Physician
Family Medicine
Dr. Michael P. Hortsch, MD
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Dr. Michael P. Hortsch practices Family Medicine. He attended Oregon Health & Science University School of Medicine. He received 3 awards: "CMS Meaningful Use Stage 1 Certification", "Physician Practice Connections Recognition Program" and "Patient-Centered Medical Home Recognition Program". Michael Hortsch is a published MD. He has 64 publications published. The most current publication "Cis-activation of L1-mediated ankyrin recruitment by TAG-1 homophilic cell adhesion." He accepts Medicare payments and is listed with Medicare.gov.
Publications
- When students struggle with gross anatomy and histology: A strategy for monitoring, reviewing, and promoting student academic success in an integrated preclinical medi...
- Learning histology - dental and medical students' study strategies.
- Correlating students' educational background, study habits, and resource usage with learning success in medical histology.
- Virtual biology: teaching histology in the age of facebook.
- Differential Effects of Human L1CAM Mutations on Complementing Guidance and Synaptic Defects in Drosophila melanogaster.
- The L1-type cell adhesion molecule neuroglian influences the stability of neural ankyrin in the Drosophila embryo but not its axonal localization.
- Sodium channel beta subunits mediate homophilic cell adhesion and recruit ankyrin to points of cell-cell contact.
- Structural and functional evolution of the L1 family: are four adhesion molecules better than one?
- Cis-activation of L1-mediated ankyrin recruitment by TAG-1 homophilic cell adhesion.
- The analysis of genomic structures in the L1 family of cell adhesion molecules provides no evidence for exon shuffling events after the separation of arthropod and cho...
- Structural requirements for outside-in and inside-out signaling by Drosophila neuroglian, a member of the L1 family of cell adhesion molecules.
- A conserved role for L1 as a transmembrane link between neuronal adhesion and membrane cytoskeleton assembly.
- The expression of MDP-1, a component of Drosophila embryonic basement membranes, is modulated by apoptotic cell death.
- Duplications in nomenclature.
- Ligation of 5' DNA overhangs to 3' DNA overhangs using short single-stranded oligonucleotide linkers.
- Ethanol does not inhibit the adhesive activity of Drosophila neuroglian or human L1 in Drosophila S2 tissue culture cells.
- LI-cadherin-mediated cell-cell adhesion does not require cytoplasmic interactions.
- The L1 family of neural cell adhesion molecules: old proteins performing new tricks.
- Neuroglian-mediated cell adhesion induces assembly of the membrane skeleton at cell contact sites.
- Liver-intestine cadherin: molecular cloning and characterization of a novel Ca(2+)-dependent cell adhesion molecule expressed in liver and intestine.
- Preparation and analysis of membranes and membrane proteins from Drosophila.
- The cytoplasmic domain of the Drosophila cell adhesion molecule neuroglian is not essential for its homophilic adhesive properties in S2 cells.
- Biologically active synthetic fragments of epidermal growth factor: localization of a major receptor-binding region.
- Appearance of functional EGF receptor kinase during rodent embryogenesis.
- Pushing the signal hypothesis: what are the limits?
- Restriction of docking protein to the rough endoplasmic reticulum: immunocytochemical localization in rat liver.
- Immunochemical analysis of rough and smooth microsomes from rat liver. Segregation of docking protein in rough membranes.
- Purification of membranes enriched in rough endoplasmic reticulum domain by using a density perturbant.
- Complete cDNA sequence coding for human docking protein.
- Characterization of secretory protein translocation: ribosome-membrane interaction in endoplasmic reticulum.
- Human ribophorins I and II: the primary structure and membrane topology of two highly conserved rough endoplasmic reticulum-specific glycoproteins.
- Transfer of secretory proteins through the membrane of the endoplasmic reticulum.
- The human docking protein does not associate with the membrane of the rough endoplasmic reticulum via a signal or insertion sequence-mediated mechanism.
- Drosophila neuroglian: a member of the immunoglobulin superfamily with extensive homology to the vertebrate neural adhesion molecule L1.
- A membrane preparation that contains proteins characteristic of the rough endoplasmic reticulum.
- A structural and functional analysis of the docking protein. Characterization of active domains by proteolysis and specific antibodies.
- Drosophila fasciclin I, a neural cell adhesion molecule, has a phosphatidylinositol lipid membrane anchor that is developmentally regulated.
