Gene mutations causing hereditary diseases in dogs

• Autorzy: Switonski M
• Języki publikacji: EN

Słowa kluczowe

EN

hereditary disease; dog; gene mutation; animal disease

• Wydawca: -
• Czasopismo: Animal Science Papers and Reports
• Rocznik: 2004
• Tom: 22
• Numer: 1
• Opis fizyczny: p.131-134,ref.

Twórcy

autor

Switonski M

• The August Cieszkowski Agricultural University of Poznan, Poznan, Poland

Bibliografia

• 1. ACLAND G.M., AGUIRRE G.D., RAY J., ZHANG Q., ALEMAN T.S., CIDECIYAN A.V.,PEARCE-KELLING S.E., ANAND V., ZENG Y., MAGUIRE A.M., JACOBSON S.G.,HAUSWIRTH W.W., BENNETT J., 2001 – Gene therapy restores vision in a canine model of childhood blindness. Nature Genetics 28, 92-95.
• 2. AGUIRRE G.D., BALDWIN V., PEARCE-KELLING S., NARFSTROM K., RAY K., ACLAND G.M., 1998 – Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect. Molecular Vision 4, 23-30.
• 3. BEATY R.M., JACKSON M., PETERSON D., BIRD A., BROWN T., BENJAMIN D.K., JUOPPERI T., KISHNANI P., BONEY A., CHEN Y.T., KOEBERL D.D., 2002 – Delivery of glucose-6-phosphatase in a canine model for glycogen storage disease, type Ia, with adeno-associated virus (AVV) vectors. Gene Therapy 9, 1015-1022.
• 4. GUYON R., LORENTZEN T.D., HITTE C., KIM L., CADIEU E., PARKER H.G., QUIGNON P., LOWE J.K., RENIER C., GELFENBEYN B., VIGNAUX F., DEFRANCE H.B., GLOUX S.,MAHAIRAS G.G., ANDRE C., GALIBERT F., OSTRANDER E.A., 2003 – A 1-Mb resolution radiation hybrid map of the canine genome. Proceedings of the National Academy of Sciences, USA 100, 5296‑5301.
• 5. KIJAS J.M.H., BAUER T.R., GAFVERT S., MARKLUND S., TROWALD-WIGH G., JOHANNISSON A., HEDHAMMAR A., BINNS M., JUNEJA R.K., HICKSTEIN D.D., ANDERSSON L., 1999 – A missence mutation in the β-2 integrin gene (ITGB2) causes canine leukocyte adhesion deficiency. Genomics 61, 101-107.
• 6. KIRKNESS E.F., BAFNA V., HALPERN A.L., LEVY S., REMINGTON K., RUSCH D.B.,DELCHER A.L., POP M., WANG W., FRASER C.M., VENTER J.C., 2003 – The dog genome:survey sequencing and comparative analysis. Science 301, 1898-1903.
• 7. MEYERS-WALLEN V.N., 2003 – Sry and Sox9 expression during canine gonadal sex determination assayed by quantitative reverse transcription-polymerase chain reaction. Molecular Reproduction and Development 65, 373-81.
• 8. MEYERS-WALLEN V.N., SCHLAFER D., BARR I., LOVELL-BADGE R., KEYZNER A., 1999 – Sry‑negative XX sex reversal in purebred dogs. Molecular Reproduction and Development 53,266-73.
• 9. ROBERTS M.C., MICKELSON J.R., PATTERSON E.E., NELSON T.E., ARMSTRONG P.J., 2001 – Autosomal dominant canine malignant hyperthermia is caused by a mutation in the gene encoding the skeletal muscle calcium release chanel (RYR1). Anesthesiology 95, 716-725.
• 10. ŚWITONSKI M., KONIECZNY P., KLUKOWSKA J., JANYGA B., AGUIRRE G., 2002 – Mikrodelecja w genie RPE65 wywołująca dziedziczną dystrofię siatkówki w polskiej populacji psów rasy briard. Medycyna Weterynaryjna 58, 946-949.
• 11. ŚWITONSKI M., SZCZERBAL I., GREWLING J., ANTOSIK P., NIZANSKI W., YANG F.,2003 – Two cases of infertile bitches with 78,XX/77,X mosaic karyotype - a need for cytogenetic evaluation of dogs with reproductive disorders. Journal of Heredity 94, 65-68.
• 12. YANG F., O’BRIEN P.C.M., MILNE B.S., GRAPHODATSKY A.S., SOLANKY N., TRIFONOV V., RENS W., SARGAN D., FERGUSON-SMITH M.A., 1999 – A complete comparative chromosome map for the dog, red fox, and human and its integration with canine genetic maps. Genomics 62, 189-202.
• 13. YANG F., MILNE B.S., SCHELLING C., DOLF G., SCHLÄPFER J., ŚWITONSKI M., LADON D., PIENKOWSKA A., BOSMA A.A., SARGAN D.R., FERGUSON-SMITH M.A., 2000 – Chromosome identification and assignment of dog DNA clones in the dog using a red fox and dog comparative map. Chromosome Research 8, 93-100.