with stage-specific differentiation and mitotic activity. Diverse tissues exhibited strong c-myb expression during development, notably tooth buds, the thyroid primordium, developing trachea and proximal branching airway epithelium, hair follicles, hematopoietic cells, and gastrointestinal crypt epithelial cells. The latter three of these all maintained high expression into adulthood, but with characteristic restriction to immature cell lineages prior to their terminal differentiation. In all sites, during fetal and adult stages, loss of c-Myb expression correlated strikingly with the initiation of terminal differentiation, but not the loss of mitotic activity. Based on these data, we hypothesize that c-Myb's function during cellular differentiation is both an activator of immature gene expression and a suppressor of terminal differentiation in diverse lineages. (+info)The postnatal development of the alimentary canal in the opossum. I. Oesophagus. (5/11754)
The oesophageal epithelium of the newborn opossum generally is two to three cells in depth and in some regions appears pseudostratified. By the 9th postnatal day the epithelium shows two distinct strata. Ciliated cells and occasional goblet cells also are observed within the epithelium during this stage and in subsequent stages. Cilia persist in the oesophagus of the adult opossum, but are restricted to the depths of the transverse folds found in the distal part of the organ. The epithelium covering the transverse folds of the adult likewise has an immature appearance. By 4-5 cm (ca. 20 days), the epithelium has assumed a more mature appearance and is of greater depth. This and later stages show three basic strata: a germinal layer, a spinous layer and, adjacent to the lumen, a flattened layer of cells that retain their nuclei. The epithelium throughout the postnatal period and in the adult does not undergo complete keratinization. The oesophageal glands begin as outgrowths from the epithelium just prior to 4-5 cm (ca. 20 days). The glands continue their development throughout the remainder of the postnatal period. The secretory units of the oesophageal glands of the the major portion of the secretory elements, and a light, rounded cell type which is less numerous and which occupies the terminal portions of the secretory units. Secretory material of the former appears complex, consisting of both neutral and acid glycoproteins. The secretory product of the light cell type is unknown at present. Both cell types are encompassed by myoepithelial cells. The relationship of the mitotic sequences to the observations made by microscopic examination of the developing oesophagus is discussed. (+info)Changes in the total number of neuroglia, mitotic cells and necrotic cells in the anterior limb of the mouse anterior commissure following hypoxic stress. (6/11754)
The effects of hypoxic stress (390 mmHg) on the total number of glia, cell division, and cell death in the anterior limb of the anterior commissure were studied. There was a significant (P less than 0-01) fall in the total number of glia following exposure to hypoxia at 390 mmHg for two days. No significant change was observed in the total number of glia between the hypoxic and recovery group one week after return to sea level (ca. 760 mmHg). No change was observed in the number of mitotic figures in the control, hypoxic or recovery groups, but significant falls were observed in the mean number of necrotic cells between both the control and hypoxic groups (P less than 0-05) and the hypoxic and recovery groups (P less than 0-012). The decrease in necrotic cells may be due to a large number of elderly and effete cells, which would normally have undergone degeneration over a period of weeks, dying rapidly after the onset of hypoxia, thus temporarily reducing the daily cell death rate. (+info)The preprophase band: possible involvement in the formation of the cell wall. (7/11754)
Numerous vesicles were observed among the microtubules of the "preprophase" band in prophase cells from root tips of Allium cepa. The content of these vesicles looks similar to the matrix of adjacent cell walls, and these vesicles often appear to be involved in exocytosis. In addition, the cell walls perpendicular to the plane of (beneath) the preprophase band are often differentially thickened compared to the walls lying parallel to the plane of the band. Our interpretation of these observations is that the preprophase band may direct or channel vesicles containing precursors of the cell wall to localized regions of wall synthesis. The incorporation of constituents of the cell wall into a narrow region defined by the position of the preprophase band may be a mechanism that ensures unidirecitonal growth of meristematic cells. (+info)Arsenic targets tubulins to induce apoptosis in myeloid leukemia cells. (8/11754)
Arsenic exhibits a differential toxicity to cancer cells. At a high concentration (>5 microM), As2O3 causes acute necrosis in various cell lines. At a lower concentration (0.5-5 microm), it induces myeloid cell maturation and an arrest in metaphase, leading to apoptosis. As2O3-treated cells have features found with both tubulin-assembling enhancers (Taxol) and inhibitors (colchicine). Prior treatment of monomeric tubulin with As2O3 markedly inhibits GTP-induced polymerization and microtubule formation in vitro but does not destabilize GTP-induced tubulin polymers. Cross-inhibition experiments indicate that As2O3 is a noncompetitive inhibitor of GTP binding to tubulin. These observations correlate with the three-dimensional structure of beta-tubulin and suggest that the cross-linking of two vicinal cysteine residues (Cys-12 and Cys-213) by trivalent arsenic inactivates the GTP binding site. Furthermore, exogenous GTP can prevent As2O3-induced mitotic arrest. (+info)Polyploidy is a condition where an organism has more than two sets of chromosomes, which are the thread-like structures that carry genetic information. It can occur in both plants and animals, although it is relatively rare in most species. In humans, polyploidy is extremely rare and usually occurs as a result of errors during cell division or abnormal fertilization.
