Random good picture Not show

151) Missense mutation A point mutation that causes a change in one amino acid of a protein.

152) The crossover operation and mutation operation of decimal code genetic algorithm and its application in the optimal problem of nonlinear function are discussed in detail.

153) Mutation of CPAP induces a neuro-developmental disorder named MCPH (autosomal recessive primary microcephaly) that causes a great reduction in brain growth in human.

154) An international team of 16 scientists today reports the first direct measurement of the general rate of genetic mutation at individual DNA letters in humans.

155) Cells with Ras gene mutation or transformed by Ras become resistant to p 53 dependent apoptosis.

156) To prevent resorting mutation, TQ 111 strain was selected for UV mutagenesis strains with.

157) The polysaccharose content of nature Cordyceps sinensis was 8.92%. The polysaccharose content of UV mutation was 8.41%. The polysaccharose content of NTG mutation was 9.08%.

158) Tobacco increased significantly the mutation rate of Salmonella typhia and the formation rate of CHO colony.

159) It appears that, like the golden zebrafish , light-skinned Europeans also have a mutation in the gene for melanosome production. This results in less pigmented skin.

160) After the ventilation supercavity formed, the ventilation mutation distinctly influenced the form, the way of gas-leakage and the stability of cavity.

161) Some monilethrix has been reported to be associated with genetic mutations on human keratins. Mutation in DSG4 has also been reported.

162) Moreover, the sensors were able to detect the transient mutation in cells(such as, the mitochysis and death of cell)because of the response time shortened to microsecond.

163) Quantum NOT gate is used to realize quantum mutation to avoid premature convergence.

164) Biological and N-terminal amino acids analysis exclude the most common As type of genotypic mutation of albumins.

165) According to comparing the zymograms of isoelectrofocusing, the relationship of enzyme activity and energy metabolism, and the relationship of enzyme activity and gene mutation were studied.

166) All of the patients who had parkin gene deletion mutation had tremor, rigidity and bradykinesia, but athetosis and family history of PD were not found.

167) This algorithm includes clonal selection, hyper - mutation and receptor editing.

168) Methods HPRT gene mutation frequency was examined by the technique of multinuclear cell assay.

169) The deletion mutation and missense mutation of COL7A1 gene result in the specific mutation in patients with clinical symptoms.

170) The mutations in patients with factor V deficiency were identified including point mutation, frameshift mutation, deletion and insertion mutation.

171) Methods: Nine heterozygous mutation carriers and nine healthy controls were investigated.

172) It's plausible that millions of years ago a single mutation resulted in two different versions of the photopigment gene becoming located on the same X chromosome.

173) So far the discussion has centered entirely around mutation in the strict sense.

174) Conclusions The splicing mutation of COL7A1 gene is the underlying cause of and specific rather than common polymorphism for the family with dystrophic epidermolysis bullosa pruriginosa subtype.

175) The dilatation process of coal mass is depicted by 3 characteristic quantities , namely, volume compression, steady dilatation and dilatation mutation.

176) Many leukemic oncogenes form as a consequence of gene fusions or mutation that result in the activation or overexpression of a tyrosine kinase.

177) Conclusion:LP is an autosomal recessive disease,(http://sentencedict.com/mutation.html) and the mutation of pathogenic gene of LP is rare in Chinese people.

178) Recent studies on adhesion molecules, cytokines and their receptors, functional mutation of chromosome DNA have provided new insights into the pathogenesis of exfoliative erythroderma.

179) People who have this mutation need less sleep than others.

180) Results A homozygous mutation at exon 13 of the proband was found by parallel TGGE. Homozygous and heterozygous mutations were also found in the family by parallel TGGE.