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Volumn 55, Issue 1, 2014, Pages 57-60

Presentation and management of trapped neutrophil syndrome (TNS) in UK border collies

Author keywords

[No Author keywords available]

Indexed keywords

CANIS FAMILIARIS;

EID: 84891662980     PISSN: 00224510     EISSN: 17485827     Source Type: Journal    
DOI: 10.1111/jsap.12134     Document Type: Article
Times cited : (11)

References (17)
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    • Neutropenia with a probable hereditary basis in Border Collies
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    • (1996) New Zealand Veterinary Journal , vol.44 , pp. 67-72
    • Allan, F.J.1    Thompson, K.G.2    Jones, B.R.3
  • 2
    • 0015831045 scopus 로고
    • A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies
    • Cohen Jr, M. M., Hall, B. D., Smith, D. W., etal. (1973) A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies. Journal of Pediatrics 83, 280-284
    • (1973) Journal of Pediatrics , vol.83 , pp. 280-284
    • Cohen Jr., M.M.1    Hall, B.D.2    Smith, D.W.3
  • 4
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    • Clinical variability of genetic isolates of Cohen syndrome
    • Douzgou, S. & Petersen, M. B. (2011) Clinical variability of genetic isolates of Cohen syndrome. Clinical Genetics 79, 501-506
    • (2011) Clinical Genetics , vol.79 , pp. 501-506
    • Douzgou, S.1    Petersen, M.B.2
  • 6
    • 3042546822 scopus 로고    scopus 로고
    • Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen Syndrome
    • Hennies, H. C., Rauch, A., Seifert, W., etal. (2004) Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen Syndrome. American Journal of Human Genetics 75, 138-145
    • (2004) American Journal of Human Genetics , vol.75 , pp. 138-145
    • Hennies, H.C.1    Rauch, A.2    Seifert, W.3
  • 7
    • 0032858635 scopus 로고    scopus 로고
    • Cohen syndrome: evaluation of its cardiac, endocrine and radiological features
    • Kivitie-Kallio, S., Eronen, M., Lipsanen-Nyman, M., etal. (1999) Cohen syndrome: evaluation of its cardiac, endocrine and radiological features. Clinical Genetics 56, 41-50
    • (1999) Clinical Genetics , vol.56 , pp. 41-50
    • Kivitie-Kallio, S.1    Eronen, M.2    Lipsanen-Nyman, M.3
  • 8
    • 0038353767 scopus 로고    scopus 로고
    • Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport
    • Kolehmainen, J., Black, G. C. M., Saarinen, A., etal. (2003) Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport. American Journal of Human Genetics 72, 1359-1369
    • (2003) American Journal of Human Genetics , vol.72 , pp. 1359-1369
    • Kolehmainen, J.1    Black, G.C.M.2    Saarinen, A.3
  • 11
    • 84863786195 scopus 로고    scopus 로고
    • Trapped neutrophil syndrome in a Border Collie dog: clinical, clinico-pathologic, and molecular findings
    • Mizukami, K., Shoubudani, T., Nishimoto, S., etal. (2012) Trapped neutrophil syndrome in a Border Collie dog: clinical, clinico-pathologic, and molecular findings. The Journal of Veterinary Medical Science 74, 797-800
    • (2012) The Journal of Veterinary Medical Science , vol.74 , pp. 797-800
    • Mizukami, K.1    Shoubudani, T.2    Nishimoto, S.3
  • 12
    • 77957154320 scopus 로고    scopus 로고
    • High frequency of COH1 intragenic deletions and duplications detected by MLPA in patients with Cohen syndrome
    • Parri, V., Katzaki, E., Uliana, V., etal. (2010) High frequency of COH1 intragenic deletions and duplications detected by MLPA in patients with Cohen syndrome. European Journal of Human Genetics 18, 1133-1140
    • (2010) European Journal of Human Genetics , vol.18 , pp. 1133-1140
    • Parri, V.1    Katzaki, E.2    Uliana, V.3
  • 14
    • 64049096972 scopus 로고    scopus 로고
    • Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1
    • Seifert, W., Holder-Espinasse, M., Kühnisch, J., etal. (2009) Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1. Human Mutation 30, E404-420
    • (2009) Human Mutation , vol.30
    • Seifert, W.1    Holder-Espinasse, M.2    Kühnisch, J.3
  • 15
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    • Cohen syndrome-associated protein, COH1, is a novel, giant Golgi matrix protein required for Golgi integrity
    • Seifert, W., Kühnisch, J., Maritzen, T., etal. (2011) Cohen syndrome-associated protein, COH1, is a novel, giant Golgi matrix protein required for Golgi integrity. Journal of Biological Chemistry 286, 37665-37675
    • (2011) Journal of Biological Chemistry , vol.286 , pp. 37665-37675
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  • 16
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    • A canine model of Cohen syndrome: trapped neutrophil syndrome
    • Shearman, J. R. & Wilton, A. N. (2011) A canine model of Cohen syndrome: trapped neutrophil syndrome. BMC Genomics 12, 258
    • (2011) BMC Genomics , vol.12 , pp. 258
    • Shearman, J.R.1    Wilton, A.N.2
  • 17
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    • Long-term management of trapped neutrophil syndrome in two border collies
    • Wouda, R. M., King, T.J. & Mackay, B. M. (2010) Long-term management of trapped neutrophil syndrome in two border collies. Australian Veterinary Practice 40, 58-63
    • (2010) Australian Veterinary Practice , vol.40 , pp. 58-63
    • Wouda, R.M.1    King, T.J.2    Mackay, B.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.