Results 91 to 100 of about 803,319 (299)
Forgery of Documents under Signature
EIRP Proceedings, 2022 In this paper we have examined the crime of forgery in private documents, in terms of elements of the structure of the crime, such as the objective side, the subjective side, forms, ways of sanctions and some procedural aspects.
Ion Rusu
doaj
Synthetic single domain antibodies for the conformational trapping of membrane proteins
eLife, 2018 Mechanistic and structural studies of membrane proteins require their stabilization in specific conformations. Single domain antibodies are potent reagents for this purpose, but their generation relies on immunizations, which impedes selections in the ...
Iwan Zimmermann +16 more
doaj +1 more source
STUDIES IN CARBOHYDRATES. PART III. INVESTIGATION OF MODAL GUM (LANNEA GRANDIS) [PDF]
, 1956 V. M. PARIKH, T. R. I NGLE, B. V. BHIDE
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Diffusion Tractography Biomarker for Epilepsy Severity in Children With Drug‐Resistant Epilepsy
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To develop a novel deep‐learning model of clinical DWI tractography that can accurately predict the general assessment of epilepsy severity (GASE) in pediatric drug‐resistant epilepsy (DRE) and test if it can screen diverse neurocognitive impairments identified through neuropsychological assessments.
Jeong‐Won Jeong +7 more
wiley +1 more source
Cell Reports, 2018 Summary: Receptors show promise for the transport of monoclonal antibodies (mAbs) across the blood-brain barrier. However, safety liabilities associated with peripheral receptor binding and Fc effector function have been reported.
Felix Weber +12 more
doaj +1 more source
Cross-modal transfer of a specific discrimination in the rabbit [PDF]
, 1969 Arthur L. Yehle, Jeannette P. Ward
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background Mitofusin 2 (MFN2) is a major causative gene for axonal Charcot – Marie – Tooth disease type 2A (CMT2A), with a wide phenotypic spectrum. Comprehensive large ‐ scale genotype – phenotype association studies are essential for understanding disease pathogenesis and improved clinical management.
Masahiro Ando +13 more
wiley +1 more source
Cross-modal generalization to tone and light in human eyelid conditioning [PDF]
, 1966 G. Alan Marlatt +4 more
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RAB39B Related Parkinsonism in an Italian Family: A Unique Use of Advanced Therapies
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Parkinson's disease (PD) is a neurodegenerative disorder that may sometimes be caused by deleterious genetic variants. Among them, RAB39B polymorphisms are known as rare causes of early‐onset PD associated with intellectual disability (Waisman's syndrome).
Caterina Del Regno +13 more
wiley +1 more source