Dr. Mark F Rogers D.P.M.
Podiatrist (Foot and Ankle Specialist)
150 W 800 N Provo UT, 84601About
Dr. Mark Rogers is a podiatrist practicing in Provo, UT. Dr. Rogers is a medical doctor specializing in the treatment of the foot , ankle and related parts of the leg. As a podiatrist, Dr. Rogers diagnoses and treats conditions of the feet. The feet are key body parts that give a person stability, absorb shock, allow for walking and standing and are necessary for overall well-being. So, the feet need expert care. Podiatrists can specialize in surgery, wound care, sports medicine, diabetic care and pediatrics.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- The use of gene ontology evidence codes in preventing classifier assessment bias.
- Genome-wide analysis of alternative splicing in Chlamydomonas reinhardtii.
- Comparative analysis of serine/arginine-rich proteins across 27 eukaryotes: insights into sub-family classification and extent of alternative splicing.
- SpliceGrapher: detecting patterns of alternative splicing from RNA-Seq data in the context of gene models and EST data.
- Deciphering the plant splicing code: experimental and computational approaches for predicting alternative splicing and splicing regulatory elements.
- An integrative approach to predicting the functional effects of non-coding and coding sequence variation.
- Probabilistic inference of biological networks via data integration.
- GTB - an online genome tolerance browser.
- HIPred: an integrative approach to predicting haploinsufficient genes.
- Recognition memory-induced gene expression in the perirhinal cortex: A transcriptomic analysis.
- Predicting the Pathogenic Impact of Sequence Variation in the Human Genome.
- Sex-specific differences in cardiovascular and metabolic hormones with integrated signalling in the paraventricular nucleus of the hypothalamus.
- Treating the placenta to prevent adverse effects of gestational hypoxia on fetal brain development.
- CScape: a tool for predicting oncogenic single-point mutations in the cancer genome.
- FATHMM-XF: accurate prediction of pathogenic point mutations via extended features.
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