نتایج جستجو برای: q14

تعداد نتایج: 206  

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

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2018

Journal: :Journal of medical genetics 1983
D A Couzin J L Watt I A Auchterlonie

A 6-year-old boy with speech delay and mild mental retardation (IQ 82) was found to have a complex double translocation involving four chromosomes and a total of five breakpoints, two being on the same arm. This resulted in the karyotype 46,XY,t(2;4;7)(7;8)(q14;q31;q11q22;q13). As far as the authors are aware this is the first time that such a complex double translocation has been reported. Bot...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2018

Journal: :Agribusiness 2023

Abstract Motivated by the long‐lasting debate on whether United States Department of Agriculture's (USDA's) World Agricultural Supply and Demand Estimates (WASDE) forecasts are optimal, we employ an unknown loss method for ex post evaluation which assumes that USDA forecasters' function is unknown. We conduct optimality tests WASDE corn, soybeans, wheat published during 1988–2019. Our results s...

Journal: :International journal of clinical and experimental pathology 2014
Khin Than Win Ming-Yuan Lee Tran-Der Tan Mung-pei Tsai Armita Bahrami Susana C Raimondi Shih-Sung Chuang

Alveolar rhabdomyosarcoma (ARMS) is remarkably rare in adults older than 45 years. Histologically, the tumor is composed of blue round cells with frequent expression of CD56 in addition to myogenic markers. Recent studies of ARMS have shown two specific recurrent translocations: PAX3-FKHR [t(2;13)(q35;q14)] or PAX7-FKHR [t(1;13)(p36;q14)]. Extranodal natural killer (NK)/T-cell lymphoma (ENKTL) ...

Journal: :Annales de genetique 2004
Monica C Varela Graziela M P Lopes Celia P Koiffmann

Prader-Willi syndrome (PWS) is a neurobehavioral disorder caused by deletions in the 15q11-q13 region, by maternal uniparental disomy of chromosome 15 or by imprinting defects. Structural rearrangements of chromosome 15 have been described in about 5% of the patients with typical or atypical PWS phenotype. An 8-year-old boy with a clinical diagnosis of PWS, severe neurodevelopmental delay, abse...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
E S Massuda E J Dunphy R A Redman J J Schreiber L E Nauta F G Barr I H Maxwell T P Cripe

Alveolar rhabdomyosarcoma (ARMS) cells often harbor one of two unique chromosomal translocations, either t(2;13)(q35;q14) or t(1;13)(p36;q14). The chimeric proteins expressed from these rearrangements, PAX3-FKHR and PAX7-FKHR, respectively, are potent transcriptional activators. In an effort to exploit these unique cancer-specific molecules to achieve ARMS-specific expression of therapeutic gen...

2016
Antonio Agostini Ludmila Gorunova Bodil Bjerkehagen Ingvild Lobmaier Sverre Heim Ioannis Panagopoulos

Lipomas are common benign soft tissue tumors whose genetic and cytogenetic features are well characterized. The karyotype is usually near- or pseudodiploid with characteristic structural chromosomal aberrations. The most common rearrangements target the high mobility group AT-hook 2 (HMGA2) gene in 12q14.3, with breakpoints occurring within or outside of the gene locus leading to deregulation o...

2008
Joanne Linnerooth-Bayer Reinhard Mechler

This paper examines the recent experience with insurance and other risk-financing instruments in developing countries in order to gain insights into the effectiveness of these instruments in reducing economic insecurity. Insurance and other risk financing strategies are viewed as efforts to recover from negative income shocks through risk pooling and transfer. Specific examples of public-privat...

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