Physician
Internal Medicine
Dr. Elaine M. Sloand, MD
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Dr. Elaine M. Sloand is an expert in the field of Internal Medicine. Dr. Elaine M. Sloand is a published physician. She has 92 papers published. The most current publication "Correction of the PNH defect by GPI-anchored protein transfer."
Publications
- Effects of granulocyte-colony-stimulating factor on Monosomy 7 aneuploidy in healthy hematopoietic stem cell and granulocyte donors.
- T-cell immune responses to Wilms tumor 1 protein in myelodysplasia responsive to immunosuppressive therapy.
- Targeting immune dysregulation in myelodysplastic syndromes.
- Alemtuzumab treatment of intermediate-1 myelodysplasia patients is associated with sustained improvement in blood counts and cytogenetic remissions.
- Graft-versus-host disease: role of inflammation in the development of chromosomal abnormalities of keratinocytes.
- Association of telomere length of peripheral blood leukocytes with hematopoietic relapse, malignant transformation, and survival in severe aplastic anemia.
- A Non-ATP-Competitive Dual Inhibitor of JAK2 and BCR-ABL Kinases: Elucidation of a Novel Therapeutic Spectrum Based on Substrate Competitive Inhibition.
- Immunosuppression for myelodysplastic syndrome: how bench to bedside to bench research led to success.
- Hypocellular myelodysplasia.
- Primitive quiescent CD34+ cells in chronic myeloid leukemia are targeted by in vitro expanded natural killer cells, which are functionally enhanced by bortezomib.
- Factors affecting response and survival in patients with myelodysplasia treated with immunosuppressive therapy.
- Myelodysplastic syndromes: introduction.
- Immunosuppressive therapy for myelodysplastic syndromes: refining the indications.
- The role of the immune system in myelodysplasia: implications for therapy.
- Cytokine gene polymorphisms in acquired bone marrow failure.
- Mobilization, collection, and immunomagnetic selection of peripheral blood CD34 cells in recovered aplastic anemia patients.
- Distinct EBV and CMV reactivation patterns following antibody-based immunosuppressive regimens in patients with severe aplastic anemia.
- CD34 cells from patients with trisomy 8 myelodysplastic syndrome (MDS) express early apoptotic markers but avoid programmed cell death by up-regulation of antiapoptoti...
- Granulocyte colony-stimulating factor preferentially stimulates proliferation of monosomy 7 cells bearing the isoform IV receptor.
- Brief communication: Successful treatment of pure red-cell aplasia with an anti-interleukin-2 receptor antibody (daclizumab).
- Preferential suppression of trisomy 8 compared with normal hematopoietic cell growth by autologous lymphocytes in patients with trisomy 8 myelodysplastic syndrome.
- Soluble urokinase activator receptor (suPAR) in stem cell mobilization.
- Distinctive gene expression profiles of CD34 cells from patients with myelodysplastic syndrome characterized by specific chromosomal abnormalities.
- Transfer of glycosylphosphatidylinositol-anchored proteins to deficient cells after erythrocyte transfusion in paroxysmal nocturnal hemoglobinuria.
- Marrow failure.
- Recombinant humanized anti-IL-2 receptor antibody (daclizumab) produces responses in patients with moderate aplastic anemia.
- Fas-mediated apoptosis is important in regulating cell replication and death in trisomy 8 hematopoietic cells but not in cells with other cytogenetic abnormalities.
- Distinct clinical outcomes for cytogenetic abnormalities evolving from aplastic anemia.
- Studies on platelet membrane glycoproteins and platelet function during hemodialysis.
- Telomere length in paroxysmal nocturnal hemoglobinuria correlates with clone size.
- Nonisotopic detection of microRNA using digoxigenin labeled RNA probes.
- Hematopoietic-specific microRNA expression in human cells.
- Absence of donor-derived keratinocyte stem cells in skin tissues cultured from patients after mobilized peripheral blood hematopoietic stem cell transplantation.
- Cytogenetic abnormalities in paroxysmal nocturnal haemoglobinuria usually occur in haematopoietic cells that are glycosylphosphatidylinositol-anchored protein (GPI-AP)...
- A pilot study of the recombinant soluble human tumour necrosis factor receptor (p75)-Fc fusion protein in patients with myelodysplastic syndrome.
- Paroxysmal nocturnal hemoglobinuria following alemtuzumab immunosuppressive therapy for myelodysplastic syndrome and complicated by recurrent life-threatening thrombos...
- Long-term follow-up of patients with moderate aplastic anemia and pure red cell aplasia treated with daclizumab.
- Increased soluble urokinase plasminogen activator receptor (suPAR) is associated with thrombosis and inhibition of plasmin generation in paroxysmal nocturnal hemoglobi...
- Treatment of severe aplastic anemia with a combination of horse antithymocyte globulin and cyclosporine, with or without sirolimus: a prospective randomized study.
- Autoimmune mechanisms in the pathophysiology of myelodysplastic syndromes and their clinical relevance.
- The relationship of aplastic anemia and PNH.
- Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome.
- Intracellular interferon-gamma in circulating and marrow T cells detected by flow cytometry and the response to immunosuppressive therapy in patients with aplastic ane...
- Clonal dominance of chronic myelogenous leukemia is associated with diminished sensitivity to the antiproliferative effects of neutrophil elastase.
- Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA.
- Genetic polymorphisms and the risk of acquired idiopathic aplastic anemia.
- Hematologic complications of HIV infection.
- Determining which patients with myelodysplastic syndrome will respond to immunosuppressive treatment.
- Successful use of balloon ablation to treat menorrhagia complicating aplastic anemia.
- Human G-CSF-mobilized CD34-positive peripheral blood progenitor cells can stimulate allogeneic T-cell responses: implications for graft rejection in mismatched transpl...
- Impaired hematopoiesis in paroxysmal nocturnal hemoglobinuria/aplastic anemia is not associated with a selective proliferative defect in the glycosylphosphatidylinosit...
- Role of Fas ligand and receptor in the mechanism of T-cell depletion in acquired immunodeficiency syndrome: effect on CD4+ lymphocyte depletion and human immunodeficie...
- Inhibition of interleukin-1beta-converting enzyme in human hematopoietic progenitor cells results in blockade of cytokine-mediated apoptosis and expansion of their pro...
- Correction of the PNH defect by GPI-anchored protein transfer.
- Pharmacologic doses of granulocyte colony-stimulating factor affect cytokine production by lymphocytes in vitro and in vivo.
- Sustained long-term hematologic recovery despite a marked quantitative defect in the stem cell compartment of patients with aplastic anemia after immunosuppressive the...
- Protease inhibitors stimulate hematopoiesis and decrease apoptosis and ICE expression in CD34(+) cells.
- Effect of amphotericin B and fluconazole on platelet membrane glycoproteins.
- Human immunodeficiency virus type 1 protease inhibitor modulates activation of peripheral blood CD4(+) T cells and decreases their susceptibility to apoptosis in vitro...
- Comparison of random-donor platelet concentrates prepared from whole blood units and platelets prepared from single-donor apheresis collections.
- 1-Deamino-8-D-arginine vasopressin (DDAVP) increases platelet membrane expression of glycoprotein Ib in patients with disorders of platelet function and after cardiopu...
- Platelet membrane glycoproteins and microvesicles in blood from postoperative salvage: a study in cardiac bypass patients.
- The role of interleukin-converting enzyme in Fas-mediated apoptosis in HIV-1 infection.
- Analysis of the expression of glycosylphosphatidylinositol anchored proteins on platelets from patients with paroxysmal nocturnal hemoglobinuria.
- Secondary colony formation after long-term bone marrow culture using peripheral blood and bone marrow of HIV-infected patients.
- Large granular lymphocyte (LGL)-like clonal expansions in paroxysmal nocturnal hemoglobinuria (PNH) patients.
- Effect of albumin on the inhibition of platelet aggregation by beta-lactam antibiotics.
- Neither human immunodeficiency virus-1 (HIV-1) nor HIV-2 infects most-primitive human hematopoietic stem cells as assessed in long-term bone marrow cultures.
- Reduction of platelet glycoprotein Ib in uraemia.
- Effect of white cells on platelets during storage.
- Transfusion of blood components to persons infected with human immunodeficiency virus type 1: relationship to opportunistic infection.
- Epidemiology of thrombocytopenia in HIV infection.
- Altered naive and memory CD4+ T-cell homeostasis and immunosenescence characterize younger patients with myelodysplastic syndrome.
- The graft-versus-leukemia effect of nonmyeloablative stem cell allografts may not be sufficient to cure chronic myelogenous leukemia.
- Safety of the blood supply.
- Preparation of IgA-deficient platelets.
- HIV testing. State of the art.
- Chemotherapy for patients with pulmonary Kaposi's sarcoma: benefit of filgrastim (G-CSF) in supporting dose administration.
- Methylene blue for neutralization of heparin.
- IgA levels in platelets washed by automated procedure.
- White cell reduction in platelet concentrates.
- [Acquired immunodeficiency syndrome].
- Transfusion in HIV disease.
- Hematopoietic stem cells and progenitors of chronic myeloid leukemia express leukemia-associated antigens: implications for the graft-versus-leukemia effect and peptid...
- Viral risks associated with blood transfusion.
- Hematopoiesis in HIV infection: use of colony stimulating factors and cytokines.
- The challenge of Pneumocystis carinii culture.
- Platelet antithrombin defect in malignancy: platelet protein alterations.
- A novel hereditary macrothrombocytopenia.
- Use of human immunodeficiency virus (HIV) human hyperimmune immunoglobulin in HIV type 1-infected children (Pediatric AIDS clinical trials group protocol 273).
- Monoclonal gammopathy-associated pure red cell aplasia.
Schools
University Of Rochester
Fell New England Deaconess
New England Deaconess
National Institute Health
Doctors Specialties
- Blood Banking
- Hematology
- Internal Medicine
Accepted Insurances
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