Results 131 to 140 of about 3,944 (168)

Proteomic profiling identifies prognostic signature for Krukenberg tumor of gastrointestinal origin. [PDF]

iScience
Wang X, Yi X, Xue Z, Liu W, Teng X, Zhang H, Guo T, Zhu Y, Wang B.   +8 more
europepmc   +1 more source

A clinically applicable method for early interstitial lung disease detection in incident rheumatoid arthritis cases: integration of protein biomarkers and clinical factors. [PDF]

Ann Med
Gou X, Jiao W, Chen H, Tan Y, Fan Q, Liu H, Liu Y, Chen J.   +7 more
europepmc   +1 more source

EmoTweetID: A dataset of Indonesian tweets for emotion classification and word embedding construction. [PDF]

Data Brief
Nugroho KS, Bachtiar FA, Mahmudy WF, Henry MM, Isnan M, Pangestu G, Pardamean B.   +6 more
europepmc   +1 more source

Hypoglycemia in Patients With LAMA2-CMD

Pediatric Neurology, 2023
Hypoglycemia has been reported in patients with LAMA2-CMD, but the frequency, risk factors, and correlation to genotype/phenotype have not been systematically assessed to date.A retrospective cohort study was performed on 48 patients with LAMA2-CMD. Patients were divided into two groups: a hypoglycemic group, with at least one episode of hypoglycemia ...
Umbertina Conti Reed, Clara Gontijo Camelo, Edmar Zanoteli   +2 more
exaly   +3 more sources

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LAMA2-related muscular dystrophy mimicking multiple sclerosis

BMJ Case Reports, 2022
Laminin-alpha2-related muscular dystrophy (LAMA2-MD) is a genetic condition due to reduced LAMA2, a protein found throughout the nervous system. Late-onset LAMA2-MD may present with proximal muscle weakness, joint contractures, neuropathy, epilepsy and/or cardiorespiratory issues, and is less common than the neonatal form. We describe a novel phenotype
Jacqueline Koshorek, Nara de Macena Sobreira, Shiv Saidha   +2 more
openaire   +2 more sources

An artificial LAMA2-GelMA hydrogel microenvironment for the development of pancreatic endocrine progenitors

Biomaterials, 2022
The biomimetic pancreatic microenvironment improves the differentiation efficiency and function of human embryonic stem cell-derived β-cells (SC-β cells). Thus, a laminin subunit alpha 2-gelatin methacrylate (LAMA2-GelMA) hybrid hydrogel as a bionics carrier for the formation and maturation of endocrine lineage was developed in our research, based on ...
Guo Qingsong, Zhiwei Wang, Yamin Li
exaly   +3 more sources

A Spectrum of Pathogenic Variants in the LAMA2 Gene in the Russian Federation

International Journal of Molecular Sciences
LAMA2-associated muscular dystrophy is a rare genetic disorder caused by pathogenic or likely pathogenic variants in the LAMA2 gene. The aim of this study is to characterize the spectrum of pathogenic/likely pathogenic variants in the LAMA2 gene among Russian patients, identify frequent pathogenic variants specific to this population, and estimate the ...
Artem Borovikov, Aysylu Murtazina, Polina Chausova   +2 more
exaly   +3 more sources

Epilepsy in LAMA2-related muscular dystrophy: A systematic review of the literature

Seizure: the Journal of the British Epilepsy Association, 2021
Epilepsy is a common, often severe, feature of LAMA2-related muscular dystrophy (LAMA2-RD) and could represent its onset and main manifestation, even in the absence of overt muscle involvement. To date, there is no systematic characterization of epilepsy in LAMA2-RD, and its impact on neurodevelopment and on the clinical course remains poorly ...
Federico Sicca, Gianluca Sesso, Andrea Salvati   +2 more
exaly   +3 more sources