Physician
Gastroenterology
Dr. Michael P. Bustin, MD
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Michael P. Bustin, MD works in the field of Gastroenterology. He researched medicine at Georgetown University School of Medicine. Georgetown University School of Medicine is ranked 49/84 in Research/PrimaryCare. Dr. Michael P. Bustin is also published. He has 71 publications published. The lastest publication: "Deficiency of fat-soluble vitamins in treated patients with pancreatic insufficiency.' Michael P. Bustin, MD is registered with Medicare and accepts Medicare payments.
Publications
- Functional interplay between histone H1 and HMG proteins in chromatin.
- Harnessing the alarmin HMGN1 for antiCancer therapy.
- The Alarmin HMGN1 Contributes to Antitumor Immunity and Is a Potent Immunoadjuvant.
- SCORHE: A novel and practical approach to video monitoring of laboratory mice housed in vivarium cage racks.
- HMGN1 Modulates Nucleosome Occupancy and DNase I Hypersensitivity at the CpG Island Promoters of Embryonic Stem Cells.
- Microtubule dynamics alter the interphase nucleus.
- Chromatin decompaction by the nucleosomal binding protein HMGN5 impairs nuclear sturdiness.
- Metabolomics Reveals a Role for the Chromatin-Binding Protein HMGN5 in Glutathione Metabolism.
- Gene network reconstruction reveals cell cycle and antiviral genes as major drivers of cervical Cancer.
- High-mobility group nucleosome-binding protein 1 acts as an alarmin and is critical for lipopolysaccharide-induced Immune responses.
- The chromatin-binding protein HMGN1 regulates the expression of methyl CpG-binding protein 2 (MECP2) and affects the behavior of mice.
- Architecture of the high mobility group nucleosomal protein 2-nucleosome complex as revealed by methyl-based NMR.
- Distinct properties of human HMGN5 reveal a rapidly evolving but functionally conserved nucleosome binding protein.
- Effects of HMGN variants on the cellular transcription profile.
- Genomic profiling of HMGN1 reveals an association with chromatin at regulatory regions.
- The role of chromatin structure in cell migration.
- UV-induced histone H2AX phosphorylation and DNA damage related proteins accumulate and persist in nucleotide excision repair-deficient XP-B cells.
- Efficient cell migration requires global chromatin condensation.
- HMGN5/NSBP1: a new member of the HMGN protein family that affects chromatin structure and function.
- High mobility group proteins.
- Regulation of chromatin structure and function by HMGN proteins.
- The nucleosome binding protein HMGN3 is expressed in pancreatic alpha-cells and affects plasma glucagon levels in mice.
- The nucleosome-binding protein HMGN2 modulates global genome repair.
- The interaction of NSBP1/HMGN5 with nucleosomes in euchromatin counteracts linker histone-mediated chromatin compaction and modulates transcription.
- The nucleosome binding protein HMGN3 modulates the transcription profile of pancreatic beta cells and affects insulin secretion.
- Nucleosome binding proteins potentiate ATM activation and DNA damage Response by modifying chromatin.
- Visualization of the expression of HMGN nucleosomal binding proteins in the developing mouse embryo and in adult mouse tissues.
- Expression of nucleosomal protein HMGN1 in the cycling mouse hair follicle.
- The dynamics of HMG protein-chromatin interactions in living cells.
- The nucleosomal binding protein NSBP1 is highly expressed in the placenta and modulates the expression of differentiation markers in placental Rcho-1 cells.
- Activation of ATM depends on chromatin interactions occurring before induction of DNA damage.
- Differential expression of the HMGN family of chromatin proteins during ocular development.
- Delineation of the protein module that anchors HMGN proteins to nucleosomes in the chromatin of living cells.
- Cell cycle-dependent binding of HMGN proteins to chromatin.
- Chromosomal protein HMGN1 enhances the heat shock-induced remodeling of Hsp70 chromatin.
