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Relevant bibliographies by topics / Bande q13

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Academic literature on the topic 'Bande q13'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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Journal articles on the topic "Bande q13"

1

Taniwaki, M., K. Nishida, T. Takashima, et al. "Nonrandom chromosomal rearrangements of 14q32.3 and 19p13.3 and preferential deletion of 1p in 21 patients with multiple myeloma and plasma cell leukemia." Blood 84, no. 7 (1994): 2283–90. http://dx.doi.org/10.1182/blood.v84.7.2283.2283.

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Abstract Structural chromosomal abnormalities and their break-points were characterized in 17 patients with multiple myeloma (MM) and 4 with plasma cell leukemia by banding. Chromosome 14q32 translocations with a variety of partners were detected in 13 patients, and a variant translocation t(8;22)(q24.1;q11) was detected in 1. Three recurrent 14q32 translocations have been identified: t(6;14)(p21.1;q32.3) occurring in 3 cases, and t(11;14)(q13;q32.3) and t(14;18) (q32.3;q21.3) each occurring in 2 cases. Translocations t(1;14)(q21;q32.3), t(3;14)(p11;q32),t(7;14)(q11.2;q32.3), and t(11;14)(q23;

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2

Taniwaki, M., K. Nishida, T. Takashima, et al. "Nonrandom chromosomal rearrangements of 14q32.3 and 19p13.3 and preferential deletion of 1p in 21 patients with multiple myeloma and plasma cell leukemia." Blood 84, no. 7 (1994): 2283–90. http://dx.doi.org/10.1182/blood.v84.7.2283.bloodjournal8472283.

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Structural chromosomal abnormalities and their break-points were characterized in 17 patients with multiple myeloma (MM) and 4 with plasma cell leukemia by banding. Chromosome 14q32 translocations with a variety of partners were detected in 13 patients, and a variant translocation t(8;22)(q24.1;q11) was detected in 1. Three recurrent 14q32 translocations have been identified: t(6;14)(p21.1;q32.3) occurring in 3 cases, and t(11;14)(q13;q32.3) and t(14;18) (q32.3;q21.3) each occurring in 2 cases. Translocations t(1;14)(q21;q32.3), t(3;14)(p11;q32),t(7;14)(q11.2;q32.3), and t(11;14)(q23;q32.3) we

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3

Bernasconi, Paolo, Irene Dambruoso, Marina Boni, et al. "Fluorescence In Situ Hybridization (FISH) Reveals Unexpected Cryptic Chromosome 11 Defects in MDS/AML Patients." Blood 108, no. 11 (2006): 4413. http://dx.doi.org/10.1182/blood.v108.11.4413.4413.

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Abstract Conventional cytogenetics (CC) discovers clonal chromosomal defects in about 40–80% of de novo MDS/AML. However, due to the poor quality of metaphases, CC is often unable to reveal cryptic defects, precisely define chromosomal breakpoints and establish the nature of marker chromosomes. All these drawbacks may be overcome by FISH, a powerful technique with high sensitivity and specificity. Abnormalities of chromosome 11 long arm and of band 11p15 are seen in 5–7% and in 0.5% of de novo MDS/AML. Herein we report two patients diagnosed as AML evolved from MDS. On CC the karyotype of the

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4

Lemons, Richard S., Rafael Espinosa, Matt Rebentisch, Frank McCormick, Martha Ladner, and Michelle M. Le Beau. "Chromosomal localization of the gene encoding GTPase-activating protein (RASA) to human chromosome 5, bands q13–q15." Genomics 6, no. 2 (1990): 383–85. http://dx.doi.org/10.1016/0888-7543(90)90581-e.

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5

Cuneo, A., C. Mecucci, S. Kerim, et al. "Multipotent stem cell involvement in megakaryoblastic leukemia: cytologic and cytogenetic evidence in 15 patients." Blood 74, no. 5 (1989): 1781–90. http://dx.doi.org/10.1182/blood.v74.5.1781.1781.

