Results 271 to 280 of about 4,192,840 (340)

Lesion Location and Functional Connections Reveal Cognitive Impairment Networks in Multiple Sclerosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cognitive impairment, fatigue, and depression are common in multiple sclerosis (MS), potentially due to disruption of regional functional connectivity caused by white matter (WM) lesions. We explored whether WM lesions functionally connected to specific brain regions contribute to these MS‐related manifestations.
Alessandro Franceschini, Paolo Preziosa, Paola Valsasina, Damiano Mistri, Monica Margoni, Federica Esposito, Massimo Filippi, Maria A. Rocca   +7 more
wiley   +1 more source

gyōza: a Snakemake workflow for modular analysis of deep-mutational scanning data. [PDF]

Genetics
Durand R, Pageau A, Landry CR.
europepmc   +1 more source

Systemic T Cell Receptor Profiling Reveals Adaptive Immune Activation and Potential Immune Signatures of Diagnosis and Brain Atrophy in Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Epilepsy is increasingly associated with immune dysregulation and inflammation. The T cell receptor (TCR), a key mediator of adaptive immunity, shows repertoire alterations in various immune‐mediated diseases. The unique TCR sequence serves as a molecular barcode for T cells, and clonal expansion accompanied by reduced overall TCR ...
Yong‐Won Shin, Sang Bin Hong, Yong Woo Shin, Inpyeong Hwang, Jaeseong Oh, Jihyeon Choi, Narae Kim, Jangsup Moon, Keun‐Hwa Jung, Kyung‐Il Park, Ki‐Young Jung, Kon Chu, Sang Kun Lee   +12 more
wiley   +1 more source

Correction: Sonongbua et al. Insights into Mitochondrial Rearrangements and Selection in Accipitrid Mitogenomes, with New Data on <i>Haliastur indus</i> and <i>Accipiter badius poliopsis</i>. <i>Genes</i> 2024, <i>15</i>, 1439. [PDF]

Genes (Basel)
Sonongbua J, Thong T, Panthum T, Budi T, Singchat W, Kraichak E, Chaiyes A, Muangmai N, Duengkae P, Sitdhibutr R, Kasorndorkbua C, Srikulnath K.   +11 more
europepmc   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas, Pablo Iruzubieta, Alberto Damborenea, Laura Pérez‐Fernández, Inmaculada Azorín, Juan Carlos Jiménez García, Ana Töpf, Pilar Martí, Lorena Fores‐Toribio, María Manterola, Rosana Blanco‐Mañez, Oihane Pikatza‐Menoio, Sonia Alonso‐Martín, Volker Straub, Aitziber L. Cortajarena, Adolfo López de Munain, David De Sancho, Lorea Blázquez, Juan J. Vilchez   +18 more
wiley   +1 more source

Evaluating the Negative-Strand Coding Potential in Plum Pox Virus. [PDF]

Mol Plant Pathol
García B, Del Álamo JV, Rincón M, Gonzalo I, Cheng X, García JA, Simón-Mateo C, Valli AA, Rodamilans B.   +8 more
europepmc   +1 more source

Electroencephalogram Sonification with Hybrid Intelligent System Design Based on Deep Network. [PDF]

J Med Signals Sens
Jalali H, Pouladian M, Nasrabadi AM, Movahed A.   +3 more
europepmc   +1 more source

TCRdb 2.0: an updated T-cell receptor sequence database. [PDF]

Nucleic Acids Res
Yue T, Chen SY, Shen WK, Liao Y, Lei Q, Guo AY.   +5 more
europepmc   +1 more source

Dockground: Expanding the Resource to Protein-DNA Complexes. [PDF]

J Mol Biol
Collins KW, Copeland MM, Kundrotas PJ, Vakser IA.   +3 more
europepmc   +1 more source

The Role of Event Number and Duration in Time-Compressed Memory Replay. [PDF]

Open Mind (Camb)
Leroy N, D'Argembeau A.
europepmc   +1 more source