Inheritance of hypodontia in Kerry Blue Terrier dogs

Genetika

Volumn 40, Issue 5, 2004, Pages 658-666

  Axenovich, T I ^a   Zorkoltseva, I V ^a   Aulchenko, Yu S ^a   Knyazev, S P ^b   Kulikova, A V ^c,d  

^a INSTITUTE OF CYTOLOGY AND GENETICS   (Russian Federation)

^b NOVOSIBIRSK STATE AGRARIAN UNIVERSITY   (Russian Federation)

^c URAL STATE AGRARIAN UNIVERSITY   (Russian Federation)

^d Sverdlovsk Regional Society of Amateur Dog Breeders   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; DOG; GENETIC HETEROGENEITY; GENETIC REGULATION; HYPODONTIA; INHERITANCE; NONHUMAN; PEDIGREE ANALYSIS; PREMOLAR TOOTH; SEGREGATION ANALYSIS; ANIMAL; ANIMAL DISEASE; CONGENITAL MALFORMATION; DOG DISEASE; GENETICS; PEDIGREE; PHENOTYPE; RECESSIVE GENE;

ANIMALIA; CANIS FAMILIARIS;

ANIMALS; ANODONTIA; BICUSPID; DOG DISEASES; DOGS; GENES, RECESSIVE; PEDIGREE; PHENOTYPE;

EID: 16644362663     PISSN: 00166758     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (32)

1. (Kuyazev S.P., Kulikova A.V., Axenovich T.I., Aulchenko Yu.S. Inheritance of oligodontia in kerry blue terrier dogs // Rus. J. Genetics. 2003. V. 39. Ka 6. P. 669-675.)
2. Stockton D.W., Das P., Goldenberg M. et al. Mutation of PAX9 is associated with oligodontia // Nat. Genet. 2000. V. 24. P. 18-19.
3. Vastardis H. The genetics of human tooth agenesis: new discoveries for understanding dental anomalies // Am. J. Orthod Dentofacial Orthop. 2000. V. 117. V. 6. P. 650-656.
4. Lidral A.C., Reising B.C. The role of MSX1 in human tooth agenesis // J. Dent. Res. 2002. V. 81. No 4. P. 274-278.
5. OMIM™. Online Mendelian Inheritance in man. http://www.ncbi.nlm.- nih.gov/Omim/
6. Pirinen S., Kentala A., Nieminen P. et al. Recessively inherited lower incisor hypodontia // J. Med. Genet. 2001. V. 38. No 8. P. 551-556.
7. Jumlongras D., Bei M., Stimson J.M. et al. A nonsense mutation in MSX1 causes Witkop syndrome // Am. J. Hum. Genet. 2001. V. 69. No 1. P. 67-74.
8. Wang H., Zhao S., Zhao W. et al. Congenital absence of permanent teeth in a six-generation Chinese kindred // Am. J. Med. Genet. 2000. V. 90. No 3. p. 193-198.
9. Ahmad W., Brancolini V., ul Faiyaz M.F. et al. A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1 // Am. J. Hum. Genet. 1998. V. 62. P. 987-991.
10. Vastardis H., Karimbux N., Guthua S.W. et al. A human MSX1 homeodomain missense causes selective tooth agenesis // Nat. Genet. 1996. V. 13. P. 417-421.
11. van den Boogaard M.J., Dorland M., Beemer F.A., van Amstel H.K. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans // Nat. Genet. 2000. V. 24. No 4. P. 342-343.
12. Nieminen P., Arte S., Tanner D. et al. Identification of a nonsense mutation in the PAX9 gene in molar oligodontia // Eur. J. Hum. Genet. 2001. V. 9. No 10. P. 743-746.
13. Frazier-Bowers S.A., Guo D.C., Cavender A. et al. A novel mutation in human PAX9 causes molar oligodontia // J. Dent. Res. 2002. V. 81. No 2. P. 129-133.
14. Das P., Hai M., Elcock C. et al. Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia // Am. J. Med. Genet. 2003. V. 1. P. 35-42.
15. Scarel R.M., Trevilatto P.C., Di Hipolito O. Jr. et al. Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia // Am. J. Med. Genet. 2000. V. 92. No 5. P. 346-349.
16. Satokata I., Maas R. Msx1 deficient mice exhibit cleft palate and abnormalities on craniofacial and tooth development // Nat. Genet. 1994. V. 6. No 4. P. 348-356.
17. Switonski M., Godynicki S., Jackowiak H. et al. X trisomy in an infertile bitch: cytogenetic, anatomic, and histologic studies // J. Hered. 2000. V. 91. No 2. P. 149-150.
18. Neyman J., Pearson E.S. On the use and interpretation of certain test criteria for the purposes of statistical inference // Biometrica. 1928. V. 20A. P. 175-263.
19. Elston R.C., Stewart J.A. General model for the genetic analysis of pedigree data // Human Heredity. 1971. V. 21. P. 523-542.
20. Elston R.C. Segregation analysis // Advances in Human Genetics. N. Y.: Plenum Press, 1981. V. 11. P. 63-120.
21. Stricker C., Fernando R.L., Elston R.C. An algorithm to approximate the likelihood for pedigree data with loops by cutting // Theoret, and Applied Genetics. 1996. V. 91. P. 1054-1063.
22. Wang T., Fernando R.L., Stricker C., Elston R.C. An approximation to the likelihood for pedigree data with loops // Theoret, and Applied Genetics. 1996. V. 93. P. 1299-1309.
23. (Aulchenko Yu.S., Axenovich T.I. An efficient algorithm for calculating the likelihood for a pedigree with short inbred loops // Rus. J. Genetics. 1999. V. 35. No 9. P. 1116-1122.)
24. Axenovich T.I., Rogatcheva M.B., Oda S., Borodin P.M. Inheritance of male hybrid sterility in the house musk shrew (Suncus murinus, Insectivora, Soricidae) // Genome. 1998. V. 41. No 6. P. 825-831.
25. Aulchenko Yu.S., Oda S.I., Rogatcheva M.B. et al. Inheritance of litter size at birth in the house musk shrew (Suncus murinus, Insectivora, Soricidae) // Genet. Res. 1998. V. 71. No 1. P. 65-72.
26. Aulchenko Y.S., Araripe L.O., D'Andrea P.S. et al. Inheritance of litter size at birth in the Brazilian grass mouse (Akodon cursor, Sigmodontinae, Rodentia) // Genet. Res. 2002. V. 80. No 1. P. 55-62.