In medicine, polyploidy is often used to describe certain types of cancer, such as breast cancer or colon cancer, that have extra sets of chromosomes. This can lead to the development of more aggressive and difficult-to-treat tumors.
However, not all cases of polyploidy are cancerous. Some individuals with Down syndrome, for example, have an extra copy of chromosome 21, which is a non-cancerous form of polyploidy. Additionally, some people may be born with extra copies of certain genes or chromosomal regions due to errors during embryonic development, which can lead to various health problems but are not cancerous.
Overall, the term "polyploidy" in medicine is used to describe any condition where an organism has more than two sets of chromosomes, regardless of whether it is cancerous or non-cancerous.
Causes of Chromosomal Instability:
1. Genetic mutations: Mutations in genes that regulate the cell cycle or chromosome segregation can lead to CIN.
2. Environmental factors: Exposure to certain environmental agents such as radiation and certain chemicals can increase the risk of developing CIN.
3. Errors during DNA replication: Mistakes during DNA replication can also lead to CIN.
Types of Chromosomal Instability:
1. Aneuploidy: Cells with an abnormal number of chromosomes, either more or fewer than the normal diploid number (46 in humans).
2. Structural changes: Deletions, duplications, inversions, translocations, and other structural changes can occur in the chromosomes.
3. Unstable chromosome structures: Chromosomes with abnormal shapes or structures, such as telomere shortening, centromere instability, or chromosome breaks, can also lead to CIN.
Effects of Chromosomal Instability:
1. Cancer: CIN can increase the risk of developing cancer by disrupting normal cellular processes and leading to genetic mutations.
2. Aging: CIN can contribute to aging by shortening telomeres, which are the protective caps at the ends of chromosomes that help maintain their stability.
3. Neurodegenerative diseases: CIN has been implicated in the development of certain neurodegenerative diseases such as Alzheimer's and Parkinson's.
4. Infertility: CIN can lead to infertility by disrupting normal meiotic recombination and chromosome segregation during gametogenesis.
Detection and Diagnosis of Chromosomal Instability:
1. Karyotyping: This is a technique used to visualize the entire set of chromosomes in a cell. It can help identify structural abnormalities such as deletions, duplications, or translocations.
2. Fluorescence in situ hybridization (FISH): This technique uses fluorescent probes to detect specific DNA sequences or proteins on chromosomes. It can help identify changes in chromosome structure or number.
3. Array comparative genomic hybridization (aCGH): This technique compares the genetic material of a sample to a reference genome to identify copy number changes.
4. Next-generation sequencing (NGS): This technique can identify point mutations and other genetic changes in DNA.
Treatment and Management of Chromosomal Instability:
1. Cancer treatment: Depending on the type and stage of cancer, treatments such as chemotherapy, radiation therapy, or surgery may be used to eliminate cancer cells with CIN.
2. Prenatal testing: Pregnant women with a family history of CIN can undergo prenatal testing to detect chromosomal abnormalities in their fetuses.
3. Genetic counseling: Individuals with a family history of CIN can consult with a genetic counselor to discuss risk factors and potential testing options.
4. Lifestyle modifications: Making healthy lifestyle choices such as maintaining a balanced diet, exercising regularly, and not smoking can help reduce the risk of developing cancer and other diseases associated with CIN.
