Results 231 to 240 of about 57,508 (269)

Rats deficient in α-galactosidase A develop ocular manifestations of Fabry disease. [PDF]

Sci Rep, 2019
Miller JJ, Aoki K, Reid CA, Tiemeyer M, Dahms NM, Kassem IS.   +5 more
europepmc   +1 more source

Lactobacillus delbrueckii: A Functional Powerhouse in Dairy Fermentation and Emerging Probiotic Applications

Food Science &Nutrition, Volume 14, Issue 2, February 2026.
Lactobacillus delbrueckii is a key lactic acid bacterium widely used in dairy fermentation, particularly in yogurt and cheese production. This graphical abstract highlights its technological roles in lactose metabolism, acidification, proteolysis, and exopolysaccharide (EPS) production, which contribute to improved texture, flavor, and nutritional ...
Yousef Nami, Anahita Barghi, Mahsa Sadeghi, Tara Farhadi, Babak Haghshenas   +4 more
wiley   +1 more source

Inhibition of Mitochondrial Complex I Impairs Release of α-Galactosidase by Jurkat Cells. [PDF]

Int J Mol Sci, 2019
Lambert JRA, Howe SJ, Rahim AA, Burke DG, Heales SJR.   +4 more
europepmc   +1 more source

Recombinant production and characterization of six novel GH27 and GH36 α-galactosidases from Penicillium subrubescens and their synergism with a commercial mannanase during the hydrolysis of lignocellulosic biomass

, 2019
Nancy Coconi Linares, Adiphol Dilokpimol, Henrik Stålbrand, Miia Mäkelä, Ronald P. de Vries   +4 more
openalex   +2 more sources

WTAP Contributes to Periodontitis Pathogenesis by Promoting PDLSC Senescence and Impairing Osteogenic Differentiation via m6A‐Dependent Regulation of TP53BP1

Immunity, Inflammation and Disease, Volume 14, Issue 2, February 2026.
ABSTRACT Background Periodontitis, a chronic inflammatory disease, represents the primary cause of tooth loss in Chinese adults. Wilms tumor 1‐associating protein (WTAP) is a key component of the N6‐methyladenosine (m6A) methyltransferase complex, and has an unclear role in periodontitis pathogenesis, particularly concerning its regulatory functions in
Menglin Xiong, Tingting Wang, Yuan Liu
wiley   +1 more source

Optimization of Saccharomyces cerevisiae α-galactosidase production and application in the degradation of raffinose family oligosaccharides. [PDF]

Microb Cell Fact, 2019
Álvarez-Cao ME, Cerdán ME, González-Siso MI, Becerra M.   +3 more
europepmc   +1 more source

A Mutant mRNA Expression in an Endomyocardial Biopsy Sample Obtained from a Patient with a Cardiac Variant of Fabry Disease Caused by a Novel Acceptor Splice Site Mutation in the Invariant AG of Intron 5 of the α-Galactosidase A Gene

, 2013
Toru Watanabe, Haruo Hanawa, Tomoyasu Suzuki, Shuang Jiao, Kaori Yoshida, Minako Ogura, Yukako Ohno, Yoshitaka Hayashi, Masahiro Ito, Takeshi Kashimura, Hiroaki Obata, Akinori Sato, Takuya Ozawa, Makoto Kodama, Hitoshi Sakuraba, Tohru Minamino   +15 more
openalex   +2 more sources

EIF4A3‐Induced Circular RNA circSnd1 Promotes Muscle Atrophy and Muscle Ageing by Stabilizing EEF1A1

Journal of Cachexia, Sarcopenia and Muscle, Volume 17, Issue 1, February 2026.
ABSTRACT Background Muscle atrophy is a common complication of ageing, and many chronic conditions, lacks defined therapeutic interventions. It is still mostly unknown how circular RNAs contribute to muscle atrophy. Methods circRNA sequencing and quantitative real‐time PCR were performed to detect the changed circRNAs in muscle atrophy models and aged ...
Jin Li, Bing Jin, Yuwei Yan, Yuying Chen, Xiaohang Yin, Xinyi Ren, Qian Li, Jingying Chen, Siqi Wang, Tingting Yang, Yanan Zhang, Qiumeng Nie, Dongchao Lu, Ming Wu, Yan Yu, Lei Chen, Tarun Keswani, Guoping Li, Dragos Cretoiu, T. Scott Bowen, Junjie Xiao, Yongjun Zheng   +21 more
wiley   +1 more source

A Novel α-Galactosidase A Splicing Mutation Predisposes to Fabry Disease. [PDF]

Front Genet, 2019
Li P, Zhang L, Zhao N, Xiong Q, Zhou YA, Wu C, Xiao H.   +6 more
europepmc   +1 more source

Physical Fitness and Physical Function in Patients With Fabry Disease: A Cross‐Sectional Multicentre Study

Journal of Cachexia, Sarcopenia and Muscle, Volume 17, Issue 1, February 2026.
ABSTRACT Background Fabry disease (FD) is a rare, X‐linked lysosomal storage disorder affecting multiple organs, including the musculoskeletal system. The physical status of FD patients remains poorly characterized. This multicentre cross‐sectional study aimed to evaluate physical fitness and function in FD patients and investigate associations with ...
Nicola Vitturi, Giorgia Gugelmo, Andrea Gasperetti, Federica Duregon, Alessandro Dalmonico, Livia Lenzini, Sara Sponchiado, Gianni Carraro, Giacomo Marchi, Mattia Cominacini, Claudia Momentè, Federica Baciga, Claudia Baschirotto, Federica Caccia, Domenico Girelli, Andrea Ermolao, Gian Paolo Fadini, Yuri Battaglia   +17 more
wiley   +1 more source