Results 261 to 270 of about 716,780 (343)
The Synergistic Taste Effect of Monosodium Glutamate and Disodium 5'-Guanylate
Shizuko Yamaguchi+3 more
openalex +2 more sources
Effects of supplemental glutamine and glutamate on growth performance, gastrointestinal development, jejunum morphology and Clostridium perfringens count in caecum of broilers [PDF]
Ebadiasl, Gholamreza
core +1 more source
Harnessing the Biological Responses Induced by Nanomaterials for Enhanced Cancer Therapy
Nanomaterial (NM)‐induced toxicity can be strategically repurposed for cancer therapy. This review summarizes the mechanism by which NMs selectively activate specific cellular processes to regulate cell fate independently. We also discussed how NMs‐induced biological responses can be leveraged as therapeutic strategies for cancer treatment.
Liting Wang+6 more
wiley +1 more source
Glutamate-Mediated Neural Alterations in Lead Exposure: Mechanisms, Pathways, and Phenotypes. [PDF]
Tamagno WA, Freeman JL.
europepmc +1 more source
We explore the hierarchical chirality transfer in self‐assembled fluorescent homopolypeptide systems for achieving aqueous circularly polarized luminescence (CPL), and reveal the α‐helix‐dominated CPL regulation mechanism during the self‐assembly process .
Jinhui Jiang+10 more
wiley +1 more source
Association of glutamine metabolites in synovial fluid with the severity of temporomandibular joint osteoarthritis. [PDF]
Song Z, Xu Y, Li C, Shao B, Gong Z.
europepmc +1 more source
Enzymatic and Physiological Properties of the Yeast Glutamate-α-Ketoadipate Transaminase
Makoto Matsuda, Maurice Ogur
openalex +1 more source
ABSTRACT Non‐syndromic Retinitis Pigmentosa (NsRP) was well known as one of the causes of visual impairment already in the 19th century. Giuseppe Albertotti, Professor of Ophthalmology at the University of Modena (Italy) in 1893, described a high prevalence of NsRP in a geographic isolate, the small village of Colloro, in northwestern Italy.
Andrea Guala+8 more
wiley +1 more source
ABSTRACT Apert syndrome is a recognizable craniofacial condition characterized by craniosynostosis, hypertelorism, exorbitism, midface hypoplasia, and complex symmetrical bony and cutaneous ‘mitten’ syndactyly of all four limbs. Around 98% of affected patients have one of two heterozygous missense variants in the FGFR2 gene, encoding either p ...
Ramy Saad+8 more
wiley +1 more source