Physician
Internal Medicine
Dr. James E. Samuelson, MD
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Doctor James E. Samuelson, MD practices Internal Medicine. He went to Wayne State University School of Medicine. Wayne State University School of Medicine is ranked 63 in research and 85 in primary care medicine He has 1 awards "CMS Meaningful Use Stage 1 Certification". Dr. James E. Samuelson has written publications. He has 47 publications published with PubMed. The lastest paper is: 'A new gene family (ariel) encodes asparagine-rich Entamoeba histolytica antigens, which resemble the amebic vaccine candidate serine-rich E. histolytica protein.'
Publications
- The Entamoeba histolytica mitochondrion-derived organelle (crypton) contains double-stranded DNA and appears to be bound by a double membrane.
- Hsp60 is targeted to a cryptic mitochondrion-derived organelle ("crypton") in the microaerophilic protozoan parasite Entamoeba histolytica.
- Primary sequences of two P-glycoprotein genes of Entamoeba histolytica.
- Physiology and molecular biology of multidrug resistance in Entamoeba histolytica.
- Cyst-specific exochitinases of Entamoebae contain unique hydrophilic repeats at their amino termini.
- Emetine-resistant mutants of Entamoeba histolytica overexpress mRNAs for multidrug resistance.
- Cloning of Entamoeba genes encoding proteolipids of putative vacuolar proton-translocating ATPases.
- Primary structure of the Entamoeba histolytica gene (Ehvma1) encoding the catalytic peptide of a putative vacuolar membrane proton-transporting ATPase (V-ATPase).
- Primary structure of an Entamoeba histolytica nicotinamide nucleotide transhydrogenase.
- Increase in mRNA of multiple Eh pgp genes encoding P-glycoprotein homologues in emetine-resistant Entamoeba histolytica parasites.
- DNA hybridization probe for clinical diagnosis of Entamoeba histolytica.
- Primary structures of alcohol and aldehyde dehydrogenase genes of Entamoeba histolytica.
- A new gene family (ariel) encodes asparagine-rich Entamoeba histolytica antigens, which resemble the amebic vaccine candidate serine-rich E. histolytica protein.
- Early lateral transfer of genes encoding malic enzyme, acetyl-CoA synthetase and alcohol dehydrogenases from anaerobic prokaryotes to Entamoeba histolytica.
- Molecular epidemiology of Entamoeba spp.: evidence of a bottleneck (Demographic sweep) and transcontinental spread of diploid parasites.
- P-glycoprotein genes of Entamoeba histolytica.
- The cDNA sequence of an abundant Entamoeba histolytica 20-kilodalton protein containing four repetitive domains.
- Cloning and expression of chitinases of Entamoebae.
- Cloning and expression of an NADP(+)-dependent alcohol dehydrogenase gene of Entamoeba histolytica.
- Cloning of the Eh cdc2 gene from Entamoeba histolytica encoding a protein kinase p34cdc2 homologue.
- Molecular cloning of a rho family gene of Entamoeba histolytica.
- Molecular cloning of a rac family protein kinase and identification of a serine/threonine protein kinase gene family of Entamoeba histolytica.
- Molecular cloning of an Entamoeba histolytica gene encoding a putative mos family serine/threonine-kinase.
- Cloning and expression of the gene for an NADP(+)-dependent aldehyde dehydrogenase of Entamoeba histolytica.
- Molecular cloning of the gene for a novel ABC superfamily transporter of Entamoeba histolytica.
- Molecular cloning of ras and rap genes from Entamoeba histolytica.
- Understanding the insertion of transporters and other membrane proteins.
- Sec-dependent membrane protein insertion: sequential interaction of nascent FtsQ with SecY and YidC.
- The role of the conserved box E residues in the active site of the Escherichia coli type I signal peptidase.
- Structures of the rare-cutting restriction endonuclease NotI reveal a unique metal binding fold involved in DNA binding.
- YidC mediates membrane protein insertion in bacteria.
- Function of YidC for the insertion of M13 procoat protein in Escherichia coli: translocation of mutants that show differences in their membrane potential dependence an...
- Engineering Escherichia coli BL21(DE3) derivative strains to minimize E. coli protein contamination after purification by immobilized metal affinity chromatography.
- Recent developments in difficult protein expression: a guide to E. coli strains, promoters, and relevant host mutations.
- Engineering BspQI nicking enzymes and application of N.BspQI in DNA labeling and production of single-strand DNA.
- Rational design of a fusion partner for membrane protein expression in E. coli.
- Discovery of natural nicking endonucleases Nb.BsrDI and Nb.BtsI and engineering of top-strand nicking variants from BsrDI and BtsI.
- BstYI bound to noncognate DNA reveals a "hemispecific" complex: implications for DNA scanning.
- Engineering a rare-cutting restriction enzyme: genetic screening and selection of NotI variants.
- Implications for switching restriction enzyme specificities from the structure of BstYI bound to a BglII DNA sequence.
- The isolation of strand-specific nicking endonucleases from a randomized SapI expression library.
- Crystal structure of BstYI at 1.85A resolution: a thermophilic restriction endonuclease with overlapping specificities to BamHI and BglII.
- Engineering strand-specific DNA nicking enzymes from the type IIS restriction endonucleases BsaI, BsmBI, and BsmAI.
- Versatility of inner membrane protein biogenesis in Escherichia coli.
- Directed evolution of restriction endonuclease BstYI to achieve increased substrate specificity.
- Direct interaction of YidC with the Sec-independent Pf3 coat protein during its membrane protein insertion.
Schools
Wayne State University School Of Medicine
Butterworth Hospital
Doctors Specialties
- Internal Medicine
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
Education
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Wayne State University School of Medicine
Hospital
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Spectrum Health - Butterworth Hospital
Drug Facts
| NPI NUMBER | 1982643466 | |
| NPPES Provider LastName | SAMUELSON | |
| NPPES Provider FirstName | JAMES | |
| NPPES Provider ZIPCode | 494189714 | |
| NPPES Provider State | MI | |
| Specialty Description | Internal Medicine | |
| Total Claim Count | 10412.0 | |
| Distinct Opioid Count | 4.0 | |
| Opioid Claim Count | 346.0 | |
| Percent Opioid Claims | 3.32 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1982643466 |
| Last Name Of The Provider | SAMUELSON |
| First Name Of The Provider | JAMES |
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