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Volumn 5, Issue 5, 1996, Pages 633-638

Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes

Author keywords

[No Author keywords available]

Indexed keywords

CELL RECEPTOR; LAMININ;

EID: 0029990051     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.5.633     Document Type: Article
Times cited : (32)

References (39)
  • 1
    • 0022939117 scopus 로고
    • The DiGeorge anomaly as a developmental field defect
    • Lammer, E. J., Opitz, J. M. (1986) The DiGeorge anomaly as a developmental field defect. Am. J. Med. Genet., Suppl. 2, 113-127.
    • (1986) Am. J. Med. Genet., Suppl. , vol.2 , pp. 113-127
    • Lammer, E.J.1    Opitz, J.M.2
  • 2
    • 0027374991 scopus 로고
    • DiGeorge syndrome: An historical review of clinical and cytogenetic features
    • Greenberg, F. (1993) DiGeorge syndrome: an historical review of clinical and cytogenetic features. J. Med. Genet., 30, 803-806.
    • (1993) J. Med. Genet. , vol.30 , pp. 803-806
    • Greenberg, F.1
  • 8
    • 0026725876 scopus 로고
    • Deletions within chromosome 22q11 in familial congenital heart disease
    • Wilson, D. I., Goodship, J. A., Burn, J., Cross, I. E. and Scambler, P. J. (1992) Deletions within chromosome 22q11 in familial congenital heart disease. Lancet, 340, 573-575.
    • (1992) Lancet , vol.340 , pp. 573-575
    • Wilson, D.I.1    Goodship, J.A.2    Burn, J.3    Cross, I.E.4    Scambler, P.J.5
  • 11
    • 0028006688 scopus 로고
    • Pulmonary atresia associated with maternal 22q11.2 deletion: Possible parent of origin effect in the conotruncal anomaly face syndrome
    • Seaver, L.H., Pierpont, J.W., Erickson, R.P., Donnerstein, R.L., Cassidy, S.B. (1994) Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome. J. Med. Genet., 31, 830-834.
    • (1994) J. Med. Genet. , vol.31 , pp. 830-834
    • Seaver, L.H.1    Pierpont, J.W.2    Erickson, R.P.3    Donnerstein, R.L.4    Cassidy, S.B.5
  • 14
    • 0029156177 scopus 로고
    • DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review
    • Demczuk, S. and Aurias, A. (1995) DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review. Ann. Genet , 38, 59-76.
    • (1995) Ann. Genet , vol.38 , pp. 59-76
    • Demczuk, S.1    Aurias, A.2
  • 18
    • 0028958564 scopus 로고
    • Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity
    • Demczuk, S. Aledo, R., Zucman, J , Delattre, O., Desmaze, C., Dauphinot, L., Jalbert, P., Rouleau, G.A., Thomas, G. and Aurias, A. (1995) Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity. Hum. Mol. Genet., 4, 551-558.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 551-558
    • Demczuk, S.1    Aledo, R.2    Zucman, J.3    Delattre, O.4    Desmaze, C.5    Dauphinot, L.6    Jalbert, P.7    Rouleau, G.A.8    Thomas, G.9    Aurias, A.10
  • 19
    • 0029065469 scopus 로고
    • Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome
    • Wadey, R., Daw, S., Taylor, C., Atif, U., Kamath, S., Halford, S., O'Donnell, H., Wilson, D., Goodship, J., Burn, J., Scambler, P. (1995) Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome. Hum. Mol. Genet , 4, 1027-1033.
    • (1995) Hum. Mol. Genet , vol.4 , pp. 1027-1033
    • Wadey, R.1    Daw, S.2    Taylor, C.3    Atif, U.4    Kamath, S.5    Halford, S.6    O'Donnell, H.7    Wilson, D.8    Goodship, J.9    Burn, J.10    Scambler, P.11
  • 20
    • 0029150085 scopus 로고
    • Localization of the human mitochondrial citrate transporter protein gene to chromosome 22q11 in the DiGeorge syndrome critical region
    • Heisterkamp, N., Mulder, M. P., Langeveld, A., Ten Hoeve, J., Wang, Z., Roe, B A. and Groffen, J. (1995) Localization of the human mitochondrial citrate transporter protein gene to chromosome 22q11 in the DiGeorge syndrome critical region Genomics, 29, 451-456.
    • (1995) Genomics , vol.29 , pp. 451-456
