Results 171 to 180 of about 16,949 (276)
Cartan subalgebras for restrictions of $\mathfrak{g}$-modules
In this paper, we deal with the $\mathcal{U}(\mathfrak{g})$-action on a $\mathfrak{g}$-module on which a larger algebra $\mathcal{A}$ acts irreducibly. Under a mild condition, we will show that the support of the $\mathcal{Z}(\mathfrak{g})$-action is a union of affine subspaces in the dual of a Cartan subalgebra modulo the Weyl group action.
openaire +2 more sources
Abstract The establishment of guidelines and curriculum standards for medical physics residency training is a critical component of setting expectations and competencies for the profession. Since the last publication of these standards, residency training has become integrated into the eligibility criteria for most medical physics certification bodies.
Jonathon A. Nye+16 more
wiley +1 more source
Energy dependence of the GAFCHROMIC LD‐V1 in the diagnostic radiographic modalities
Abstract The GAFCHROMIC LD‐V1 radiochromic film is widely used in dosimetry because it can provide high‐resolution two‐dimensional dose distributions without processing. This study aimed to evaluate the response characteristics at different effective energies, from the low‐energy range of mammography to the high‐energy range of computed tomography. Net
Tatsuhiro Gotanda+9 more
wiley +1 more source
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao+34 more
wiley +1 more source
Verma modules over generalized Virasoro algebras Vir[G]
Jun Hu, Xiandong Wang, Kaiming Zhao
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FGF14 GAA Intronic Expansion in Unsolved Adult‐Onset Ataxia in the Care4Rare Canada Consortium
ABSTRACT Background and Objectives Spinocerebellar ataxias (SCA) represent a clinically and genetically heterogeneous group of progressive neurodegenerative diseases with prominent cerebellar atrophy. Recently, a novel pathogenic repeat expansion in intron 1 of FGF14 was identified, causing adult‐onset SCA (SCA27B). We aimed to determine the proportion
Alexanne Cuillerier+20 more
wiley +1 more source
Restrictions to G(𝔽p) and G(r) of rational G-modules [PDF]
Eric M. Friedlander
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Essential g-radical supplemented modules [PDF]
Celıl Nebıyev, Hasan Hüseyın Ökten
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Early Language Impairment as an Integral Part of the Cognitive Phenotype in Huntington's Disease
ABSTRACT Objective Huntington's disease (HD) speech/language disorders have typically been attributed to motor and executive impairment due to striatal dysfunction. In‐depth study of linguistic skills and the role of extrastriatal structures in HD is scarce.
Arnau Puig‐Davi+13 more
wiley +1 more source
Some properties of (amply) g-radical supplemented modules [PDF]
Berna Koşar, Ayten Peki̇n
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