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It displayed cross-binding activity with human norovirus but not to a structurally similar virus, feline calicivirus.
Feline infectious agents offer powerful natural models of deadly human diseases, which include feline immunodeficiency virus, feline sarcoma virus and feline leukemia virus.
Apoptosis is an integral part of pathogenesis of many viruses such as human immunodeficiency virus type 1, chicken anemia virus, feline leukemia virus, and papillomavirus.
Lions (Panthera leo) are susceptible to viral diseases of domestic carnivores, including infections with canine distemper virus, feline parvovirus, feline retroviruses, feline herpesvirus, and feline calicivirus (FCV) (1 – 4 ).
Surfactin is also active against several viruses, including the Semliki Forest virus, Herpes simplex virus (HSV-1 and HSV 2), Simian immunodeficiency virus, Vesicular stomatitis virus, Feline calicivirus, and the Murine encephalomyocarditis virus.
In contrast to retroviral vectors, lentiviral vectors are capable of delivering genes to both dividing and nondividing cells and are predominantly based on human immunodeficiency virus type 1, although other lentiviral vectors based on simian immunodeficiency virus, feline immunodeficiency virus, and equine infectious anaemia virus have been described.
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The domestic cat has offered enormous genomic potential in the veterinary description of over 250 hereditary disease models as well as the occurrence of several deadly feline viruses (feline leukemia virus -- FeLV, feline coronavirus -- FECV, feline immunodeficiency virus - FIV) that are homologues to human scourges (cancer, SARS, and AIDS respectively).
Other viruses including feline immunodeficiency virus [55], foamy viruses [56], [57], Kaposi's sarcoma associated herpes virus [58], [59], human papillomavirus [60], [61], visna virus [62] or human T-cell leukemia/lymphoma virus type I (HTLV-I) [63], [64] use AP-1 factors either to regulate their own replication or to interfere with host cell gene regulation.
Lions, especially in captivity, are vulnerable to the canine distemper virus (CDV), feline immunodeficiency virus (FIV), and feline infectious peritonitis (FIP).
Because the peptide sequence from the canine parvovirus is also found in two other pathogens, mink enteritis virus and feline panleukopenia virus, the researchers expected that an injection of the chimeric particles would protect the corresponding species--dog, mink, and cat--against the viral diseases.
The virus causes feline panleukopenia, a serious and highly contagious disease that can cause a wide range of symptoms, including vomiting, dehydration, fever and neurological symptoms.
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