نتایج جستجو برای: 1q

تعداد نتایج: 809  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تحصیلات تکمیلی علوم پایه زنجان - دانشکده ریاضی و کامپیوتر 1389

/ j( %( - d e $ m* e g( 1n . o m* - ) ep j+ o1n . ( - 1q ??+ ??* + / - d e $ e g( 1n . r ( os@ ep ( 5 59* a o5% : 6 /: & 5 & + 6 oep ( a ( 0( + 5< t( oa - ()* -+ -2 - ? g ??= : u 1 ??+ 1n . r ( -2 e6 -+ -2 - ? . v o?? & ( ( /: ()* -+ % - ? ??p - o + * ? e70 s+* ? ??57 m* e g( + -+ 1;w g* ? ( ?? i + *...

Journal: :Neuro-oncology 2013
Xiaohui Ren Haihui Jiang Xiangli Cui Yong Cui Jun Ma Zhongli Jiang Dali Sui Song Lin

BACKGROUND This study aimed to evaluate the prognostic significance of co-polsomy of chromosome 1q and 19p in 1p/19q codeleted oligodendroglial tumors (ODGs). METHODS In a series of 148 ODGs with 1p/19q deletion, co-polysomy of 1q and 19p was detected by fluorescence in situ hybridization (FISH). Log-rank analysis and Cox regression methods were used to compare Kaplan-Meier plots and identify...

Journal: :The Journal of Experimental Medicine 1963
I. H. Lepow G. B. Naff E. W. Todd J. Pensky C. F. Hinz

A euglobulin fraction of human C'1 has been chromatographically resolved into three distinct activities, designated C'1q, C'1r, and C'1s, in the order of their elution from DEAE cellulose. All three of these activities have been shown to participate in various hemolytic reactions requiring C'1, including the cold phase of the Donath-Landsteiner reaction, and to be necessary for generation of C'...

2013
Ju Young Kim

BACKGROUND Allostatic load (AL) measures overall physiological wear and tear on one's body, as a preclinical marker of pathophysiologic processes that precede the onset of disease. We studied the association of dietary habits with AL. METHODS Consecutive patients visiting a tertiary hospital Health Promotion Center from September 2009 to February 2010, older than 20 years with metabolic syndr...

Journal: :Histopathology 2002
I Zudaire M D Odero C Caballero C Valenti J M Martínez-Penuela J Isola M J Calasanz

AIMS The aim of this work is the study of the prognostic significance of the chromosomal aberrations described in a series of invasive ductal breast carcinomas. METHODS AND RESULTS We analysed by comparative genomic hybridization a group of 70 formalin-fixed paraffin-embedded invasive ductal breast carcinomas. Aberrations showed a frequency similar to previous studies using frozen tumours. In...

Journal: :Theoretical Computer Science 2022

A length n binary word is q-decreasing, q?1, if every of its maximal factors the form 0a1b satisfies a=0 or q?a>b. In particular, in 1-decreasing words run 0s immediately followed by a strictly shorter 1s. We show constructively that these are bijection with having no occurrences 1q+1, and thus they enumerated (q+1)-generalized Fibonacci numbers. give some enumerative results reveal similaritie...

Journal: :Cancer research 2003
Mattias Höglund David Gisselsson Gunnar B Hansen Torbjörn Säll Felix Mitelman

Ovarian carcinoma has the highest mortality of all of the gynecologic cancers. The chromosomal changes in this tumor type are highly complex, and the karyotypes typically show severe aneuploidy. Despite the abundance of cytogenetic information, with approximately 400 published karyotypes, very little is known about the mode of karyotypic evolution and the possible presence of cytogenetic pathwa...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 1995
I Bièche M H Champème R Lidereau

Alterations of the long arm of chromosome 1 are the most frequent cytogenetic abnormalities found in human breast carcinoma. We examined genetic alterations on chromosome 1q in 124 human breast tumors, using restriction fragment length polymorphism markers mapping to the long arm (13 markers) and short arm (4 markers). Imbalance of heterozygosity at one or more loci on the long arm was observed...

Journal: :Blood 2004
Carmela Lanzara Antonella Roetto Filomena Daraio Silvain Rivard Romina Ficarella Hervey Simard Timothy M Cox Mario Cazzola Alberto Piperno Anne-Paule Gimenez-Roqueplo Paola Grammatico Stefano Volinia Paolo Gasparini Clara Camaschella

Juvenile or type 2 hemochromatosis (JH) is transmitted as a recessive trait that leads to severe iron overload and organ damage typically before age 30 years. Linkage to a locus on chromosome 1q has been found in most patients with JH. The recently identified causal gene encodes hemojuvelin, a protein with a proposed crucial role in iron metabolism. A second, rare type of JH, with clinical expr...

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