Animal cells possess thousands of long non-coding (lnc) RNAs, such as antisense
noncoding RNA in the INK4 locus (ANRIL), which have regulatory roles in the cells' …

Vitiligo is a multifactorial skin disease with established role of genetics and autoimmunity in
its pathogenesis. Vitamin D receptor (VDR) polymorphisms have been suggested to …

The presence of single nucleotide variations in the coding region of micro-RNA (miRNA)-
encoding genes plays a significant role in the expression and function of these molecules in …

Background In meta-analyses of genetic association studies, ancestry and ethnicity are not
accurately investigated. Ethnicity is usually classified using conventional race/ethnic …

The functional variant of the Klotho" KL-VS" stretch, which includes six polymorphisms in
linkage disequilibrium, is reportedly associated with healthy aging and longevity in …

Gene families are considered as groups of homologous genes which they share very similar
sequences and they may have identical functions. Members of gene families may be found …

نداد تسد زا ینعی نینج طقــس تروص هب هک تسا هدش اب نینج دلوت ای یرادراــب 24 ای 20 هتفه زا
لبق یرادراــب رد نینج طقس زورب.] 1 [دــشاب یم رتمک ای مرگ 500 نزو% 10-15 دودح ناهج رسارس رد …‎

ینژ هداوناخ 1 یاراد هک تسا هدش لیکشت نژ یدادعت زا. دنشاب یم درکلمع رد یناشوپ مه و دوخ یلاوت رد
یدایز یژولومه نوزگا نامه ای نیئتورپ هدننک دک یحاون رد رتشیب تهابش نیا یگدش فعاضم دادخر …‎

Background and purpose: Congenital Myasthenic Syndrome (CMS) is a rare genetic
disease with autosomal recessive inheritance pattern which is caused by mutations in the …

Abstract Background and purpose: Congenital Myasthenic Syndrome (CMS) is a rare
genetic disease with autosomal recessive inheritance pattern which is caused by mutations …