نتایج جستجو برای: hereditary rings

تعداد نتایج: 132578  

The purpose of this paper is to introduce some new classes of rings and modules that are closely related to the classes of almost Dedekind domains and almost Dedekind modules. We introduce the concepts of $\phi$-almost Dedekind rings and $\Phi$-almost Dedekind modules and study some properties of this classes. In this paper we get some equivalent conditions for $\phi$-almost Dedekind rings and ...

Journal: :international journal of group theory 2015
claude carlet yin tan

we give a survey of recent applications of group rings to combinatorics and tocryptography, including their use in the di erential cryptanalysis of block ciphers.

Journal: :The Journal of Cell Biology 1995
H Mehlin B Daneholt U Skoglund

The transport of Balbiani ring (BR) premessenger RNP particles in the larval salivary gland cells of the dipteran Chironomus tentans can be followed using electron microscopy. A BR RNP particle consists of an RNP ribbon bent into a ringlike structure. Upon translocation through the nuclear pore complex (NPC), the ribbon is straightened and enters the central channel of the NPC with the 5' end o...

Journal: :Organic letters 2016
Yu-Ting Dong Quan Jin Ling Zhou Jie Chen

An efficient N-heterocyclic carbene (NHC) catalyzed sulfenylation reaction of α,β-unsaturated aldehydes with N-(arylthio)phthalimide has been developed. A wide variety of α-thioenals can be obtained with good to excellent yields and excellent Z-configuration.

2004

In this paper we construct a q-deformation of the Witt-Burnside ring of a profinite group over a commutative ring, where q ranges over the ring of integers. When q = 1, this coincides with the Witt-Burnside ring introduced by A. To achieve our goal we show that there exists a q-deformation of the necklace ring of a profinite group over a commutative ring. As in the classical case, i.e., the cas...

2009
M. N. DAIF

The following result is proved: Let R be a 2-torsion free semiprime ring, and let T : R → R be an additive mapping, related to a surjective homomorphism θ : R → R, such that 2T (x2) = T (x)θ(x) + θ(x)T (x) for all x ∈ R. Then T is both a left and a right θ-centralizer.

Journal: :iranian journal of otorhinolaryngology 0
bijan khademi department of otorhinolaryngology, shiraz institute for cancer research, shiraz university of medical sciences, shiraz, iran venon asefi otorhinolaryngologist, shiraz, iran mehdi tarzi otorhinolaryngologist, shiraz, iran

introduction: maxillary osteomyelitis is a rare phenomenon. if it occurs, evaluation for underlying disease especially osteopetrosis must be considered. osteomyelitis occurs as a complication in 10% of the cases of osteopetrosis. case report: this is a case report of maxillary osteomyelitis presented in a 15-year old boy with osteopetrosis.  in this case, the disease represented mainly with fac...

Journal: :iranian journal of immunology 0
shervin shahinpour research center for immunod eficiencies, pediatrics ce nter of excel lence, children's medical c enter, tehran university of medical sciences, tehran marzieh tavakol department of allergy and clinical immunology, shahid bahonar hospital, alborz u niversity of medical sciences, karaj, iran hassan abolhass ani research center for immunod eficiencies, pediatrics ce nter of excel lence, children's medical c enter, tehran university of medical sciences, tehran payam mohammadinejad research center for immunod eficiencies, pediatrics ce nter of excel lence, children's medical c enter, tehran university of medical sciences, tehran masoud movahedi research center for immunod eficiencies, pediatrics ce nter of excel lence, children's medical c enter, tehran university of medical sciences, tehran saba arshi allergy and clinical immunology department of rasole-akram hospital, iran university of medical sciences, tehran, iran asghar aghamohammadi

background: hereditary angioedema (hae) is a rare autosomal dominant primary immunodeficiency with complement system defect characterized by recurrent episodes of angioedema involving the skin or mucosa of the upper respiratory and gastrointestinal tracts. objective: to characterize the clinical and laboratory data of hereditary angioedema in iran. methods: patients with probable diagnosis of a...

Journal: :caspian journal of neurological sciences 0
karim nikkhah ali ghabeli-juibary resident of neurology, department of neurology, student research committee, school of medicine, mashhad university of medical sciences, mashhad, iran; [email protected] ariane sadr-nabavi

hereditary spastic paraplegias are highly heterogeneous neurodegenerative disorders with some special mutations. we report on a patient with pescavus, distal a myotrophy, hyper extended fingers, and pectus excavatum. neurological examination showed that he had proximal lower limbs weakness with a positive gower sign, exaggerated lower limbs deep tendon reflexes with spasticity, distal muscle wa...

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