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Abstract Cytologic and cytogenetic results obtained from patients fulfilling the FAB criteria for the diagnosis of acute nonlymphocytic leukemia (ANLL) of megakaryocytic lineage (ANLL-M7) are reported. Eleven cases were de novo ANLL-M7, of whom three presented with acute myelofibrosis. Four cases were megakaryoblastic transformations of chronic myelogenous leukemia (two cases), refractory anemia with excess of blasts (one case), and polycythemia vera (one case). Four patients showed a minority of granular blasts, with occasional Auer rods in one. Positive myeloperoxidase and/or sudan black-B s

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Cuneo, A., C. Mecucci, S. Kerim, et al. "Multipotent stem cell involvement in megakaryoblastic leukemia: cytologic and cytogenetic evidence in 15 patients." Blood 74, no. 5 (1989): 1781–90. http://dx.doi.org/10.1182/blood.v74.5.1781.bloodjournal7451781.

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Cytologic and cytogenetic results obtained from patients fulfilling the FAB criteria for the diagnosis of acute nonlymphocytic leukemia (ANLL) of megakaryocytic lineage (ANLL-M7) are reported. Eleven cases were de novo ANLL-M7, of whom three presented with acute myelofibrosis. Four cases were megakaryoblastic transformations of chronic myelogenous leukemia (two cases), refractory anemia with excess of blasts (one case), and polycythemia vera (one case). Four patients showed a minority of granular blasts, with occasional Auer rods in one. Positive myeloperoxidase and/or sudan black-B stainings

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7

Redner, Robert L., Lydia C. Contis, Carol Evans, Maureen E. Sherer, and Sofia Shekhter-Levin. "A Novel t(3;17) Variant of Acute Promyelocytic Leukemia with Rearrangement of the RARA Locus." Blood 104, no. 11 (2004): 4428. http://dx.doi.org/10.1182/blood.v104.11.4428.4428.

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Abstract The vast majority of patients with Acute Promyelocytic Leukemia (APL, FAB M3) have the t(15;17)(q12;q21) chromosomal translocation. This introduces the gene for PML into the retinoic acid receptor alpha (RARA) locus, which leads to expression of a PML-RARA fusion. There is convincing evidence that expression of PML-RARA underlies the APL phenotype. Yet, there have been identified rare cases of APL that do not manifest t(15;17). Many of these cases exhibit cryptic rearrangements of PML and RARA. However, in a number of cases it has clearly been shown that a fusion protein different tha

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8

Luke, Sunny, Ram S. Verma, Rhandy Pebenito, and Michael J. Macera. "Inversion-duplication of bands q13→q21 of human chromosome 9." American Journal of Medical Genetics 40, no. 1 (1991): 57–60. http://dx.doi.org/10.1002/ajmg.1320400111.

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9

Shardy, Deborah L., Mohammed F. Azim, Rizwan C. Naeem, and Sharon E. Plon. "Identification of the Novel Chromosomal Translocation t(17;19)(q23;q13) in a Pediatric Patient with Acute Myeloid Leukemia." Blood 106, no. 11 (2005): 4344. http://dx.doi.org/10.1182/blood.v106.11.4344.4344.

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Abstract Chromosomal rearrangements have been associated with many hematologic malignancies. Identification of the genes involved in several of these rearrangements has provided information about the development of malignancy and has led to therapeutic interventions. Historically, a considerable number of pediatric acute myeloid leukemia (AML) cases have been reported as cytogenetically normal. However, with improved cytogenetic techniques and the use of fluorescent in situ hybridization (FISH), new translocations are now being identified. We present the case of a 10-year-old male with AML (FA

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10

Kottaridis, Panagiotis, Diana Brazma, Julie Howard-Reeves, Helen Mazzullo, and Elisabeth P. Nacheva. "A Cell Line SYRMO Derived From AML with EVI 1 Rearrangements Following Imatinib Mesylate Therapy for Chronic Myeloid Leukaemia." Blood 116, no. 21 (2010): 4470. http://dx.doi.org/10.1182/blood.v116.21.4470.4470.

