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Volumn 120, Issue 1-2, 2008, Pages 117-122

Three autosomal chromosome translocations associated with repeated early embryonic loss (REEL) in the domestic horse (Equus caballus)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; AUTOSOME; AUTOSOME ABERRATION; BACTERIAL ARTIFICIAL CHROMOSOME; CHROMOSOME 10; CHROMOSOME 15; CHROMOSOME 16; CHROMOSOME 3P; CHROMOSOME 3Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME MAP; CHROMOSOME TRANSLOCATION; EMBRYO MEMBRANE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE SEQUENCE; HORSE; KARYOTYPE; NONHUMAN; PRIORITY JOURNAL;

EID: 43449136491     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000118749     Document Type: Article
Times cited : (36)

References (23)
  • 1
    • 0024058933 scopus 로고
    • Embryonic loss in mares. Incidence, possible causes, and diagnostic considerations
    • Ball BA: Embryonic loss in mares. Incidence, possible causes, and diagnostic considerations. Vet Clin North Am Equine Pract 4:263-290 (1988).
    • (1988) Vet Clin North Am Equine Pract , vol.4 , pp. 263-290
    • Ball, B.A.1
  • 4
    • 0037398042 scopus 로고    scopus 로고
    • The first generation whole genome radiation hybrid map in the horse identifies conserved segments in human and mouse genomes
    • Chowdhary BP, Raudsepp T, Kata SR, Goh G, Millon LV, et al: The first generation whole genome radiation hybrid map in the horse identifies conserved segments in human and mouse genomes. Genome Res 13:742-751 (2003).
    • (2003) Genome Res , vol.13 , pp. 742-751
    • Chowdhary, B.P.1    Raudsepp, T.2    Kata, S.R.3    Goh, G.4    Millon, L.V.5
  • 5
    • 0037847425 scopus 로고    scopus 로고
    • Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C-alpha-formylglycine generation enzyme
    • Dierks T, Schmidt B, Borissenkio LV, Pent J, Preusser A, et al: Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C-alpha-formylglycine generation enzyme. Cell 113:435-444 (2003).
    • (2003) Cell , vol.113 , pp. 435-444
    • Dierks, T.1    Schmidt, B.2    Borissenkio, L.V.3    Pent, J.4    Preusser, A.5
  • 6
    • 0031263425 scopus 로고    scopus 로고
    • ISCNH: International system for cytogenetic nomenclature of the domestic horse. Bowling AT, Breen M, Chowdhary BP, Hirota K, Lear TL, et al (committee). Chromosome Res 5:433-453 (1997).
    • ISCNH: International system for cytogenetic nomenclature of the domestic horse. Bowling AT, Breen M, Chowdhary BP, Hirota K, Lear TL, et al (committee). Chromosome Res 5:433-453 (1997).
  • 7
    • 0036519027 scopus 로고    scopus 로고
    • Use of Zoo-FISH to characterize a reciprocal translocation in a thoroughbred mare: T(1;16)(q16;q21.3)
    • Lear TL, Layton G: Use of Zoo-FISH to characterize a reciprocal translocation in a thoroughbred mare: t(1;16)(q16;q21.3). Equine Vet J 43:207-209 (2002).
    • (2002) Equine Vet J , vol.43 , pp. 207-209
    • Lear, T.L.1    Layton, G.2
  • 8
    • 0032609068 scopus 로고    scopus 로고
    • Autosomal trisomy in a Thoroughbred colt: 65,XY,+31
    • Lear TL, Cox JH, Kennedy GA: Autosomal trisomy in a Thoroughbred colt: 65,XY,+31. Equine Vet J 31:85-88 (1999).
    • (1999) Equine Vet J , vol.31 , pp. 85-88
    • Lear, T.L.1    Cox, J.H.2    Kennedy, G.A.3
  • 9
    • 0033937026 scopus 로고    scopus 로고
    • Horse v-fes feline sarcoma viral oncogene homologue; pyruvate kinase muscle type 2; plasminogen, beta spectrin, non-erythrocytic 1, thymidiliate synthetase; and microsatellite LEX078 map to 1q14-q15, 1q21, 31q12-q14, 15q22, 8q12-q14 and 14qter, respectively
    • Lear TL, Piumi F, Terry R, Guerin G, Bailey E: Horse v-fes feline sarcoma viral oncogene homologue; pyruvate kinase muscle type 2; plasminogen, beta spectrin, non-erythrocytic 1, thymidiliate synthetase; and microsatellite LEX078 map to 1q14-q15, 1q21, 31q12-q14, 15q22, 8q12-q14 and 14qter, respectively. Chromosome Res 8:361 (2000).
