Cargando…

Chromosomal aberrations detected by Fluorescence in situ hybridization in 344 Brazilian chronic lymphocytic leukemia patients

Detalles Bibliográficos
Autores principales:	Zorovich, Maria Eduarda Sanseverino de Lourenço da Motta, Dourado, Denise Albuquerque, Chauffaille, Maria de Lourdes Lopes Ferrari
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Sociedade Brasileira de Hematologia e Hemoterapia 2017
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693278/ https://www.ncbi.nlm.nih.gov/pubmed/29150118 http://dx.doi.org/10.1016/j.bjhh.2017.05.008

Ejemplares similares

Diversity of breakpoints of variant Philadelphia chromosomes in chronic myeloid leukemia in Brazilian patients
por: Chauffaille, Maria de Lourdes Lopes Ferrari, et al.
Publicado: (2015)

Fluorescence in situ hybridisation for interphase chromosomal aberration-based biological dosimetry
por: Meher, Prabodha Kumar, et al.
Publicado: (2023)

Investigation of chromosomal aberrations in Egyptian hepatocellular carcinoma patients by fluorescence in situ hybridization
por: Aly, Magdy S., et al.
Publicado: (2010)

Detection of chromosome aberrations in interphase nuclei using fluorescence in situ hybridization technique.
por: Song, H. G., et al.
Publicado: (1993)

Fluorescence in situ hybridisation analysis of chromosomal aberrations in gastric tissue: the potential involvement of Helicobacter pylori
por: Williams, L, et al.
Publicado: (2005)

Comparison of Next-Generation Sequencing and Fluorescence In Situ Hybridization for Detection of Segmental Chromosomal Aberrations in Neuroblastoma
por: Kim, Eojin, et al.
Publicado: (2021)

The treatment of acute lymphoblastic leukemia has come a long way but the best is yet to come
por: Chauffaille, Maria de Lourdes Lopes Ferrari
Publicado: (2013)

Fluorescent in situ Hybridization on Mitotic Chromosomes of Mosquitoes
por: Timoshevskiy, Vladimir A., et al.
Publicado: (2012)

Investigation of Chromosome 1 Aberrations in the Lymphocytes of Prostate Cancer and Benign Prostatic Hyperplasia Patients by Fluorescence in situ Hybridization
por: Miszczyk, Justyna, et al.
Publicado: (2021)

Comparison of chromosomal aberrations detected by fluorescence in situ hybridization with clinical parameters, DNA ploidy and Ki 67 expression in renal cell carcinoma.
por: Wada, Y., et al.
Publicado: (1998)

When karyotype is decisive for myelodysplastic syndromes diagnosis
por: Perazzio, Aline dos Santos Borgo, et al.
Publicado: (2019)

Is karyotyping still needed in the diagnosis and monitoring of chronic myeloid leukemia?
por: Chauffaille, Maria de Lourdes L.F.
Publicado: (2017)

Marrow iron staining should always be performed to diagnose Myelodysplastic/myeloproliferative neoplasia with ring sideroblasts and thrombocythemia.
por: Chauffaille, Maria de Lourdes Lopes Ferrari, et al.
Publicado: (2019)

Identifying the similarities and differences between single nucleotide polymorphism array (SNPa) analysis and karyotyping in acute myeloid leukemia and myelodysplastic syndromes
por: Noronha, Thiago Rodrigo de, et al.
Publicado: (2015)

Characterization of axolotl lampbrush chromosomes by fluorescence in situ hybridization and immunostaining
por: Keinath, Melissa C., et al.
Publicado: (2021)

The use of fluorescence in situ hybridisation combined with premature chromosome condensation for the identification of chromosome damage.
por: Evans, J. W., et al.
Publicado: (1991)

Karyotypic and fluorescent in situ hybridization study of the centromere of chromosome 7 in secondary myeloid neoplasms
por: Tanizawa, Roberta Sandra da Silva, et al.
Publicado: (2011)

Application of Fluorescence In Situ Hybridization (FISH) Technique for the Detection of Genetic Aberration in Medical Science
por: Ratan, Zubair Ahmed, et al.
Publicado: (2017)

