메뉴 건너뛰기




Volumn 10, Issue 6, 2000, Pages 425-429

Immunohistochemical staining of dystrophin on formalin-fixed paraffin-embedded sections in Duchenne/Becker muscular dystrophy and manifesting carriers of Duchenne muscular dystrophy

Author keywords

Catalyzed signal amplification system; Dystrophin; Immunohistochemical staining; Muscle tissue

Indexed keywords

ANTIBODY; DYSTROPHIN; MONOCLONAL ANTIBODY; PEROXIDASE;

EID: 0034255708     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(99)00116-9     Document Type: Article
Times cited : (16)

References (19)
  • 1
    • 0023614188 scopus 로고
    • Dystrophin: The protein product of the Duchenne muscular dystrophy locus
    • Hoffman E.P., Brown R.H., Kunkel L.M. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell. 51:1987;919-928.
    • (1987) Cell , vol.51 , pp. 919-928
    • Hoffman, E.P.1    Brown, R.H.2    Kunkel, L.M.3
  • 2
    • 0024466501 scopus 로고
    • The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion
    • Koenig M., Beggs A.H., Moyer M., et al. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Am J Hum Genet. 45:1989;498-506.
    • (1989) Am J Hum Genet , vol.45 , pp. 498-506
    • Koenig, M.1    Beggs, A.H.2    Moyer, M.3
  • 3
    • 0024815723 scopus 로고
    • Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications
    • denDunnen J.T., Grootscholten P.M., Bakker E., et al. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. Am J Hum Genet. 45:1989;835-847.
    • (1989) Am J Hum Genet , vol.45 , pp. 835-847
    • Dendunnen, J.T.1    Grootscholten, P.M.2    Bakker, E.3
  • 4
    • 0025320994 scopus 로고
    • Duplicational mutation at the Duchenne muscular dystrophy locus: Its frequency, distribution, origin, and phenotypegenotype correlation
    • Hu X., Ray P.N., Murphy E.G., Thompson M.W., Worton R. Duplicational mutation at the Duchenne muscular dystrophy locus: Its frequency, distribution, origin, and phenotypegenotype correlation. Am J Hum Genet. 46:1990;682-695.
    • (1990) Am J Hum Genet , vol.46 , pp. 682-695
    • Hu, X.1    Ray, P.N.2    Murphy, E.G.3    Thompson, M.W.4    Worton, R.5
  • 5
    • 0028343781 scopus 로고
    • Heteroduplex analysis of the Dystrophin gene: Application to point mutation and carrier detection
    • Prior T.W., Papp A.C., Syder P.J., et al. Heteroduplex analysis of the Dystrophin gene: application to point mutation and carrier detection. Am J Med Genet. 50:1994;68-73.
    • (1994) Am J Med Genet , vol.50 , pp. 68-73
    • Prior, T.W.1    Papp, A.C.2    Syder, P.J.3
  • 6
    • 0029020724 scopus 로고
    • The identification of point mutations in Duchenne muscular dystrophy patients by using reverse-transcription PCR and the protein truncation test
    • Gardner R.J., Bobrow M., Roberts R.G. The identification of point mutations in Duchenne muscular dystrophy patients by using reverse-transcription PCR and the protein truncation test. Am J Hum Genet. 57:1995;311-320.
    • (1995) Am J Hum Genet , vol.57 , pp. 311-320
    • Gardner, R.J.1    Bobrow, M.2    Roberts, R.G.3
  • 7
    • 0030817080 scopus 로고    scopus 로고
    • Novel point mutations in the dystrophin gene
    • Sitnik R., Campiotto S., Vainzof M., et al. Novel point mutations in the dystrophin gene. Hum Mutat. 10:1997;217-222.
    • (1997) Hum Mutat , vol.10 , pp. 217-222
    • Sitnik, R.1    Campiotto, S.2    Vainzof, M.3
  • 8
    • 0023718395 scopus 로고
    • Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface
    • Bonilla E., Samitt C.E., Miranda A.F., et al. Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface. Cell. 54:1988;447-452.
    • (1988) Cell , vol.54 , pp. 447-452
    • Bonilla, E.1    Samitt, C.E.2    Miranda, A.F.3
  • 9
    • 0024537135 scopus 로고
    • Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy
    • Arahata K., Ishihara T., Kamakura K., et al. Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy. N Engl J Med. 320:1989;138-142.
    • (1989) N Engl J Med , vol.320 , pp. 138-142
    • Arahata, K.1    Ishihara, T.2    Kamakura, K.3