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Abstract Abstract 4470 Chronic Myeloid Leukaemia (CML) is a malignant disorder of the haematopoeitic stem cell, usually characterised by the t(9;22) giving rise to the Philadelphia chromosome (Ph), and by the BCR-ABL gene rearrangement at the molecular level. Imatinib mesylate (IM), which targets the tyrosine kinase (TK) activity of BCR-ABL, has become the first line therapy for CML patients. Dasatinib or Nilotinib is now indicated as a second line therapy for patients who develop resistance or intolerance to IM. Here we report the case of a 51 year old woman who was diagnosed in Cyprus (2007)

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Dissertations / Theses on the topic "Bande q13"

1

Szepetowski, Pierre. "Les cancers du sein : place de la genetique moleculaire dans la definition de nouvelles voies de recherche : exemple de la region chromosomique 11q13." Nice, 1991. http://www.theses.fr/1991NICE6801.

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2

Bekri, Soumeya. "Remaniements de la bande q13 du chromosome 11 dans les hémopathies B et les cancers du sein." Aix-Marseille 2, 1997. http://www.theses.fr/1997AIX22057.

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Nous nous sommes interesses, au cours de ce travail, a la caracterisation de deux types de remaniements de la bande q13 du chromosome 11 : les amplifications genomiques et les translocations, lorsqu'elles sont associees respectivement a des cancers du sein et a des hemopathies b. Notre but ultime est d'identifier le ou les gene(s) localise(s) dans les segments chromosomiques rearranges et dont le dysfonctionnement serait implique dans une des etapes de ces processus cancereux. La premiere partie de nos travaux a concerne l'etude des remaniements de la bande q13 du chromosome 11, et en particul

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3

COURSEAUX, ANOUK. "Caracterisation structurale et fonctionnelle de la region proximale de la bande q13 du chromosome 11 humain : etude de son implication dans divers types de pathologies." Nice, 1996. http://www.theses.fr/1996NICE5031.

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La bande q13 du chromosome 11 tient une place importante en pathologie humaine. De nombreuses alterations genomiques y ont ete associees a des maladies et syndromes varies ainsi qu'a diverses pathologies cancereuses humaines, faisant d'elle une des regions les plus intensivement etudiees. Notre interet premier pour cette region du genome etait fonde sur l'existence d'evenements multiples d'amplification dans des carcinomes humains impliquant tout ou partie de 11q13. La complexite apparemment croissante de ces phenomenes d'amplification m'a conduit a orienter mes activites vers l'etablissement

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4

FERNANDES, MARIE. "Etude comparative de deux regions chromosomiques conservees au cours de l'evolution : la bande q13 du chromosome 11 humain et la region pericentromerique du chromosome 19 de la souris." Aix-Marseille 2, 1997. http://www.theses.fr/1997AIX22059.

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La comparaison des genomes permet non seulement d'etudier la phylogenie des especes mais egalement d'identifier des genes impliques dans des processus biologiques conserves au cours de l'evolution. Les approches moleculaires comparatives peuvent etre menees chez les organismes complexes a trois niveaux de resolution : la cytogenetique, la cartographie et la sequence des macromolecules (adn, proteines). Nos travaux concernent la cartographie physique comparative de deux regions chromosomiques homologues entre l'homme et la souris : la bande q13 du chromosome 11 humain (hsa11q13) et la region pe

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5

Zhu, Ying. "Deletion of chromosome bands 11q22-q23 in lymphoproliferative disorders and the genetics of mantle cell lymphoma." Helsinki : University of Helsinki, 2002. http://ethesis.helsinki.fi/julkaisut/laa/haart/vk/zhu/.

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6

McIntosh, Gary Gordon. "Evaluation of the clinical and biological significance of overexpression of... genes at the int-2/hst-1 oncogene amplification locus on band q13 of chromosome 11 in human breast cancer." Thesis, University of Newcastle Upon Tyne, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321591.

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7

Chapman, Robert Macdonald. "Investigation of the chromosome 13 band q14 lesions in B-cell chronic lymphocytic leukaemia : evidence for a novel tumour suppressor gene." Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242548.

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