    • (2000) Chromosome Res , vol.8 , pp. 361
    • Lear, T.L.1    Piumi, F.2    Terry, R.3    Guerin, G.4    Bailey, E.5
  • 11
    • 0029922369 scopus 로고    scopus 로고
    • Tandem 1:30 translocation: A new structural abnormality in the horse (Equus caballus)
    • Long SE: Tandem 1:30 translocation: a new structural abnormality in the horse (Equus caballus). Cytogenet Cell Genet 72:162-163 (1996).
    • (1996) Cytogenet Cell Genet , vol.72 , pp. 162-163
    • Long, S.E.1
  • 13
    • 0036707817 scopus 로고    scopus 로고
    • Cytogenetic localization of 136 genes in the horse: Comparative mapping with the human genome
    • Milenkovic D, Oustry-Vaiman A, Lear TL, Billault A, Mariat D, et al: Cytogenetic localization of 136 genes in the horse: comparative mapping with the human genome. Mamm Genome 13:524-534 (2002).
    • (2002) Mamm Genome , vol.13 , pp. 524-534
    • Milenkovic, D.1    Oustry-Vaiman, A.2    Lear, T.L.3    Billault, A.4    Mariat, D.5
  • 16
    • 85012752328 scopus 로고    scopus 로고
    • Power MM: Horse chromosomes, in McFeely RA (ed): Advances in Veterinary Science and Comparative Medicine, 34: Domestic Animal Cytogenetics, pp 131-167 (Academic Press, Inc., San Diego 1990).
    • Power MM: Horse chromosomes, in McFeely RA (ed): Advances in Veterinary Science and Comparative Medicine, Vol 34: Domestic Animal Cytogenetics, pp 131-167 (Academic Press, Inc., San Diego 1990).
  • 17
    • 0026126777 scopus 로고
    • The first description of a balanced reciprocal translocation t(1q;3q) and its clinical effects in a mare
    • Power MM: The first description of a balanced reciprocal translocation t(1q;3q) and its clinical effects in a mare. Equine Vet J 23:146-149 (1991).
    • (1991) Equine Vet J , vol.23 , pp. 146-149
    • Power, M.M.1
  • 19
    • 0026499315 scopus 로고
    • Putative fragile sites in the horse karyotype
    • Rønne M: Putative fragile sites in the horse karyotype. Hereditas 117:127-136 (1992).
    • (1992) Hereditas , vol.117 , pp. 127-136
    • Rønne, M.1
  • 20
    • 0015246254 scopus 로고
    • A rapid banding technique for human chromosomes
    • Seabright M: A rapid banding technique for human chromosomes. Lancet 2:971-972 (1971).
    • (1971) Lancet , vol.2 , pp. 971-972
    • Seabright, M.1
  • 21
    • 0028988724 scopus 로고
    • The oxytocin receptor gene (OXTR) localizes to human chromosome 3p25 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids
    • Simmons CF Jr, Clancy TE, Quan R, Knoll JHM: The oxytocin receptor gene (OXTR) localizes to human chromosome 3p25 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids. Genomics 26:623-623 (1995).
    • (1995) Genomics , vol.26 , pp. 623-623
    • Simmons Jr, C.F.1    Clancy, T.E.2    Quan, R.3    Knoll, J.H.M.4
  • 22
    • 0002528624 scopus 로고
    • Genetic risks of familial reciprocal and Robertsonian translocation carriers
    • Daniel A, Liss A eds, John Wiley and Sons Ltd, New York
    • Stene J, Stengel-Rutkowski S: Genetic risks of familial reciprocal and Robertsonian translocation carriers, in Daniel A, Liss A (eds): The Cytogenetics of Mammalian Autosomal Rearrangements, pp 3-72 (John Wiley and Sons Ltd, New York 1988).
    • (1988) The Cytogenetics of Mammalian Autosomal Rearrangements , pp. 3-72
    • Stene, J.1    Stengel-Rutkowski, S.2
  • 23
    • 84860368996 scopus 로고    scopus 로고
    • Vanderwall DK, Newcombe JR, in Samper JC, Pycock JF, McKinnon AO, (eds): Current therapy in equine reproduction, early embryonic loss, pp 374-383 (Saunders Elsevier, St. Louis 2007).
    • Vanderwall DK, Newcombe JR, in Samper JC, Pycock JF, McKinnon AO, (eds): Current therapy in equine reproduction, early embryonic loss, pp 374-383 (Saunders Elsevier, St. Louis 2007).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.