Results 31 to 40 of about 604,221 (250)

Two New Types of Rings Constructed from Quasiprime Ideals

open access: yesInternational Journal of Mathematics and Mathematical Sciences, 2011
Keigher showed that quasi-prime ideals in differential commutative rings are analogues of prime ideals in commutative rings. In that direction, he introduced and studied new types of differential rings using quasi-prime ideals of a differential ring.
Manal Ghanem, Hassan Al-Ezeh
doaj   +1 more source

Epilepsy‐Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Pathogenic variants in SCN1A, which encodes the voltage‐gated sodium channel NaV1.1, are associated with multiple epilepsy syndromes exhibiting a range of clinical severity. SCN1A variants are reported in different syndromes, including Dravet syndrome, which is associated with loss‐of‐function, whereas neonatal/infantile‐onset ...
Lanie N. Liebovitz   +3 more
wiley   +1 more source

Ferrocene-Containing Pseudorotaxanes in Crystals: Aromatic Interactions with Hammett Correlation

open access: yesMolecules, 2022
Single crystals of pseudorotaxanes, [(FcCH2NH2CH2Ar)(DB24C8)][PF6] (DB24C8 = dibenzo[24]crown-8, Fc = Fe(C5H4)(C5H5), Ar = -C6H3-3,4-Cl2, -C6H3-3,4-F2, -C6H4-4-F, -C6H4-4-Cl, -C6H4-4-Br, -C6H3-3-F-4-Me, -C6H4-4-I) and [(FcCH2NH2CH2C6H4-4-Me)(DB24C8)][Ni ...
Yuji Suzaki   +6 more
doaj   +1 more source

PF-circRNA-Supplementary Tables.pdf

open access: yes, 2022
PF-circRNA-Supplementary Table 1 and ...
Jinqing Li (12509803)
core   +1 more source

Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce   +72 more
wiley   +1 more source

Profiles of Kelch mutations in Plasmodium falciparum across South Asia and their implications for tracking drug resistance

open access: yesInternational Journal for Parasitology: Drugs and Drug Resistance, 2019
Artemisinin-based combination therapy (ACT) offers highly successful treatment of malaria. Emergence and spread of Plasmodium falciparum (Pf) parasites with decreased susceptibility to ACT in South-East Asia has caused concern worldwide.
Jyoti Chhibber-Goel, Amit Sharma
doaj   +1 more source

Comparative Evaluation of the Angiogenic Potential of Hypoxia Preconditioned Blood-Derived Secretomes and Platelet-Rich Plasma: An In Vitro Analysis

open access: yesBiomedicines, 2020
Blood-derived factor preparations are being clinically employed as tools for promoting tissue repair and regeneration. Here we set out to characterize the in vitro angiogenic potential of two types of frequently used autologous blood-derived secretomes ...
Philipp Moog   +8 more
doaj   +1 more source

Spectral Study of some Charge Transfer Complexes Derived from Schiff base of 3- Methoxy -4-hydroxy benzaldehyde with some Electrone acceptors. [PDF]

open access: yesمجلة جامعة الانبار للعلوم الصرفة, 2012
:A new series of Schiff bases were obtained by condensation of 3- methoxy -4-hydroxy benzaldehyde (vanillin) with seven aromatic amine .These bases were identified by infrared spectra and melting point .
Laila A. Jubur   +1 more
doaj   +1 more source

SPG4 and Dementia: Expanding the Clinical Spectrum

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza   +19 more
wiley   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

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