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IRA HOLT, M.D.
M.D.
Internal Medicine Physician
NPI: 1881791358Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
00003739(AL)
Research & Publications (20)
Muscleblind-like proteins: similarities and differences in normal and myotonic dystrophy muscle.
PMID 19095965·Am J Pathol·2009
8-other
Defective mRNA in myotonic dystrophy accumulates at the periphery of nuclear splicing speckles.
PMID 17825047·Genes Cells·2007
8-other
Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium composition.
PMID 16697197·Neuromuscul Disord·2006
7-preclinical
Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo.
PMID 12783988·J Cell Sci·2003
7-preclinical
How does a g993t mutation in the emerin gene cause Emery-Dreifuss muscular dystrophy?
PMID 11587540·Biochem Biophys Res Commun·2001
8-other
The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin.
PMID 11313760·Eur J Hum Genet·2001
7-preclinical
Coupled leading- and lagging-strand synthesis of mammalian mitochondrial DNA.
PMID 10721989·Cell·2000
7-preclinical
163rd ENMC International Workshop: nucleoid and nucleotide biology in syndromes of mitochondrial DNA depletion myopathy 12-14 December 2008, Naarden, The Netherlands.
PMID 19464176·Neuromuscul Disord·2009
8-other
Analysis of mitochondrial DNA by two-dimensional agarose gel electrophoresis.
PMID 19513665·Methods Mol Biol·2009
7-preclinical
Human heart mitochondrial DNA is organized in complex catenated networks containing abundant four-way junctions and replication forks.
PMID 19525233·J Biol Chem·2009
7-preclinical
Inhibition of mitochondrial fission favours mutant over wild-type mitochondrial DNA.
PMID 19561330·Hum Mol Genet·2009
8-other
MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.
PMID 19436705·PLoS Genet·2009
7-preclinical
Mice expressing an error-prone DNA polymerase in mitochondria display elevated replication pausing and chromosomal breakage at fragile sites of mitochondrial DNA.
PMID 19244310·Nucleic Acids Res·2009
7-preclinical
The accessory subunit of mitochondrial DNA polymerase gamma determines the DNA content of mitochondrial nucleoids in human cultured cells.
PMID 19625489·Nucleic Acids Res·2009
8-other
The conserved translocase Tim17 prevents mitochondrial DNA loss.
PMID 18826960·Hum Mol Genet·2009
8-other
Cytoplasmic CUG RNA foci are insufficient to elicit key DM1 features.
PMID 19092997·PLoS One·2008
7-preclinical
The mitochondrial transcription termination factor mTERF modulates replication pausing in human mitochondrial DNA.
PMID 17884915·Nucleic Acids Res·2007
8-other
Analysis of replicating mitochondrial DNA by two-dimensional agarose gel electrophoresis.
PMID 18314729·Methods Mol Biol·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 18704 HIGHWAY 11 N
VANCE, AL 35490 - Phone
- (205) 481-8510
Quick Facts
- NPI
- 1881791358
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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