    • Heisterkamp, N.1    Mulder, M.P.2    Langeveld, A.3    Ten Hoeve, J.4    Wang, Z.5    Roe, B.A.6    Groffen, J.7
  • 23
    • 0023665902 scopus 로고
    • An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs
    • Kozak, M. (1987) An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res. 15, 8125-8148.
    • (1987) Nucleic Acids Res. , vol.15 , pp. 8125-8148
    • Kozak, M.1
  • 24
    • 0024618904 scopus 로고
    • Overlapping genes of Drosophila melanogaster, organization of the z600-gonadal-Etp28/29 gene cluster
    • Schulz, R. A. and Butler, B.A. (1989) Overlapping genes of Drosophila melanogaster, organization of the z600-gonadal-Etp28/29 gene cluster. Genes Dev. 3, 232-242
    • (1989) Genes Dev. , vol.3 , pp. 232-242
    • Schulz, R.A.1    Butler, B.A.2
  • 26
    • 0023924807 scopus 로고
    • Human laminin B2 chain. Comparison of the complete amino acid sequence with the B1 chain reveals variability in sequence homology between different structural domains
    • Pikkarainen, T., Kallunki, T. and Tryggvason, K. (1988) Human laminin B2 chain. Comparison of the complete amino acid sequence with the B1 chain reveals variability in sequence homology between different structural domains. J Biol. Chem., 263, 6751-6758.
    • (1988) J Biol. Chem. , vol.263 , pp. 6751-6758
    • Pikkarainen, T.1    Kallunki, T.2    Tryggvason, K.3
  • 28
    • 0026442649 scopus 로고
    • Laminins and other strange proteins
    • Engel, J (1992) Laminins and other strange proteins. Biochemistry, 31, 10643-10651.
    • (1992) Biochemistry , vol.31 , pp. 10643-10651
    • Engel, J.1
  • 29
    • 0028869111 scopus 로고
    • Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome
    • Lévy, A., Demczuk, S., Aurias, A., Dépetris, D., M.-G. Mattei and Philip, N. (1995) Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome. Hum. Mol. Genet., 4, 2417.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 2417
    • Lévy, A.1    Demczuk, S.2    Aurias, A.3    Dépetris, D.4    Mattei, M.-G.5    Philip, N.6
  • 33
    • 0028133599 scopus 로고
    • Junctional epidermolysis bullosa inversa (locus EBR2A) assigned to 1q31 by linkage and asscciation of LAMCI
    • Gedde-Dahl, T., Dupuy, B M., Jonassen, R., Winberg, J.-O., Anton-Lamprecht, I. and Olaisen, B. (1994) Junctional epidermolysis bullosa inversa (locus EBR2A) assigned to 1q31 by linkage and asscciation of LAMCI. Hum. Mol. Genet., 3, 1387-1391.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1387-1391
    • Gedde-Dahl, T.1    Dupuy, B.M.2    Jonassen, R.3    Winberg, J.-O.4    Anton-Lamprecht, I.5    Olaisen, B.6
  • 34
    • 0024992614 scopus 로고
    • Role of neural crest in congenital heart disease
    • Kirby, M.L., Waldo, K.L. (1990) Role of neural crest in congenital heart disease. Circulation, 82, 332-340
    • (1990) Circulation , vol.82 , pp. 332-340
    • Kirby, M.L.1    Waldo, K.L.2
  • 36
    • 0027184851 scopus 로고
    • Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly
    • Palacios, J., Gamallo, C., García, M., Rodriguez, J. I. (1993) Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly Am. J. Med. Genet., 46, 641-646.
    • (1993) Am. J. Med. Genet. , vol.46 , pp. 641-646
    • Palacios, J.1    Gamallo, C.2    García, M.3    Rodriguez, J.I.4
  • 37
    • 0028204058 scopus 로고
    • Neural crest cell interactions with laminin: Structural requirements and localization of the binding site for α1β1 integrin
    • Lallier, T., Deutzmann, R., Perris, R. and Bronner-Fraser, M. (1994) Neural crest cell interactions with laminin: structural requirements and localization of the binding site for α1β1 integrin. Dev Biol., 162, 451-464.
    • (1994) Dev Biol. , vol.162 , pp. 451-464
    • Lallier, T.1    Deutzmann, R.2    Perris, R.3    Bronner-Fraser, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.