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FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Generalized vitiligo in Chinese patients is linked to other autoimmune diseases, especially in familial cases.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Specific genes influence hair growth and quality in goats and sheep.

The analysis found genes linked to skin and hair development are more active in Pashmina goats, which may explain their long-fiber production.

Human skin xenografting could improve our understanding of skin development, renewal, and healing.

Drug repurposing speeds up drug development, saves money, and has led to about a third of new drug approvals.

The document discussed hair loss causes and treatments but didn't give a final summary.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Notch signalling helps skin cells differentiate and prevents tumors.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Certain immune cells in the skin release a protein that stops hair growth by keeping hair stem cells inactive.

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

Certain genes and pathways are crucial for high-quality brush hair in Yangtze River Delta White Goats.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Ro stress hindered ginseng root growth and ginsenoside production, but increased certain hormones and affected gene regulation related to plant growth and stress responses.

Genes affecting wool fiber thickness in Angora rabbits were identified, which could help breed finer wool.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

The cause of Frontal fibrosing alopecia, a type of hair loss, is complex, likely involving immune responses and genetics, but is not fully understood.

3D imaging of skin biopsies offers better accuracy but is time-consuming and can't clear melanin.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.