- Migration cues induce chromatin alterations.
- HMG chromosomal proteins in development and Disease.
- Chromosomal protein HMGN1 modulates the phosphorylation of serine 1 in histone H2A.
- High mobility group box-1 protein induces the migration and activation of human dendritic cells and acts as an alarmin.
- Determinants of histone H1 mobility and chromatin binding in living cells.
- Distinct domains in high mobility group N variants modulate specific chromatin modifications.
- A role for chromosomal protein HMGN1 in corneal maturation.
- Down-regulation of nucleosomal binding protein HMGN1 expression during embryogenesis modulates Sox9 expression in chondrocytes.
- Chromosomal protein HMGN1 modulates the expression of N-cadherin.
- Chromosomal protein HMGN1 enhances the acetylation of lysine 14 in histone H3.
- Increased tumorigenicity and sensitivity to ionizing radiation upon loss of chromosomal protein HMGN1.
- The dynamics of histone H1 function in chromatin.
- Chromosomal protein HMGN1 modulates histone H3 phosphorylation.
- Global nature of dynamic protein-chromatin interactions in vivo: three-dimensional genome scanning and dynamic interaction networks of chromatin proteins.
- Dynamic interaction of HMGA1a proteins with chromatin.
- Network of dynamic interactions between histone H1 and high-mobility-group proteins in chromatin.
- Chromosomal proteins HMGN3a and HMGN3b regulate the expression of glycine transporter 1.
- Immunochemical analysis of chromatin.
- Preparation and functional analysis of HMGN proteins.
- Chromatin decompaction method by HMGN proteins.
- Developmental role of HMGN proteins in Xenopus laevis.
- HMGN dynamics and chromatin function.
- The role of DNA methylation in setting up chromatin structure during development.
- Retroposed copies of the HMG genes: a window to genome dynamics.
- Chromosomal protein HMGN1 enhances the rate of DNA repair in chromatin.
- Inflammation-promoting activity of HMGB1 on human microvascular endothelial cells.
- At the crossroads of necrosis and apoptosis: signaling to multiple cellular targets by HMGB1.
- Mitotic phosphorylation of chromosomal protein HMGN1 inhibits nuclear import and promotes interaction with 14.3.3 proteins.
- Immunohistochemical localization of the nucleosome-binding protein HMGN3 in mouse brain.
- Competition between histone H1 and HMGN proteins for chromatin binding sites.
- Histone cross-linking by transglutaminase.
- Metastable macromolecular complexes containing high mobility group nucleosome-binding chromosomal proteins in HeLa nuclei.
- Modulation of HMG-N2 binding to chromatin by butyrate-induced acetylation in human colon adenocarcinoma cells.
- Deficiency of fat-soluble vitamins in treated patients with pancreatic insufficiency.
- Management of common non-malignant GI problems in the elderly.
Schools
Georgetown University
Conn Health Center
University MD Hospital
Procedures Preformed
- Colonoscopy, Proctosigmoidoscopy, and Sigmoidoscopy
- Endoscopy (Esophagus, Stomach, Small Intestine)
- Manometry
Conditions Treated
- Abdominal Pain
- Anemia
- Barrett's Esophagus
- Benign Neoplasm of the Digestive System
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Doctors Specialties
- Gastroenterology
Accepted Insurances
Education
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University of Maryland -
University of Connecticut -
Georgetown University School of Medicine
Hospital
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Baptist Hospital of Miami -
University of Miami Hospital
Drug Facts
| NPI NUMBER | 1861403206 | |
| NPPES Provider LastName | BUSTIN | |
| NPPES Provider FirstName | MICHAEL | |
| NPPES Provider ZIPCode | 331251673 | |
| NPPES Provider State | FL | |
| Specialty Description | Gastroenterology | |
| Total Claim Count | 2503.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1861403206 |
| Last Name Of The Provider | BUSTIN |
| First Name Of The Provider | MICHAEL |
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