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Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Changing light exposure can affect hair growth timing in goats, possibly due to a key gene, CSDC2.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Advanced therapies like gene, cell, and tissue engineering show promise for hair regrowth in alopecia, but their safety and effectiveness need more verification.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

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

ELL is crucial for gene transcription related to skin cell growth.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

The gene HDC is important for the development of hair follicles in newborn mice.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.