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MCHR2 gene duplications may be linked to alopecia areata.

Only two of the four keratin genes are expressed in wool fibers.

Tanning ability is linked to specific DNA changes in skin genes.

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

Specific keratin gene mutations can cause monilethrix.

Key genes can rewire networks, changing skin appendage types.

The research helps in creating genetically modified animals to study hair growth.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

PCOS shares similar genetic traits across different diagnosis criteria and is linked to other health conditions.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

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

Scientists discovered two versions of a new human hair keratin gene.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Two siblings have a rare hair condition caused by a new genetic variant.

Hoxd gene regulation in mammals and birds is robust despite differences in DNA sequences, due to 3D chromatin structures.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

Mitochondrial genes help predict breast cancer outcomes and spread.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

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

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Recent selection on immune response genes was identified across seven ethnicities.

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

Researchers identified genes and proteins that may influence wool thickness in sheep.