Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Rossana Bonomi"'
1
Simultaneous PML/RARα and AML1/ETO expression with t(15;17) at onset and relapse with only t(8;21) in an acute promyelocytic leukemia patient
Autor: Ana Inés Landoni, Hugo Giordano, Enrique Bódega, Rossana Bonomi, Marı́a del Rosario Uriarte, Robert E. Gallagher, Marı́a del Pilar Moreno
Publikováno v: Cancer Genetics and Cytogenetics. 123:41-43
We report a patient with acute promyelocytic leukemia with the common translocation (15;17) and PML-RARAalpha fusion gene. In relapse, blasts showed typical FAB M2 morphologic features, and the karyotype was 45,X, -Y,t(8;21). A reexamination of the l
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18df0a9b24f809266a8a385a5b488541
https://doi.org/10.1016/s0165-4608(00)00297-1
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2
Duplication of band 12q24 in acute myeloblastic leukemia
Autor: Therry Leblanc, Roland Berger, Maryvonne Le Coniat, Rossana Bonomi
Publikováno v: Cancer genetics and cytogenetics. 108(1)
Cytogenetic studies of two patients with acute myeloblastic leukemia, classified as M1 and M2, showed a partial duplication of the distal part of the long arm of chromosome 12 (12q24) as the sole detectable chromosome abnormality. High white blood ce
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbbc5f616f5a6b69d531f20514508cbc
https://pubmed.ncbi.nlm.nih.gov/9973928
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3
PML/Rara and Rara/PML Chimeric Genes On Derivative Chromosome 17 In a Patient With Acute Promyelocytic Leukemia With Atypical t(15;17)(q11;q21)
Autor: Analía Sanguinetti, Gerardo Romanelli, Victoria Elizondo, Rossana Bonomi, Daniela Infante, Cecilia Canessa, Solange Simonet, Lem Martinez, Pablo Lopez, Isabel Moro, M. Rosario Uriarte Escuder
Publikováno v: Blood. 122:4960-4960
Introduction Acute promyelocytic leukemia (APL) of the WHO classification is genetically characterized by the t(15;17)(q22;q21) chromosomal translocation involving the retinoic acid receptor alpha (RARA) located on band 17q21 and the promyelocytic le
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::417a4d897fbc8fa3134163cb584ad501
https://doi.org/10.1182/blood.v122.21.4960.4960
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4
Microphotometric scanning of chromatid gaps and breaks induced by AluI and BamHI in Chinese hamster ovary cells
Autor: Wilner Martínez-López, Gustavo A. Folle, Máximo E. Drets, Rossana Bonomi
Publikováno v: Brazilian Journal of Genetics, Volume: 19, Issue: 4, Pages: 577-582, Published: 1996
Brazilian Journal of Genetics v.19 n.4 1996
Brazilian Journal of Genetics
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Chromatid gaps and breaks induced by the restriction endonucleases AluI and BamHI in the long arm of chromosome 1 of Chinese hamster ovary cells were microphotometrically scanned and mapped to a quantitative G-band map. More than 50% of chromatid bre
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb2b20a3707fea88b25c493a476b4742
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84551996000400007&lng=en&tlng=en
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5
BCR/ABL Fusion Gene On Constitutional Der(14;22) Roberstsonian Translocation in a Case of Chronic Myeloid Leukemia with Masked Philadelphia Chromosome
Autor: Victoria Elizondo, Solange Simonet, M. Rosario Uriarte Escuder, Isabel Moro, Juan Zunino, Pablo Lopez, Gerardo Romanelli, Rossana Bonomi, Daniela Infante, Marina Lafage, Natacha Gardiol
Publikováno v: Blood. 120:4822-4822
Abstract 4822 Chronic myeloid leukemia (CML) is characterized by the Philadelphia chromosome (Ph) observed in more than 90% of patients with CML as a result of t(9;22)(q34;q11), leading to the formation of the BCR/ABL chimeric gene. The remaining 5
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::601a4c1c10022fa412ba475a1891787a
https://doi.org/10.1182/blood.v120.21.4822.4822
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6
A novel BCR-ABL fusion transcript (e15a2) in 2 patients with atypical chronic myeloproliferative syndrome
Autor: María Moreno, Marı́a del Rosario Uriarte, Rossana Bonomi, Adriana Cardeza, Marı́a Noel Cortinas
Publikováno v: Blood. 97:3668-3669
The BCR-ABL chimeric gene results from a reciprocal translocation, t(9;22)(q34;q11). The breakpoint on chromosome 9 is in the majority of cases 5′ to ABL exon 2, whereas the breakpoints on chromosome 22 can occur in various regions within the BCR g
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f4dc4803ac969d9d5eaf181c2e87b8d5
https://doi.org/10.1182/blood.v97.11.3668
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7
Concomitant Detection of BCR-ABL Translocation and JAK2 V617F Mutation In 6 Myeloproliferative Neoplasm at Diagnosis
Autor: Maria Noel Zubillaga, Susana Boschi, Santiago Pomoli, Victoria Elizondo, Lem Martinez, Gonzalo Manrique, Lilián Díaz, Rossana Bonomi, Verónica Pérez, M. Rosario Uriarte Escuder, Mónica Cappetta, Ines Prosper
Publikováno v: Blood. 116:4832-4832
Abstract 4832 Background Myeloproliferatives neoplasms (MPN) are clonal stem cell disorders characterized by proliferation of one or more of the myeloid lineages, associated with genetic abnormalities that include translocations or point mutations of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::12f85f2fa69ac0ee252cbaaaea5f86f3
https://doi.org/10.1182/blood.v116.21.4832.4832
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8
Variant Philadelphia Translocation with BCR/ABL Fusion Gene Site In 10q24 In a Case of Chronic Myeloid Leukemia
Autor: Daniela Infante, Lem Martinez, Pablo Lopez, Isabel Moro, Rossana Bonomi, M. Rosario Uriarte Escuder, Ines Prosper, Victoria Elizondo, Solange Simonet, Gerardo Romanelli
Publikováno v: Blood. 116:4839-4839
Abstract 4839 Introduction. Chronic myeloid leukemia (CML) is characterized by the Philadelphia chromosome (Ph) observed in more than 90% of patients with CML as a result of t(9;22)(q34;q11), leading to the formation of chimeric gene BCR/ABL encoding
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e89a6d627c075bf1d04f84e04415c18b
https://doi.org/10.1182/blood.v116.21.4839.4839
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9
Bone marrow reconstitution with normal autologous cells demonstrated by VNTR analysis after allogeneic bone marrow transplatation for chronic myelogenous leukemia
Autor: HN Seuánez, C Azambuja, Rossana Bonomi, M del Rosario Uriarte
Publikováno v: Leukemia. 11:2213-2214
Bone marrow reconstitution with normal autologous cells demonstrated by VNTR analysis after allogeneic bone marrow transplatation for chronic myelogenous leukemia
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b5eb7a784be6754d437a0a0bb572500f
https://doi.org/10.1038/sj.leu.2400821
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10
Is trisomy 4 a secondary chromosomal abnormality in acute myeloblastic leukemia?
Autor: Roland Berger, Rossana Bonomi, Maryvonne Le Coniat
Publikováno v: Cancer Genetics and Cytogenetics. 79:186-187
Cytogenetic studies were carried out in a patient with acute monocytic leukemia (AML-M5) at diagnosis and in relapse. While no chromosome abnormality was detected initially, isolated trisomy 4 was found in relapse. The primary or secondary nature of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68c5f321a58573e47e6cac94b5fae39a
https://doi.org/10.1016/0165-4608(94)00126-v
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