نتایج جستجو برای: key deletion

تعداد نتایج: 628265  

Journal: :J. Comb. Optim. 2003
Arkadii G. D'yachkov Péter L. Erdös Anthony J. Macula Vyacheslav V. Rykov David C. Torney Chang-Shung Tung Pavel A. Vilenkin P. Scott White

We describe how deletion-correcting codes may be enhanced to yield codes with double-strand DNA-sequence codewords. This enhancement involves abstractions of the pertinent aspects of DNA; it nevertheless ensures specificity of binding for all pairs of single strands derived from its codewords—the key desideratum of DNA codes– i.e. with binding feasible only between reverse complementary strands...

احمدی, رضوان, صالحی, زیور, ظهیری, زیبا, فرجی سراوانی, مهدیه,

Background and purpose: Spontaneous abortion (SA) is pregnancy termination prior to 20 weeks gestation or with a fetus born weighing less than 500 grams. The etiology of spontaneous abortion (SA) remains unclear, but it may be related to a possible genetic predisposition. The glutathione Stransferases (GSTs) are a family of enzymes involved in the detoxification of a wide range of chemicals....

Fatemeh Sarkargar, Hossein Khodai , Mahta Mazaheri , Razieh Sadat Tabatabaei,

Abstract Background: Haemophilia A (HA) is an X-linked bleeding disorder caused by the absence or reduced activity of coagulation factor VIII (FVIII). Coagulation factors are a group of related proteins that are essential for the formation of blood clots. The aim of this study was to genotype the coagulation factor VIII gene mutations using Inverse Shifting PCR (IS-PCR) in an Iranian family ...

Background Autosomal recessive polycystic kidney disease (ARPKD) is caused by mutations in the PKHD1gene. In the present study, we describe a severe case of ARPKD carrying a point mutation and a novel four-exon deletion of PKHD1 gene. Materials and Methods The PKHD1, PKD1 and PKD2 ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس 1390

میزان شیوع ناباروری مردان در بین زوجهای جوان 15- 10درصد تخمین زده می شود و در این بین عوامل ژنتیکی در حدود 10 درصد علل ناباروری در مردان را سبب می شوند. به همین جهت در مطالعه حاضر بر اساس مطالعات گذشته در جمعیت مردان نابارور ژاپنی، فراوانی چهار پلی مورفیسم و دو جهش در پروتامینها شامل c321t در ژن prm1 و c248t در ژن prm2 و g deletion at 1036 and 1046، g1272c و t1019g در ژن tnp2 برای اولین بار در ...

Journal: :genetics in the 3rd millennium 0
امید آریانی omid ariani مرتضی بنیادی morteza bonyadi center of excellence for molecular analysis of smn gene biodiversity, department of genetics, faculty of natural sciences, university of tabriz, tabriz, iran محمد برزگر mohammad barzegar

spinal muscular atrophy (sma) is an autosomal recessive neuromuscular disorder characterized by degeneration of spinal cord anterior horn cells, leading to muscular atrophy. sma is clinically classified into three sub-groups based on the age of onset and severity. the majority of patients with sma have homozygous deletions of exons 7 and 8 of the survival motor neuron (smn) gene. the purpose of ...

2007
Chun-Wei Lin Tzung-Pei Hong Wen-Hsiang Lu

The frequent pattern tree (FP-tree) is an efficient data structure for association-rule mining without generation of candidate itemsets. It, however, needed to process all transactions in a batch way. In addition to record insertion, record deletion is also commonly seen in real-application. In this paper, we propose the structure of prelarge trees for efficiently handling deletion of records b...

2012
Raquel Assis Alexey S. Kondrashov

Gene conversion is the unidirectional transfer of genetic information between orthologous (allelic) or paralogous (nonallelic) genomic segments. Though a number of studies have examined nucleotide replacements, little is known about length difference mutations produced by gene conversion. Here, we investigate insertions and deletions produced by nonallelic gene conversion in 338 Drosophila and ...

2018
Chee Wai Chua Nusrat J Epsi Eva Y Leung Shouhong Xuan Ming Lei Bo I Li Sarah K Bergren Hanina Hibshoosh Antonina Mitrofanova Michael M Shen

Master regulatory genes of tissue specification play key roles in stem/progenitor cells and are often important in cancer. In the prostate, androgen receptor (AR) is a master regulator essential for development and tumorigenesis, but its specific functions in prostate stem/progenitor cells have not been elucidated. We have investigated AR function in CARNs (CAstration-Resistant Nkx3.1-expressin...

2014
Shuai Le Xinyue Yao Shuguang Lu Yinling Tan Xiancai Rao Ming Li Xiaolin Jin Jing Wang Yan Zhao Nicholas C. Wu Renate Lux Xuesong He Wenyuan Shi Fuquan Hu

Bacteria develop a broad range of phage resistance mechanisms, such as prevention of phage adsorption and CRISPR/Cas system, to survive phage predation. In this study, Pseudomonas aeruginosa PA1 strain was infected with lytic phage PaP1, and phage-resistant mutants were selected. A high percentage (~30%) of these mutants displayed red pigmentation phenotype (Red mutant). Through comparative gen...

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