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1,821 Possible Causes for Triplicate

  • Influenza

    The bars indicate the standard deviations calculated for triplicates.[doi.org] Each experiment was performed in triplicate. Propagation of influenza viruses and rhinoviruses was performed using MDCK and HeLa Ohio cells, respectively.[doi.org] 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[doi.org]

  • Malignant Neoplasm

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

  • Appendicitis

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

  • Meningitis

    All ELISA experiments were performed in triplicate.[journals.plos.org]

  • 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[dx.doi.org] HEK293T cells (3 10 5 cells/well) were co-transfected in triplicate with the TLR expression plasmids.[doi.org] Data are presented as the means SD of triplicate cultures. *p 0.05 were considered significant when compared to empty vector.[doi.org]

  • 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[familydiagnosis.com] We present three brothers and their mother with triplication of 4q.[ashg.org] Symptoms of Chromosome 4q32.1-q32.2 triplication syndrome Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of head or neck Downslanted palpebral[familydiagnosis.com]

  • Partial Trisomy 21

    Only the terminal band 21q22 was not in triplicate.[ncbi.nlm.nih.gov] 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[biomed.papers.upol.cz] 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[content.iospress.com]

  • 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[ncbi.nlm.nih.gov] Chromosome 1p36.22p36.21 duplications/triplication causes Setleis syndrome (focal facial dermal dysplasia type III) .[indiana.pure.elsevier.com] 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[ncbi.nlm.nih.gov]

  • 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[ncbi.nlm.nih.gov] Other rare PLP1 abnormalities have been also identified, including X-chromosome translocations, triplications, and a partial duplication, all involving PLP1.[ncbi.nlm.nih.gov] Other causes of PMD include PLP1 deletions, triplications and point mutations.[ncbi.nlm.nih.gov]

  • 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.[en.wikipedia.org] 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.[mayomedicallaboratories.com] "Microduplication and triplication of 22q11. 2: a highly variable syndrome." The American Journal of Human Genetics 76.5 (2005): 865-876.[thinkgenetic.com]

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