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Journal articles on the topic 'Canine transmissible venereal tumor'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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1

Carreira, Vinicius Soares, Heitor Flávio Ferrari, Ingeborg Maria Langohr, et al. "Leishmaniasp. Amastigotes Identification in Canine Transmissible Venereal Tumor." Case Reports in Veterinary Medicine 2014 (2014): 1–4. http://dx.doi.org/10.1155/2014/603852.

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Leishmaniasis is a vector-borne disease withLeishmania chagasibeing the etiological agent of canine visceral leishmaniasis in South America. Canine venereal tumor is a transplantable round cell tumor of histiocytic origin which is mostly observed in sexually active male and female intact dogs. It has been shown thatLeishmaniaamastigotes have higher tropism for the canine male genital tract tissues and venereal leishmaniasis transmission has been documented in dogs but, to date, a canine venereal tumor-dependent transmission route has not been fully demonstrated. In this report, a 10-year-old,

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2

Guvenc, T., M. Haligur, and M. N. Orman. "Mitosis and apoptosis in canine cutaneous histiocytoma and transmissible venereal tumour." Acta Veterinaria Hungarica 50, no. 3 (2002): 315–21. http://dx.doi.org/10.1556/avet.50.2002.3.8.

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Cell proliferation and apoptosis in canine cutaneous histiocytomas and transmissible venereal tumours were examined in twenty cases. The Ki-67 immunohistochemistry and Tunel methods were used to detect mitotic activity and apoptosis, respectively. The number of Ki-67 immunoreactive cells was 11.65 (±1.1706) in canine cutaneous histiocytomas and 17 (±2.1751) in transmissible venereal tumours. The mean values of apoptotic cells for canine cutaneous histiocytomas and transmissible venereal tumours were 13.25 (±1.8758) and 8.52 (±1.1007), respectively. It was considered that mitotic activity and a

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3

Pashkevych, Iryna, Volodymyr Stybel, and Natalia Soroka. "DIAGNOSTIC METHODS OF CANINE TRANSMISSIBLE VENEREAL SARCOMA." EUREKA: Health Sciences 3 (May 31, 2018): 67–76. http://dx.doi.org/10.21303/2504-5679.2018.00567.

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Modern diagnostic of oncological diseases, along with classical clinical and morphological methods, provides for the mandatory use of instrumental immunological, immunocytochemical and molecular genetic research methods. The main tasks of such a complex of diagnostic measures are aimed at monitoring oncological diseases at all stages of the diagnostic and treatment process, namely: the detection of a tumor at early stages of its development and the study of changes in metabolic processes in the body under the influence of neoplasms, morphological confirmation of the diagnosis, identification o

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4

Mozos, E., A. Méndez, J. C. Gómez-Villamandos, J. Martín de las Mulas, and J. Pérez. "Immunohistochemical Characterization of Canine Transmissible Venereal Tumor." Veterinary Pathology 33, no. 3 (1996): 257–63. http://dx.doi.org/10.1177/030098589603300301.

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The collective immunohistochemical expression of human lysozyme, human alpha-1-antitrypsin, human CD3 antigen, calf vimentin, human keratins, human lambda light chains, canine immunoglobulins IgG, IgM, and bovine protein S-100 has been analyzed on formalin-fixed, paraffin-embedded tissue sections of 25 spontaneous canine transmissible venereal tumors (CTVT) from both genital and extragenital locations using the avidin-biotin-peroxidase complex technique. Lysozyme immunoreactivity was detected in 10/25 CTVT, alpha-1-antitrypsin in 14/25 CTVT, and vimentin in 25/25 CTVT. All CTVT cells were nega

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5

Flórez, Mauricio Montoya, Francisco Pedraza, Fabrizio Grandi, and Noeme S. Rocha. "Cytologic subtypes of canine transmissible venereal tumor." Veterinary Clinical Pathology 41, no. 1 (2012): 4–5. http://dx.doi.org/10.1111/j.1939-165x.2012.00401.x.

