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1,821 Possible Causes for Triplicate

  • Influenza

    The bars indicate the standard deviations calculated for triplicates.[] Each experiment was performed in triplicate. Propagation of influenza viruses and rhinoviruses was performed using MDCK and HeLa Ohio cells, respectively.[] Influenza A virus RNA was quantified in triplicate in a single experimental run by performing a one-step TaqMan real-time reverse transcriptase (RT) PCR using a Quantitect[]

  • Malignant Neoplasm

    All assays were performed in triplicate and repeated in at least three independent experiments.[] Each transfection assay was performed in triplicate and repeated in at least three independent experiments and using two different Hmga1 / ES cell clones.[]

  • Appendicitis

    Congenital appendiceal disorders Appendiceal congenital disorders are extremely rare but occasionally reported (eg, agenesis, duplication, triplication).[]

  • Meningitis

    All ELISA experiments were performed in triplicate.[]

  • Tuberculosis

    […] pool as described before. 31 IFN-γ ELISPOT responses to medium controls were consistently 6 splenocytes was represented as the average spot forming cells (SFC) s.d.s in triplicate[] HEK293T cells (3 10 5 cells/well) were co-transfected in triplicate with the TLR expression plasmids.[] Data are presented as the means SD of triplicate cultures. *p 0.05 were considered significant when compared to empty vector.[]

  • Chromosome 4q32.1-q32.2 Triplication Syndrome

    More Symptoms of Chromosome 4q32.1-q32.2 triplication syndrome » Genetics of Chromosome 4q32.1-q32.2 triplication syndrome Associated cytogenetic location Location: 4q32.1[] We present three brothers and their mother with triplication of 4q.[] Symptoms of Chromosome 4q32.1-q32.2 triplication syndrome Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of head or neck Downslanted palpebral[]

  • Partial Trisomy 21

    Only the terminal band 21q22 was not in triplicate.[] Nimblegen targeted chromosome 21 array specified the range of duplication from the centromere to the band 21q21.3 (19 Mb) in the first case and the range of duplication and triplication[] An elderly man with phenotypic DS and partial trisomy of chromosome 21 (PT21) lacked triplication of APP affo rding an opportunity to study the role of this gene in the pathogenesis[]

  • Setleis Syndrome

    Chromosomal microarray analyses revealed unique copy number variants of 1p36 in two individuals with duplications at 1p36.22p36.21 and one with a triplication at 1p36.22p36.21[] Chromosome 1p36.22p36.21 duplications/triplication causes Setleis syndrome (focal facial dermal dysplasia type III) .[] The syndrome results from recessive mutations in the TWIST2 gene, encoding a basic helix-loop-helix transcription factor or de novo genomic duplication or triplication, which[]

  • Pelizaeus-Merzbacher Disease

    Further examination revealed an underlying genomic organization, duplication-inverted triplication-duplication (DUP-TRP/INV-DUP), in which a triplicated segment was nested[] Other rare PLP1 abnormalities have been also identified, including X-chromosome translocations, triplications, and a partial duplication, all involving PLP1.[] Other causes of PMD include PLP1 deletions, triplications and point mutations.[]

  • 22q11.2 Duplication Syndrome

    "Microduplication and triplication of 22q11.2: a highly variable syndrome". Am. J. Hum. Genet. 76 (5): 865–76. doi:10.1086/429841. PMC 1199375. PMID 15800846.[] Yobb TM, Sommerville MJ, Willatt L, et al: Microduplication and triplication of 22q11.2: a highly variable syndrome. Am J Hum Genet 2005;76:865-876 3.[] "Microduplication and triplication of 22q11. 2: a highly variable syndrome." The American Journal of Human Genetics 76.5 (2005): 865-876.[]

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