Results 91 to 100 of about 63,430 (242)
Aims Insomnia is a common sleep disorder, affecting up to 20% of the world population and adversely impacting productivity, health, and overall well‐being. Although pharmacologic options exist to treat insomnia, the health‐related quality of life for patients who are prescribed hypnotics is no higher than for those who are not, revealing a significant ...
Garth T. Whiteside+5 more
wiley +1 more source
Full-length nuclear receptor allosteric regulation. [PDF]
Choi WJ, Haratipour Z, Blind RD.
europepmc +1 more source
Identification of Regions of the Tomato γ-Glutamyl Kinase That Are Involved in Allosteric Regulation by Proline [PDF]
Tomomichi Fujita+5 more
openalex +1 more source
The Role of Ribosome Recycling in Human Diseases This diagram highlights how disruptions in ribosome translation and recycling can negatively impact cellular and organismal health. Usually, these processes operate efficiently to maintain cellular protein homeostasis.
Foozhan Tahmasebinia, Zhihao Wu
wiley +1 more source
Allosteric regulation of tRNA import: interactions between tRNA domains at the inner membrane of Leishmania mitochondria [PDF]
Srikanta Goswami
openalex +1 more source
Abstract Post‐translational modifications (PTMs) play a pivotal role in epigenetic regulation and are key pathways for modulating protein functionality. PTMs involve the covalent attachment of distinct chemical groups, such as succinyl, crotonyl, and lactyl, at specific protein sites, which alter protein structure, function, stability, and activity ...
Ting Wu+16 more
wiley +1 more source
Allosteric regulation and inhibition of protein kinases. [PDF]
Mingione VR+3 more
europepmc +1 more source
Structure and allosteric regulation of the αXβ2 integrin I domain [PDF]
Thomas Vorup‐Jensen+4 more
openalex +1 more source
Periodontitis treatment and microbiome in a patient with FAM20A mutation: Case study of 1.5 years
Abstract Background Enamel‐renal‐gingival syndrome (ERGS) is an autosomal recessive disorder caused by mutations in the FAMily with sequence similarity 20A (FAM20A) gene, and is characterized by amelogenesis imperfecta, delayed or failed tooth eruption, and periodontitis.
John Rong Hao Tay+2 more
wiley +1 more source
Disease-causing cystathionine β-synthase linker mutations impair allosteric regulation. [PDF]
Roman JV+4 more
europepmc +1 more source