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6

McKay, Heather. "Canine transmissible venereal tumour disease." BSAVA Companion 2018, no. 2 (2018): 23. http://dx.doi.org/10.22233/20412495.0218.23.

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7

Chu, R. M., T. J. Sun, H. Y. Yang, et al. "Heat shock proteins in canine transmissible venereal tumor." Veterinary Immunology and Immunopathology 82, no. 1-2 (2001): 9–21. http://dx.doi.org/10.1016/s0165-2427(01)00327-0.

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8

Ayala-Díaz, Sergio, Diego Alberto Vergara Medina, Marcela Lizano, and Joaquín Manzo-Merino. "Transmissible Cancer: A Canine Transmissible Venereal Tumor during Pregnancy, Case Report." Cancer Science & Research 1, no. 1 (2018): 1–4. http://dx.doi.org/10.33425/2639-8478.1004.

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9

Ganguly, B., U. Das, and A. K. Das. "Canine transmissible venereal tumour: a review." Veterinary and Comparative Oncology 14, no. 1 (2013): 1–12. http://dx.doi.org/10.1111/vco.12060.

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10

Moro, J. V., M. Tinucci-Costa, A. C. T. Silveira, D. G. Gerardi, and A. C. Alessi. "Reactivity of p53 protein in canine transmissible venereal tumor." Arquivo Brasileiro de Medicina Veterinária e Zootecnia 62, no. 2 (2010): 318–23. http://dx.doi.org/10.1590/s0102-09352010000200011.

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The expression of p53 protein was evaluated in canine transmissible venereal tumor (CTVT), as following: natural occurrence (n=8); resistant to chemotherapy (n=4); and allogeneic transplanted in progression (n=8), stable (n=8), and regression (n=8)stages. The collected specimens were submitted to GM1 immunohistochemical reaction. Results showed a mean percentage of immunomarked cells around 18.6% in CTVT of natural occurrence, 23.8% in CTVT resistant to chemotherapy, 22.9% in allogeneic transplanted CTVT in both progression and stable stages, and 35.8% in transplanted CTVT in regression stage.

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11

Santos, F. G. A., L. Moro, G. D. Cassali, et al. "Cell proliferation markers in the transplanted canine transmissible venereal tumor." Arquivo Brasileiro de Medicina Veterinária e Zootecnia 63, no. 6 (2011): 1345–52. http://dx.doi.org/10.1590/s0102-09352011000600010.

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Adult male mongrel dogs were subcutaneously transplanted with the canine transmissible venereal tumor (TVT) on the hypogastric region. Twelve specimens of tumors were collected, half during the proliferative phase and the other half during the regressive phase. Fragments of the tumor were fixed in 10% buffered formalin and routinely processed for light microscopy. Sections of 4µm were stained by Schorr or AgNOR or either immunostained for MIB1 (Ki67). Schorr stain, AgNOR and MIB1 showed an increased proliferative activity through mitotic index, nuclear argyrophilic protein stain and cycling tu

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12

Rogers, KS, MA Walker, and HB Dillon. "Transmissible venereal tumor: a retrospective study of 29 cases." Journal of the American Animal Hospital Association 34, no. 6 (1998): 463–70. http://dx.doi.org/10.5326/15473317-34-6-463.

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Twenty-nine cases of naturally occurring, transmissible venereal tumor were studied retrospectively. The external genitalia was the primary site of tumor involvement in 27 dogs, with the remaining two dogs having primary intranasal involvement. Extragenital tumor involvement was identified in six cases, including five cases with metastatic disease. Fifteen cases were treated effectively with radiation therapy alone. Radiation therapy also was effective in four cases that were resistant to chemotherapy. Four of five cases treated with at least four doses of vincristine as a solitary agent also

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13

Duzanski, A. P., H. B. Fêo, L. M. Montoya, C. V. Seullner, and N. S. Rocha. "Canine Transmissible Venereal Tumor: Is Its Biological Behavior Changing?" Anatomical Record 300, no. 6 (2017): 1009–10. http://dx.doi.org/10.1002/ar.23527.

