메뉴 건너뛰기




Volumn 4, Issue 6, 2010, Pages 352-357

Cytogenetic and genetic studies in a hypospadic horse (Equus caballus, 2n = 64)

Author keywords

Chromosome deletion; Gene mutation; Horse; Hypospadias; MAMLD1

Indexed keywords

EQUIDAE; EQUUS CABALLUS; FRIESIA;

EID: 78049322862     PISSN: 16615425     EISSN: 16615433     Source Type: Journal    
DOI: 10.1159/000319527     Document Type: Article
Times cited : (11)

References (25)
  • 2
    • 63449116753 scopus 로고    scopus 로고
    • 11p microdeletion including WT1 but not PAX6, presenting with cataract, mental retardation, genital abnormalities and seizures: A case report
    • Almind GJ, Brøndum-Nielsen K, Bangsgaard R, Baekgaard P, Grønskov K: 11p microdeletion including WT1 but not PAX6, presenting with cataract, mental retardation, genital abnormalities and seizures: a case report. Mol Cytogenet 2: 6 (2009).
    • (2009) Mol Cytogenet , vol.2 , pp. 6
    • Almind, G.J.1    Brøndum-Nielsen, K.2    Bangsgaard, R.3    Baekgaard, P.4    Grønskov, K.5
  • 3
    • 6344229471 scopus 로고    scopus 로고
    • Linkage between cryptorchidism, hypospadias, and GGN repeat length in the androgen receptor gene
    • Aschim EL, Nordenskjold A, Giwercman A, Lundin KB, Ruhayel Y, et al: Linkage between cryptorchidism, hypospadias, and GGN repeat length in the androgen receptor gene. J Clin Endocr Metab 89: 5105-510 9 (2004).
    • (2004) J Clin Endocr Metab , vol.89 , pp. 5105-5109
    • Aschim, E.L.1    Nordenskjold, A.2    Giwercman, A.3    Lundin, K.B.4    Ruhayel, Y.5
  • 4
    • 1842826354 scopus 로고    scopus 로고
    • Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity
    • Aslan H, Karaca N, Basaran S, Ermis H, Ceylan Y: Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity. BMC Pregnancy and Childbirth 3: 1-6 (2003).
    • (2003) BMC Pregnancy and Childbirth , vol.3 , pp. 1-6
    • Aslan, H.1    Karaca, N.2    Basaran, S.3    Ermis, H.4    Ceylan, Y.5
  • 5
    • 67650066484 scopus 로고    scopus 로고
    • Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability
    • Belligni EF, Biamino E, Molinatto C, Messa J, Pierluigi M, et al: Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability. It J Pediatr 35: 9-18 (2009).
    • (2009) It J Pediatr , vol.35 , pp. 9-18
    • Belligni, E.F.1    Biamino, E.2    Molinatto, C.3    Messa, J.4    Pierluigi, M.5
  • 6
    • 34248161063 scopus 로고    scopus 로고
    • Clinical, cytogenetic and hormonal findings in a stallion with hypospadias-a case report
    • Bleul U, Theiss F, Rutten M, Kahn W: Clinical, cytogenetic and hormonal findings in a stallion with hypospadias-a case report. Vet J 173: 679-682 (2007).
    • (2007) Vet J , vol.173 , pp. 679-682
    • Bleul, U.1    Theiss, F.2    Rutten, M.3    Kahn, W.4
  • 7
    • 43449098565 scopus 로고    scopus 로고
    • Clinical, cytogenetic and molecular evaluation in a dog with bilateral cryptorchidism and hypospadias
    • Cassata R, Iannuzzi A, Parma P, De Lorenzi L, Peretti V, et al: Clinical, cytogenetic and molecular evaluation in a dog with bilateral cryptorchidism and hypospadias. Cytogenet Genome Res 120: 140-143 (2008).
    • (2008) Cytogenet Genome Res , vol.120 , pp. 140-143
    • Cassata, R.1    Iannuzzi, A.2    Parma, P.3    De Lorenzi, L.4    Peretti, V.5
  • 8
    • 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
  • 9
    • 0018569779 scopus 로고
    • A gene for hypospadias in a child with presumed tetra-somy 18p
    • Cote GB, Petmezaki S, Bastakis N: A gene for hypospadias in a child with presumed tetra-somy 18p. Am J Med Genet 4: 141-146 (1979).
    • (1979) Am J Med Genet , vol.4 , pp. 141-146
    • Cote, G.B.1    Petmezaki, S.2    Bastakis, N.3
  • 10
    • 77951276881 scopus 로고    scopus 로고
    • Substitution of Ile(707) for Leu in Klentaq DNA polymerase reduces the amplification capacity of the enzyme
    • Davalieva K, Efremov DG: Substitution of Ile(707) for Leu in Klentaq DNA polymerase reduces the amplification capacity of the enzyme. Prilozi 30: 57-69 (2009).
    • (2009) Prilozi , vol.30 , pp. 57-69
    • Davalieva, K.1    Efremov, D.G.2
  • 11
    • 0242607574 scopus 로고    scopus 로고
    • Microduplication 22q11.2, an emerging syndrome: Clinical, cy-togenetic, and molecular analysis of thirteen patients
    • Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM et al: Microduplication 22q11.2, an emerging syndrome: clinical, cy-togenetic, and molecular analysis of thirteen patients. Am J Hum Genet 73: 1027-1040 (2003).
    • (2003) Am J Hum Genet , vol.73 , pp. 1027-1040
    • Ensenauer, R.E.1    Adeyinka, A.2    Flynn, H.C.3    Michels, V.V.4    Lindor, N.M.5
  • 14
    • 33746358497 scopus 로고    scopus 로고
    • Deletion mapping of critical region for hypospadias, penoscrotal transposition and imperforate anus on human chromosome 13
    • Garcia NM, Allgood J, Santos LJ, Lonergan D, Batanian JR, et al: Deletion mapping of critical region for hypospadias, penoscrotal transposition and imperforate anus on human chromosome 13. J Pediatr Urol 2: 233-242 (2006).
    • (2006) J Pediatr Urol , vol.2 , pp. 233-242
    • Garcia, N.M.1    Allgood, J.2    Santos, L.J.3    Lonergan, D.4    Batanian, J.R.5
  • 15
    • 56649088076 scopus 로고    scopus 로고
    • Tools of the trade: Diagnostics and research in domestic animal cytogenetics
    • Iannuzzi L, Di Berardino D: Tools of the trade: diagnostics and research in domestic animal cytogenetics. J Appl Genet 49: 357-366 (2008).
    • (2008) J Appl Genet , vol.49 , pp. 357-366
    • Iannuzzi, L.1    Di Berardino, D.2
  • 16
    • 0031263425 scopus 로고    scopus 로고
    • International system for cytogenetic nomenclature of the domestic horse
    • ISCNH Committee
    • ISCNH: International system for cytogenetic nomenclature of the domestic horse (AT Bowling, M Breen, BP Chowdhary, et al., Committee). Chromosome Res 5: 433-443 (1997).
    • (1997) Chromosome Res , vol.5 , pp. 433-443
    • Bowling, A.T.1    Breen, M.2    Chowdhary, B.P.3
  • 17
    • 33750489078 scopus 로고    scopus 로고
    • R-spond in1 is essentia l i n sex determination skin differentiation and malignancy
    • Parma P, Radi O, Vidal V, Chaboissier MC, Del-lambr a E , et al: R-spond in1 is essentia l i n sex determination, skin differentiation and malignancy. Nat Genet 38: 1304-1309 (2006).
    • (2006) Nat Genet , vol.38 , pp. 1304-1309
    • Parma, P.1    Radi, O.2    Vidal, V.3    Chaboissier, M.C.4    Del-Lambra, E.5
  • 18
    • 33745226965 scopus 로고    scopus 로고
    • Subtelomere FISH analysis of 11 688 cases: An evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities
    • Ravnan JB, Tepperberg JH, Papenhausen P, Lamb AN, Hedrick J, et al: Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities. J Med Genet 43: 478-489 (2006).
    • (2006) J Med Genet , vol.43 , pp. 478-489
    • Ravnan, J.B.1    Tepperberg, J.H.2    Papenhausen, P.3    Lamb, A.N.4    Hedrick, J.5
  • 22
    • 50649094002 scopus 로고    scopus 로고
    • A new susceptibility locus for hypospadias on chromosome 7q32.2-q36.1
    • Thai HTT, Soderhall C, Lagerstedt K, Omrani MD, Frisen L, et al: A new susceptibility locus for hypospadias on chromosome 7q32.2-q36.1. Hum Genet 124: 155-160 (2008).
    • (2008) Hum Genet , vol.124 , pp. 155-160
    • Htt, T.1    Soderhall, C.2    Lagerstedt, K.3    Omrani, M.D.4    Frisen, L.5
  • 23
    • 0032192178 scopus 로고    scopus 로고
    • Cloning and characterization of the equine F18 gene, which has a novel exon
    • Tozaki T, Hirota K, Mashima S, Tomita M, Mu-koyama H: Cloning and characterization of the equine F18 gene, which has a novel exon. Animal Genet 29: 381-384 (1998).
    • (1998) Animal Genet , vol.29 , pp. 381-384
    • Tozaki, T.1    Hirota, K.2    Mashima, S.3    Tomita, M.4    Mu-Koyama, H.5
  • 24
    • 0037270548 scopus 로고    scopus 로고
    • Ile-Leu substitution (I415L) in germline E-cadherin gene (CDH1) in Japanese familial gastric cancer
    • Wang Y, Song JP, Ikeda M, Shinmura K, Yokota J, Sugimura H: Ile-Leu substitution (I415L) in germline E-cadherin gene (CDH1) in Japanese familial gastric cancer. Jpn J Clin Oncol 33: 17-20 (2003).
    • (2003) Jpn J Clin Oncol , vol.33 , pp. 17-20
    • Wang, Y.1    Song, J.P.2    Ikeda, M.3    Shinmura, K.4    Yokota, J.5    Sugimura, H.6
  • 25
    • 20544435269 scopus 로고    scopus 로고
    • 3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome
    • Willatt L, Cox J, Barber J, Cabanas ED, Collins A, et al: 3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome. Am J Hum Genet 77: 154-160 (2005).
    • (2005) Am J Hum Genet , vol.77 , pp. 154-160
    • Willatt, L.1    Cox, J.2    Barber, J.3    Cabanas, E.D.4    Collins, A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.