- Drosophila fasciclin I is a novel homophilic adhesion molecule that along with fasciclin III can mediate cell sorting.
- Membrane biogenesis during B cell differentiation: most endoplasmic reticulum proteins are expressed coordinately.
- Molecular genetics of neuronal recognition in Drosophila: evolution and function of immunoglobulin superfamily cell adhesion molecules.
- Drosophila neurotactin, a surface glycoprotein with homology to serine esterases, is dynamically expressed during embryogenesis.
- Sticky molecules in not-so-sticky cells.
- Cell and substrate adhesion molecules in Drosophila.
- Differential splicing generates a nervous system-specific form of Drosophila neuroglian.
- Annulin, a protein expressed at limb segment boundaries in the grasshopper embryo, is homologous to protein cross-linking transglutaminases.
- Female receptivity phenotype of icebox mutants caused by a mutation in the L1-type cell adhesion molecule neuroglian.
- The Drosophila L1CAM homolog Neuroglian signals through distinct pathways to control different aspects of mushroom body axon development.
- Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila.
- Fasciclin II: the NCAM ortholog in Drosophila melanogaster.
- Pathogenic human L1-CAM mutations reduce the adhesion-dependent activation of EGFR.
- The interaction between L1-type proteins and ankyrins--a master switch for L1-type CAM function.
- Phosphorylation of L1-type cell-adhesion molecules--ankyrins away!
- A conserved role for Drosophila Neuroglian and human L1-CAM in central-synapse formation.
- Genetic analysis of an overlapping functional requirement for L1- and NCAM-type proteins during sensory axon guidance in Drosophila.
- Drosophila contactin, a homolog of vertebrate contactin, is required for septate junction organization and paracellular barrier function.
- Neuroglian stabilizes epithelial structure during Drosophila oogenesis.
- Activation of EGF receptor kinase by L1-mediated homophilic cell interactions.
- Septate and paranodal junctions: kissing cousins.
- Drosophila Echinoid is an antagonist of Egfr signalling, but is not a member of the L1-type family of cell adhesion molecules.
- Neuroglian activates Echinoid to antagonize the Drosophila EGF receptor signaling pathway.
- Neural cell adhesion molecules--brain glue and much more!
- The axonal localization of large Drosophila ankyrin2 protein isoforms is essential for neuronal functionality.
- Structural requirements for interaction of sodium channel beta 1 subunits with ankyrin.
Schools
Oregon Health Sciences University
San Joaquin Genl Hospital
Doctors Specialties
- Family Medicine
Accepted Insurances
- Choice Plus POS II
- Assurant Health
- Blue Card PPO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Commercial Insurance Company
- First Choice Health PPO
- First Health (Coventry Health Care) PPO
- GEHA
- Health Plan of Oregon PPO
- HealthNet
- Medicare Advantage PFFS
- Humana
- Kaiser Permanente
- Connect
- Mail Handlers Benefit Plan (MHBP)
- MedHealthInsurance
- Medicaid
- Medicare MCR
- MultiPlan PPO
- PHCS Network PPO
- ODS Health Plan
- Preferred PSN
- Heritage Plus
- Heritage Signature
- Personal Option EPO
- Preferred PPO
- Preferred Provider Network PPN
- Tricare
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- PacifiCare HMO
- United Healthcare
- Wisconsin Physicians Service
Awards
- CMS Meaningful Use Stage 1 Certification
- Physician Practice Connections Recognition Program
- Patient-Centered Medical Home Recognition Program
Education
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San Joaquin General Hospital -
Oregon Health & Science University School of Medicine
Hospital
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Providence St. Vincent Medical Center
Drug Facts
| NPI NUMBER | 1326090291 | |
| NPPES Provider LastName | HORTSCH | |
| NPPES Provider FirstName | MICHAEL | |
| NPPES Provider ZIPCode | 97223 | |
| NPPES Provider State | OR | |
| Specialty Description | Family Practice | |
| Total Claim Count | 6420.0 | |
| Distinct Opioid Count | 7.0 | |
| Opioid Claim Count | 271.0 | |
| Percent Opioid Claims | 4.22 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1326090291 |
| Last Name Of The Provider | HORTSCH |
| First Name Of The Provider | MICHAEL |
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