نتایج جستجو برای: 520g

تعداد نتایج: 19  

ژورنال: طب انتظامی 2016

سرطان کولورکتال(CRC)  سومین سرطان شایع در دنیا می‌باشد و میزان مرگ‌ومیر آن تقریباً 50 درصد بیماران است. باوجود پیشرفت‌ها در روش‌های درمانی باز هم در اکثر تومورها برداشتن تومور طی عمل جراحی تنها راه مؤثر درمانی به‌حساب می‌آید بااین‌حال حدود 40-30 درصد بیماران پس از جراحی عود را نشان می‌دهند. ازاین‌رو نیاز بسیار زیادی به یافتن علل اصلی عود سرطان کولورکتال احساس می‌شود که البته متأسفانه کمتر به آن ...

Journal: :Human mutation 2005
Unda Todt Martin Dichgans Karin Jurkat-Rott Axel Heinze Giovanni Zifarelli Jan B Koenderink Ingrid Goebel Vera Zumbroich Anne Stiller Alfredo Ramirez Thomas Friedrich Hartmut Göbel Christian Kubisch

Migraine is a recurrent neurovascular disease. Its two most common forms-migraine without aura (MO) and migraine with aura (MA)-both show familial clustering and a complex pattern of inheritance. Familial hemiplegic migraine (FHM) is a rare monogenic subform caused by mutations in the calcium channel gene CACNA1A or the Na(+)/K(+)-ATPase gene ATP1A2. An involvement of FHM genes in the pathogene...

Journal: :Diabetes care 2001
M C Ng S C Lee G T Ko J K Li W Y So Y Hashim A H Barnett I R Mackay J A Critchley C S Cockram J C Chan

OBJECTIVE We examined the prevalence of different forms of diabetes in Hong Kong Chinese patients with familial early-onset type 2 diabetes and compared their clinical features with patients with familial late-onset type 2 diabetes. RESEARCH DESIGN AND METHODS A total of 145 young patients with early-onset diabetes (age and age at diagnosis < or = 40 years) and a family history of diabetes we...

Journal: :Scientific reports 2016
Qing-Yun Wang Bei Hu Hui Liu Liang Tang Wei Zeng Ying-Ying Wu Zhi-Peng Cheng Yu Hu

Hemophilia B (HB) is an X-linked recessive bleeding disorder caused by mutations in the coagulation factor IX (FIX) gene. Genotyping patients with HB is essential for genetic counseling and provides useful information for patient management. In this study, the F9 gene from 23 patients with HB was analyzed by direct sequencing. Nineteen point mutations were identified, including a novel missense...

2012
Wen Wang Lan-Juan Zhao Ye-Xiong Tan Hao Ren Zhong-Tian Qi

The deregulation of microRNA (miRNA) is frequently associated with a variety of cancers, including hepatocellular carcinoma (HCC). In this study, we identified 10 upregulated miRNAs (miR-217, miR-518b, miR-517c, miR-520g, miR-519a, miR-522, miR-518e, miR-525-3p, miR-512-3p and miR-518a-3p) and 10 downregulated miRNAs (miR-138, miR-214, miR-214#, miR-27a#, miR-199a-5p, miR-433, miR-511, miR-592,...

2012
Esterina D’Asti Delphine Garnier Tae H. Lee Laura Montermini Brian Meehan Janusz Rak

The brain is a frequent site of neoplastic growth, including both primary and metastatic tumors. The clinical intractability of many brain tumors and their distinct biology are implicitly linked to the unique microenvironment of the central nervous system (CNS) and cellular interactions within. Among the most intriguing forms of cellular interactions is that mediated by membrane-derived extrace...

Journal: :Annals of the Rheumatic Diseases 2021

Background: Using transcriptomic data at initiation of therapy, we recently identified differentially expressed genes (DEGs) that separated IL-17Ai response from non-response 1 . Integration cell-type-specific DEGs with protein-protein interactions (PPIs) and further comprehensive pathway enrichment analysis revealed Rho GTPase signaling exhibited a strong signal specific to particularly the ge...

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