401 results on '"Maciejewski, J P"'
Search Results
52. Clonality of the stem cell compartment during evolution of myelodysplastic syndromes and other bone marrow failure syndromes
53. Survival of AML patients receiving HLA-matched sibling donor allogeneic bone marrow transplantation correlates with HLA-Cw ligand groups for killer immunoglobulin-like receptors
54. Erratum: Epistasis between TIFAB and miR-146a: neighboring genes in del(5q) myelodysplastic syndrome
55. Dendritic cells in autologous hematopoietic stem cell transplantation for diffuse large B-cell lymphoma: graft content and post transplant recovery predict survival
56. Differential gene expression in hematopoietic progenitors from paroxysmal nocturnal hemoglobinuria patients reveals an apoptosis/immune response in ‘normal’ phenotype cells
57. Liquid metal induced embrittlement in fuel line braze joints
58. Large granular lymphocyte (LGL)-like clonal expansions in paroxysmal nocturnal hemoglobinuria (PNH) patients
59. Constitution and telomere dynamics of bone marrow stromal cells in patients undergoing allogeneic bone marrow transplantation
60. Intracellular cytokines of peripheral blood lymphocytes in nephrotic syndrome
61. Stable quasicrystalline phase in Al-Cu-Fe-Cr coating materials
62. Cytomegalovirus-Specific Regulatory and Effector T Cells Share TCR Clonality—Possible Relation to Repetitive CMV Infections
63. Deletions of Xp22.2 including PIG-A locus lead to paroxysmal nocturnal hemoglobinuria
64. Intravenous aminophylline increases the degree of saturation of urine with calcium phosphate and struvite
65. Significant disease burden in paroxysmal nocturnal haemoglobinuria (PNH) patients with lower levels of haemolysis, mild anaemia and minimal transfusion: clinical improvement with eculizumab therapy: 180
66. Double-negative regulatory T cells induce allotolerance when expanded after allogeneic haematopoietic stem cell transplantation
67. Slightly dilated acute obstructive failure of congenital solitary kidney
68. Comparative analysis of the influences of IL-1, IL-3 and GM-CSF on the commitment of granulocyte-macrophage progenitors in vitro
69. Erratum: Disruption of SF3B1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells
70. An Investigation of Sputtered Al-Cu-Fe-Cr Quasicrystalline Films Via Synchrotron Diffraction
71. Erratum: Regulation of IL-2 expression by transcription factor BACH2 in umbilical cord blood CD4+T cells
72. Case of the month: a 4-year-old girl with cardiac insufficiency and intermittent fever
73. Risk of developing chronic myeloid neoplasms in well-differentiated thyroid cancer patients treated with radioactive iodine
74. A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia
75. Distinct clinical and biological implications of various DNMT3A mutations in myeloid neoplasms
76. Differences in genomic patterns and clinical outcomes between African-American and White patients with myelodysplastic syndromes
77. Clinicopathologic and molecular characterization of myeloid neoplasms with isolated t(6;9)(p23;q34)
78. The complexity of interpreting genomic data in patients with acute myeloid leukemia
79. Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents
80. Complete mutational spectrum of the autophagy interactome: a novel class of tumor suppressor genes in myeloid neoplasms
81. Epistasis between TIFAB and miR-146a: neighboring genes in del(5q) myelodysplastic syndrome
82. Activating somatic mutations outside the SH2-domain of STAT3 in LGL leukemia
83. Comprehensive quantitative proteomic profiling of the pharmacodynamic changes induced by MLN4924 in acute myeloid leukemia cells establishes rationale for its combination with azacitidine
84. An International MDS/MPN Working Group's perspective and recommendations on molecular pathogenesis, diagnosis and clinical characterization of myelodysplastic/myeloproliferative neoplasms
85. Prognostic signature and clonality pattern of recurrently mutated genes in inactive chronic lymphocytic leukemia
86. Genomic patterns associated with hypoplastic compared to hyperplastic myelodysplastic syndromes
87. Runx1 repression by histone deacetylation is critical for Setbp1-induced mouse myeloid leukemia development
88. The relationship of TP53 R72P polymorphism to disease outcome and TP53 mutation in myelodysplastic syndromes
89. FAS-MEDIATED MODULATION OF BCR/ABL IN CHRONIC MYELOGENOUS LEUKEMIA RESULTS IN DIFFERENTIAL EFFECTS ON APOPTOSIS
90. Human Cytomegalovirus, Human Herpesvirus 8 and Other Herpesviruses (Part III, Section 2, Chapter 75)
91. Disruption of SF3B1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells
92. The analysis of clonal diversity and therapy responses using STAT3 mutations as a molecular marker in large granular lymphocytic leukemia
93. PRPF8 defects cause missplicing in myeloid malignancies
94. A phase II multicenter rabbit anti-thymocyte globulin trial in patients with myelodysplastic syndromes identifying a novel model for response prediction
95. Baseline characteristics and disease burden in patients in the International Paroxysmal Nocturnal Hemoglobinuria Registry
96. Risk of developing chronic myeloid neoplasms in well-differentiated thyroid cancer patients treated with radioactive iodine
97. A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia
98. Distinct clinical and biological implications of various DNMT3A mutations in myeloid neoplasms
99. Novel somatic mutations in large granular lymphocytic leukemia affecting the STAT-pathway and T-cell activation
100. CSF3R T618I co-occurs with mutations of splicing and epigenetic genes and with a new PIM3 truncated fusion gene in chronic neutrophilic leukemia
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