Results 71 to 80 of about 23,762 (307)

Interpretable Machine Learning for Solvent‐Dependent Carrier Mobility in Solution‐Processed Organic Thin Films

open access: yesAdvanced Intelligent Discovery, EarlyView.
This work establishes a correlation between solvent properties and the charge transport performance of solution‐processed organic thin films through interpretable machine learning. Strong dispersion interactions (δD), moderate hydrogen bonding (δH), closely matching and compatible with the solute (quadruple thiophene), and a small molar volume (MolVol)
Tianhao Tan, Lian Duan, Dong Wang
wiley   +1 more source

Types of canine hormonal dwarfism through case reports

open access: yes, 2022
Background. Hormonal dwarfism refers to a group of rare endocrinopathies characterized by a growth disorder generally due to an isolated or multiple deficiencies of anterior pituitary hormones and it may present as different clinical presentations ...
Herrera Barbuzano, Nereida
core  

Imaging in short stature

open access: yesIndian Journal of Endocrinology and Metabolism, 2012
Short stature can be a sign of disease, disability, and social stigma causing psychological stress. It is important to have an early diagnosis and treatment.
Vikas Chaudhary, Shahina Bano
doaj   +1 more source

An Autonomous Large Language Model‐Agent Framework for Transparent and Local Time Series Forecasting

open access: yesAdvanced Intelligent Discovery, EarlyView.
Architecture of the proposed large language model (LLM)‐based agent framework for autonomous time series forecasting in thermal power generation systems. The framework operates through a vertical pipeline initiated by natural language queries from users, which are processed by the LLM Agent Core powered by Llama.cpp and a ReAct loop with persistent ...
William Gouvêa Buratto   +5 more
wiley   +1 more source

An Unusual Combination of Primordial Dwarfism with Isolated Cleft Palate

open access: yes, 2012
Primordial dwarfism is a rare anomaly with over 200 sub-types, which results in a relatively small body size in all stages of life, beginning at the intrauterine period. The life expectancy for these patients is around 30 years but very few survive their
K. Agarwal   +3 more
core   +1 more source

Assessing the Feasibility of Wearable Devices for Physiological Monitoring and Heat Risk Prediction in Outdoor Agricultural Workers

open access: yesAmerican Journal of Industrial Medicine, EarlyView.
ABSTRACT Background Outdoor agricultural workers experience significant heat exposure, yet few studies have evaluated whether wearable sensors can reliably measure continuous physiological responses in real field conditions. This pilot study examined the feasibility and predictive utility of core temperature, hydration, heart rate, and movement data ...
Sinan Sousan   +10 more
wiley   +1 more source

Induction of Autopolyploidy and Preliminary Investigation of the Dwarfing Mechanism in Hedychium coccineum

open access: yesPlants
In this study, Hedychium coccineum tetraploid plants and octaploid plants induced by colchicine were used as materials. The ploidy levels were precisely identified by combining root tip squash and flow cytometry analyses, and the differences between ...
Fang Wang   +7 more
doaj   +1 more source

The Arabidopsis Gain-of-Function Mutant ssi4 Requires RAR1 and SGT1b Differentially for Defense Activation and Morphological Alterations

open access: yesMolecular Plant-Microbe Interactions, 2008
A gain-of-function mutation in resistance (R) gene SSI4 causes constitutive activation of defense responses, spontaneous necrotic lesion formation, enhanced resistance against virulent pathogens, and a severe dwarf phenotype.
Fasong Zhou   +5 more
doaj   +1 more source

35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT HUWE1 (HECT, UBA, and WWE Domain Containing E3 Ubiquitin Protein Ligase1, OMIM 300697), located at Xp11.22, encodes a ubiquitin ligase that is highly conserved across species. Genetic variants in HUWE1 described in multiple independent studies cause X‐linked intellectual disability, including in the patients identified by Juberg, Marsidi, and ...
Mindy H. Li   +25 more
wiley   +1 more source

Case Report: Dual pathogenic mechanism of a PRKG2 missense variant underlies an attenuated phenotype of acromesomelic dysplasia

open access: yesFrontiers in Genetics
Acromesomelic dysplasia comprises a group of rare skeletal disorders characterized by dwarfism with anomalies predominantly affecting the middle and distal segments of the limbs.
Daria Akimova   +5 more
doaj   +1 more source

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