کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5589037 | 1569465 | 2016 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Recent advance in the molecular genetics of Wilson disease and hereditary hemochromatosis
ترجمه فارسی عنوان
پیشرفت اخیر در ژنتیک مولکولی بیماری ویلسون و هموکروماتوز ارثی
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
HFEhepcidin antimicrobial peptideHJVSLC40A1TGNTfR2ATP7BATPase - ایتیپیایزها Wilson disease - بیماری ویلسونGenetic mutation - جهش ژنتیکیTrans-Golgi network - شبکه Trans-GoljiBiological function - عملکرد بیولوژیکیHAMP - هامپhemojuvelin - همسایهHemochromatosis - هموکروماتوزhereditary hemochromatosis - هموکروماتوز ارثیTransferrin receptor 2 - گیرنده انتقالن 2
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
ژنتیک
چکیده انگلیسی
Metabolic liver diseases such as Wilson disease (WD) and hereditary hemochromatosis (HH) possess complicated pathogenesis and typical hereditary characteristics with the hallmarks of a deficiency in metal metabolism. Mutations in genes encoding ATPase, Cu + transporting, beta polypeptide (ATP7B) and hemochromatosis (HFE) or several non-HFE genes are considered to be causative for WD and HH, respectively. Although the identification of novel mutations in ATP7B for WD and HFE or the non-HFE genes for HH has increased, especially with the application of whole genome sequencing technology in recent years, the biological function of the identified mutations, as well as genotype-phenotype correlations remain to be explored. Further analysis of the causative gene mutation would be critical to clarify the mechanisms underlying specific disease phenotypes. In this review, we therefore summarize the recent advances in the molecular genetics of WD and HH including the updated mutation spectrums and the correlation between genotype and phenotype, with an emphasis on biological functional studies of the individual mutations identified in WD and HH. The weakness of the current functional studies and analysis for the clinical association of the individual mutation was also discussed. These works are essential for the understanding of the association between genotypes and phenotypes of these inherited metabolic liver diseases.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Medical Genetics - Volume 59, Issue 10, October 2016, Pages 532-539
Journal: European Journal of Medical Genetics - Volume 59, Issue 10, October 2016, Pages 532-539
نویسندگان
Tingxia Lv, Xiaojin Li, Wei Zhang, Xinyan Zhao, Xiaojuan Ou, Jian Huang,