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The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

A gene variation is linked to hair thickness in Asians.

Genomic research can help improve the quality and production of natural fibers in animals.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

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

Researchers found a genetic region that influences the number of coat layers in dogs.

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

The EDAR gene greatly affects hair thickness in Asian populations.

Scientists found a gene in mice that causes early hearing loss.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Nerve signals are crucial for hair follicle stem cells to become skin stem cells and help in wound healing.

PDGF signaling is crucial for maintaining and renewing hair follicle stem cells, which could help treat hair loss.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Activin activation in skin cells speeds up wound healing without affecting scar quality.

Using special RNA to target a mutant gene fixed hair problems in mice.

Tissue-derived extracellular vesicles are crucial for cancer diagnosis, prognosis, and treatment.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

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