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Only a few hair-specific keratins are linked to inherited hair disorders.

New genetic locations explain much of hair color variation in Europeans.

A specific gene mutation causes congenital hair loss.

Hair follicle studies suggest that maintaining telomere length could help treat hair loss and graying, but it's uncertain if mouse results apply to humans.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Estrogen and prolactin may play bigger roles in female hair loss than previously thought.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

AR gene not major factor in female hair loss; different from male hair loss.

Longer CAG repeats in gene linked to more severe hair loss in females.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Estrogens can improve skin aging but carry risks; more research is needed on safer treatments.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Alopecia areata causes hair loss, has no cure, and various treatments exist.

Androgens have complex effects on hair growth, promoting it in some areas but causing hair loss in others, and our understanding of this is still evolving.

The document concludes that hair is complex, with a detailed growth cycle, structure, and clinical importance, affecting various scientific and medical fields.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Wnt signaling may be linked to heart diseases in aging and could be a target for future treatments.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.