Oligonucleotide Fluorescence In Situ Hybridization: An Efficient Chromosome Painting Method in Plants
por: Harun, Arrashid, et al.
Publicado: (2023)

Limitations of performance status assessment in elderly with acute myeloid leukemia
por: Carbonell, Ana Lúcia Ippolito, et al.
Publicado: (2015)

The association of three DNA repair genes polymorphisms on the frequency of chromosomal alterations detected by fluorescence in situ hybridization
por: Santiago, Fábio, et al.
Publicado: (2021)

Chromosomal Aberrations in Cattle
por: Holečková, Beáta, et al.
Publicado: (2021)

Diagnostic Utility of Multiprobe Fluorescence in situ Hybridization Assay for Detecting Cytogenetic Aberrations in Acute Leukemia
por: Kim, Bo-Ram, et al.
Publicado: (2014)

Combined Fluorescent-Chromogenic In Situ Hybridization for Identification and Laser Microdissection of Interphase Chromosomes
por: Paz, Nerea, et al.
Publicado: (2013)

FISHIS: Fluorescence In Situ Hybridization in Suspension and Chromosome Flow Sorting Made Easy
por: Giorgi, Debora, et al.
Publicado: (2013)

An assessment of chromosomal alterations detected by fluorescence in situ hybridisation in pancreatobiliary tract malignancy
por: Pu, Xiaohong, et al.
Publicado: (2020)

Conventional Karyotyping and Fluorescence In Situ Hybridization for Detection of Chromosomal Abnormalities in Multiple Myeloma
por: Crabtree, Matthew, et al.
Publicado: (2022)

BCR/ABL1 fluorescence in situ hybridization fusion signals on both copies of chromosome 22 in a Philadelphia-masked chronic myeloid leukemia case: implication for the therapy
por: Soriani, Silvia, et al.
Publicado: (2021)

Increased angiogenesis in primary myelofibrosis: latent transforming growth factor-β as a possible angiogenic factor
por: Ponce, Cesar Cilento, et al.
Publicado: (2014)

Chemopreventive Potential of Synergy1 and Soybean in Reducing Azoxymethane-Induced Aberrant Crypt Foci in Fisher 344 Male Rats
por: Gourineni, V. P., et al.
Publicado: (2011)

Catalog of Chromosome Aberrations in Cancer
por: Secker-Walker, Lorna M
Publicado: (1996)

SEX CHROMOSOME ABERRATIONS IN SCHIZOPHRENIA
por: Chatterjee, S. B., et al.
Publicado: (1980)

JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases
por: de Noronha, Thiago Rodrigo, et al.
Publicado: (2019)

Additional information offered by single nucleotide polymorphism array advantages in two myelodysplastic syndromes with excess blasts cases and future perspectives
por: Noronha, Thiago Rodrigo de, et al.
Publicado: (2019)

Chromosomal analysis of non-small-cell lung cancer by multicolour fluorescent in situ hybridisation
por: Berrieman, H K, et al.
Publicado: (2004)

Recent advances in rice genome and chromosome structure research by fluorescence in situ hybridization (FISH)
por: Ohmido, Nobuko, et al.
Publicado: (2010)

Mapping pachytene chromosomes of coffee using a modified protocol for fluorescence in situ hybridization
por: Iacia, Ana Amélia Sanchez, et al.
Publicado: (2013)

FMS-related tyrosine kinase 3 internal tandem duplication (FLT3-ITD): a villain among others
por: de Arruda, Vanessa Y.N., et al.
Publicado: (2017)

Molecular genetic tests for JAK2V617F, Exon12_JAK2 and MPLW515K/L are highly informative in the evaluation of patients suspected to have BCR-ABL1-negative myeloproliferative neoplasms
por: dos Santos, Marcos Tadeu, et al.
Publicado: (2014)

Diagnosis and treatment of chronic lymphocytic leukemia: recommendations from the Brazilian Group of Chronic Lymphocytic Leukemia
por: Rodrigues, Celso Arrais, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_b3g08n56hs959h1gg5qhg9bjj8