Puumala virus

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    Human gene therapy is when genetic material is introduced into human cells to treat a genetic disease. Instead of traditionally treating the symptoms, gene therapy aims to treat the disease’s root cause by directly altering genes and correcting defects. Therefore, gene therapy is only viable for certain diseases. Disorders from mutations in single genes are the most treatable, whereas disorders that involve many genes and environmental factors are trickier. There are two types of gene therapy:

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    The idea of extending human’s life has been a controversy for many years, since the scientific revolution of 1543. Since then, our medical field has brought new technology, that offers us to make this idea possible. However, this technology has brought up stakeholders that are among the medical community and patients, since they are using our genes and changing them to creating a longer life. Scientist call this process gene editing which is "the ability to precisely and accurately change any part

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    Kosoy et al. [11] described the presence of Bartonella in 13 insectivorous and frugivorous bat species sampled across 25 localities in Kenya. A total of 331 blood samples were re-suspended in brain-heart infusion (BHI) broth and plated on agar supplemented with 10% rabbit blood, of which 106 (30.2%) were culture positive. Bartonella isolates were obtained from 23 (26%) straw-colored fruit bat (Eidolon helvum), 22 (21%) Egyptian fruit bats (Rousettus aegyptiacus), four (44%) African sheath-tailed

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    reassortment within this genus has resulted in the arisal of virulent reassortants, including a novel virus that emerged as a cause of hemorrhagic fever in the late 1990’s. While several orthobunyaviruses are endemic in North America and are intermittently associated with human and animal disease, the potential for reassortment among endemic Bunyamwera orthobunyaviruses such as Cache Valley virus (CVV) and Tensaw virus (TENV) is currently not well understood. CVV is notable

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    Human Embryos

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    Introduction The concept of altering human genomic DNA has been around for decades, with pioneering studies in the late eighties illustrating the insertion of homologous DNA sequences at defined locations within mammalian chromosomes (Smithies et al., 1985). Only now, are these rudimentary techniques being replaced with rapid, inexpensive, and more efficient tools for genome editing (Zhang et al., 2014). Tools like CRISPR/ Cas9, which, were once a bacterial defense mechanism but have since been

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    autoimmune diseases. Exposure to infectious agents (viral or bacterial) in CD, has also been suggested as a factor causing tissue damage and inflammation, which could affect the host’s immune tolerance to gluten (Bethune and Khosla, 2008). Hepatitis C Virus (HCV) may be considered as a suitable candidate. It was hypothesized that some viruses including HCV may have amino-acid sequences homologous to some gliadin epitopes;

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    Gene Therapy

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    retinal pigment epithelium. About 10% of people with Leber congenital amaurosis (LCA), an inherited disorder that causes vision loss starting in childhood, have an altered form of the gene RPE65. The researchers hoped to halt this process by using a virus to shuttle a functional RPE65 gene into the retina. This strategy, in which genes are used to treat or prevent a disease is known as gene therapy. Clinical trials of experimental gene therapy for LCA and other diseases that affect the retina has been

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    Tree bark skin is a very rare disorder. This disorder is associated with a high risk of carcinoma of the skin. This disorder usually starts on the hands and feet. The condition usually affects people in the ages 1-20, but can also affect you during your middle age. The cause of this condition is inactivating PH mutation in usually ever1-2 genes, these are adjacent to one another.Image result for tree bark skinImage result for tree bark skin The way they determine if you have this condition

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    welly. Even though there isn't a cure infected “patients are given supported hospital care” (Marburg virus disease history,sThe CDC states that “Marburg is a rare severe Hemorrhagic fever”(Marburg Hemorrhagic fever). Marburg was first recognized in 1967 in Germany.Fruit bats maybe the reservoir of Marburg. The first people who caught Marburg we’re exposed to monkeys. Scientist say that this virus is transmitted through direct contact of body fluids.Marburg has countless amounts of symptoms, has no

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    Gene Replacement Therapy

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    The objective of gene replacement therapy is to alter the defective gene to achieve a permanent cure for the diagnosed patient by identifying the faulty gene and providing a corrected copy of the gene without affecting the genomic sequence. Clinical trials initiated gene replacement experimentation, primarily leading to significant progress but not yet accomplished.“The most recent clinical trial for the treatment of hemophilia with gene transfer showed transient achievement of efficacy in the highest

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