نتایج جستجو برای: q32

تعداد نتایج: 835  

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2019

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

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

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2010

2013
Magdalena Witkowska Piotr Smolewski

Nowadays, it is believed that the main role in the development of gastric mucosa-associated lymphoid tissue (MALT) lymphoma plays Helicobacter pylori infection. This world-wide distributed bacteria is in charge of most cases of not only upper gastrointestinal tract disorders but also some of extragastric problems. Constant stimulation of the immune system causes a B-lymphocytes proliferation, w...

2012
Ivyna Bong Pau Ni Ng Ching Ching Chang Kian Meng Zubaidah Zakaria

More than 50% of myeloma cases have normal karyotypes under conventional cytogenetic analysis due to low mitotic activity and content of plasma cells in the bone marrow. We used a polymerase chain reaction (PCR)-based translocation detection assay to detect BCL1/JH t(11;14) (q13;q32) in 105 myeloma patients, and randomly selected 8 translocation positive samples for array comparative genomic hy...

Journal: :Molecular vision 2005
Vedam Lakshmi Ramprasad Sarangapani Sripriya George Ronnie Derek Nancarrow Sandeep Saxena Arvind Hemamalini Dipak Kumar Lingam Vijaya Govindasamy Kumaramanickavel

PURPOSE Congenital microcoria is a rare autosomal dominant developmental disorder of the iris associated with myopia and juvenile open angle glaucoma. Linkage to the chromosomal locus 13q31-q32 has previously been reported in a large French family. In the current study, a three generation Asian Indian family with 15 congenital microcoria (pupils with a diameter <2 mm) affected members was studi...

2012
Yoonmi Seok Juwon Kim Jong Rak Choi Yu Ri Kim Seo-Jin Park Sue Jung Kim Jaewoo Song Kyung-A Lee

The coexistence of CCND1/IGH and MYC rearrangements in mantle cell lymphoma (MCL) is a rare finding associated with a very poor prognosis. In this study, a patient with blastoid variant (MCL) is reported. The disease was clinically aggressive and refractory to chemotherapy, and the patient only survived for 1 month following diagnosis. Conventional cytogenetic study, FISH, and multicolor FISH (...

Journal: :European journal of dermatology : EJD 2005
Jeong Hee Cho-Vega Francisco Vega Georgios Rassidakis L Jeffrey Medeiros

Primary cutaneous marginal zone B-cell lymphoma (PCMZL) is included as one of the major types of primary cutaneous B-cell lymphoma in the revised World Health Organization-European Organization for Research and Treatment of Cancer classification. Clinically, PCMZL is an indolent disease and has an excellent prognosis. PCMZL is composed of a polymorphous infiltrate that includes centrocyte-like,...

Journal: :The hematology journal : the official journal of the European Haematology Association 2000
X Troussard H Avet-Loiseau M Macro M P Mellerin M Malet M Roussel B Sola

INTRODUCTION Chromosomal abnormalities are detected in 50 to 70% of patients with multiple myeloma (MM). By conventional cytogenetic analysis, a t(11;14)(q13;q32) is observed at a frequency of 3 to 14%. MATERIALS AND METHODS To demonstrate a cyclin D1 expression in MM patients or MM cell lines, 14 patients with multiple myeloma (MM) and nine human multiple myeloma cell lines (HMCL) were scree...

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