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Volumn 106, Issue 3, 2000, Pages 311-313

Illegitimate splicing of the NF1 gene in healthy individuals mimics mutation-induced splicing alterations in NF1 patients

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA;

EID: 0034112646     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390051043     Document Type: Article
Times cited : (49)

References (10)
  • 1
    • 0030746291 scopus 로고    scopus 로고
    • Inhibition of nonsense-mediated messenger RNA decay in clinical samples facilitates detection of human MSH2 mutations with an in vivo fusion protein assay and conventional techniques
    • Andreutti-Zaugg C, Scott RJ, Iggo R (1997) Inhibition of nonsense-mediated messenger RNA decay in clinical samples facilitates detection of human MSH2 mutations with an in vivo fusion protein assay and conventional techniques. Cancer Res 57:3288-3293
    • (1997) Cancer Res , vol.57 , pp. 3288-3293
    • Andreutti-Zaugg, C.1    Scott, R.J.2    Iggo, R.3
  • 2
    • 0033927894 scopus 로고    scopus 로고
    • Towards a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1
    • Eisenbarth I, Bayer K, Krone W, Assum G (2000) Towards a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1. Am J Hum Genet (in press)
    • (2000) Am J Hum Genet (In Press)
    • Eisenbarth, I.1    Bayer, K.2    Krone, W.3    Assum, G.4
  • 4
    • 0030698051 scopus 로고    scopus 로고
    • Aberrant splicing of the TSG101 and FHIT genes occurs frequently in multiple malignancies and in normal tissues and mimics alterations previously described in tumours
    • Gayther SA, Barski P, Batley SJ, Li L, de Foy KAF, Cohen SN, Ponder BAJ, Caldas C (1997) Aberrant splicing of the TSG101 and FHIT genes occurs frequently in multiple malignancies and in normal tissues and mimics alterations previously described in tumours. Oncogene 15:2119-2126
    • (1997) Oncogene , vol.15 , pp. 2119-2126
    • Gayther, S.A.1    Barski, P.2    Batley, S.J.3    Li, L.4    De Foy, K.A.F.5    Cohen, S.N.6    Ponder, B.A.J.7    Caldas, C.8
  • 7
    • 0031439698 scopus 로고    scopus 로고
    • Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 gene
    • Messiaen L, Callens T, De Paepe A, Craen M, Mortier G (1997) Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 gene. Hum Genet 101:75-80
    • (1997) Hum Genet , vol.101 , pp. 75-80
    • Messiaen, L.1    Callens, T.2    De Paepe, A.3    Craen, M.4    Mortier, G.5
  • 8
    • 0031657522 scopus 로고    scopus 로고
    • Neurofibromatosis type 1 (NF1): A protein truncation assay yielding identification of mutations in 73% of patients
    • Park VM, Pivnick EK (1998) Neurofibromatosis type 1 (NF1): a protein truncation assay yielding identification of mutations in 73% of patients. J Med Genet 35:813-820
    • (1998) J Med Genet , vol.35 , pp. 813-820
    • Park, V.M.1    Pivnick, E.K.2
  • 9
    • 0030024492 scopus 로고    scopus 로고
    • Molecular genetics of neurofibromatosis type 1 (NF1)
    • Shen MH, Harper PS, Upadhyaya M (1996) Molecular genetics of neurofibromatosis type 1 (NF1). J Med Genet 33:2-17
    • (1996) J Med Genet , vol.33 , pp. 2-17
    • Shen, M.H.1    Harper, P.S.2    Upadhyaya, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.