نتایج جستجو برای: q12

تعداد نتایج: 725  

Journal: :American journal of blood research 2012
Lu Li Fan Zhou Jian Hou

More than 50% of adult patients with acute myeloid leukemia (AML) carry chromosome abnormalities, like t(8;21)(q22;q22), t(15;17), t(8;21)inv(16) or t(16;16). t(10;17) translocation was very rare in AML. There are only 10 such cases reported in the literature. Here, we describe a case of acute myeloid leukemia with t(10;17)(p13;q12) chromosome translocation, who had complete remission after one...

2009
Volker Beckmann Claudio Soregaroli

Ex-ante regulations and ex-post liabilities for using a new technology will induce additional costs for adopters. The standard model is advanced by including irreversibility and uncertainty and taking into account transaction costs of negotiating possible cost reductions. The case analysed is the coexistence policy for GM crops in the European Union. Results show, the design of the rules and re...

Journal: :Journal of medical genetics 1977
H J Kim L Y Hsu L C Goldsmith L Strauss K Hirschhorn

A newborn infant with clinical and pathological findings typical trisomy 13 and 22 syndromes had an extra chromosome which was a derivative chromosome from maternal balanced translocation affecting Nos. 13 and 22; 47,XY,+der(22),t(13:22)(q22:q12)Mat. The presence of extra specific euchromatic regions of No. 13(13q22 and/or 13q34) and No. 22 (22q11) seem to be responsible for the trisomy 13 and ...

Journal: :Pathology international 2013
Rita Abi-Raad Guy J Manetti John W Colberg Jason L Hornick Jaimin G Shah Manju L Prasad

Ewing sarcoma (ES)/primitive neuroectodermal tumor (PNET) is a malignant small round blue cell neoplasm of presumed neuroectodermal origin that affects bones and soft tissue in children and young adults. Nearly 80% of the patients are younger than 20 years. The tumor cells characteristically express CD99 (MIC2 antigen), a glycoprotein localized on cell membrane. The defining feature of ES/PNET ...

Journal: :Animal genetics 1995
L K Park P Moran D A Dightman

Chromosome location: The location of the canine gene is unknown; the corresponding human gene maps to 17q21 (Law et a1. 1986). or to 17ql1.1-q12 (Xu et a1. 1988). Acknowledgement: This work was supported by a grant from the American Kennel Club. References Hogg D. et a1. (1986J JBioI Chern 261,12420-7. Law M.L. et al. (1986J Cytogenet Cell Genet 42,202-7. Xu W. et al. (1988J Proc Nat! Acad Sci ...

2005
Yasuhiko Kaneko Glauco Frizzera Setsuko Edamura Nobuo Maseki Masaharu Sakurai Yoshihiro Komada Minoru Sakurai Haruki Tanaka Masamichi Sasaki Taizan Suchi Atsushi Kikuta Haruki Wakasa Hiroshi Hojo Shuki Mizutani

We report a novel chromosome translocationt(2;5)(p23;q35) or its variant. t(2;5;13)(p23;q35;q12)-in 3 patients with peripheral T-celI lymphoma. All 3 were female children who had peripheral lymphadenopathy without organomegaly and underwent complete remission with or without chemotherapy. Their tumors were characterized histologically by predominant large cells, at times showing phagocytosis, a...

Journal: :Management of the personnel and intellectual resources in Russia 2023

The level of staff involvement is a very important tool for personnel management and business in general. It needs to be researched, improved maintained ensure the growth companies. article provides an overview main domestic foreign models that allow assessing state involvement, exploring structure finding its bottlenecks opportunities development. examines composition focus Q12 Gallup engageme...

2012
Jan Cameron Erik Christensen Allan M. Sinclair

conjecture Jan Cameron ∗, Erik Christensen †, Allan M. Sinclair ‡,Roger R. Smith §,Stuart White ¶,Alan D. Wiggins ‖ ∗Department of Mathematics, Vassar College, Poughkeepsie, NY 12604, U.S.A.,†Institute for Mathematiske Fag, University of Copenhagen, Copenhagen, Denmark.,‡School of Mathematics, University of Edinburgh, JCMB, King’s Buildings, Mayfield Road, Edinburgh, EH9 3JZ, Scotland.,§Departm...

2012
Kalliopi Apostolopoulou Ioannis S Pateras Athanassios Kotsinas Vassilis G Gorgoulis

Other names: DKFZp547O146; FBI-1; FBI1; LRF; MGC99631; ZBTB7; ZNF857A; pokemon HGNC (Hugo): ZBTB7A Location: 19p13.3 Local order EEF2 (19pter-q12) eukaryotic translation elongation factor 2 SNORD37 (19p13.3) small nucleolar RNA, C/D box 37 PIAS4 (19p13.3) protein inhibitor of activated STAT, 4 ZBTB7A (19p13.3) zinc finger and BTB domain containing 7A MAP2K2 (19q13.3) mitogen-activated protein k...

Journal: :Journal of medical genetics 1987
N Okada T Hasegawa M Osawa Y Fukuyama

A rare chromosome abnormality consisting of interstitial deletion 3q was found in a malformed girl. Chromosome analysis using G and Q banding showed deletion of bands 3q12----3q21: 46,XX,del(3)(pter----q12::q21----qter). The clinical features of the proband included severe psychomotor retardation, craniofacial asymmetry, hypertelorism, epicanthus, high arched palate, progressive scoliosis, mult...

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