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The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A gene mutation in Lama3 is linked to a common type of hair loss.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

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

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Genetic discoveries are leading to new treatments for alopecia areata.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Sox6 is important in heart and kidney health, affecting diseases like diabetes, heart disease, and high blood pressure.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

No significant link between male pattern baldness and COVID-19 severity was found.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Afro-textured hair needs personalized care due to its unique genetic traits.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Identified genes linked to male-pattern baldness may help develop new treatments.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

DNA markers can help predict male pattern baldness, useful in criminal and missing person cases.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

Androgenetic alopecia is linked to heart disease, metabolic issues, and mental health problems.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.