Results 241 to 250 of about 773,961 (344)

Twinkle Light‐Inspired Aggregation‐Induced Emission “Lighting‐Up” Bacteriophages to Enhance Immunoassays via Spontaneous Amino‐Yne Click Reaction

Aggregate, EarlyView.
Herein, we present a twinkle‐light‐inspired “lighting‐up” bifunctional bacteriophage for fluorescence immunoassays via a spontaneous amino‐yne click reaction, and demonstrate its versatile potential for the highly sensitive detection of various targets, ranging from small molecules to pathogenic microorganisms, in complex samples.
Xiaoyi Lv, Xirui Chen, Qi Chen, Qing Liu, Mingjian Yao, Weipeng Tong, Hao Fang, Yiping Chen, Yonghua Xiong, Ben Zhong Tang, Xiaolin Huang   +10 more
wiley   +1 more source

Early and Accurate Pathogen Identification Based on mNGS: Key to Timely Therapy for Mycoplasma Prosthetic Joint Infection. [PDF]

Orthop Surg
Lin Z, Chen Y, Yu Z, Zhang Z, Lin Y, Zhang W, Li W, Guo Y, Fang X.   +8 more
europepmc   +1 more source

Adapting Image‐Based Models for 1D Data via Spider Plot Transformation and Transfer Learning

Advanced Intelligent Systems, EarlyView.
A novel method enables the use of pretrained image‐based neural networks for complex 1D data, including Raman and mid‐infrared spectra, electrocardiograms, and mass spectrometry. 2D spider plots with false‐color fill enable transfer lerning, therefore enhancing data augmentation and model explainability across diverse spectral and time series datasets.
Azadeh Mokari, Oleg Ryabchykov, Thomas Bocklitz   +2 more
wiley   +1 more source

PLLA Coating of Lyophilized Human Bone Allograft for Long-term Release of Antibiotics. [PDF]

In Vivo
Barbeck M, Zhang J, Stojanovic S, Radenkovic M, Najman S, Foth A, Jung O, Beuer F, Xiong X.   +8 more
europepmc   +1 more source

Mycosis Fungoides, Sézary Syndrome, and Cutaneous B‐Cell Lymphomas: 2025 Update on Diagnosis, Risk‐Stratification, and Management

American Journal of Hematology, EarlyView.
ABSTRACT Disease Overview Primary cutaneous lymphomas are a rare and heterogeneous group of extranodal lymphomas that require the integration of clinical and histopathologic data for classification and treatment. Diagnosis Diagnosis and disease classification is based on histopathologic review and immunohistochemical staining of an appropriate skin ...
Alexandra C. Hristov, Trilokraj Tejasvi, Ryan A. Wilcox   +2 more
wiley   +1 more source

Toward the Characterization of the Human Core Ocular Surface Microbiome. [PDF]

Invest Ophthalmol Vis Sci
Morandi SC, Uldry AC, Eldridge N, Kreuzer M, Herzog EL, Zinkernagel M, Zysset-Burri DC.   +6 more
europepmc   +1 more source

The evolutionary history of methicillin-resistant Staphylococcus aureus (MRSA)

Proceedings of the National Academy of Sciences of the United States of America, 2002
M. Enright, D. Robinson, Gaynor A. Randle, E. Feil, H. Grundmann, B. Spratt, C. Walsh   +6 more
semanticscholar   +1 more source

Prenatal Brain Abnormalities in Sodium‐Dependent Multivitamin Transporter Deficiency

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT In treatable neurometabolic disorders, early diagnosis and prompt initiation of treatment are key to improved survival and outcomes. Biallelic variants in SLC5A6 cause sodium‐dependent multivitamin transporter deficiency (OMIM # 618973), which is treatable with high‐dose pantothenic acid, biotin, and alpha lipoic acid.
Eri Ogawa, Kenjiro Kosaki, Toshiki Takenouchi   +2 more
wiley   +1 more source

Mesh-Augmented Ventral Hernia Repair Despite Iatrogenic <i>Staphylococcus aureus</i>-Peritonitis Due to Progressive Pneumoperitoneum: A Case Report. [PDF]

Surg Case Rep
Klewitz R, Menzel M, Holzner P, Fichtner-Feigl S, Hipp J.   +4 more
europepmc   +1 more source

Genotype–Phenotype Correlations, Mortality, and Clinical Insights in Keratitis–Ichthyosis–Deafness Syndrome: A Comprehensive Review and Case Report

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero, Marco Antonio Hernández Lepe, José de Jesús Manríquez Torres, Diego Daniel Aguirre‐Gómez, Natsuo Hayashi‐Mercado, Genaro Rodríguez Uribe, Tadeo Cerón, María Ruiz‐Gamboa, Jesús Alonso Gándara‐Mireles, Ismael Lares‐Asseff, Verónica Loera‐Castañeda, Jorge Alvelais‐Palacios, Lucrecia Arzamendi‐Cepeda, Lidia Magdalena Castañeda‐González, Adolfo García‐Barrón, Francisco Yamal Quiroz Herrera, Francisco González‐Salazar, Horacio Almanza‐Reyes   +17 more
wiley   +1 more source