In conclusion, chromosomal instability is a common feature of many human diseases, including cancer, and can be caused by a variety of factors. The diagnosis and management of CIN require a multidisciplinary approach that includes cytogenetic analysis, molecular diagnostics, and clinical evaluation. Understanding the causes and consequences of CIN is crucial for developing effective therapies and improving patient outcomes.
There are several types of aneuploidy, including:
1. Trisomy: This is the presence of an extra copy of a chromosome. For example, Down syndrome is caused by an extra copy of chromosome 21 (trisomy 21).
2. Monosomy: This is the absence of a chromosome.
3. Mosaicism: This is the presence of both normal and abnormal cells in the body.
4. Uniparental disomy: This is the presence of two copies of a chromosome from one parent, rather than one copy each from both parents.
Aneuploidy can occur due to various factors such as errors during cell division, exposure to certain chemicals or radiation, or inheritance of an abnormal number of chromosomes from one's parents. The risk of aneuploidy increases with age, especially for women over the age of 35, as their eggs are more prone to errors during meiosis (the process by which egg cells are produced).
Aneuploidy can be diagnosed through various methods such as karyotyping (examining chromosomes under a microscope), fluorescence in situ hybridization (FISH) or quantitative PCR. Treatment for aneuploidy depends on the underlying cause and the specific health problems it has caused. In some cases, treatment may involve managing symptoms, while in others, it may involve correcting the genetic abnormality itself.
In summary, aneuploidy is a condition where there is an abnormal number of chromosomes present in a cell, which can lead to various developmental and health problems. It can occur due to various factors and can be diagnosed through different methods. Treatment depends on the underlying cause and the specific health problems it has caused.
Mitosis
Mitosis inducer protein kinase cdr2
Cdc14
Cell division
Catastrophin
Meiosis
Entomophthora
J. Richard McIntosh
Michele Banks
Mitotic stingaree
OutlookSoft
Conly Rieder
Induced cell cycle arrest
Glossary of mycology
Ciliate
Dimethyl tetrachloroterephthalate
Peter K. Hepler
Sporogenesis
Wnt signaling pathway
Trypanosoma brucei
William R. Brinkley
Ectopic thymus
Kriegeriales
Gamete
Paramecium
Proliferative index
Eduard Strasburger
Survivin
Interphase
Homologous chromosome
Mitosis: Metaphase and Anaphase | SparkNotes
Biology Quiz : Mitosis - Worksheet / Test Paper
Digital Wish - Lesson Plans: Mitosis
mitosis fonts Search like Mitosis
GitHub - seanmtracey/image-mitosis: Use the power of the cloudz to generate map tiles super-quick (hopefully...)
Snapshot: Phosphoregulation of Mitosis | Garvan Institute of Medical Research
APS -APS March Meeting 2023
- Event - Structural changes in chromosomes driven by multiple condensin motors during mitosis
Chromator is required for proper microtubule spindle formation and mitosis in Drosophila | www.ibmc.up.pt
Go to DNA replication and spindle checkpoints cooperate during S phase to delay mitosis and preserve genome integrity.
Comparing Mitosis and Meiosis
mitosis - CEH
Mitosis - Presentation Genetics
Volume 22 Issue 3, March 2004
Focus on Mitosis - TOPS
Mitosis Chapter 13 | researchpaper123.com
MR002 - Mitosis, Onion Root Tip - Valley Microscope
Study Guides
Mitosis, microtubules, and the matrix<...
Are there 92 chromosomes in mitosis? - Lukes Epworth Answers
Onion Mitosis, l.s., Showing All Stages, H&E Stain
What is the main difference between mitosis and meiosis? - AnswersAll
Mitosis Worksheet & Diagram Identification Answer Key
A Step-by-step Explaination of the Stages of Mitosis - Biology Wise
Dose-Dependent Transmissibility of Chromosome Aberrations in Human Lymphocytes at First Mitosis. II. Biological Effectiveness...
Partner switching for Ran during the mitosis dance<...
Emergency Response Safety and Health Database: Glossary | NIOSH | CDC
Effect of plumbagin on cell growth and mitosis - ABIM - An Annotated Bibliography of Indian Medicine
Greenwich Academic Literature Archive - Phytoene and phytofluene overproduction by Dunaliella salina using the mitosis...