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14

Rodrigues, Geórgia Nadalini, Antonio Carlos Alessi, and José Luiz Laus. "INTRAOCULAR TRANSMISSIBLE VENEREAL TUMOR IN A DOG." Ciência Rural 31, no. 1 (2001): 141–43. http://dx.doi.org/10.1590/s0103-84782001000100023.

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Canine transmissible venereal tumor (TVT) is a round cell neoplasm occurring on the external genital mucosa of male and female dogs. Transmission is by cell implantation during coitus, licking, or other interaction between an affected dog and a susceptible host. Metastasis of the tumor rarely occurs. This report describes an unusual presentation of TVT with intraocular involvement and inguinal lymph nodes metastasis. The subject was a six-year-old, intact, male, Brazilian Terrier dog with a history of abnormal masses in the right eye, penis and several subcutaneous nodules in the inguinal area

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15

Ayala-Díaz, Sergio, Roberto Jiménez-Lima, Katia M. Ramírez-Alcántara, et al. "Presence of Papillomavirus DNA sequences in the canine transmissible venereal tumor (CTVT)." PeerJ 7 (October 25, 2019): e7962. http://dx.doi.org/10.7717/peerj.7962.

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Background The canine transmissible venereal tumor (CTVT) or Sticker’s sarcoma is a neoplastic disease affecting dogs. This disease is presented as a tumoral mass in the genital organs of both, male and female individuals. Up to date, there is no clear evidence indicating a viral agent as the causative mediator for CTVT development. Purpose The present work aims to analyze 21 samples from canines with CTVT for molecular identification of Papillomavirus DNA sequences. In addition, microbiological analysis, cytologic and histopathologic evaluations were also performed. Results All patients showe

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16

Marchal, T., L. Chabanne, C. Kaplanski, D. Rigal, and J. P. Magnol. "Immunophenotype of the canine transmissible venereal tumour." Veterinary Immunology and Immunopathology 57, no. 1-2 (1997): 1–11. http://dx.doi.org/10.1016/s0165-2427(96)05757-1.

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17

Osorio-Morales, Lina Fernanda, and Francisco Pedraza-Ordóñez. "Electrochemotherapy Treatment of Canine Transmissible Venereal Tumors." Artificial Organs 41, no. 12 (2017): 1185. http://dx.doi.org/10.1111/aor.13062.

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18

Choi, Y., N. Ishiguro, M. Shinagawa, et al. "Molecular structure of canine LINE-1 elements in canine transmissible venereal tumor." Animal Genetics 30, no. 1 (1999): 52–53. http://dx.doi.org/10.1046/j.1365-2052.1999.00400.x.

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19

Antonov, Anton. "Successful Treatment of Canine Transmissible Venereal Tumor Using Vincristine Sulfate." Advances in Research 5, no. 5 (2015): 1–5. http://dx.doi.org/10.9734/air/2015/20017.

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20

FARJANIKISH, Ghasem. "Morphoathological Description of an Extra Genital Canine Transmissible Venereal Tumor." İstanbul Üniversitesi Veteriner Fakültesi Dergisi 43, no. 23931 (2016): 0. http://dx.doi.org/10.16988/iuvfd.266473.

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21

Kabuusu, Richard M., Sachin Kumthekar, Josephine Tang, et al. "Clinicopathological changes during canine transmissible venereal tumor treatment with vincristine." Indian Journal of Veterinary Pathology 43, no. 2 (2019): 132. http://dx.doi.org/10.5958/0973-970x.2019.00027.0.

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22

ISHIKAWA, Toshio, Hirotsugu YAMAMOTO, and Yoshiki SUGIYAMA. "A Case of Abdominal Canine Transmissible Venereal Tumor after Uterectomy." Journal of the Japan Veterinary Medical Association 48, no. 9 (1995): 686–88. http://dx.doi.org/10.12935/jvma1951.48.686.

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23

Frampton, Dan, Hagen Schwenzer, Gabriele Marino, et al. "Molecular Signatures of Regression of the Canine Transmissible Venereal Tumor." Cancer Cell 33, no. 4 (2018): 620–33. http://dx.doi.org/10.1016/j.ccell.2018.03.003.

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24

Veloso, Jéssica Fontes, Thais Nascimento de Andrade Oliveira, Lorena Priscila Andrade, et al. "Three Cases of Exclusively Extragenital Canine Transmissible Venereal Tumor (cTVT)." Acta Scientiae Veterinariae 46 (May 29, 2018): 8. http://dx.doi.org/10.22456/1679-9216.86846.

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Background: Canine Transmissible Venereal Tumor (cTVT) is a neoplasia that affects mainly the genital organs of dogs, but can rich extragenital sites as well. It´s a tumor characterized microscopically by the presence of vacuolized round cells. Transmission occurs by implantation of these cells in non-affected tissues and the treatment is based on vincristine chemotherapy.Cases: Case 1. A 5-year-old intact male Poodle, presenting an increase volume of nasal plane came for veterinary care at a private veterinary clinic. The animal had bilateral bloody nasal secretion and dyspnea. The external g

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25

Flórez, Luis M. M., Haline F. Ballestero, Anderson P. Duzanski, et al. "Immunocytochemical characterization of primary cell culture in canine transmissible venereal tumor." Pesquisa Veterinária Brasileira 36, no. 9 (2016): 844–50. http://dx.doi.org/10.1590/s0100-736x2016000900009.

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Abstract: Immunochemistry with anti-vimentin, anti-lysozyme, anti-alpha 1 antitrypsin, anti-CD3 and anti-CD79α antibodies has been used for characterization of primary cell culture in the transmissible venereal tumor (TVT). Samples for primary cell culture and immunohistochemistry assays were taken from eight dogs with cytological and clinical diagnosis of TVT. To validate the immunochemical results in the primary cell culture of TVT, a chromosome count was performed. For the statistical analysis, the Mann-Whitney test with p<0.05 was used. TVT tissues and culture cells showed intense anti-

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26

Thatcher, Graham, Cecilia Robat, and Cynthia Bell. "Diagnosis and Management of an Oronasal Fistula Secondary to Nasal Transmissible Venereal Tumor in a Dog." Journal of Veterinary Dentistry 37, no. 4 (2020): 220–26. http://dx.doi.org/10.1177/0898756420987011.

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Canine transmissible venereal tumor (CTVT) is a contagious tumor commonly seen in populations of sexually intact dogs that have close contact with each other. CTVT is one of only 3 known naturally transmissible, contagious tumors in which the mutated tumor cell is thought to have originated in an individual canid about 11000 years ago. Clinical history, signalment, cytological and histologic evaluation are typically sufficient for reaching a diagnosis, although immunohistochemistry(IHC) may be necessary for unique presentations of this neoplasm. This case report describes the diagnosis of an o

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27

Adrian, FEGHIU, CRÎNGANU Dan, DUMITRESCU Florin, PASCAL Manuela, VASILESCU Florina, and MILITARU Manuella. "Nasal Transmissible Venereal Tumor In A Jack Russel Terrier Bitch." Acta Veterinaria 65, no. 1 (2015): 143–48. http://dx.doi.org/10.1515/acve-2015-0012.

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Abstract A two-year old Jack Russell Terrier female with left-sided epistaxis was brought to the Clinic of the Bucharest Faculty of Veterinary Medicine. Endoscopy of the left nasal cavity revealed a cauliflower-like mass. Cytological and histopathological features were specific to canine transmissible venereal tumour (CTVT). Tumor tissue showed positive immunoreactivity to anti-vimentin monoclonal antibody (90%) and Ki67 (35%) and samples were negative for anti-cytokeratin monoclonal antibody. Chemotherapy with vincristine sulphate at a dose of 0.025 mg/kg i.v./week for 6 administrations was s

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28

Yadav, Anup, Praveen Kumar, Sandeep Panihar, et al. "Clinico-Histopathological Studies in Canine Transmissible Venereal Tumour." International Journal of Current Microbiology and Applied Sciences 7, no. 11 (2018): 2714–19. http://dx.doi.org/10.20546/ijcmas.2018.711.310.

