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Volumn 42, Issue 3, 1997, Pages 528-531

Genomic organization and complete nucleotide sequence of the human PWP2 gene on chromosome 21

Author keywords

[No Author keywords available]

Indexed keywords

TRYPTOPHAN;

EID: 0031570671     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4761     Document Type: Article
Times cited : (5)

References (19)
  • 1
    • 0028064998 scopus 로고
    • An autosomal locus causing autoimmune disease: Autoimmune polyglandular disease type I assigned to chromosome 21
    • 1. Aaltonen, J., Björses, P., Sandkuijl, L., Perheentupa, J., and Peltonen, L. (1994). An autosomal locus causing autoimmune disease: Autoimmune polyglandular disease type I assigned to chromosome 21. Nature Genet. 8: 83-87.
    • (1994) Nature Genet. , vol.8 , pp. 83-87
    • Aaltonen, J.1    Björses, P.2    Sandkuijl, L.3    Perheentupa, J.4    Peltonen, L.5
  • 4
    • 0023305876 scopus 로고
    • Pattern matching of biological sequences with limited storage
    • 4. Gotoh, O. (1987). Pattern matching of biological sequences with limited storage. Comput. Appl. Biosci. 3: 17-20.
    • (1987) Comput. Appl. Biosci. , vol.3 , pp. 17-20
    • Gotoh, O.1
  • 5
    • 0027184311 scopus 로고
    • A NotI restriction map of the entire long arm of human chromosome 21
    • 5. Ichikawa, H., Hosoda, F., Arai, Y., Shimizu, K., Ohira, M., and Ohki, M. (1993). A NotI restriction map of the entire long arm of human chromosome 21. Nature Genet. 4: 361-366.
    • (1993) Nature Genet. , vol.4 , pp. 361-366
    • Ichikawa, H.1    Hosoda, F.2    Arai, Y.3    Shimizu, K.4    Ohira, M.5    Ohki, M.6
  • 7
    • 0031588567 scopus 로고    scopus 로고
    • Localization of 16 exons to a 450-kb region involved in the autoimmune polyglandular disease type i (APECED) on human chromosome 21q22.3
    • 7. Kudoh, J., Nagamine, K., Asakawa, S., Abe, I., Kawasaki, K., Maeda, H., Tsujimoto, S., Minoshima, S., Ito, F, and Shimizu, N. (1997). Localization of 16 exons to a 450-kb region involved in the autoimmune polyglandular disease type I (APECED) on human chromosome 21q22.3. DNA Res. 4: 45-52.
    • (1997) DNA Res. , vol.4 , pp. 45-52
    • Kudoh, J.1    Nagamine, K.2    Asakawa, S.3    Abe, I.4    Kawasaki, K.5    Maeda, H.6    Tsujimoto, S.7    Minoshima, S.8    Ito, F.9    Shimizu, N.10
  • 9
    • 0030586239 scopus 로고    scopus 로고
    • Cloning the cDNA of human PWP2, which encodes a protein with WD repeats and maps to 21q22.3
    • 9. Lalioti, M. D., Chen, H., Rossier, C., Shafaatian, R., Reid, J. D., and Antonarakis, S. E. (1996). Cloning the cDNA of human PWP2, which encodes a protein with WD repeats and maps to 21q22.3. Genomics 35: 321-327.
    • (1996) Genomics , vol.35 , pp. 321-327
    • Lalioti, M.D.1    Chen, H.2    Rossier, C.3    Shafaatian, R.4    Reid, J.D.5    Antonarakis, S.E.6
  • 11
    • 0030583302 scopus 로고    scopus 로고
    • Isolation of cDNA for a novel human protein KNP-I that is homologous to the E. Coli SCRP-27A protein from the autoimmune polyglandular disease type I (APECED) region of chromosome 21q22.3
    • 11. Nagamine, K., Kudoh, J., Minoshima, S., Kawasaki, K., Asakawa, S., Ito, F., and Shimizu, N. (1996). Isolation of cDNA for a novel human protein KNP-I that is homologous to the E. coli SCRP-27A protein from the autoimmune polyglandular disease type I (APECED) region of chromosome 21q22.3. Biochem. Biophys. Res. Commun. 225: 608-616.
    • (1996) Biochem. Biophys. Res. Commun. , vol.225 , pp. 608-616
    • Nagamine, K.1    Kudoh, J.2    Minoshima, S.3    Kawasaki, K.4    Asakawa, S.5    Ito, F.6    Shimizu, N.7
  • 12
    • 0028076764 scopus 로고
    • The ancient regulatory-protein family of WD-repeat proteins
    • 12. Neer, E. J., Schmidt, C. J., Nambudripad, R., and Smith, T. F. (1994). The ancient regulatory-protein family of WD-repeat proteins. Nature 371: 297-300.
    • (1994) Nature , vol.371 , pp. 297-300
    • Neer, E.J.1    Schmidt, C.J.2    Nambudripad, R.3    Smith, T.F.4
  • 14
    • 0029977272 scopus 로고    scopus 로고
    • A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3
    • 14. Sertié, A. L., Quimby, M., Moreira, E. S., Murray, J., Zatz, M., Antonarakis, S. E., and Passos-Bueno, M. R. (1996). A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3. Hum. Mol. Genet. 5: 843-847.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 843-847
    • Sertié, A.L.1    Quimby, M.2    Moreira, E.S.3    Murray, J.4    Zatz, M.5    Antonarakis, S.E.6    Passos-Bueno, M.R.7
  • 16
    • 0026351408 scopus 로고
    • Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach
    • 16. Uberbacher, E. C., and Mural, R. J. (1991). Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach. Proc. Natl. Acad. Sci. USA 88: 11261-11265.
    • (1991) Proc. Natl. Acad. Sci. USA , vol.88 , pp. 11261-11265
    • Uberbacher, E.C.1    Mural, R.J.2
  • 17
    • 0030070163 scopus 로고    scopus 로고
    • Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan
    • 17. Veske, A., Oehlmann, R., Younus, F., Mohyuddin, A., Müller-Myhsok, B., Mehdi, S. Q., and Gal, A. (1996). Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan. Hum. Mol. Genet. 5: 165-168.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 165-168
    • Veske, A.1    Oehlmann, R.2    Younus, F.3    Mohyuddin, A.4    Müller-Myhsok, B.5    Mehdi, S.Q.6    Gal, A.7
  • 18
    • 0029812436 scopus 로고    scopus 로고
    • A periodic tryptophan protein 2 gene homologue (PWP2H) in the candidate region of progressive myoclonus epilepsy on 21q22.3
    • 18. Yamakawa, K., Gao, D.-Q., and Korenberg, J. R. (1996). A periodic tryptophan protein 2 gene homologue (PWP2H) in the candidate region of progressive myoclonus epilepsy on 21q22.3. Cytogenet. Cell Genet. 74: 140-145.
    • (1996) Cytogenet. Cell Genet. , vol.74 , pp. 140-145
    • Yamakawa, K.1    Gao, D.-Q.2    Korenberg, J.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.