Metaphase3
- 16. During mitosis, loosely arranged strands of chromosomes become coiled, shortened and distinct during the metaphase. (syvum.com)
- The rate of loop extrusion is smaller at the start of mitosis and increases as the cells approach the metaphase. (aps.org)
- A liver biopsy performed showed changes consistent with chronic hepatitis C along with many scattered mitoses arrested in metaphase in the hepatocytes that have been referred to as "ring" mitoses. (nih.gov)
Phase of mitosis3
- Prophase is the first phase of mitosis. (syvum.com)
- Students should divide the poster board into five sections (one for each phase of mitosis) and use what they have learned to depict each phase. (digitalwish.com)
- This is the phase of mitosis where the cell performs its normal activities for life. (sliderbase.com)
Asexual reproduction1
- Benchmark Number: SC.7.L.16.3 Benchmark Description: Compare and contrast the general processes of sexual reproduction requiring meiosis and asexual reproduction requiring mitosis. (digitalwish.com)
Phases of mitosis3
- Students will also develop and perform a skit about the phases of mitosis. (digitalwish.com)
- This lesson will introduce students to the step-by-step phases of mitosis in an effort to imprint on the young mind the idea that each cell is highly organized. (digitalwish.com)
- Through the use of microslide viewers, students studied the phases of mitosis in both plant and animal cell division. (topsprogram.ca)
Assembly in mitosis2
- We found Sgt1 to be required for proper centrosome maturation and mitotic spindle assembly in mitosis. (wixsite.com)
- After establishing my lab, we discovered the role of RanGTPase in regulating spindle assembly in mitosis. (nih.gov)
Meiosis3
- This diagram shows a diploid nucleus (2n=8) in which chromosome replication has occurred in preparation for mitosis (top) and meiosis (bottom). (researchpaper123.com)
- Mitosis and meiosis are two important processes of cell division. (ahmadcoaching.com)
- The importance of mitosis and meiosis to an organism is apparent to living organisms considering that chromosomes contain genes and proper distribution of genes is vital for viable daughter cells. (ahmadcoaching.com)
Interphase1
- 14. The interphase and mitosis together constitute the cell cycle. (syvum.com)
Prophase1
- The prophase is the longest stage of mitosis. (syvum.com)
Genome1
- During mitosis, a cell divides its duplicated genome into two identical daughter cells. (garvan.org.au)
Chromosomes5
- 7. During which stage of mitosis do chromatids separate to form two sets of daughter chromosomes? (syvum.com)
- 13. During which stage of mitosis does longitudinal splitting of the chromosomes occur? (syvum.com)
- In this part of the lesson, students will create physical representations of mitosis on poster board, using a variety of the materials listed in the Planning Ahead section (e.g., yarn to represent chromosomes, lifesavers to represent centromeres). (digitalwish.com)
- Before a cell divides, it undergoes a process called mitosis that copies its chromosomes and produces two identical nuclei. (nih.gov)
- Mitosis represents that part of the cell cycle where the replicated chromosomes are separated into two identical nuclei. (byui.edu)
Hepatocyte1
- In this example, the high frequency of mitosis (arrows) is a repair response following hepatocyte loss secondary to treatment with a hepatotoxicant. (nih.gov)
Mitotic1
- However, the extent to which plant mitosis differs from that of animals at the level of the protein repertoire is uncertain, largely because of the difficulty in the identification and in vivo characterization of mitotic genes of plants . (bvsalud.org)
Biology1
- Here, we discuss protocols for mitosis imaging that can be combined with endogenous green fluorescent protein (GFP) tagging or conditional RNA interference ( RNAi ) in the moss Physcomitrella patens, which is an emergent model plant for cell and developmental biology . (bvsalud.org)
CELLS14
- Agents that affect MITOSIS of CELLS. (nih.gov)
- Images of Hela cells expressing a live cell fluorescent mitosis biosensor as they go through cell division. (nature.com)
- A new fluorescent biosensor allows mitosis to be monitored simultaneously in a large number of cells. (nature.com)
- Finally, we have identified the human homologues for some of the new genes and downregulation of these in HeLa cells also resulted in severely defective chromosome congression and segregation during mitosis. (wixsite.com)
