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Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Certain gene variations are found in people with polycystic ovary syndrome.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

A certain gene variation can affect protein production and is linked to male pattern baldness.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

The article concludes that better understanding gene regulation related to seasonal changes can offer insights into the mechanisms of seasonal timing in mammals.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

Nanoparticulate systems improve drug delivery by controlling release, protecting drugs, changing absorption and distribution, and concentrating drugs in targeted areas.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

Gene differences found in hair follicles linked to male baldness.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Gene regulation could revolutionize hair color by altering pigmentation from within.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

ESR2 gene linked to female-pattern hair loss.

Mutations in the P2RY5 gene cause hereditary woolly hair.

The gelatin/β-TCP scaffold with nanoparticles improves wound healing and skin regeneration.

S100A3 protein is crucial for hair shaft formation in mice.

Genetically-altered adult stem cells can help in wound healing and are becoming crucial in regenerative medicine and drug design.

Gene linked to common hair loss found, may lead to new treatments.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.

The method safely and efficiently delivers genes to the skin but may not work for conditions needing high levels of gene products.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.