Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms 喜欢 0 阅读量: 24 作者: Cremonesi,L 摘要: Abnormalities of the L1CAM gene, a member of the immunoglobulin gene superfamily of neural-cell adhesion molecules, are ...
Mutation of the start codon in the FRDA1 gene: linkage analysis of three pedigrees with the ATG to ATT transversion points to a unique common ancestor. Hum Genet. 1998;103(1):102–5.Zuhlke C, Laccone F, Cossee M, Kohlschutter A, Koenig M, Schwinger E. Mutation of the start codon...
The numbers 0, 803, 857 and 2 777 indicate the position of the "A" of the "ATG" start codon, the T-DNA insertion sites in bcl1 and SALK_109281, and the "G" of the "TAG" stop codon in the BCL1 gene, respectively. The bar and NPTII genes are represented by the purple and ...
We report herein the interaction of a rare initiation codon mutation of the α2 gene and α0-thal in a Thai boy with Hb H disease. This finding highlights a wide variety of molecular pathology of the α-globin genes underlying α-thal syndrome in Southeast Asia....
control of the CET1 promoter were constructed by integrating a DNA fragment containing the CET1 promoter, which was obtained by PCR using the plasmid pFA6a-kanMX6-pCET1-VN [14] and the oligonucleotides CET1pro-ATG34-Fw and -Rv, into the upstream of the start codon of chromosomal ATG34....
Start today. Try it now Create an account Ask a question Our experts can answer your tough homework and study questions. Ask a question Search AnswersLearn more about this topic: Transfer RNA | tRNA Overview, Structure & Function from Chapter 9 / Lesson 6 298K ...
De novo initiation codon mutation (ATG 3 ACG) of the beta-globin gene causing beta-thalassemia in a Swiss family - Beris, Darbellay, et al. - 1993 () Citation Context ...ll known to result in little or no protein translation (discussed in Kozak, 1996). Genetic diseases where the start...
A De NOWPhenylketonuria Mutation: ATG (Met) to ATA (Ile) in the Start Codon of the Phenylalamine Hydroxylase GeneFIGURE 2. Diagnosis of the M11 mutation by PCR in the PKU family. Genomic DNA was amplified using the 1A2 and the 182 primers, and digested with the restriction enzyme Nspl...
Improved fusion protein expression of EGFP via the mutation of both Kozak and the initial ATG codon. Cell Mol Biol Lett. 2007; 12:362-9. [PubMed: 17318296]C. Dai, Z. Cao, Y. Wu, H. Yi, D. Jiang, W. Li, Improved fusion protein expression of EGFP via the mutation of both Koz...
De novo mutation of the beta-globin gene initiation codon (ATG-->AAG) in a Northern European boy. Am J Hematol. 1997; 56 :179–82.Waye JS, Eng B, Patterson M, Barr RD & Chui DH. De novo mutation of the beta-globin gene initiation codon (ATG-->AAG) in a Northern European...