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29

Harmelin, A., J. H. Pinthus, N. Katzir, et al. "Use of a murine xenograft model for canine transmissible venereal tumor." American Journal of Veterinary Research 62, no. 6 (2001): 907–11. http://dx.doi.org/10.2460/ajvr.2001.62.907.

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30

Pereira, J. S., A. B. F. Silva, A. L. B. Martins, A. M. R. Ferreira, and D. E. Brooks. "Immunohistochemical characterization of intraocular metastasis of a canine transmissible venereal tumor." Veterinary Ophthalmology 3, no. 1 (2000): 43–47. http://dx.doi.org/10.1046/j.1463-5224.2000.00097.x.

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31

Champour, Mohsen, Najmoddin Ojrati, Arefeh Nikrou, Hedyeh Rahimian, and Maysam Tehrani-Sharif. "First report of diffuse cutaneous canine transmissible venereal tumor in Iran." Comparative Clinical Pathology 24, no. 4 (2014): 741–44. http://dx.doi.org/10.1007/s00580-014-1973-z.

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32

Mascarenhas, Mariana B., Paulo V. Peixoto, Regina R. Ramadinha, et al. "Immunohistochemical, lectin histochemical and ultrastructural studies of canine transmissible venereal tumor in Brazil." Pesquisa Veterinária Brasileira 37, no. 6 (2017): 613–20. http://dx.doi.org/10.1590/s0100-736x2017000600014.

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ABSTRACT: Canine transmissible venereal tumor (CTVT) is a naturally occurring contagious round-cell neoplasia, with poorly understood origin and transmission. This study aims to further investigate the tumor nature through immunohistochemistry, lectin histochemistry and transmission electron microscopy (TEM) analysis, and to provide support for diagnostic and differential diagnoses of CTVT. Immunohistochemistry was performed in 10 genital and six exclusively extragenital tumors, which were previously diagnosed by citology and histopathology. CTVT samples were incubated with biotinylated antibo

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33

Sandusky, G. E., W. W. Carlton, and K. A. Wightman. "Immunohistochemical Staining For S100 Protein in the Diagnosis of Canine Amelanotic Melanoma." Veterinary Pathology 22, no. 6 (1985): 577–81. http://dx.doi.org/10.1177/030098588502200611.

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Formalin-fixed, paraffin-embedded tissue samples of canine amelanotic melanomas and normal canine tissues were studied immunohistochemically for the presence of S100 protein. Use of the avidin-biotin complex procedure demonstrated variable amounts of S100 protein in the tumor cell cytoplasm and nuclei in 26 of 31 tumors. S100 protein was not observed in some other common canine skin tumors stained by the avidin-biotin complex technique. These were a mast cell tumor, fibrosarcoma, mammary gland adenocarcinoma, histiocytoma, transmissible venereal tumor, and a thyroid gland adenocarcinoma. Among

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Sandusky, G. E., W. W. Carlton, and K. A. Wightman. "Diagnostic Immunohistochemistry of Canine Round Cell Tumors." Veterinary Pathology 24, no. 6 (1987): 495–99. http://dx.doi.org/10.1177/030098588702400604.

