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

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

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

Mutations in specific genes cause different types of ectodermal dysplasias.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Increased EGFR gene variations may predict chemotherapy outcomes in small cell lung cancer patients.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

BRG1 is essential for skin cells to move and heal wounds properly.

Specific genes influence hair and cashmere growth in Laiwu black goats.

The protein StAR is found in 17 different organs and can affect hair loss and brain functions, but its full role is not yet fully understood.

Basal cell carcinomas and squamous cell carcinomas have different gene activity patterns, suggesting unique treatment approaches.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

Slug (Snai2) helps regulate hair growth timing in mice.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

LGR5 and LGR6 are expressed differently in various skin tumors, which may offer clues about their origins.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

Nonionic liposomes are the best for delivering genes to skin cells.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

The research identified new skin traits in mice, some linked to human skin conditions.

The study found 65 intermediate filament genes, including new keratins, and suggested updating keratin naming.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Genes linked to wool fineness in sheep have been identified.

The three estrogen receptor genes are highly expressed in zebrafish neuromasts during development.

EDA2R gene linked to hair loss.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.