| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.2741/2812 |
| P698 | PubMed publication ID | 17981680 |
| P2093 | author name string | James G Patton | |
| Amanda S Solis | |||
| Nikki Shariat | |||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1926-1942 | |
| P577 | publication date | 2008-01-01 | |
| P1433 | published in | Frontiers in Bioscience | Q5506062 |
| P1476 | title | Splicing fidelity, enhancers, and disease | |
| P478 | volume | 13 |
| Q50553789 | A founder synonymous COL7A1 mutation in three Danish families with dominant dystrophic epidermolysis bullosa pruriginosa identifies exonic regulatory sequences required for exon 87 splicing. |
| Q39680958 | Adaptive Gene Loss? Tracing Back the Pseudogenization of the Rabbit CCL8 Chemokine |
| Q92311837 | Association of TLR4 and TLR9 gene polymorphisms and haplotypes with cervicitis susceptibility |
| Q27675089 | Asyn-anticonformational difference allows SRSF2 to recognize guanines and cytosines equally well |
| Q36306493 | Bicodon bias can determine the role of synonymous SNPs in human diseases |
| Q36996416 | Cannabinoid receptor genotype moderation of the effects of childhood physical abuse on anhedonia and depression |
| Q41844784 | Conservation/Mutation in the splice sites of cytokine receptor genes of mouse and human |
| Q35891898 | Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele |
| Q34964532 | Divergence of exonic splicing elements after gene duplication and the impact on gene structures. |
| Q57639981 | Exon skipping-mediated dystrophin reading frame restoration for small mutations |
| Q42332000 | Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes |
| Q37761136 | Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics |
| Q92135212 | Impact of matrix metalloproteinase-11 gene polymorphisms on development and clinicopathologcial variables of uterine cervical cancer in Taiwanese women |
| Q33699177 | Moving on from GWAS: functional studies on the G6PC2 gene implicated in the regulation of fasting blood glucose |
| Q33930004 | Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels |
| Q42131969 | Occult hepatitis B infection: an evolutionary scenario |
| Q37483533 | PSF suppresses tau exon 10 inclusion by interacting with a stem-loop structure downstream of exon 10. |
| Q34349200 | Personalized exon skipping strategies to address clustered non-deletion dystrophin mutations |
| Q38089634 | Silencing human genetic diseases with oligonucleotide-based therapies. |
| Q36577263 | TRAIL and TRAIL receptors splice variants during long-term interferon β treatment of patients with multiple sclerosis: evaluation as biomarkers for therapeutic response |
| Q28474475 | Targeted genome-wide enrichment of functional regions |
| Q33690608 | The intronic splicing code: multiple factors involved in ATM pseudoexon definition |
| Q27302868 | The soluble form of the EIAV receptor encoded by an alternative splicing variant inhibits EIAV infection of target cells |
Search more.