Associate Professor, Medicine, Indiana University School of Medicine
Nephrology
Dr. Robert L. Bacallao, MD
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Robert Bacallao is an expert in the field of Nephrology. He studied medicine at University of Illinois College of Medicine at Chicago. University of Illinois College of Medicine at Chicago is ranked 49 in research and 85 in primary care medicine Robert Bacallao is a published doctor. He published 63 publications, including: 'Role of the matrix in autosomal dominant polycystic kidney disease.' Robert Bacallao accepts Medicare.
Publications
- Management of Pain in ADPKD and Anatomy of Renal Innervation.
- Dichloroacetate treatment accelerates development of pathology in rodent autosomal recessive polycystic Kidney disease.
- Caveat Emptor:If you have PKD be careful of what your drink?
- Inversin modulates the cortical actin network during mitosis.
- A Method to Facilitate and Monitor Expression of Exogenous Genes in the Rat Kidney Using Plasmid and Viral Vectors.
- A Telomerase Immortalized Human Proximal Tubule Cell Line With a Truncation Mutation (Q4004X) in Polycystin-1.
- High resolution 4-dimension imaging of metanephric embryonic Kidney morphogenesis.
- Calcimimetics inhibit Renal pathology in rodent nephronophthisis.
- MMP-9 gene deletion mitigates microvascular loss in a model of ischemic acute Kidney injury.
- Ectopic expression of cadherin 8 is sufficient to cause cyst formation in a novel 3D collagen matrix Renal tubule culture.
- Impaired endothelial proliferation and mesenchymal transition contribute to vascular rarefaction following acute Kidney injury.
- Rab10 associates With primary cilia and the exocyst complex in renal epithelial cells.
- The biomarker enriched proteome of autosomal dominant polycystic Kidney disease cyst fluid.
- Attenuated, flow-induced ATP release contributes to absence of flow-sensitive, purinergic Cai2+ signaling in human ADPKD cyst epithelial cells.
- Characterization of the renal cyst fluid proteome in autosomal dominant polycystic Kidney disease (ADPKD) patients.
- Autosomal recessive polycystic Kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases confe...
- Pulmonary immunity to viral infection: adenovirus infection of lung dendritic cells renders T cells nonresponsive to interleukin-2.
- Real-time three-dimensional imaging of lipid signal transduction: apical membrane insertion of epithelial Na(+) channels.
- Renal cysts of inv/inv mice resemble early infantile nephronophthisis.
- Nucleotide depletion increases trafficking of gentamicin to the Golgi complex in LLC-PK1 cells.
- Functional studies of the Kidney of living animals using multicolor two-photon microscopy.
- Distal ureter morphogenesis depends on epithelial cell remodeling mediated by vitamin A and Ret.
- Inversin forms a complex With catenins and N-cadherin in polarized epithelial cells.
- The gene mutated in autosomal recessive polycystic Kidney disease encodes a large, receptor-like protein.
- Direct in situ reverse transcriptase-polymerase chain reaction.
- ADPKD: a human Disease altering Golgi function and basolateral exocytosis in renal epithelia.
- Compromised cytoarchitecture and polarized trafficking in autosomal dominant polycystic Kidney disease cells.
- Cablin: a novel protein of the capillary basal lamina.
- Role of the matrix in autosomal dominant polycystic Kidney disease.
- Optical methods in Renal research.
- Apiconuclear organization of microtubules does not specify protein delivery from the trans-Golgi network to different membrane domains in polarized epithelial cells.
- NHE-1 protein in vascular smooth muscle and lymphocytes from the spontaneously Hypertensive rat.
- Recent advances in the understanding of polycystic Kidney disease.
- Actin and villin compartmentation during ATP depletion and recovery in Renal cultured cells.
- Uncoupling of the molecular ''fence'' and paracellular ''gate'' functions in epithelial tight junctions.
- Assignment of the human Na+/glucose cotransporter gene SGLT1 to chromosome 22q13.1.
- Cell polarity in human renal Cystic disease.
- Biology of polycystic Kidney disease.
- Method for recovering ATP content and mitochondrial function after chemical anoxia in Renal cell cultures.
- The pathogenesis of polycystic Kidney disease.
- Impaired tubulogenesis of cyst-derived cells from autosomal dominant polycystic Kidneys.
- ATP depletion: a novel method to study junctional properties in epithelial tissues. II. Internalization of Na+,K(+)-ATPase and E-cadherin.
- ATP depletion: a novel method to study junctional properties in epithelial tissues. I. Rearrangement of the actin cytoskeleton.
- Filling in the matrix of Kidney disease.
- The role of the cytoskeleton in Renal development.
- Hematuria, proteinuria, and hypertension in a patient with multiple organ system Disease.
- The secY protein can act post-translationally to promote bacterial protein export.
- Molecular events in the organization of Renal tubular epithelium: from nephrogenesis to regeneration.
- Preservation of biological specimens for observation in a confocal fluorescence microscope and operational principles of confocal fluorescence microscopy.
- The subcellular organization of Madin-Darby canine Kidney cells during the formation of a polarized epithelium.
- Multiple methods of visualizing the yeast vacuole permit evaluation of its morphology and inheritance during the cell cycle.
- pH-induced microtubule-dependent redistribution of late endosomes in neuronal and epithelial cells.
- A polycystin-1 multiprotein complex is disrupted in polycystic Kidney disease cells.
- Cellular and subcellular localization of the ARPKD protein; fibrocystin is expressed on primary cilia.
- Novel light microscopy imaging techniques in nephrology.
- Mispolarization of desmosomal proteins and altered intercellular adhesion in autosomal dominant polycystic Kidney disease.
- Imaging gene expression.
- Differential expression of Renal proteins in a rodent model of Meckel syndrome.
- Cystic Kidney diseases and planar cell polarity signaling.
- Human ADPKD primary cyst epithelial cells With a novel, single codon deletion in the PKD1 gene exhibit defective ciliary polycystin localization and loss of flow-induc...
- Adult human CD133/1(+) Kidney cells isolated from papilla integrate into developing Kidney tubules.
- Lysophosphatidic acid is a modulator of cyst growth in autosomal dominant polycystic Kidney disease.
Schools
University Of Illinois College Of Medicine Chicago
University Of Illinois
University Of California Los Angeles
Procedures Preformed
- Hemodialysis
Conditions Treated
- Amyloidosis
- Calcium Metabolism Disorders
- Chronic Kidney Diseases
- Congenital Cystic Kidney Disease
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Doctors Specialties
- Nephrology
Accepted Insurances
Education
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UCLA Medical Center -
University of Illinois College of Medicine at Chicago -
University of Illinois College of Medicine
Drug Facts
| NPI NUMBER | 1295792760 | |
| NPPES Provider LastName | BACALLAO | |
| NPPES Provider FirstName | ROBERT | |
| NPPES Provider ZIPCode | 462025188 | |
| NPPES Provider State | IN | |
| Specialty Description | Nephrology | |
| Total Claim Count | 214.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1295792760 |
| Last Name Of The Provider | BACALLAO |
| First Name Of The Provider | ROBERT |
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