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Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

SQSTM1 gene issues may increase the risk of alopecia areata.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

A genetic marker linked to a type of hair loss was found in most patients studied.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

Activating Tgr5 may help treat hair loss and bone loss.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Blocking α-toxin helps heal Staphylococcus aureus-infected wounds faster in both normal and diabetic mice, with different effects on their immune responses.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Blocking certain receptors in the lungs might help treat a specific type of asthma.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Engineered bacteria can deliver antioxidants to protect skin.

A vitamin D receptor mutation causes rickets and affects immune responses.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

HLA-DRB5 and other genes may be linked to alopecia universalis.

AMPK activation may reduce melanoma risk in red-haired individuals.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.