- The cells of the zygote then divide by mitosis (which does not change the ploidy level) to produce an adult organism (still 2n) of the next generation. (researchpaper123.com)
- A cell divides during mitosis to produce two identical daughter cells. (ahmadcoaching.com)
- Mitosis is responsible for regeneration, healing of the wound, and replacement of older cells. (ahmadcoaching.com)
- While during wound healing mitosis adds new cells to the damaged tissue site. (ahmadcoaching.com)
- Mitosis adds new cells to the growing body and different cells are specialized to perform different functions. (ahmadcoaching.com)
- A single cutting of a plant is transformed into a whole new plant due to the addition of new cells produced by mitosis. (ahmadcoaching.com)
- Similarly, during the process of cloning a single cell is divided into multiple identical cells by the mitosis process. (ahmadcoaching.com)
- Any malfunctioning in mitosis leads to unwanted tumors or cancer in which cells divide uncontrollably and form clusters of cells. (ahmadcoaching.com)
- The whitefish embryo is a good place to look at mitosis because these cells are rapidly dividing as the fish embryo is growing. (valleymicroscope.com)
- The authors interpret the mechanism of multinucleation to be due to failure of cells to divide following mitosis. (cdc.gov)
Search1
- Type Mitosis: The Game in Search bar and install it. (appsformacpc.com)
Tumors1
- Malfunction in mitosis leads to unwanted tumors or cancer. (ahmadcoaching.com)
Liver3
- While occasional mitoses can be seen in a normal liver, finding more than one or two mitoses per 10 high-power fields is not typical for adult rodents. (nih.gov)
- The current liver biopsy was compared with the biopsy from 7 years ago, which appeared similar, however, ring mitoses were absent. (nih.gov)
- Ring mitosis have been associated with colchicine-mediated tissue injury in various other sites, and their presence is felt to represent colchicine-induced liver injury in this case. (nih.gov)
Cell division3
- Mitosis, or cell division, is a messy process. (crev.info)
- The proper execution of each step of mitosis is important for normal cell division. (ahmadcoaching.com)
- An agent that prevents or interferes with cell division (mitosis). (cdc.gov)
Centrosome1
- The SnapShot begins in late G2 phase, with the activation of the central driver of mitosis, cyclin dependent kinase 1 (CDK1) at the centrosome. (garvan.org.au)
Organization1
- We created a theoretical framework that describes the loop extrusion (LE) by multiple condensin I and II motors in order to investigate the changes in chromosome organization during mitosis. (aps.org)
Https1
- Access it online or download it at https://books.byui.edu/bio_180/122_mitosis . (byui.edu)
Occur1
- If mitosis doesn't occur, then healing of the wound would be impossible. (ahmadcoaching.com)
Tissue1
- Mitosis is involved in tissue culturing and cloning processes. (ahmadcoaching.com)
Lesson1
- In this lesson, students will make physical representations of mitosis. (digitalwish.com)
Processes1
- This system has potential for use in the high-throughput study of mitosis and other intracellular processes, as is being done with various animal cell lines . (bvsalud.org)
Study2
- Figure 1 Increased mitosis (arrows) in a male F344/N rat from an acute repeated-dose study. (nih.gov)
- Two specimens are commonly used by biologists to study mitosis: the blastula of a whitefish and the root tip of an onion. (valleymicroscope.com)
Process3
- The mitosis process is significant for multicellular organisms. (ahmadcoaching.com)
- During the process of mitosis, no crossing over takes place. (ahmadcoaching.com)
- Some living organisms reproduce asexually by the process called mitosis. (ahmadcoaching.com)
Site1
- In the online version, hovering the mouse over a track highlights all related events, while clicking on a phosphosite opens a popup detailing the role of this site in regulating mitosis. (garvan.org.au)
Events1
- A key mechanism controlling mitosis is the precise temporal addition and removal of over 32,000 phosphorylation events by a network of kinases and counterbalancing phosphatases. (garvan.org.au)
Development2
- The growth and development of a multicellular organism are courtesy of mitosis. (ahmadcoaching.com)
- The development and growth of multicellular organisms require mitosis. (ahmadcoaching.com)
Show1
- 2015). Here, we show phosphoevents currently believed to be key regulators of mitosis. (garvan.org.au)
Broken1
- 1. During which stage of mitosis is the nuclear membrane broken into fragments? (syvum.com)