Associate Professor, Pathology, University of Utah School of Medicine
Pathology
Dr. David W. Bahler, MD
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David W. Bahler, MD is an expert in the field of Pathology. He attended University of Rochester School of Medicine and Dentistry. Dr. David W. Bahler is also published. He has 58 publications published. The lastest publication: "Clonal salivary gland infiltrates associated with myoepithelial sialadenitis (Sjgren's syndrome) begin as nonmalignant antigen-selected expansions.' David Bahler accepts all Medicare patients.
Publications
- A Limited Plasma Cell Flow Cytometry Panel With Reflex CD138 Immunohistochemistry Is an Optimal Workflow Process for Evaluating Plasma Cell Neoplasms in Bone Marrow Sp...
- Myelofibrotic Transformations of Polycythemia Vera and Essential Thrombocythemia are Morphologically, Biologically, and Prognostically Indistinguishable From Primary M...
- Recurrent reciprocal RNA chimera involving YPEL5 and PPP1CB in chronic lymphocytic Leukemia.
- A Quantitative Allele-Specific PCR Test for the BRAF V600E Mutation Using a Single Heterozygous Control Plasmid for Quantitation: A Model for qPCR Testing without Stan...
- Improved flow cytometric detection of ZAP-70 in chronic lymphocytic Leukemia using experimentally optimized isotypic control antibodies.
- A pyrosequencing-based test for detection and relative quantification of the BCR-ABL1 T315I point mutation.
- Clinical laboratory analysis of immunoglobulin heavy chain variable region genes for chronic lymphocytic Leukemia prognosis.
- Immunomagnetic bead separation of mononuclear cells from contaminating granulocytes in cryopreserved blood samples.
- Use of similar immunoglobulin VH gene segments by MALT Lymphomas of the ocular adnexa.
- Small B-cell neoplasms with typical mantle cell lymphoma immunophenotypes often include chronic lymphocytic Leukemias.
- Fatal non-transplant-related epstein-barr virus-associated atypical lymphoid proliferations in infants and children: a clinicopathologic study.
- Whole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic Leukemia.
- CD158k/KIR3DL2 is a useful marker for identifying neoplastic T-cells in Sézary syndrome by flow cytometry.
- A new DNA-based test for detection of nucleophosmin exon 12 mutations by capillary electrophoresis.
- Optimization of flow cytometric measurement of ZAP-70 in chronic lymphocytic Leukemia.
- Quantitation of plasma cells in bone marrow aspirates by flow cytometric analysis compared with morphologic assessment.
- Flow cytometric analysis of different CD14 epitopes can help identify immature monocytic populations.
- T-cell large granular lymphocyte Leukemias have multiple phenotypic abnormalities involving pan-T-cell antigens and receptors for MHC molecules.
- Hairy cell Leukemia variant: fact or fiction.
- Indolent mantle cell Lymphoma with nodal involvement and mutated immunoglobulin heavy chain genes.
- Analysis of CD10+ hairy cell Leukemia.
- Importance of CD117 in the evaluation of Acute leukemias by flow cytometry.
- Splenic marginal zone Lymphomas appear to originate from different B cell types.
- Rapidly progressive, Acute polyradiculopathies and cranial neuropathies resulting from leptomeningeal nasal-type NK cell lymphoma.
- The induction of rules for predicting chemical carcinogenesis in rodents.
- Symbolic, neural, and Bayesian machine learning models for predicting carcinogenicity of chemical compounds.
- Recurrent Epstein-Barr virus-associated lesions in organ transplant recipients.
- T cell antigen receptor vaccines for active therapy of T cell malignancies.
- Histological and immunoglobulin VH gene analysis of interfollicular small lymphocytic Lymphoma provides evidence for two types.
- Transformation of mycosis fungoides: T-cell receptor beta gene analysis demonstrates a common clonal origin for plaque-type mycosis fungoides and CD30+ large-cell lymp...
- Salivary gland mucosa-associated lymphoid tissue Lymphoma immunoglobulin V(H) genes show frequent use of V1-69 with distinctive CDR3 features.
- Epstein-Barr virus-negative post-transplant lymphoproliferative Disorders: a distinct entity?
- Clonal salivary gland infiltrates associated with myoepithelial sialadenitis (Sjögren's syndrome) begin as nonmalignant antigen-selected expansions.
- Salivary gland lymphoid infiltrates associated with lymphoepithelial lesions: a clinicopathologic, immunophenotypic, and genotypic study.
- Ongoing Ig gene hypermutation in salivary gland mucosa-associated lymphoid tissue-type Lymphomas.
- A clonally distinct recurrence of Burkitt's Lymphoma at 15 years.
- Heterogeneity and clonal variation related to cell surface expression of a mouse lung tumor-associated antigen quantified using flow cytometry.
- Enhanced immune recognition of H-2 antigen-deficient murine lung carcinoma cells following treatment with dimethyl sulfoxide.
- Reduced tumorigenicity of a spontaneous mouse lung carcinoma following H-2 gene transfection.
- Lysis of a lung carcinoma by poly I:C-induced natural killer cells is independent of the expression of class I histocompatibility antigens.
- Dimethyl sulfoxide induces expression of H-2 antigens on mouse lung carcinoma cells.
- Molecular analysis of deficient class I H-2 antigen expression by mouse lung carcinoma cells.
- Analysis of Plasmodium falciparum growth in culture using acridine orange and flow cytometry.
- Follicular Lymphoma: a model of lymphoid tumor progression in man.
- Ig VH gene expression among human follicular Lymphomas.
- Diversity of T-cell antigen receptor variable genes used by mycosis fungoides cells.
- Clonal evolution of a follicular Lymphoma: evidence for antigen selection.
- Antigen selection in human Lymphomagenesis.
- Flow cytometric analysis of BCL-2 can distinguish small numbers of Acute lymphoblastic leukaemia cells from B-cell precursors.
- Analysis of immunoglobulin V genes suggests cutaneous marginal zone B-cell Lymphomas recognise similar antigens.
- Expression of T-plastin, FoxP3 and other tumor-associated markers by leukemic T-cells of cutaneous T-cell Lymphoma.
- Array CGH analysis of chronic lymphocytic Leukemia reveals frequent cryptic monoallelic and biallelic deletions of chromosome 22q11 that include the PRAME gene.
- Atypical 11q deletions identified by array CGH may be missed by FISH panels for prognostic markers in chronic lymphocytic Leukemia.
- Laboratory practice guidelines for detecting and reporting BCR-ABL drug resistance mutations in chronic myelogenous leukemia and Acute lymphoblastic leukemia: a report...
- Flow cytometric detection and serotyping of enterovirus for the clinical laboratory.
- Combined testing for CCAAT/enhancer-binding protein alpha (CEBPA) mutations and promoter methylation in Acute myeloid leukemia demonstrates shared phenotypic features.
- Diffuse large B-cell Lymphoma with aberrant expression of the T-cell antigens CD2 and CD7.
Schools
UmdnjSom
Conditions Treated
- Acute Leukemia
- Anemia
- Leukocytosis
- Lymphocytosis
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Doctors Specialties
- Hematology
- Hematopathology
- Pathology
Accepted Insurances
Education
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University of Pennsylvania Health System -
University of Rochester School of Medicine and Dentistry
Hospital
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University of Utah Health Care - Hospital and Clinics
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1346330974 |
| Last Name Of The Provider | BAHLER |
| First Name Of The Provider | DAVID |
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