Search

everythinglearnresearchcommunity

for

Search:↓

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

MDSC-Exo can treat autoimmune alopecia areata and promote hair regrowth in mice.

Long non-coding RNAs help regulate wool fineness in Gansu alpine fine-wool sheep.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

17β-estradiol boosts APE1/Ref-1 secretion in cells and mice via a calcium-dependent pathway.

A new method quickly detects hair changes from EGFR inhibitors using a microscope.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

EF and PXE not closely related.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

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

The DiLiCre mouse model is an effective tool for precise genome editing using light.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Spironolactone, a heart and liver drug, has new uses including cancer treatment, viral infection prevention, and skin condition improvement.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

ILC1-like cells can cause alopecia areata by themselves.

EDA is vital for bone and cartilage formation and could help treat skeletal disorders.

Noncoding RNAs help determine cashmere quality in goats.

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

Sheep exosomes can enhance hair growth in mice.

The study found markers indicating that cells responsible for hair color are differentiating in specific areas of the hair follicle.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A 308 nm excimer laser successfully treated a boy with a rare skin condition after about a year of weekly sessions.

Exosome treatments may cause mild inflammation, new blood vessel growth, and hair growth, detectable by ultrasound.

TRα and CRABPII genes change their activity levels during goat fetal skin development.