نتایج جستجو برای: q21

تعداد نتایج: 1024  

2013
Ayda Bennour Ikram Tabka Yosra Ben Youssef Zahra Kmeira Abderrahim Khelif Ali Saad Halima Sennana

The acquisition of secondary chromosomal aberrations in chronic myeloid leukemia (CML) patients with Philadelphia chromosome-positive (Ph+) karyotype signifies clonal evolution associated with the progression of the disease to its accelerated or blastic phase. Therefore, these aberrations have clinical and biological significance. T(3;12)(q26;p13), which is a recurrent chromosomal aberration ob...

Journal: :Oncology reports 2012
Giuseppina Liguori Monica Cantile Margherita Cerrone Elvira La Mantia Maurizio Di Bonito Fabrizio Zanconati Maria Pia Curcio Gabriella Aquino Anna La Mura Rosa Giannatiempo Annarosaria De Chiara Angela Lombardi Gerardo Botti Antonio D'Antonio Michele Caraglia Renato Franco

Primary breast mucosa-associated lymphoid tissue (MALT) lymphomas are uncommon and restricted diagnostic criteria should be used to exclude breast involvement by systemic lymphomas. The molecular pathogenesis of primary breast MALT lymphomas is not clear because of the rarity of the disease. Generally the molecular studies of MALT lymphoma in extr...

Journal: :Cancer research 1990
H Konishi M Sakurai H Nakao N Maseki Y Kaneko Y Yagiri K Notohara G Frizzera

Clonal chromosomal abnormalities were found in tumor tissue of 43 (84%) of 51 patients with non-Hodgkin's lymphoma (B-cell, 32; T-cell, 15) from an adult T-cell leukemia/lymphoma-nonendemic area in western mainland Japan. Four tumors were tetraploid, and the other 39 had a chromosome number in the diploid range. Trisomies 3, 5, 7, 18, and X, monosomy 13, and loss of an X in female and a Y in ma...

2012
Giovanni Carulli Alessandra Marini Maria I. Ferreri Antonio Azzarà Virginia Ottaviano Tiziana Lari Melania Rocco Stefano Giuntini Mario Petrini

About 5% of adult B-cell acute lymphoblastic leukemias (B-ALL) are characterized by t(4;11)(q21;q23), which confers peculiar features to this B-ALL subtype, including a very immature immunophenotype and poor prognosis. We describe the case of a 21-year-old female who presented with B-ALL carrying the t(4;11)(q21;q23) and blasts positive for CD19, TdT, CD79a, CD38, HLA-DR. Before completing the ...

Journal: :Blood 1994
K Suzukawa E Parganas A Gajjar T Abe S Takahashi K Tani S Asano H Asou N Kamada J Yokota

Structural alterations occur in the long arm of chromosome 3 in approximately 2% of patients with acute myelogenous leukemia (AML) or myelodysplastic syndrome (MDS). The major alterations are inv(3)(q21q26) and t(3:3)(q21;q26) and are often classified as the 3q21q26 syndrome. We previously reported that the EVI1 gene is transcriptionally activated in AMLs with t(3;3)(q21;q26) and inv(3)(q21q26)...

Journal: :Blood 1985
C D Bloomfield O M Garson L Volin S Knuutila A de la Chapelle

A number of specific chromosomal abnormalities have been associated with distinctive clinical and/or morphological subtypes of acute nonlymphocytic leukemia (ANLL) in recent years. We have studied three patients with ANLL and t(1;3)(p36;q21). Each had weakness as their major complaint, a moderately severe anemia and, for ANLL, a relatively high platelet count. All three demonstrated abnormaliti...

Journal: :Journal of Thoracic Oncology 2021

IntroductionRovalpituzumab tesirine (Rova-T) is an antibody-drug conjugate targeting DLL3, a Notch pathway ligand highly expressed on SCLC cells. Rova-T was evaluated alone or in combination with platinum-based chemotherapy (cisplatin carboplatin combined etoposide [CE]) frontline treatment of extensive-stage SCLC.MethodsOne cycle CE pre-enrollment permitted (later mandated). The following four...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2014

Journal: :international journal of reproductive biomedicine 0
zia eslami mohammad hasan sheikhha seyed mehdi kalantar seyed mohammad seyedhasani

background: carriers of translocations may have an increased risk of an unbalanced progeny due to imbalances and delays in meiosis. case: a 24-year-old pregnant iranian female was referred to the genetic department of yazd clinical and research centre for infertility because of her pregnancy history. she had three previous pregnancies, two of which ended in abortion. the one live born infant wa...

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