DYM: Difference between revisions
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edited opening sentence to make clear that article is about both protein and the gene that encodes it |
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*{{cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8 }} |
*{{cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8 }} |
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*{{cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, ''et al.'' |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3 }} |
*{{cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, ''et al.'' |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3 }} |
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*{{cite journal | author=Ehtesham N, Cantor RM, King LM, ''et al.'' |title=Evidence that Smith-McCort dysplasia and Dyggve-Melchior-Clausen dysplasia are allelic disorders that result from mutations in a gene on chromosome 18q12. |journal=Am. J. Hum. Genet. |volume=71 |issue= 4 |pages= 947–51 |year= 2002 |pmid= 12161821 |doi=10.1086/342669 }} |
*{{cite journal | author=Ehtesham N, Cantor RM, King LM, ''et al.'' |title=Evidence that Smith-McCort dysplasia and Dyggve-Melchior-Clausen dysplasia are allelic disorders that result from mutations in a gene on chromosome 18q12. |journal=Am. J. Hum. Genet. |volume=71 |issue= 4 |pages= 947–51 |year= 2002 |pmid= 12161821 |doi=10.1086/342669 | pmc=378548 }} |
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*{{cite journal | author=Thauvin-Robinet C, El Ghouzzi V, Chemaitilly W, ''et al.'' |title=Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1. |journal=J. Med. Genet. |volume=39 |issue= 10 |pages= 714–7 |year= 2002 |pmid= 12362026 |doi=10.1136/jmg.39.10.714 }} |
*{{cite journal | author=Thauvin-Robinet C, El Ghouzzi V, Chemaitilly W, ''et al.'' |title=Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1. |journal=J. Med. Genet. |volume=39 |issue= 10 |pages= 714–7 |year= 2002 |pmid= 12362026 |doi=10.1136/jmg.39.10.714 | pmc=1734996 }} |
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*{{cite journal | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }} |
*{{cite journal | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 }} |
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*{{cite journal | author=Cohn DH, Ehtesham N, Krakow D, ''et al.'' |title=Mental retardation and abnormal skeletal development (Dyggve-Melchior-Clausen dysplasia) due to mutations in a novel, evolutionarily conserved gene. |journal=Am. J. Hum. Genet. |volume=72 |issue= 2 |pages= 419–28 |year= 2003 |pmid= 12491225 |doi=10.1086/346176 }} |
*{{cite journal | author=Cohn DH, Ehtesham N, Krakow D, ''et al.'' |title=Mental retardation and abnormal skeletal development (Dyggve-Melchior-Clausen dysplasia) due to mutations in a novel, evolutionarily conserved gene. |journal=Am. J. Hum. Genet. |volume=72 |issue= 2 |pages= 419–28 |year= 2003 |pmid= 12491225 |doi=10.1086/346176 | pmc=420018 }} |
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*{{cite journal | author=El Ghouzzi V, Dagoneau N, Kinning E, ''et al.'' |title=Mutations in a novel gene Dymeclin (FLJ20071) are responsible for Dyggve-Melchior-Clausen syndrome. |journal=Hum. Mol. Genet. |volume=12 |issue= 3 |pages= 357–64 |year= 2003 |pmid= 12554689 |doi=10.1093/hmg/ddg029 }} |
*{{cite journal | author=El Ghouzzi V, Dagoneau N, Kinning E, ''et al.'' |title=Mutations in a novel gene Dymeclin (FLJ20071) are responsible for Dyggve-Melchior-Clausen syndrome. |journal=Hum. Mol. Genet. |volume=12 |issue= 3 |pages= 357–64 |year= 2003 |pmid= 12554689 |doi=10.1093/hmg/ddg029 }} |
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*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }} |
*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }} |
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*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }} |
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }} |
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*{{cite journal | author=Clark TA, Schweitzer AC, Chen TX, ''et al.'' |title=Discovery of tissue-specific exons using comprehensive human exon microarrays. |journal=Genome Biol. |volume=8 |issue= 4 |pages= R64 |year= 2007 |pmid= 17456239 |doi= 10.1186/gb-2007-8-4-r64 }} |
*{{cite journal | author=Clark TA, Schweitzer AC, Chen TX, ''et al.'' |title=Discovery of tissue-specific exons using comprehensive human exon microarrays. |journal=Genome Biol. |volume=8 |issue= 4 |pages= R64 |year= 2007 |pmid= 17456239 |doi= 10.1186/gb-2007-8-4-r64 | pmc=1896007 }} |
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Revision as of 08:11, 19 June 2010
Template:PBB Dymeclin is a protein that in humans is encoded by the DYM gene.[1]
References
Further reading
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