Professor, Internal Medicine, University of Arkansas COM
Gastroenterology
Dr. Jonathan A. Dranoff, MD
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Dr. Jonathan A. Dranoff is an expert in the field of Gastroenterology. He studied medicine at Boston University School of Medicine. Boston University School of Medicine has a rank of 30 in research and a 52 in primary care He over the years received 2 awards: "CMS Meaningful Use Stage 1 Certification" and "Elected Member". Jonathan Dranoff is a published doctor and has 46 publications published. The lastest was: 'Expression and subcellular localization of the ryanodine receptor in rat pancreatic acinar cells.' Dr. Jonathan A. Dranoff accepts Medicare.
Publications
- Strategies and endpoints of antifibrotic drug trials: Summary and recommendations from the AASLD Emerging Trends Conference, Chicago, June 2014.
- Beyond scar formation: Portal myofibroblast-mediated angiogenesis in the fibrotic liver.
- MCP-1 downregulates MMP-9 export via vesicular redistribution to lysosomes in rat portal fibroblasts.
- Expression of mediators of purinergic signaling in human liver cell lines.
- How does coffee prevent liver fibrosis? biological plausibility for recent epidemiological observations.
- Posttranslational regulation of tissue inhibitor of metalloproteinase-1 by calcium-dependent vesicular exocytosis.
- Contribution of Myofibroblasts of Different Origins to Liver Fibrosis.
- CXCL12 induces hepatic stellate cell conTraction through a calcium-independent pathway.
- Advances in cholangiocyte immunobiology.
- Activated Hepatic Stellate Cells Upregulate Transcription of Ecto-5'-nucleotidase/CD73 via Specific SP1 and SMAD Promoter Elements.
- Role of purinergic P2X receptors in the control of liver homeostasis.
- Co-expression of ecto-5'-nucleotidase/CD73 with specific NTPDases differentially regulates adenosine formation in the rat liver.
- New insights on the pathogenesis of biliary Cirrhosis provided by studies in FXR knockout mice.
- Portal fibroblasts: Underappreciated mediators of biliary fibrosis.
- Transcriptional regulation of IL-6 in bile duct epithelia by extracellular ATP.
- Adenosine induces loss of actin stress fibers and inhibits conTraction in hepatic stellate cells via Rho inhibition.
- IL-6 downregulates transcription of NTPDase2 via specific promoter elements.
- Transforming growth factor-beta and substrate stiffness regulate portal fibroblast activation in culture.
- Molecular basis for calcium signaling in hepatic stellate cells.
- The spatial distribution of inositol 1,4,5-trisphosphate receptor isoforms shapes Ca2+ waves.
- Cloning, purification, and identification of the liver canalicular ecto-ATPase as NTPDase8.
- Adenosine inhibits cytosolic calcium signals and chemotaxis in hepatic stellate cells.
- Secretion of MCP-1/CCL2 by bile duct epithelia induces myofibroblastic transdifferentiation of portal fibroblasts.
- The anti-apoptotic protein Mcl-1 inhibits mitochondrial Ca2+ signals.
- Portal fibroblasts regulate the proliferation of bile duct epithelia via expression of NTPDase2.
- Expression of P2Y nucleotide receptors and ectonucleotidases in quiescent and activated rat hepatic stellate cells.
- The ecto-nucleoside triphosphate diphosphohydrolase NTPDase2/CD39L1 is expressed in a novel functional compartment within the liver.
- Isolation of primary rat liver fibroblasts.
- The type II inositol 1,4,5-trisphosphate receptor can trigger Ca2+ waves in rat hepatocytes.
- NT5E Mutations That Cause Human Disease Are Associated with Intracellular Mistrafficking of NT5E Protein.
- Intracellular calcium signals regulate growth of hepatic stellate cells via specific effects on cell cycle progression.
- Prevention of liver fibrosis by the purinoceptor antagonist pyridoxal-phosphate-6-azophenyl-2'',4''-disulfonate (PPADS).
- Autocrine release of TGF-beta by portal fibroblasts regulates cell growth.
- Ectonucleotidase NTPDase2 is selectively down-regulated in biliary Cirrhosis.
- Succinate is a paracrine signal for liver damage.
- Stimulation of bile duct epithelial secretion by glybenclamide in normal and cholestatic rat liver.
- Expression and subcellular localization of the ryanodine receptor in rat pancreatic acinar cells.
- Regulation of bile acid transport: beyond molecular cloning.
- Short-term regulation of bile acid uptake by microfilament-dependent translocation of rat ntcp to the plasma membrane.
- Transnasal endoscopy for enteral feeding tube placement in critically ill patients.
- A primitive ATP receptor from the little skate Raja erinacea.
- It''s swell to have ATP in the liver.
- Polarized expression and function of P2Y ATP receptors in rat bile duct epithelia.
- Establishment and Characterization of Rat Portal Myofibroblast Cell Lines.
- Pathological Changes in Pulmonary Circulation in Carbon Tetrachloride (ccl4)-Induced Cirrhotic Mice.
Schools
Med Coll Of Pa
Boston University School Of Public Health
Yale University School Of Med
Procedures Preformed
- Colonoscopy, Proctosigmoidoscopy, and Sigmoidoscopy
- Endoscopy (Esophagus, Stomach, Small Intestine)
- Liver Biopsy
Conditions Treated
- Abdominal Pain
- Anemia
- Barrett's Esophagus
- Benign Neoplasm of the Digestive System
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Doctors Specialties
- Gastroenterology
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
- Elected Member
Education
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Yale University School of Medicine -
Boston University School of Medicine
Drug Facts
| NPI NUMBER | 1669458469 | |
| NPPES Provider LastName | DRANOFF | |
| NPPES Provider FirstName | JONATHAN | |
| NPPES Provider ZIPCode | 722057101 | |
| NPPES Provider State | AR | |
| Specialty Description | Gastroenterology | |
| Total Claim Count | 220.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1669458469 |
| Last Name Of The Provider | DRANOFF |
| First Name Of The Provider | JONATHAN |
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