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Sixty-five canine skin neoplasms studied using immunocytochemistry, included 22 histiocytomas, 18 amelanotic melanomas, 14 cutaneous lymphosarcomas, six mast cell tumors, and five transmissible venereal tumors. Formalin-fixed, paraffin-embedded sections were stained using the avidin-biotin-peroxidase complex (ABC) immunoperoxidase technique for reactivity with S-100 protein, kappa and lambda immunoglobulin light chains, alpha-1-antitrypsin, alpha-1-antichymotrypsin, leukocyte common antigen (LCA), neuron-specific enolase, keratin, cytokeratin, muramidase, and vimentin. Detection of S-100, kapp

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35

Santos, F. G. A., A. C. Vasconcelos, J. E. S. Nunes, et al. "Apoptosis in the transplanted canine transmissible venereal tumor during growth and regression phases." Arquivo Brasileiro de Medicina Veterinária e Zootecnia 60, no. 3 (2008): 607–12. http://dx.doi.org/10.1590/s0102-09352008000300013.

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Twelve male, mongrel, adult dogs were subcutaneously transplanted with cells originated from two canine transmissible venereal tumors (TVT). The aim was to demonstrate and to quantify the occurrence of apoptosis in the TVT regression. After six months of transplantation, a tumor sample was obtained from each dog, being six dogs with TVT in the growing phase and six in the regression phase as verified by daily measurements. Samples were processed for histological and ultrastructural purposes as well as for DNA extraction. Sections of 4µm were stained by HE, Shorr, methyl green pyronine, Van Gie

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36

Arcila-Villa, Antony, Carmen Dussán-Lubert, and Francisco Pedraza-Ordoñez. "Distribution and prevalence of transmissible venereal tumor in the Colombian canine population." Revista Colombiana de Ciencias Pecuarias 31, no. 3 (2018): 180–87. http://dx.doi.org/10.17533/udea.rccp.v31n3a02.

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37

SETTHAWONGSIN, Chanokchon, Somporn TECHANGAMSUWAN, Sirikachorn TANGKAWATTANA, and Anudep RUNGSIPIPAT. "Cell-based polymerase chain reaction for canine transmissible venereal tumor (CTVT) diagnosis." Journal of Veterinary Medical Science 78, no. 7 (2016): 1167–73. http://dx.doi.org/10.1292/jvms.15-0710.

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38

Choi, Young Ki, and Chul Joong Kim. "Sequence analysis of canine LINE-1 elements and p53 gene in canine transmissible venereal tumor." Journal of Veterinary Science 3, no. 4 (2002): 285. http://dx.doi.org/10.4142/jvs.2002.3.4.285.

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39

Wunderlich, V. "Anton Sticker (1861–1944) und das Sticker-Sarkom des Hundes." Tierärztliche Praxis Ausgabe K: Kleintiere / Heimtiere 40, no. 06 (2012): 432–37. http://dx.doi.org/10.1055/s-0038-1623673.

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ZusammenfassungDas Sticker-Sarkom (neuere Bezeichnung CTVT für canine transmissible venereal tumor) ist ein histiozytärer venerischer Tumor, der unter Hunden durch direkten Kontakt übertragen wird. Seit kurzem ist gesichert, dass alle weltweit vorkommenden Tumoren dieses Typs ursprünglich von dem Tumor eines Tieres abstammen. Das beim Kontakt übertragene infektiöse Agens ist die Krebszelle selbst. Damit stellt das StickerSarkom die älteste bekannte Krebslinie und heute zugleich das beste Modell für infektiöse Krebszellen dar. Das Sarkom ist nach dem deutschen Veterinärund Humanmediziner Anton

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40

Mascarenhas, Mariana B., Paulo V. Peixoto, Regina R. Ramadinha, et al. "Immunohistochemical study of genital and extragenital forms of canine transmissible venereal tumor in Brazil." Pesquisa Veterinária Brasileira 34, no. 3 (2014): 250–54. http://dx.doi.org/10.1590/s0100-736x2014000300009.

