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A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

In STSD patients, the body compensates for low androgen levels by increasing another enzyme's activity.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

GFRα2 is essential for controlling neuron size but not for target innervation in certain sensory neurons.

Asparagus racemosus root extract reduced sebum and pore size in men but not in women.

Taking 5-ARI before prostate laser surgery may lead to more blood changes, longer surgery, and more urinary issues.

R-Spondin-1 is important for skin health and could help diagnose and treat various skin conditions.

The activity of a specific rat enzyme in the prostate and epididymis is highly dependent on the acidity level.

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe side effects.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Squaric acid dibutylester helps hair growth by increasing certain immune cells in the skin.

5alpha-reductase 2 is crucial for proper male brain development and sexual differentiation.

ALRV5XR significantly improves hair density in women with hair loss and is well-tolerated.

CD19-CAR T cell therapy may help regenerate skin in systemic sclerosis.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

5-alpha-reductase inhibitors help treat urinary symptoms from an enlarged prostate.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

CARASIL can cause different symptoms even with the same genetic mutation.

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

Tofacitinib can cause a rare rash called SDRIFE, which resolves after stopping the drug.

Ca 45 mainly enters rat skin and eye through biosynthesis and may be adsorbed in cartilage and glands.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.