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Volumn 56, Issue 2, 1999, Pages 179-183

Genomic structure, chromosomal mapping, and expression pattern of human DCAMKL1 (KIAA0369), a homologue of DCX (XLIS)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN KINASE (CALCIUM,CALMODULIN);

EID: 0033104802     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1998.5673     Document Type: Article
Times cited : (36)

References (14)
  • 3
    • 0029000061 scopus 로고
    • Lissencephaly and other malformations of cortical development: 1995 update
    • Dobyns W. B., Truwit C. L. Lissencephaly and other malformations of cortical development: 1995 update. Neuropediatrics. 23:1995;132-147.
    • (1995) Neuropediatrics , vol.23 , pp. 132-147
    • Dobyns, W.B.1    Truwit, C.L.2
  • 4
    • 0029032393 scopus 로고
    • Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q
    • Eiberg H., Berendt I., Mohr J. Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q. Nat. Genet. 10:1995;354-356.
    • (1995) Nat. Genet. , vol.10 , pp. 354-356
    • Eiberg, H.1    Berendt, I.2    Mohr, J.3
  • 7
    • 0031040866 scopus 로고    scopus 로고
    • Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome
    • Lo Nigro C., Chong S. S., Smith A. C. M., Dobyns W. B., Ledbetter D. H. Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome. Hum. Mol. Genet. 6:1997;157-164.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 157-164
    • Lo Nigro, C.1    Chong, S.S.2    Smith, A.C.M.3    Dobyns, W.B.4    Ledbetter, D.H.5
  • 8
    • 0031589004 scopus 로고    scopus 로고
    • Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro
    • Nagase T., Ishikawa K., Nakajima D., Ohira M., Seki N., Miyajima N., Tanaka A., Kotani H., Nomura N., Ohara O. Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro. DNA Res. 4:1997;141-150.
    • (1997) DNA Res. , vol.4 , pp. 141-150
    • Nagase, T.1    Ishikawa, K.2    Nakajima, D.3    Ohira, M.4    Seki, N.5    Miyajima, N.6    Tanaka, A.7    Kotani, H.8    Nomura, N.9    Ohara, O.10
  • 9
    • 0031588576 scopus 로고    scopus 로고
    • Construction and characterization of human brain cDNA libraries suitable for analysis of cDNA clones encoding relatively large proteins
    • Ohara O., Nagase T., Ishikawa K., Nakajima D., Ohira M., Seki N., Nomura N. Construction and characterization of human brain cDNA libraries suitable for analysis of cDNA clones encoding relatively large proteins. DNA Res. 4:1997;53-59.
    • (1997) DNA Res. , vol.4 , pp. 53-59
    • Ohara, O.1    Nagase, T.2    Ishikawa, K.3    Nakajima, D.4    Ohira, M.5    Seki, N.6    Nomura, N.7
  • 10
    • 0031613727 scopus 로고    scopus 로고
    • Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to doublecortin
    • Omori Y., Suzuki M., Ozaki K., Harada Y., Nakamura Y., Takahashi E.-I., Fujiwara T. Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to doublecortin. J. Hum. Genet. 43:1998;169-177.
    • (1998) J. Hum. Genet. , vol.43 , pp. 169-177
    • Omori, Y.1    Suzuki, M.2    Ozaki, K.3    Harada, Y.4    Nakamura, Y.5    Takahashi, E.-I.6    Fujiwara, T.7
  • 13
    • 0025884458 scopus 로고
    • Deletion of chromosome 13 in Moebius syndrome
    • Slee J. J., Smart R. D., Viljoen D. L. Deletion of chromosome 13 in Moebius syndrome. J. Med. Genet. 28:1991;413-414.
    • (1991) J. Med. Genet. , vol.28 , pp. 413-414
    • Slee, J.J.1    Smart, R.D.2    Viljoen, D.L.3
  • 14
    • 0017626152 scopus 로고
    • Three-generation pedigree of a Moebius syndrome variant with chromosome translocation
    • Ziter F. A., Wiser W. C., Robinson A. Three-generation pedigree of a Moebius syndrome variant with chromosome translocation. Arch. Neurol. 34:1977;437-442.
    • (1977) Arch. Neurol. , vol.34 , pp. 437-442
    • Ziter, F.A.1    Wiser, W.C.2    Robinson, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.