778 results on '"Bernstein, Irwin D."'
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102. SIRT1 is dispensable for function of hematopoietic stem cells in adult mice
103. Drug Transporter ABCB1 SNP Predicts Outcome in Patients with Acute Myeloid Leukemia Treated with Gemtuzumab Ozagamicin: A Report from Children's Oncology Group AAML0531 Trial
104. Angiopoietin-like proteins stimulate HSPC development through interaction with notch receptor signaling
105. Author response: Angiopoietin-like proteins stimulate HSPC development through interaction with notch receptor signaling
106. Infusion of a Non HLA-Matched Off-the-Shelf Ex Vivo Expanded Cord Blood Progenitor Cell Product Following Myeloablative Cord Blood Transplantation Is Safe, Decreases the Time to Hematopoietic Recovery, and Results in Excellent Overall Survival
107. Notch Signaling By Either Notch1 or Notch2 Mediates Expansion of AGM-Derived Long-Term HSC Populations in Vitro
108. E47 controls the developmental integrity and cell cycle quiescence of multipotential hematopoietic progenitors1
109. PASSIVE IMMUNOTHERAPY WITH MONOCLONAL ANTIBODIES TO DIFFERENTIATION ANTIGENS
110. Therapy of Acute Leukemia with Monoclonal Antibodies and Immunoconjugates
111. High-Dose Radioimmunotherapy of B Cell Lymphomas1
112. Antibody-targeted therapy
113. Clonal development, stem-cell differentiation, and clinical remissions in acute nonlymphocytic leukemia
114. Maturation of hematopoietic stem cells from prehematopoietic stem cells is accompanied by up-regulation of PD-L1
115. Dose Dependent Enhancement Of Neutrophil Recovery By Infusion Of Notch Ligand Ex Vivo Expanded Cord Blood Progenitors: Results Of a Multi-Center Phase I Trial
116. Novel Long-Term Co-Culture Approach Identifies Prognostically Important Heterogeneity Of Stem/Progenitor Cell Involvement In Human Acute Myeloid Leukemia
117. AGM-Derived Endothelial Cells and Notch Ligands Provide Embryonic Hematopoietic Stem Cell-Supportive Niches In Vitro
118. Induction of Multipotential Hematopoietic Progenitors from Human Pluripotent Stem Cells via Respecification of Lineage-Restricted Precursors
119. Transmembrane protein 88: a Wnt regulatory protein that specifies cardiomyocyte development
120. SGN-CD33A: a novel CD33-targeting antibody–drug conjugate using a pyrrolobenzodiazepine dimer is active in models of drug-resistant AML
121. Notch-HES1 signaling axis controls hemato-endothelial fate decisions of human embryonic and induced pluripotent stem cells
122. Visualizing human ESC-derived hematopoiesis
123. NOTCH signaling specifies arterial-type definitive hemogenic endothelium from human pluripotent stem cells
124. Activation of Notch Signaling Mediates Ex Vivo Expansion of Multilineage, Engrafting Murine Hematopoietic Progenitors From Embryonic Sources.
125. SGN-CD33A: A Novel CD33-Directed Antibody-Drug Conjugate, Utilizing Pyrrolobenzodiazepine Dimers, Demonstrates Preclinical Antitumor Activity Against Multi-Drug Resistant Human AML
126. Activation of Notch Signaling During Ex Vivo Expansion Maintains Donor Muscle Cell Engraftment
127. Engineering Stem Cell Expansion
128. Infusion of Mismatched Ex Vivo Expanded and Cryopreserved Murine Hematopoietic Progenitors Rescues Mice After Lethal Radiation Exposure,
129. Infusion of “off-the-shelf” Third Party Ex Vivo Expanded Cord Blood Progenitor Cells As Supportive Care Following Clofarabine with High Dose Cytarabine and Granulocyte Colony-Stimulating Factor Priming for the Treatment of AML,
130. Prognostic implications of the IDH1 synonymous SNP rs11554137 in pediatric and adult AML: a report from the Children's Oncology Group and SWOG
131. AF1q/MLLT11 regulates the emergence of human prothymocytes through cooperative interaction with the Notch signaling pathway
132. Cryopreserved Ex-Vivo Expanded Murine Hematopoietic Progenitors Can Engraft Across MHC Barriers and Improve Survival In a Murine Model of Acute Radiation Syndrome.
133. Sequential Acquisition of Somatic Mutations In Progenitors with Differential Proliferative Potential In Human Acute Myeloid Leukemia
134. Prognostic Implications of the IDH1 synonymous SNP rs11554137 In Pediatric and Adult AML: a Children's Oncology Group and Southwest Oncology Group Study
135. Endothelial Cells Are Essential for the Self-Renewal and Repopulation of Notch-Dependent Hematopoietic Stem Cells
136. Notch2 Signaling Inhibits Differentiation and Promotes Self Renewal of Hematopoietic Stem and Progenitor Cells During Marrow Regeneration.
137. The transcription factor E47 controls the cell cycle quiescence and development of multipotent hematopoietic progenitors (138.3)
138. Hematopoietic Stem Cell Function and Survival Depend on c-Myc and N-Myc Activity
139. Priming with Myeloid Growth Factors Enhances CD33 Expression, Decreases P-Glycoprotein Activity, and Improves Efficacy of Gemtuzumab Ozogamicin against Acute Myeloid Leukemia (AML) Colony Forming Cells (CFC)
140. Notch-Mediated Expansion of Human Cord Blood Progenitor Cells Results in Rapid Myeloid Reconstitution in Vivo Following Myeloablative Cord Blood Transplantation
141. Enhanced T Cell Reconstitution by Cord Blood Progenitors Expanded Ex-Vivo Using the Notch Ligand Delta1
142. Facilitation of Thymic and Bone Marrow Engraftment by Hematopoietic Progenitors Expanded Ex-Vivo Using the Notch Ligand Delta1
143. E47 Controls the Developmental Integrity and Cell Cycle Quiescence of Multipotential Hematopoietic Progenitors
144. Simultaneously targeting CD45 significantly increases cytotoxicity of the anti-CD33 immunoconjugate, gemtuzumab ozogamicin, against acute myeloid leukemia (AML) cells and improves survival of mice bearing human AML xenografts
145. Loss of TLE1 and TLE4 from the del(9q) commonly deleted region in AML cooperates with AML1-ETO to affect myeloid cell proliferation and survival
146. Phosphorylated ITIMs Enable Ubiquitylation of an Inhibitory Cell Surface Receptor
147. Gene Conversion Is a Late Event in Evolution of High Risk AML.
148. The HSP 90 Inhibitor, 17-AAG, Increases Gemtuzumab Ozogamicin-Induced Cytotoxicity in Acute Myeloid Leukemia (AML) Cells.
149. ITIM-dependent endocytosis of CD33-related Siglecs: role of intracellular domain, tyrosine phosphorylation, and the tyrosine phosphatases, Shp1 and Shp2
150. The Interaction of the Wnt and Notch Pathways Modulates Natural Killer Versus T Cell Differentiation
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