Sentence examples for * ctg in from inspiring English sources

However, the French RCT only included women with abnormal CTG in labor with or without meconium-stained amniotic fluid, but excluded normal CTG cases 10, criteria that in many cases are violations of the ST analysis clinical guidelines and recommendations 23, 24.

This paper presents a random-walk-based feature extraction method called commute time guided transformation (CTG) in the graph embedding framework.

Therefore, we consider that the anesthesia for the AVM embolization should have been managed with the use of FHR monitoring device such as cardiotocography (CTG) in case of non-reassuring fetal status because some obstetric anesthesia texts recommend FHR monitoring for the viable-age fetus during non-obstetric surgery [11, 12].

In addition, an in-frame insertion/deletion (CTG) in the signal-peptide domain was noted in both populations.

The origin of DM is an expansion of the trinucleotide sequence CTG in the 3'-untranslated region (UTR) of the DMPK gene.

For this purpose pET28b_l-l-GFP-l plasmid DNA was amplified by PCR using as primers the primer TT506 525 (Hind III) R (5'-AAG CTT CCT ACG AGG AAG AGT AAT TTT AGA TTG AAG ATT ATA ATC AAC AAT AAT TTT ATC AAG AGA ATA ATT TCG TCT CGG ATC CCG ACC CAT TTG CTG) in combination with the primer pET28 (Mlu I) 3F (5'-AAT GAT CAG CCC ACT GAC GC).

Aims: A one-day workshop was hosted by the Symptom Control Committee of the National Cancer Institute of Canada, Clinical Trials Group (NCIC-CTG), in conjunction with the October 2002 annual meeting of the Canadian Association of Radiation Oncologists in Toronto, Ontario.

The 18 CTG codons in Cre were mutagenized in a similar manner and the system was used to delete XYL2.

21 The frequent use of oxytocin (89%), use of oxytocin without indications of labour dystocia (28%) and overdosage (39%) in women with insufficient CTG tracings in our study are alarming findings.

Additionally, a T/G SNP in the variable "CTT" repeat unit of alleles "25" and "26" at locus DYS481 resulted in the presence of a leading "CTG" repeat in both of these alleles.

Myotonic dystrophy type 1 (DM1), the commonest type of muscular dystrophy in adults, is caused by expansion of CTG repeats in the 3′UTR of the DMPK gene.