Results 101 to 110 of about 7,517 (194)
Establishment of a method for detecting nucleotide polymorphism of SLC39A13 gene based on ARMS-PCR [PDF]
In order to achieve its nucleotide polymorphism (SNP) accurate typing, this paper establishes a molecular diagnostic technique based on fluorescent quantitative PCR for accurate genotyping of the nucleotide polymorphism (SNP) at the rs755555 locus of the
Bingqian GUO +5 more
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Editorial: Phosphorylation-Dependent Peptidyl-Prolyl Cis/Trans Isomerase PIN1
Jormay Lim, Tae Ho Lee, Futoshi Suizu
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Measures obtained from two DRG by individual were pooled, and we also pooled affected dogs and controls. We used PPIB (Peptidylprolyl Isomerase B) as control and all genes of the locus (GDNF-AS, GDNF, WDR70, NUP155, SLC1A3) were tested 3 times with 3 ...
David Silversides (3515558) +20 more
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Treatment of schistosomiasis, a widespread human parasitic disease caused by the helminth parasites of the genus Schistosoma, relies mainly on one chemotherapeutic agent, praziquantel, although several other compounds exert anti-parasitic effects.
BOUMIS G +6 more
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Peptidylprolyl isomerase A (PPIA) is a key molecule involved in various biological functions and has been implicated in multiple diseases. However, the biological significance of PPIA in pan-cancer remains unclear.
Yuanqian Yao, Xueqing Gong, Hui Li
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BackgroundAccurate evaluation of gene expression requires normalization relative to the expression of reliable reference genes. Expression levels of "classical" reference genes can differ, however, across experimental conditions.
Rumei Li +11 more
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NMR assignments of the FK506-binding domain of FK506-binding protein 35 from Plasmodium vivax
PvFKBP35 is a member of the FK506 binding protein family (FKBP) from Plasmodium vivax. The FK506- binding domain of PvFKBP35 shows a canonical peptidylprolyl cis–trans isomerase (PPIase) activity.
Yoon, Ho Sup, Shin, Joon, Alag, Reema
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Characterisation of the PrtM maturase of Streptococcus equi; a proven virulence factor in strangles
Streptococcus equi subspecies equi (S. equi) is the pathogen responsible for the prevalent and highly contagious equine disease called strangles. Strangles has been reported worldwide as a cause of a high level of animal suffering and economic loss.
Ikolo, Felicia
core
Primer sequences used for qPCR analysis.
POLR2A - polymerase (RNA) II (DNA directed) polypeptide A; TMEM222 - transmembrane protein 222; MVK - mevalonate kinase; DEFB1 - defensin beta 1; PPIA - peptidylprolyl isomerase; GAPDH - glyceraldehyde-3-phosphate dehydrogenase; RPLP0 - ribosomal protein,
Annette V. Jacobsen (677206) +3 more
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p53 mRNA expressions were normalized to that of glyceraldehyde-3-phosphate dehydrogenase (Gapdh) (A), hypoxanthine guanine phosphoribosyl transferase (Hprt) (B) and peptidylprolyl isomerase A (Ppia) (C) (*p n = 5 for control group, n = 5 for the sham ...
Kazuhiko Kibayashi (2823470) +4 more
core +1 more source

