نتایج جستجو برای: q27
تعداد نتایج: 214 فیلتر نتایج به سال:
یکی از مهمترین مسائلی که به طور روزمره کلیه کشورهای جهان با آن سروکار دارند ،مسئله تامین انرژی می باشد.کاهش ذخایر منابع فسیلی و افزایش قیمت نفت و فرآورده های آن از یک سو ولزوم توجه به کاهش آلودگی های زیست محیطی ناشی از سوخت های فسیلی از سوی دیگر ،کشورهای جهان را ترغیب به استفاده از انرژیهای تجدید شونده وپاک نموده است.از جمله منابع تجدیدشونده که امروزه مورد توجه بسیاری از کشورهای اروپایی وآمریکا...
This article reviews the performance of the World Trade Organization in the oversight of national regulatory decisions affecting agricultural and food trade. A picture emerges of modest international disciplines on the regulatory decisions of sovereign nations and the need for ongoing improvements. A road map to regulations is presented and empirical assessments of the effects of technical regu...
BCL6. Blood. 2000;96:2907-2909. 5. Kramer MH, Hermans J, Wijburg E, et al. Clinical relevance of BCL2, BCL6, and MYC rearrangements in diffuse large B-cell lymphoma. Blood. 1998;92: 3152-3162. 6. Ueda C, Akasaka T, Kurata M, et al. The gene for interleukin-21 receptor is the partner of BCL6 in t(3;16)(q27;p11), which is recurrently observed in diffuse large B-cell lymphoma. Oncogene. 2002;21:36...
We have identified a novel lysosome-associated membrane glycoprotein localized on chromosome 3q26.3-q27, DC-LAMP, which is homologous to CD68. DC-LAMP mRNA is present only in lymphoid organs and DC. A specific MAb detects the protein exclusively in interdigitating dendritic cells. Expression of DC-LAMP increases progressively during in vitro DC differentiation, but sharply upon activation with ...
BACKGROUND A recent genome-wide association study has identified a new genetic variant rs7758229 in SLC22A3 for colorectal cancer susceptibility in a Japanese population, but it is unknown whether this newly identified variant is associated with colorectal cancer in other populations, including the Chinese population. METHODS We examined the associations between rs7758229 and colorectal cance...
Polymicrogyria is a malformation of cortical development characterized by loss of the normal gyral pattern, which is replaced by many small and infolded gyri separated by shallow, partly fused sulci, and loss of middle cortical layers. The pathogenesis is unknown, yet emerging data supports the existence of several loci in the human genome. We report on the clinical and brain imaging features, ...
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