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Publications tagged with this subject: 13

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1. Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin

2. Severe congenital microcephaly with AP4M1 mutation, a case report

3. Identification of a large intronic transposal insertion in SLC17A5 causing sialic acid storage disease

4. Arginine CGA codons as a source of nonsense mutations: a possible role in multivariant gene expression, control of mRNA quality, and aging

5. Nuclear genetic codes with a different meaning of the UAG and the UAA codon

6. The drive to generate multiple forms of oncogenic cyclin D1 transcripts in mantle cell lymphoma

7. Gene expression patterns of chicken neuregulin 3 in association with copy number variation and frameshift deletion

8. Case report: maternal mosaicism resulting in inheritance of a novel GATA6 mutation causing pancreatic agenesis and neonatal diabetes mellitus

9. NMD monitors translational fidelity 24/7

10. Identification of alternatively spliced transcripts of rice phytochelatin synthase 2 gene OsPCS2 involved in mitigation of cadmium and arsenic stresses

11. Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

12. Sialotranscriptomics of Rhipicephalus zambeziensis reveals intricate expression profiles of secretory proteins and suggests tight temporal transcriptional regulation during blood-feeding

13. Two novel C-terminal frameshift mutations in the β-globin gene lead to rapid mRNA decay


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