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Hydroxychloroquine may help treat benign prostatic hyperplasia by reducing inflammation and promoting cell death.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The Graft Quality Index grades hair transplant grafts to predict placement difficulty and surgery results.

The humanized AA mouse model is better for testing new alopecia areata treatments.

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

AR-27 E-Chol siRNA can effectively regrow hair by reducing androgen receptor gene activity.

The Itpr3 gene causes a specific hair pattern in mice.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

The agouti gene may help understand and treat obesity.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Two new IRAK4-inhibitors effectively reduced skin inflammation and immune response markers in healthy volunteers.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

AMP-303 injections can increase hair growth in androgenetic alopecia with minimal side effects.

A compromised gut may trigger the autoimmune hair loss condition Alopecia Areata.

The KRTAP36-2 gene in sheep affects wool yield.

Red fluorescence in AGA scalps is linked to different microbes.

Imiquimod cream can cause hair loss.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Hair loss in male pattern baldness involves muscle degeneration and increased scalp fat.

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Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

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

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

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

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