Memlükler Dönemi (648-923/1250-1517) Tarih ve Tabakât Eserlerine Dair
نویسندگان
چکیده
منابع مشابه
Op-brai150057 1505..1517
Non-progressive cerebellar ataxias are a rare group of disorders that comprise approximately 10% of static infantile encephalopathies. We report the identification of mutations in PMPCA in 17 patients from four families affected with cerebellar ataxia, including the large Lebanese family previously described with autosomal recessive cerebellar ataxia and short stature of Norman type and localiz...
متن کاملBio013276 1509..1517
Pseudohypoaldosteronism type II (PHAII) is a hereditary hypertensive disease caused by mutations in four different genes: with-no-lysine kinases (WNK) 1 and 4, Kelch-like family member 3 (KLHL3), and cullin 3 (Cul3). Cul3 and KLHL3 form an E3 ligase complex that ubiquitinates and reduces the expression level of WNK4. PHAIIcausing mutations in WNK4 and KLHL3 impair WNK4 ubiquitination. However, ...
متن کاملVzj50063 641..648
The objective of this study was to examine the pore-scale distribution and morphology of organic immiscible liquid in natural porous media containing three immiscible fluids. High-resolution, threedimensional images of an organic liquid (tetrachloroethene) in both three-phase (water–air–organic liquid) and two-phase (water–organic liquid) systems were obtained using synchrotron X-ray microtomog...
متن کامل648-658 Tan
Purpose: Critical bending moment (CBM), the moment at which the external nonaxial load applied overcomes screw joint preload and causes loss of contact between the mating surfaces of the implant screw joint components, was measured with 2 types of implants and 2 types of abutments. Materials and Methods: Using 4 test groups of 5 implant-abutment pairs, CBM at the implant-abutment screw joint wa...
متن کاملDmm021972 1517..1529
Tuberous sclerosis complex (TSC) is an autosomal dominant syndrome that is best characterised by neurodevelopmental deficits and the presence of benign tumours (called hamartomas) in affected organs. This multi-organ disorder results from inactivating point mutations in either the TSC1 or the TSC2 genes and consequent activation of the canonical mammalian target of rapamycin complex 1 signallin...
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ژورنال
عنوان ژورنال: İslam Tetkikleri Dergisi
سال: 2020
ISSN: 2687-5616,2717-6967
DOI: 10.26650/iuitd.2020.678998