578 results on '"Xue, Yongquan"'
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152. The Chandra Deep Field-South Survey: 4 Ms Source Catalogs
153. Effectiveness of First and Second Line Nilotinib in Chronic Myeloid Leukemia (CML) Patients with Atypical e1a2 BCR-ABL Transcripts
154. A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia
155. Engineering a methymycin/pikromycin-calicheamicin hybrid: construction of two new macrolides carrying a designed sugar moiety
156. Mechanistic studies of desosamine biosynthesis: C-4 deoxygenation precedes C-3 transamination
157. Tetraploid clone characterized by two t(15;17) in five cases of acute promyelocytic leukemia
158. Y-chromosome loss as the sole karyotypic anomaly with 3′RARα submicroscopic deletion in a case of M3r subtype of acute promyelocytic leukemia
159. An X-Ray Detected Group of Quiescent Early-Type Galaxies atz= 1.6 in the Chandra Deep Field South
160. THE X-RAY STAR FORMATION STORY AS TOLD BY LYMAN BREAK GALAXIES IN THE 4 Ms CDF-S
161. Isodicentric 20q− in two cases of B-cell acute lymphocytic leukemia with the respective t(9;20)(p11;q11.2) and t(9;22)(q34;q11.2)
162. Translocation (14;14)(q11;q32) with simultaneous involvement of the IGH and CEBPE genes in B-lineage acute lymphoblastic leukemia
163. Absence of BRAF V600E mutation in hematologic malignancies excluding hairy-cell leukemia
164. Establishment and characterization of a novel acute myeloid leukemia cell line, JIH-4, carrying a t(16;21)(p11.2;q22) and expressing the FUS-ERG fusion
165. Clinical, Biological Profile and Outcome of Biphenotypic Acute Leukemia: a Case Series.
166. VARIABLE O VI AND N V EMISSION FROM THE X-RAY BINARY LMC X-3: HEATING OF THE BLACK HOLE COMPANION
167. Pulmonary Alveolar Proteinosis as a Terminal Complication in a Case of Myelodysplastic Syndrome with idic(20q–)
168. Study On the Clonal Origin of Dysplastic Cells by Fluorescence in Situ Hybridization in Myelodysplastic Syndromes.
169. Chromosome Study On Chronic Lymphocytic Leukemia Using CpG- Oligodeoxynucleotide as Immunostimulant Agent.
170. A Novel Recurrent Chromosomal Inversion, Inversion(9)(p21q34), in Ph-Positive Leukemia Patients.
171. Two novel translocations disrupt the RUNX1 gene in acute myeloid leukemia
172. Establishment and characterization of a new human acute myelocytic leukemia cell line SH-2 with a loss of Y chromosome, a derivative chromosome 16 resulting from an unbalanced translocation between chromosomes 16 and 17, monosomy 17, trisomy 19, and p53 alteration
173. Modelling the broad-band spectral energy distribution of the microquasars XTE J1550−564 and H 1743−322
174. The Establishment and Characterization of a Human Acute Myelocytic Leukemia Cell Line, SH-2 Carrying t(16;17))(q24;q12) Translocation.
175. Der(20)idic(20)(p11)del(20)(q11q13) Is Seen Not Only in Myeloid Disorders but Also in Lymphoid Disorders: A Report of Further Seven Cases.
176. Two Novel Translocations That Disrupt the RUNX1 Gene in Acute Myeloid Leukemia.
177. Modeling the Hard States of XTE J1550−564 during Its 2000 Outburst
178. CytCD79a expression in acute leukemia with t(8;21): biphenotypic or myeloid leukemia?
179. Accretion Disk Spectra of the Brightest Ultraluminous X‐Ray Source in M82
180. A novel t(4;12)(q11;q13) in a patient with acute myeloid leukemia
181. Minimally Differentiated Acute Myeloid Leukemia with t(12;22)(p13;q11) Translocation Showing Primary Multidrug Resistance and Expressing Multiple Multidrug-Resistant Proteins
182. Fluorescence In Situ Hybridization Studies in 22 Cases of Plasma Cell Leukemia.
183. Trisomy 22 as the Sole Abnormality Is an Important Marker for Inversion 16 in Acute Myeloid Leukemia.
184. Dicentric (7;9)(p11;p11) is a rare but recurrent abnormality in acute lymphoblastic leukemia: a study of 7 cases
185. X‐Ray Spectral Variability of TeV Blazars during Rapid Flares
186. FISH studies identify the i(20q−) anomaly as a der(20)del(20)(q11q13)idic(20)(p11)
187. Hot One‐Temperature Accretion Flows Revisited
188. Multiplex Fluorescence In Situ Hybridization (M-FISH) in the Detection of Complex Karyotypic Abnormalities of Acute Myeloid Leukemia and Myelodysplastic Syndromes.
189. Fluorescence In Situ Hybridization Detected MRD and Chimerism in Patients with Hematologic Malignancies after allo-HSCT.
190. Interphase Fluorescence In Situ Hybridization Detection of Cytogenetic Abnormalities in B-Cell Chronic Lymphocytic Leukemia.
191. Preliminary Study of Inducing Differentiation and Apoptosis in a Novel Human Acute Monocytic Leukemic Cell Line SHI-1.
192. Gene expression profiling of the bone marrow mononuclear cells from patients with myelodysplastic syndrome
193. X‐Ray Flares from Markarian 501
194. Y-chromosome loss in acute promyelocytic leukemia
195. Generation of the NUP98-TOP1 fusion transcript by the t(11;20) (p15;q11) in a case of acute monocytic leukemia
196. Constitutional Robertsonian translocations in (9;22)-positive chronic myelogenous leukemia
197. Pentasomy 8q Resulting from Duplication of Isochromosome 8q in Chronic Myelomonocytic Leukemia
198. AML1 and ETO genes implicated in an acute myeloblastic leukemia patient with t(8;19)
199. The Streptomyces venezuelae pikAV gene contains a transcription unit essential for expression of enzymes involved in glycosylation of narbonolide and 10-deoxymethynolide
200. t(8;21;8)(p23;q22;q22): A New Variant form of t(8;21) Translocation in Acute Myeloblastic Leukemia with Maturation
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