Search

everythinglearnresearchcommunity

for

Search:↓

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

MOF controls skin development by regulating genes for mitochondria and cilia.

Finasteride improves heart function and repairs damage after heart attack in mice.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

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

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Wnt/ß-catenin signaling is crucial for regulating skin stem cells and hair growth, with the right levels and timing needed for proper function.

The gene Prss53 affects hair shape and bone development in rabbits.

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.

Wounds heal without scarring in early development but later result in scars, and studying Wnt signaling could help control scarring.

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

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

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

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

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

DKK-1 gene linked to hair loss in AGA and AA patients; more research needed for potential therapy.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Chicken feather gene mutation helps understand human hair disorders.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

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.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The document concludes that understanding hair biology is key to treating hair disorders, with gene therapy showing potential as a future treatment.

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.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

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

Mice without the IL-6 gene had more hair growth after injury due to higher activity of a related protein, Stat3.