Results 21 to 30 of about 1,305 (130)
Genetic Links Between Hydrogen Sulfide Pathways and Risk of Alzheimer's Disease and Related Risk Factors: A Phenome‐Wide Approach [PDF]
Abstract Background Hydrogen sulfide (H2S) is a promising therapeutic drug target for various pathologies, including Alzheimer's disease (AD) and related dementias (ADRD). The newly recognized gasotransmitter freely permeates cellular membranes and is vital to maintaining homeostasis, primarily via smooth muscle relaxation and vasodilatory mechanisms ...
Brady J, Reay W.
europepmc +2 more sources
Vitiligo is a prevalent depigmentation disorder affecting around 1% of the general population. So far, various Genome Wide Association Studies (GWAS) and Candidate Gene Association Studies (CGAS) have identified several single nucleotide variants (SNVs ...
Tithi Dutta +5 more
doaj +1 more source
A disease-modifying treatment for Alzheimer's disease : focus on the trans-sulfuration pathway
High homocysteine levels in Alzheimer's disease (AD) result from low activity of the trans-sulfuration pathway. Glutathione levels are also low in AD. L-cysteine is required for the synthesis of glutathione.
Abohamza, Eid +2 more
core +2 more sources
Introduction. The mesentery is one of recently described separate organs which functions and its ability to protect injury are still unclear. Adipocytes are a part of mesentery (MAC), however, it is a little known about their age-related changes ...
Oleh Revenko +3 more
doaj +1 more source
Background Infertility is a global reproductive-health problem, and diminished ovarian reserve (DOR) is one of the common causes of female infertility.
Li Dong +6 more
doaj +1 more source
Discovering drugs that efficiently treat brain diseases has been challenging. Genetic variants that modulate the expression of potential drug targets can be utilized to assess the efficacy of therapeutic interventions.
Denis A Baird +22 more
doaj +1 more source
Isolated sulfite oxidase deficiency (ISOD) is a devastating, neurometabolic disorder caused by mutations in the SUOX gene necessary for the final step in the sulfur-containing amino acid catabolic pathway.
Monica Boyer +3 more
doaj +1 more source
peer reviewedIsolated sulfite oxidase deficiency (ISOD) is a rare hereditary metabolic disease caused by absence of functional sulfite oxidase (SO) due to mutations of the SUOX gene.
Thaqi, Besarta +9 more
core +1 more source
Multimodal Integration of Genomic Data Reveals Regulatory Mechanisms at the Polycystic Ovary Syndrome (PCOS)-Associated 12q13.2 Locus. [PDF]
Polycystic ovary syndrome (PCOS) is a complex endocrine disorder affecting reproductive-aged women. Previous studies have identified genomic associations at chromosome 12q13.2, but the functional mechanisms underlying these associations remain unclear ...
Harris RA, McAllister JM, Strauss JF.
europepmc +2 more sources
Local surface plasmon resonance (LSPR)-enhanced catalysis has brought a substantial amount of opportunities across various disciplines such as photocatalysis, photodetection, and photothermal therapeutics.
Yuan Chen (9740) +3 more
core +1 more source

