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Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.

Glycogen helps E. coli cells divide unevenly and organize their contents.

The study found an efficient method to extract antioxidants from Hibiscus leaves.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

The ethanol patch test reliably identifies ALDH phenotype.

Certain genes may promote longer root hairs in plants when phosphorus is low.

p2y5, now called LPA6, is a receptor important for human hair growth.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

DHEA boosts bone cell growth and differentiation in elderly stem cells.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

6-O glucose linoleate helps human hair grow and produce lipids.

K6hf is a unique protein found only in a specific layer of hair follicles.

A new genetic mutation was found causing hair and eye issues in a boy.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

FERONIA regulates plant growth, pollen interactions, and sugar signaling.

CDH3-related disease causes worsening eye and hair issues.

Biliverdin IXβ and IXδ help Pseudomonas aeruginosa adapt to chronic infections.

Human hair keratin scaffold material degrades in muscles mainly through the ubiquitin system with lysosome help.

Inhibiting ODC can prevent UV-induced skin cancer.

A new mutation in the HR gene causes hair loss in a specific family.

Mutations in the SNRPE gene cause hereditary hair loss.

Enzyme purified and characterized for minoxidil sulphation in rat liver.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.