>
Fa
|
Ar
|
En
journal of human genetics
سال:2015 - دوره:60 - شماره:11
Associations of human leukocyte antigens with autoimmune diseases: challenges in identifying the mechanism
- صفحه:697-702
Distribution of HLA haplotypes across Japanese Archipelago: similarity, difference and admixture
- صفحه:683-690
Functional and genetic diversity of leukocyte immunoglobulin-like receptor and implication for disease associations
- صفحه:703-708
Genetics of autoimmune diseases: insights from population genetics
- صفحه:657-664
Human immune system diversity and its implications in diseases
- صفحه:655-656
Human leukocyte antigen polymorphisms and personalized medicine for rheumatoid arthritis
- صفحه:691-696
Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients
- صفحه:723-728
Overexpression of microRNA-133a inhibits ischemia-reperfusion-induced cardiomyocyte apoptosis by targeting DAPK2
- صفحه:709-716
Setleis syndrome due to inheritance of the 1p36.22p36.21 duplication: evidence for lack of penetrance
- صفحه:717-722
The genomic landscape of human immune-mediated diseases
- صفحه:675-681
The impact of next-generation sequencing technologies on HLA research
- صفحه:665-673
Copyright 2023
Islamic World Science Citation Center
All Rights Reserved
