نتایج جستجو برای: hereditary stability

تعداد نتایج: 382625  

2002
A. F. Ivanov

This paper surveys some results in stochastic differential delay equations beginning with ”On stationary solutions of a stochastic differential equations” by K. Ito and M. Nisio, 1964, and also some results in stochastic stability beginning with the ”Stability of positive supermartingales” by R. Bucy, 1964. The problems discussed in this survey are the existence and uniqueness of solutions of s...

2004
V. Kolmanovskii L. Shaikhet

Many stability results in the theory of stochastic hereditary systems and their applications were obtained by construction of appropriate Lyapunov functionals. One general method of Lyapunov functionals construction was proposed and developed by the authors during last decade for stability investigation of deterministic and stochastic functional-differential and difference equations. In this pa...

Journal: :Blood 2007
Colin P Johnson Massimiliano Gaetani Vanessa Ortiz Nishant Bhasin Sandy Harper Patrick G Gallagher David W Speicher Dennis E Discher

Pathogenic mutations in alpha and beta spectrin result in a variety of syndromes, including hereditary elliptocytosis (HE), hereditary pyropoikilocytosis (HPP), and hereditary spherocytosis (HS). Although some mutations clearly lie at sites of interaction, such as the sites of spectrin alpha-betatetramer formation, a surprising number of HE-causing mutations have been identified within linker r...

Journal: :Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 2018

بهاری, امیر, رضایی, محمد صادق, غفاری, جواد,

Hereditary angioedema is a rare disorder of complement system which is often seen with autosomal dominant hereditary. Clinical characteristics include non- pruritic and non-pitting mucocutaneous edema that could involve all parts of the body. This study reports seven cases of hereditary angioedema with classical manifestations accompanied by low function of C1INH (type 2). One death occurred du...

Journal: :Blood 1978
A C Greenquist S B Shohet S E Bernstein

In contrast to the disease in humans, hereditary spherocytosis in the common house mouse produces an extreme spherocytosis. The cells show a broad distribution in size ranging from microcytic to macrocytic. Of particular interest is the finding of a substantial reduction in the major membrane polypeptide called spectrin, supporting a critical role for this protein in the control of erythrocyte ...

Journal: :Cell 2003
Keith W. Caldecott

DNA single-strand break repair (SSBR) is critical for the survival and genetic stability of mammalian cells. Three papers have recently associated mutations in putative human SSBR genes with hereditary spinocerebellar ataxia. The emerging links between SSBR and neurodegenerative disorders are discussed.

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه بیرجند - دانشکده علوم 1391

in this thesis, we consider a mathematical model of cancer with completely unknown parameters. we study the stability of critical points which are biologically admissible. then we consider a control on the system and introduce situations at which solutions are attracted to critical points and so the cancer disease has auto healing. the lyapunov stability method is used for estimating the un...

Journal: :Neuron 2013
Robert A. Carrillo Kaushiki Menon Kai Zinn

In this issue of Neuron, Nahm et al. (2013) examine the Drosophila ortholog of spartin, the human gene mutated in a form of hereditary spastic paraplegia. Spartin inhibits BMP signaling and upregulation of BMP signaling may increase microtubule stability and neurodegeneration.

Journal: :iranian journal of radiology 0
abdolrahman rostamian department of rheumatology, vali-asr hospital, imam khomeini hospital complex, tehran university of medical sciences, tehran, iran; center for research on occupational disease, tehran university of medical sciences, tehran, iran hamed mazoochy department of orthopedics, imam khomeini hospital complex, tehran university of medical sciences, tehran, iran shafieh movassaghi department of rheumatology, vali-asr hospital, imam khomeini hospital complex, tehran university of medical sciences, tehran, iran seyed mohammad javad mortazavi department of orthopedics, imam khomeini hospital complex, tehran university of medical sciences, tehran, iran elham sadeghzadeh department of rheumatology, vali-asr hospital, imam khomeini hospital complex, tehran university of medical sciences, tehran, iran fatemeh shahbazi department of rheumatology, vali-asr hospital, imam khomeini hospital complex, tehran university of medical sciences, tehran, iran; department of biology, payame noor university, karaj, iran; department of biology, payame noor university, karaj, iran , +98-2161192376

coexisting ankylosing spondylitis and hereditary multiple exostoses have rarely been reported (three patients) previously. a 27-year-old man with hereditary multiple exostoses is presented as a fourth report. at the age of 15 years, the patient had multiple exostoses around the knee, ankle and shoulder joints. he was diagnosed with ankylosing spondylitis 3 years ago. the patient’s sister and hi...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید