Cultural expression

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    A chordoma is a rare type of bone tumor that grows along the spine or skull base. Since it originates from stems notochord cell lines, chordomas are normally present in the midline on the axial skeleton and become very difficult to detect during the early stages of life. Generally, 50% of cases occur in the sacrococcygeal region, 35% in Spenoccipital region and 15% in the rest of the column, especially in the 2nd cervical vertebra transverse process level and sinuses. Chordomas represent less than

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    Melanoma Outline

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    cancer-driving genes from number of mutated genes Literature Review • By integration vectors, mutations in host genes can induce cancer • Enhance levels of transcription and translation • Generate transcripts or inactivate tumour suppressor gene (TSG) expression • Intragenic insertions can interfere with splicing of genes • For screening mutagenesis, prefer to insert the transposon into the gene • Transposons offer a great scope to detect tags to find insertion

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    For our gene and protein lab, my group decided and I to research the deadly, yet rare, disease, known as Huntington's disease. Huntington's disease is an extremely rare condition when your nerve cells in your brain break down overtime. Also, “HD” has a treatment that could aid someone, but it unfortunately cannot be cured. Huntington’s Disease typically begins when someone is thirty or forty years of age and can last years to a life time. Furthermore, the disease is caused by an HTT gene that has

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    Aurora Kinase B Structure In humans, aurora kinase B associates itself with the INCENP complex (inner centromere protein)+. Aurora kinase B is a protein consisting of 344 amino acids. The protein has 13 alpha helices, 7 beta pleated sheets and one turn. The amino acid sequence is as follows: Residues 1 – 50 MAQKENSYPW PYGRQTAPSG LSTLPQRVLR KEPVTPSALV LMSRSNVQPT 51 – 100 AAPGQKVMEN SSGTPDILTR HFTIDDFEIG RPLGKGKFGN VYLAREKKSH 101 – 150 FIVALKVLFK SQIEKEGVEH QLRREIEIQA HLHHPNILRL YNYFYDRRRI

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    Cisplatin

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    CHAPTER 1 INTRODUCTION Cisplatin is a platinum-based chemotherapeutic agent with proven efficacy against solid tumors. However, the clinical use of cisplatin is limited by the development of permanent hearing loss in cancer patients. There is currently no drug approved by the US Food and Drug Administration for cisplatin-induced hearing loss (1, 2). Multiple studies have shown that cisplatin profoundly damages outer hair cells (OHCs) present in the hook region, basal and middle turns of the cochlea

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    Pkc Carraway Lab Report

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    When the PKCγ-Cγ3 images are viewed separately, in the trials with the constitutively active PLCγ1 (A25E) mutant positive control, we will see the PKCγ (indicated by the pink color of Cγ3) move closer to the edges of the cell (which are defined by phase microscopy). In the same trials, the fascin-FTIC images will show the location a fascin to be near the edges of the cell as well (as indicated by the green FTIC). Once these two images are layered over one another, will show an overlap of the to colors

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    Accumulation of both genetic and epigenetic deregulation results in genome alterations (10). Both of the gene mutations and epigenetic modifications have been initially considered as two separate mechanisms contributing to carcinogenesis. However, current evidence has revealed an interference between gene mutations and epigenetic modifications in cancer formation. Therefore, it has been suggested that gene mutations lead to distribution of several epigenetic patterns as well as mutagenesis and genome

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    Introduction Neurofibromatosis (NF) Type I is a common autosomal dominant genetic disorders. NF Type I has a prevalence rate of approximately 1/3000-4000 individuals. NF Type I is caused mutations in the NFI gene. This gene provides instructions for making the protein neurofibromin. Neurofibromin is produced in many cells, including nerve cells and specialized cells that surround nerves such as, oligodendrocytes and Schwann cells. This protein acts as a tumor suppressor that keeps cells from growing

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    Identify and define at least three key terms used within the field of genetics. 1. Gene- a piece of DNA that will carry the information it needs to make a specific protein. 2. Genotype- The genetic makeup of an individual 3. Generalist Genes Hypothesis- genes that affect one ability are largely the same genes that affect other abilities, even though there are some genetic effects that are specific to each ability. After defining your terms of choice, discuss how the authors Haworth, Kovas et

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    Cray Fish Hematopoiesis

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    In order to study the molecules regulator in hematopoiesis by an in vitro culture, crayfish hematopoietic cytokines, astakine1 have been identified (5). Astakine1 is an invertebrate prokineticin, which plays an important role in hematopoiesis regulation in crustacean. Astakine1 was original purified from plasma and plasma levels of astakine1 was increased after LPS stimulation. The injected-animals with purified or recombinant astakine1 were resulted in a dramatic increase in total hemocyte count

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