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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.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

BST2 is a key marker for hair loss disease alopecia areata.

ApoBDs, once seen as waste, are now viewed as potential tools for disease treatment and tissue repair.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Abrocitinib helped a 14-year-old girl with severe alopecia areata regrow her hair significantly.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

WNT10A and EBF1 interaction affects hair growth in male-pattern baldness.

CCCA mainly affects Black women and is linked to high-tension hairstyles, heating tools, chemical relaxants, and genetics.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

Zinc deficiency causes reversible hair loss by disrupting hair growth and stem cell function.

Most patients successfully switched from the original adalimumab to a biosimilar with few reverting due to reduced effectiveness or side effects.

The XBB lineage of the Omicron variant spread rapidly in Southeastern Wisconsin.

The document concludes that early and accurate diagnosis of hair loss on the top of the scalp in Black men is important to distinguish CCCA from other types of hair loss.

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Higher FABP4 levels may indicate more severe alopecia areata.

MOF controls skin development by regulating genes for mitochondria and cilia.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

MPA increases cancer spread by boosting Eph A2 activity.

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.