  • 10
    • 0026625337 scopus 로고
    • The use of catalyzed reporter deposition as a means of signal amplification in a variety of formats
    • Bobrow M.N., Litt G.J., Shaughnessy K.J., Mayer P.C., Conlon J. The use of catalyzed reporter deposition as a means of signal amplification in a variety of formats. J Immunol Methods. 150:1992;145-149.
    • (1992) J Immunol Methods , vol.150 , pp. 145-149
    • Bobrow, M.N.1    Litt, G.J.2    Shaughnessy, K.J.3    Mayer, P.C.4    Conlon, J.5
  • 11
    • 0026686751 scopus 로고
    • Biotin amplification of biotin and horseradish peroxidase signals in histochemical stains
    • Adams J.C. Biotin amplification of biotin and horseradish peroxidase signals in histochemical stains. J Histochem Cytochem. 40:1992;1457-1463.
    • (1992) J Histochem Cytochem , vol.40 , pp. 1457-1463
    • Adams, J.C.1
  • 12
    • 0024245082 scopus 로고
    • Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification
    • Chamberlain J.S., Gibbs R.A., Ranier J.E., Nguyen P.N., Caskey C.T. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic Acids Res. 16:1988;11141-11156.
    • (1988) Nucleic Acids Res , vol.16 , pp. 11141-11156
    • Chamberlain, J.S.1    Gibbs, R.A.2    Ranier, J.E.3    Nguyen, P.N.4    Caskey, C.T.5
  • 13
    • 0025244924 scopus 로고
    • Detection of 98% of DMD/ BMD gene deletions by polymerase chain reaction
    • Beggs A.H., Koenig M., Boyce F.M., Kunkel L.M. Detection of 98% of DMD/ BMD gene deletions by polymerase chain reaction. Hum Genet. 86:1990;45-48.
    • (1990) Hum Genet , vol.86 , pp. 45-48
    • Beggs, A.H.1    Koenig, M.2    Boyce, F.M.3    Kunkel, L.M.4
  • 15
    • 0032525109 scopus 로고    scopus 로고
    • Demonstration of Kaposi's sarcoma-associated herpes virus cyclin D homolog in cutaneous Kaposi's sarcoma by colorimetric in situ hybridization using a catalyzed signal amplification system
    • Reed J.A., Nador R.G., Spaulding D., Tani Y., Cesarman E., Knowles D.M. Demonstration of Kaposi's sarcoma-associated herpes virus cyclin D homolog in cutaneous Kaposi's sarcoma by colorimetric in situ hybridization using a catalyzed signal amplification system. Blood. 91:1998;3825-3832.
    • (1998) Blood , vol.91 , pp. 3825-3832
    • Reed, J.A.1    Nador, R.G.2    Spaulding, D.3    Tani, Y.4    Cesarman, E.5    Knowles, D.M.6
  • 16
    • 0030700222 scopus 로고    scopus 로고
    • Expression of epidermal growth factor receptor in fetal mouse submandibular gland detected by a biotinyltyramide-based catalyzed signal amplification method
    • Gresik E.W., Kashimata M., Kadoya Y., Mathews R., Minami N., Yamashina S. Expression of epidermal growth factor receptor in fetal mouse submandibular gland detected by a biotinyltyramide-based catalyzed signal amplification method. J Histochem Cytochem. 45:1997;1651-1657.
    • (1997) J Histochem Cytochem , vol.45 , pp. 1651-1657
    • Gresik, E.W.1    Kashimata, M.2    Kadoya, Y.3    Mathews, R.4    Minami, N.5    Yamashina, S.6
  • 17
    • 0029893802 scopus 로고    scopus 로고
    • Application of catalyzed signal amplification in immunodetection of gonadotropin subunits in clinically nonfunctioning pituitary adenomas
    • Sanno N., Teramoto A., Sugiyama M., Itoh Y., Osamura Y. Application of catalyzed signal amplification in immunodetection of gonadotropin subunits in clinically nonfunctioning pituitary adenomas. Clin Pathol. 106:1996;16-21.
    • (1996) Clin Pathol , vol.106 , pp. 16-21
    • Sanno, N.1    Teramoto, A.2    Sugiyama, M.3    Itoh, Y.4    Osamura, Y.5
  • 18
    • 0023134993 scopus 로고
    • Localization and cloning of Xp2l deletion breakpoints involved in muscular dystrophy
    • Monaco A.P., Bertelson C.J., Coletti-Feener C., Kunkel L.M. Localization and cloning of Xp2l deletion breakpoints involved in muscular dystrophy. Hum Genet. 75:1987;221-227.
    • (1987) Hum Genet , vol.75 , pp. 221-227
    • Monaco, A.P.1    Bertelson, C.J.2    Coletti-Feener, C.3    Kunkel, L.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.