Dr. Michael Todd Howard M.D.
Family Practitioner | Adult Medicine
3525 Riley Street Baton Rouge LA, 70805About
Dr. Michael Howard is a family practitioner practicing in Baton Rouge, LA. Dr. Howard specializes in comprehensive health care for people of all ages. In addition to diagnosing and treating illnesses, family practitioners also put focus on preventative care with routine checkups, tests and personalized coaching on how to maintain a healthy lifestyle. Dr. Howard possesses immense general knowledge on maintaining health and today, family practitioners provide more care for the underserved and rural populations than any other medical specialty.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Readthrough of dystrophin stop codon mutations induced by aminoglycosides.
- Efficient stimulation of site-specific ribosome frameshifting by antisense oligonucleotides.
- Programmed ribosomal frameshifting in decoding the SARS-CoV genome.
- Recoding elements located adjacent to a subset of eukaryal selenocysteine-specifying UGA codons.
- Polyamine sensing during antizyme mRNA programmed frameshifting.
- Epitopes derived by incidental translational frameshifting give rise to a protective CTL response.
- The Blue Obelisk-interoperability in chemical informatics.
- Antisense-induced ribosomal frameshifting.
- Polyamine analogs with xylene rings induce antizyme frameshifting, reduce ODC activity, and deplete cellular polyamines.
- A recoding element that stimulates decoding of UGA codons by Sec tRNA[Ser]Sec.
- DMD pseudoexon mutations: splicing efficiency, phenotype, and potential therapy.
- Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle.
- A mutation in the SEPN1 selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads to SEPN1-related myopathy.
- DMD exon 1 truncating point mutations: amelioration of phenotype by alternative translation initiation in exon 6.
- Divergent regulation of the key enzymes of polyamine metabolism by chiral alpha-methylated polyamine analogues.
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