نتایج جستجو برای: wolfram mine
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BACKGROUND Wolfram Syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized by Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness identified by the acronym "DIDMOAD". The WS gene, WFS1, encodes a transmembrane protein called Wolframin, which recent evidence suggests may serve as a novel endoplasmic reticulum calcium channel in pancreatic β-cells and neuro...
Introduction. One of the major problems in reductive proof theory in the early 1970s was to give a proof-theoretic reduction of classical theories of iterated arithmetical inductive definitions to corresponding constructive systems. This problem was solved in [BFPS] in various ways which all where based on the method of cut-elimination (normalization, reps.) for infinitary Tait-style sequent ca...
BACKGROUND Wolfram Syndrome (WFS:OMIM 222300) is an autosomal recessive, progressive, neurologic and endocrinologic degenerative disorder caused by mutations in the WFS1 gene, encoding the endoplasmic reticulum (ER) protein wolframin, thought to be involved in the regulation of ER stress. This paper reports a cross section of data from the Washington University WFS Research Clinic, a longitudin...
One of the key advantages of the Bayesian paradigm is the ability to incorporate past experiences and expert opinion into statistical analyses. However, the principled, precise distillation of expert opinion into a probability distribution, a task known as prior elicitation, is challenging and involves considerations from psychology, computational science, software engineering, and other relate...
Wolfram syndrome (MIM 222300) is the association ofjuvenile onset diabetes mellitus and optic atrophy, also known as DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness). Patients present with diabetes mellitus followed by optic atrophy in the first decade, cranial diabetes insipidus and sensorineural deafness in the second decade, dilated renal outflow tracts early in t...
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