Novel mutation of the cyclin-dependent kinase 4 gene in a Chinese patient with intimal sarcoma of the pulmonary artery

The long arm of human chromosome 12 contains a region that has been found to be amplified in a number of different tumors, including osteosarcomas and soft tissue sarcomas. There are more than 5 genes located in this area such as CDK2, CDK4, WNT1, MDM2 and WNTIOb. CDK4 gene consists of eight exons,...

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Vydáno v:Chinese medical journal Ročník 122; číslo 9; s. 1107 - 1109
Hlavní autoři: Gao, Feng, Liu, Qi-cai, Wang, Mi, Wang, Zhi-qiang, Huang, Yi, Zhou, Xiao-hui, Zhang, Sheng
Médium: Journal Article
Jazyk:angličtina
Vydáno: China Department of Gene Diagnosis First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian 350005, China%Department of Neurology First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian 350005, China%Department of Chemistry First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian 350005, China%Department of Laboratory Medicine First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian 350005, China 05.05.2009
Department of Pathology First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian 350005, China%Department of Laboratory Medicine First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian 350005, China
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ISSN:0366-6999, 2542-5641, 2542-5641
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Popis
Shrnutí:The long arm of human chromosome 12 contains a region that has been found to be amplified in a number of different tumors, including osteosarcomas and soft tissue sarcomas. There are more than 5 genes located in this area such as CDK2, CDK4, WNT1, MDM2 and WNTIOb. CDK4 gene consists of eight exons, of which the start codon is located in the beginning of exon 2 and the stop codon in the a member of the Ser-Thr catalytic domain extends beginning of exon 8. CDK4 is protein kinase family and its from amino acid 6 to 295.
Bibliografie:CDK4 gene
intimal sarcoma, pulmonary artery
11-2154/R
CDK4 gene; intimal sarcoma, pulmonary artery; clinical character
clinical character
R781.5
R739.410.2
ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:0366-6999
2542-5641
2542-5641
DOI:10.3760/cma.j.issn.0366-6999.2009.09.018