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Aiming to provide insight and discussing the problems related to the diagnosis and differential diagnosis of canine transmissible venereal tumor (CTVT), especially in its extragenital form, immunohistochemical evaluation was performed and a comparison was established by analysis of the microscopic appearance of 10 genital CTVTs and 13 exclusively extragenital CTVTs previously diagnosed by cytology and histopathology. CTVTs samples were incubated with biotinylated antibodies raised against specific membrane (anti-macrophage) and cytoplasmic antigens (anti-lysozyme, anti-S-100 protein, anti-vime

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41

Baez-Ortega, Adrian, Kevin Gori, Andrea Strakova, et al. "Somatic evolution and global expansion of an ancient transmissible cancer lineage." Science 365, no. 6452 (2019): eaau9923. http://dx.doi.org/10.1126/science.aau9923.

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The canine transmissible venereal tumor (CTVT) is a cancer lineage that arose several millennia ago and survives by “metastasizing” between hosts through cell transfer. The somatic mutations in this cancer record its phylogeography and evolutionary history. We constructed a time-resolved phylogeny from 546 CTVT exomes and describe the lineage’s worldwide expansion. Examining variation in mutational exposure, we identify a highly context-specific mutational process that operated early in the cancer’s evolution but subsequently vanished, correlate ultraviolet-light mutagenesis with tumor latitud

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42

Hiblu, Murad A., Nizar M. Khabuli, and Abdurraouf O. Gaja. "Canine transmissible venereal tumor: First report of three clinical cases from Tripoli, Libya." Open Veterinary Journal 9, no. 2 (2019): 103. http://dx.doi.org/10.4314/ovj.v9i2.1.

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43

Sánchez-Servín, Abel, Simón Martínez, Emilio Córdova-Alarcon, and Raúl Fajardo. "TP53 Polymorphisms allow for genetic sub-grouping of the canine transmissible venereal tumor." Journal of Veterinary Science 10, no. 4 (2009): 353. http://dx.doi.org/10.4142/jvs.2009.10.4.353.

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44

Chikweto, Alfred, Sachin Kumthekar, Hugh Larkin, et al. "Genital and Extragenital Canine Transmissible Venereal Tumor in Dogs in Grenada, West Indies." Open Journal of Veterinary Medicine 03, no. 02 (2013): 111–14. http://dx.doi.org/10.4236/ojvm.2013.32018.

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45

Scarpelli, Karime C., Maria L. Valladão, and Konradin Metze. "Predictive factors for the regression of canine transmissible venereal tumor during vincristine therapy." Veterinary Journal 183, no. 3 (2010): 362–63. http://dx.doi.org/10.1016/j.tvjl.2008.11.009.

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46

Amber, E. I., R. A. Henderson, J. B. Adeyanju, and E. O. Gyang. "Single-Drug Chemotherapy of Canine Transmissible Venereal Tumor With Cyclophosphamide, Methotrexate, or Vincristine." Journal of Veterinary Internal Medicine 4, no. 3 (1990): 144–47. http://dx.doi.org/10.1111/j.1939-1676.1990.tb00887.x.

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47

Scarpelli, Karime C., Maria Luiza C. R. Valladão, Edson M. Scarpelli, and Konradin Metze. "Seasonality of side effects during chemotherapy of canine transmissible venereal tumor with vincristine." Veterinary Immunology and Immunopathology 128, no. 1-3 (2009): 340. http://dx.doi.org/10.1016/j.vetimm.2008.10.276.

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Katzir, N., G. Rechavi, J. B. Cohen, et al. ""Retroposon" insertion into the cellular oncogene c-myc in canine transmissible venereal tumor." Proceedings of the National Academy of Sciences 82, no. 4 (1985): 1054–58. http://dx.doi.org/10.1073/pnas.82.4.1054.

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Marino, G., G. Gaglio, and A. Zanghì. "Clinicopathological study of canine transmissible venereal tumour in leishmaniotic dogs." Journal of Small Animal Practice 53, no. 6 (2012): 323–27. http://dx.doi.org/10.1111/j.1748-5827.2012.01201.x.

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Batatnuzi, E. K., and F. Kristensen. "Urinary tract infection: The role of canine transmissible venereal tumour." Journal of Small Animal Practice 37, no. 6 (1996): 276–79. http://dx.doi.org/10.1111/j.1748-5827.1996.tb02378.x.

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