نتایج جستجو برای: rhce
تعداد نتایج: 123 فیلتر نتایج به سال:
Two distinct RHCE alleles in cis to weak D type 31 alleles in individuals from different ethnicities
More and more cultural heritage organizations see a great opportunity by opening up their collections via the Web to expand their userbase. In this paper we look at our current work in a specific use case, a cultural heritage organization called RHCe that wanted to open up its photo and video archives to the public. We demonstrate in this paper how we can utilize metadata to offer a homogeneous...
Costs of accountable care organization participation for primary care providers: early stage results
BACKGROUND Little is known about the impact of joining an Accountable Care Organization (ACO) on primary care provider organization's costs. The purpose of this study was to determine whether joining an ACO is associated with an increase in a Rural Health Clinic's (RHC's) cost per visit. METHODS The analyses focused on cost per visit in 2012 and 2013 for RHCs that joined an ACO in 2012 and co...
This study aims (1) to examine the trends and patterns of colorectal cancer screening (CCS) of Medicare beneficiaries in rural areas by state and year (before and after Affordable Care Act [ACA] enactment) and (2) to investigate the contextual, organizational, and aggregated patient characteristics influencing variations in care received by patients of rural health clinics (RHCs). The following...
The molecular backgrounds of variants encountered in Afro-Caribbean black individuals and associated with the production of clinically significant antibodies against high-incidence antigens (anti-RH18, anti-RH34) and against Rhe epitopes were determined. We showed that RH:-18 phenotypes are produced by 3 distinct RHCE alleles: ceEK carrying 48G>C (exon 1), 712A>G, 787A>G, 800T>A (exon 5); ceBI ...
Rhnull disease, which includes the amorph and regulator types, is a rare genetic disorder characterized by stomatocytosis and chronic hemolytic anemia. We studied here a German family transmitting a putative amorph Rhnull disease gene and identified a rare mutation causing the loss-offunction phenotype. We analyzed the genomic and transcript structure of RH30, RH50, and CD47, the three loci tho...
A two-locus gene conversion model with selection and its application to the human RHCE and RHD genes
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