Mutational analysis of the DTDST gene in a fetus with achondrogenesis type 1B. Am J Med Genet 1998;78:58-60.Cai G, Nakayama M, Hiraki Y, Ozono K. 1998. Mutational analysis of the DTDST gene in a fetus with achondro- genesis type 1B. Am J Med Genet 78:58-60....
南昌大学医学院硕士学位论文骨畸形发育不良硫酸盐转移因子(DTDST)基因突变与先天性马蹄内翻足(CTEV)的相关性研究姓名:***请学位级别:硕士专业:儿科学指导教师:**乐20090601摘要摘要目的:先天性马蹄内翻足(congenitaltalipesequinovarus,CTEV)在小儿骨科学中是最常见的畸形之一,发病率为1~3‰,发病率在各种族间存在...
The diastrophic dysplasia sulfate transporter (DTDST) gene encodes a transmembrane protein that transports sulfate into chondrocytes to maintain adequate sulfation of proteoglycans. Mutations in this gene are responsible for four recessively inherited chondrodysplasias that include diastrophic dysplasia, multip...
摘要: Identifies DTDST mutations in subjects with recessive multiple epiphyseal dysplasia. Association of skeletal dysplasia with morbidity; Diagnosis of the disease; Factors that determines body height in MED. 展开 关键词: audit clinical governance quality research and development service evaluation DOI:...
This experiment is aim at study the VCAM-1 gene\'s sequential expression intibial dyschondroplasia(TD) of broiler,and further to explore the pathogenesis of thetibial dyschondroplasiaof broiler. 本实验目的在于研究血管粘附分子-1(VCAM-1)基因在肉鸡胫骨软骨发育不良(TibialDyschondroplasia,TD)中不同阶...
搜索智能精选 题目汉语中的“基因”来自英语的gene,从该词产生的方式看,“基因”属于()A.纯粹音译词 B.音译兼意译词 C.意译词 D.仿译词 答案B
The protein encoded by this gene is similar in sequence to histidyl-tRNA synthetase, which hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). The encoded protein is found in the cytoplasm. [provided by RefSeq, Jul 2008] 第一抗体就是平常所说的抗体,即能和抗原特异性结合。
PROBLEM TO BE SOLVED: To obtain the subject new vector containing a DNA sequence encoding a mammalian sulfate transporter, not containing the DNA sequence of 5' non- translation region of the gene and useful for detection of a therapeutic agent for a bone or cartilage disease, a gene ...
2001. Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene: correlation between sulfate transport activity and chondrodysplasia phenotype. Hum. Mol. Genet. 10(14): 1485-1490. doi:10.1093/hmg/10.14.1485. PMID: 11448940.
The vector for expression is obtained by cloning the vector by using a cDNA derived from a rat osteoblast-like cell as a template and a partial sequence of the DTDST gene as a primer, incorporating the obtained DTDST gene to a cassette cosmid derived from an adenovirus genome, and ...