Bezerra MA,Albuquerque DM,Santos MN.Two new unstable haemoglobins leading to chronic haemolytic anaemia:Hb Caruaru [beta122 (GH5) Phe-->Ser], a probable case of germ line mutation, and Hb Olinda [beta22 (B4) 25 (B7)], a deletion of a 12 base-pair sequence.European Journal of ...
2. 2. A Ser for Gly substitution at position 13 (10 of the A helix) was found in a polypeptide with the overall sequence of the β B globin. 3. 3. On the basis of the nucleotide sequence of the β B-globin gene, a C to T transition occurring on a CpG doublet is considered ...
Objective To observe the expression of chromosome region maintenance 1(CRM1) and P-p27ser10) in epithelial ovarian cancer(EOC) tissues, and to discuss their influence on the proliferation of EOC SKOV3 cell line. Methods We analyzed the associat...
‐(Ser) 3 ‐J18 peptide was labeled with 99m Tc using EDDA /tricine as coligands. The in vitro and in vivo studies of this radiolabeled peptide were performed for cellular‐specific binding and tumor targeting in A‐549 cells and tumor‐bearing mice, respectively. The high radiochemical pur...
Takezaki T, Gao CM, Wu JZ, Li ZY, Wang JD, Ding JH, Liu YT, Hu X, Xu TL, Tajima K, Sugimura H (2002) hOGG1 ser326cys polymorphism and modification by environmental factors of stomach cancer risk in Chinese. Int J Cancer 99:624–627 View Article...
Cloning and Sanger sequencing revealed that the proband had a c.166A T (p.Thr56Ser) mutation in exon 4 of GYPB * S . When antibody screening of 60 455 blood donors was performed using the proband RBC s, no antibodies were detected. GYPB *S with c.166T should encode an unusual S...
Results: [99mTc-EDDA/tricin/HYNIC-(Ser)3-D-Phe13]BN(7-14) and [99mTc-EDDA/tricin/ HYNIC-(Gly)3-D-Phe13]BN (7-14) were obtained with radiochemical purities of >95%. Results of invitro studies demonstrated a high stability in serum and saline. Conclusion: Radiolabeling of this novel...
Pro-allele carriers of Ser307Pro polymorphism had larger right inferior temporal surface area than Ser/Ser carriers in the patients with schizophrenia; however, no significant difference was found in the same area in the healthy controls. The Ala851Ser polymorp...
A correction to the article "Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy," by Helen A. L. Tuppen and colleagues that was published online on February 29, 2012 is presented....
del Castillo, Maternally inherited nonsyndromic hearing impairment in a Spanish family with the 7510T > C mutation in the mitochondrial tRNASer(UCN) gene, J. Med. Genet. 39 (2002) e82.del Castillo F.J., Villamar M., Moreno-Pelayo M.A., Almela J.J., Morera C., Adiego I., Moreno...