учебник по алгебре 8 класс мордкович читать часть 2
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учебник по алгебре 8 класс мордкович читать часть 2, A novel homozygous ZNF469 variant causing brittle cornea , Anti-ZNF469 | Atlas Antibodies | Biomol.com, Common Genetic Variants Near the Brittle Cornea Syndrome , Systematically Displaying the Pathogenesis of Keratoconus via , Identification of Single-Nucleotide Polymorphisms in ZNF469 , ZNF469 Human Gene Knockout Kit (CRISPR) from OriGene Technologies, .
The index case had a history of bilateral keratoglobus, corneal perforations, bilateral hypoacusia, and skeletal anomalies. His two children exhibited topographic anomalies compatible with keratoconus suspects as well as mild skeletal anomalies. Genetic analysis identified a novel homozygous c.2340delC variant in the ZNF469 gene, which predicts a p.(Arg781Glufs*19) truncated protein. Sanger sequencing identified heterozygosity for the c.2340delC variant in DNA from both siblings., Ectatic corneal disease (ECD) includes a clinically heterogeneous group of eye diseases characterized by progressive thinning and subsequent bulging of the corneal structure. Keratoconus (KC), keratoglobus, and pellucid marginal degeneration are …, Buy Anti-ZNF469, item number: ATA-HPA077792.100 from Atlas Antibodies at Biomol! Polyclonal Antibody against Human ZNF469, Gene description: zinc finger protein 469, Alternative Gene Names: KIAA1858, Zfp469, Validated….
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. Alpha 2.0. Login Register., Davidson AE, Borasio E, Liskova P, Khan AO, Hassan H, Cheetham ME, et al. Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus. Invest Ophthalmol Vis Sci. (2015) 56:578–86. 10.1167/iovs.14-15792 [Google Scholar] 203., Thoracic aortic aneurysms and dissections often have inter-related pathologies that are increasingly recognized to have a genetic basis. A patient with a vascular history consisting of a spontaneous aorto-iliac dissection and thoracic aortic aneurysm belonged to a family with a significant self-reported history of aneurysmal disease. Suspecting a genetic component, genetic investigation was , Compare ZNF469 Human Gene Knockout Kit (CRISPR) KN435404 from OriGene Technologies on Biocompare.com ZNF469 - KN2.0, Human gene knockout kit via CRISPR, non-homology mediated Welcome Guest, , .