نتایج جستجو برای: chromosome 10q
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72% of balanced spermatozoa (Figure 1). No further rearrangement involving chromosome 10 and 18 has been found. Hybridization with X, Y, 18, 13, and 21 chromosome probes revealed no significant increase of gametes with numerical abnormalities (data not shown). Microarray-based comparative genomic hybridization was performed using Agilent® oligonucleotide arrays according to the manufacturer’s i...
Our article ‘‘A map of dependencies among three-valued logics’’ (Information Sciences, vol. 250, 161–177, 2013) contains some typing mistakes that may affect a proper understanding of the paper. They are corrected here. Table 1 (Table 8 in [1]) Relations among implications. N. How it can be obtained Name 1 Residuation applied to p⁄1q = :((:p? 12:q)? 12:q) 2 (p? 3q)^(:q? 3:p), (p? 4q)^(:q? 4:p) ...
The apolipoprotein E (APOE) gene has been consistently shown to be a major genetic risk factor; however, all cases of Alzheimer's disease (AD) cannot be attributed to the epsilon4 variant of APOE, because about half of AD patients have the APOE-epsilon3*3 genotype. To identify an additional genetic risk factor(s), we performed large-scale single nucleotide polymorphism (SNP)-based association a...
زمینه مطالعه : امروزه استفاده از کوآنزیم 10q به عنوان مکمل خوراکی یا تزریقی در بهبود ناباروری در مردان بسیار موثر بوده است. نقش اصلی 10coq ، حضور در زنجیره انتقال الکترون در طی فرایند تنفس سلولی به منظور تولید انرژی در غشای میتوکندری است. هدف: هدف از انجام این مطالعه بررسی اثرات کوآنزیم 10q بر خصوصیات مورفولوژیک بیضه و هیستولوژیک لوله های اسپرم ساز شترمرغ بود. روش کار: 18 شترمرغ نر شش ماهه، از ...
Alzheimer's disease (AD) is the most common cause of dementia. It is characterized by beta-amyloid (A beta) plaques, neurofibrillary tangles and the degeneration of specifically vulnerable brain neurons. We observed high expression of the cholesterol 25-hydroxylase (CH25H) gene in specifically vulnerable brain regions of AD patients. CH25H maps to a region within 10q23 that has been previously ...
The Usher syndromes (USH) are a group of autosomal recessive diseases characterized by progressive pigmentary retinopathy and sensorineural hearing loss. Five USH genes have been mapped and at least one additional gene is known to exist. By homozygosity mapping in a consanguineous family, a sixth USH gene has been localized. Clinical findings in the four affected children are consistent with es...
Loss of heterozygosity (LOH) on several loci and mutations on PTEN tumor suppressor gene (10q23.3) occur frequently in sporadic gliomas. We have performed polymerase chain reaction (PCR)-LOH analysis using microsatellite markers and single-stranded conformational polymorphism (SSCP) analysis to determine the incidence of allelic losses on chromosome 10q, 9p, 17p and 13q and mutations of exons 5...
BACKGROUND Loss of heterozygosity (LOH) on chromosomal regions is crucial in tumor progression and this study aimed to identify genome-wide LOH in pancreatic cancer. MATERIALS AND METHODS Single-nucleotide polymorphism (SNP) profiling data GSE32682 of human pancreatic samples snap-frozen during surgery were downloaded from Gene Expression Omnibus database. Genotype console software was used t...
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