نتایج جستجو برای: pick c

تعداد نتایج: 1066027  

2009
Mirmojtaba Gharibi

Iranian National Petrochemical Company (NPC) has recently started a fast development. Because of the imbalance in development of NPC, despite of its reputation and history, is not able to recruit qualified workforce. Managers concern the future of the industry as this flow of low qualified human resources accedes to the top of the organizational pyramid. In this paper, a system dynamics model h...

Journal: :journal of cellular and molecular anesthesia 0
masoud nashibi anesthesiology research center, shahid beheshti university of medical sciences, tehran, iran ardeshir tajbakhsh anesthesiology research center, shahid beheshti university of medical sciences, tehran, iran farhad safari anesthesiology research center, shahid beheshti university of medical sciences, tehran, iran kamran mottaghi anesthesiology research center, shahid beheshti university of medical sciences, tehran, iran

nieman-pick disease type c is a rare, autosomal recessive, neurometabolic disorder associated with the accumulation of unesterified cholesterol in lysosomes and late endosomes. because of multiple organ involvement and wide range of clinical manifestations, these patients will demand multiple diagnostic and therapeutic procedures requiring anesthesia. sincepathogenesis of this disease is still ...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 1999
F B Scalco R Giugliani P Tobo J C Coelho

Niemann-Pick type C (NPC) fibroblasts present a large concentration of cholesterol in their cytoplasm due to a still unidentified deficiency in cholesterol metabolism. The influence of dimethylsulfoxide (DMSO) on the amount of intracellular cholesterol was measured in 8 cultures of normal fibroblasts and in 7 fibroblast cultures from NPC patients. DMSO was added to the fibroblast cultures at th...

Journal: :Journal of medical genetics 1981
P Donnai D Donnai R Harris R Stephens E Young S Campbell

An Ashkenazi Jewish woman had a child with Niemann-Pick disease in her first marriage. She subsequently remarried a man who was also heterozygous for the condition and conceived twins. Prenatal diagnostic tests were performed and one twin was shown to be homozygous and the other heterozygous for Niemann-Pick disease. The problems of prenatal diagnosis and counselling in twin pregnancies are dis...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Dennis C Ko Jonathan Binkley Arend Sidow Matthew P Scott

The neurodegenerative disease Niemann-Pick Type C2 (NPC2) results from mutations in the NPC2 (HE1) gene that cause abnormally high cholesterol accumulation in cells. We find that purified NPC2, a secreted soluble protein, binds cholesterol specifically with a much higher affinity (K(d) = 30-50 nM) than previously reported. Genetic and biochemical studies identified single amino acid changes tha...

Journal: :Blood 2010
Jakub Tolar Mary Eapen Paul J Orchard Bruce R Blazar

performance of the GM-CSF affinity column used to isolate antibodies. If used repeatedly, is it possible that a proportion of high affinity anti–GM-CSF AAs from PAP sera used as a positive control would be retained on the GM-CSF column and released slowly during subsequent purifications of HC IgG? If PAP anti–GMCSF IgG contamination did occur, not only would it account for the immunoblot data g...

2011
Hans H Klünemann

Niemann-Pick type C disease (NPC) is a rare and progressive genetic condition that is associated with an abnormal accumulation of lysosomal lipids in the body, which manifests as a variety of neurological symptoms that range greatly in severity. Management focuses largely on treating symptoms, but recent developments have led to disease-specific therapy that can slow or stabilise the progressio...

2016
Steven U. Walkley Cristin D. Davidson Jonathan Jacoby Philip D. Marella Elizabeth A. Ottinger Christopher P. Austin Forbes D. Porter Charles H. Vite Daniel S. Ory

Rare disease represents one of the most significant issues facing the medical community and health care providers worldwide, yet the majority of these disorders never emerge from their obscurity, drawing little attention from the medical community or the pharmaceutical industry. The challenge therefore is how best to mobilize rare disease stakeholders to enhance basic, translational and clinica...

Journal: :International Journal of Molecular Sciences 2018

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